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  • Lunar and Planetary Science and Exploration  (269)
  • Mice  (169)
  • 2005-2009  (438)
  • 1980-1984
  • 2007  (438)
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  • 2005-2009  (438)
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  • 101
    Publication Date: 2007-07-07
    Description: The airway epithelium plays an essential role in innate immunity to lung pathogens. Ribonucleoprotein particles primarily composed of major vault protein (MVP) are highly expressed in cells that encounter xenobiotics. However, a clear biologic function for MVP is not established. We report here that MVP is rapidly recruited to lipid rafts when human lung epithelial cells are infected with Pseudomonas aeruginosa, and maximal recruitment is dependent on bacterial binding to the cystic fibrosis transmembrane conductance regulator. MVP was also essential for optimal epithelial cell internalization and clearance of P. aeruginosa. These results suggest that MVP makes a substantial contribution to epithelial cell-mediated resistance to infection.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685177/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685177/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kowalski, Michael P -- Dubouix-Bourandy, Anne -- Bajmoczi, Milan -- Golan, David E -- Zaidi, Tanweer -- Coutinho-Sledge, Yamara S -- Gygi, Melanie P -- Gygi, Steven P -- Wiemer, Erik A C -- Pier, Gerald B -- R01 HL 58398-08/HL/NHLBI NIH HHS/ -- R01 HL058398/HL/NHLBI NIH HHS/ -- R37 HL 32854-22/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2007 Jul 6;317(5834):130-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17615361" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cystic Fibrosis Transmembrane Conductance Regulator/genetics/metabolism ; Epithelial Cells/metabolism/microbiology ; Humans ; Immunity, Innate ; Lung/immunology/microbiology ; Lung Diseases/*immunology/metabolism/microbiology ; Membrane Microdomains/metabolism ; Mice ; Pseudomonas Infections/*immunology/metabolism/microbiology ; Pseudomonas aeruginosa/*immunology/metabolism ; RNA, Small Interfering/genetics ; Respiratory Mucosa/immunology/*metabolism/*microbiology ; Signal Transduction ; Vault Ribonucleoprotein Particles/*physiology
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  • 102
    Publication Date: 2007-11-10
    Description: Variants in the FTO (fat mass and obesity associated) gene are associated with increased body mass index in humans. Here, we show by bioinformatics analysis that FTO shares sequence motifs with Fe(II)- and 2-oxoglutarate-dependent oxygenases. We find that recombinant murine Fto catalyzes the Fe(II)- and 2OG-dependent demethylation of 3-methylthymine in single-stranded DNA, with concomitant production of succinate, formaldehyde, and carbon dioxide. Consistent with a potential role in nucleic acid demethylation, Fto localizes to the nucleus in transfected cells. Studies of wild-type mice indicate that Fto messenger RNA (mRNA) is most abundant in the brain, particularly in hypothalamic nuclei governing energy balance, and that Fto mRNA levels in the arcuate nucleus are regulated by feeding and fasting. Studies can now be directed toward determining the physiologically relevant FTO substrate and how nucleic acid methylation status is linked to increased fat mass.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668859/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668859/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gerken, Thomas -- Girard, Christophe A -- Tung, Yi-Chun Loraine -- Webby, Celia J -- Saudek, Vladimir -- Hewitson, Kirsty S -- Yeo, Giles S H -- McDonough, Michael A -- Cunliffe, Sharon -- McNeill, Luke A -- Galvanovskis, Juris -- Rorsman, Patrik -- Robins, Peter -- Prieur, Xavier -- Coll, Anthony P -- Ma, Marcella -- Jovanovic, Zorica -- Farooqi, I Sadaf -- Sedgwick, Barbara -- Barroso, Ines -- Lindahl, Tomas -- Ponting, Chris P -- Ashcroft, Frances M -- O'Rahilly, Stephen -- Schofield, Christopher J -- 068086/Wellcome Trust/United Kingdom -- 077016/Wellcome Trust/United Kingdom -- G108/617/Medical Research Council/United Kingdom -- G9824984/Medical Research Council/United Kingdom -- MC_U137761446/Medical Research Council/United Kingdom -- U54 GM064346/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2007 Nov 30;318(5855):1469-72. Epub 2007 Nov 8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Chemistry Research Laboratory and Oxford Centre for Integrative Systems Biology, University of Oxford, 12 Mansfield Road, Oxford, Oxon OX1 3TA, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17991826" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Brain/enzymology/metabolism ; Cell Nucleus/enzymology ; Computational Biology ; DNA/*metabolism ; DNA Methylation ; DNA, Single-Stranded/metabolism ; Eating ; Energy Metabolism ; Fasting ; Ferrous Compounds/metabolism ; Hypothalamus/enzymology/metabolism ; Ketoglutaric Acids/*metabolism ; Male ; Mice ; Mixed Function Oxygenases ; Molecular Sequence Data ; Oxo-Acid-Lyases/chemistry/*genetics/*metabolism ; RNA, Messenger/genetics/metabolism ; Recombinant Proteins/metabolism ; Succinic Acid/metabolism ; Thymine/analogs & derivatives/metabolism
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  • 103
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-02-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miller, Greg -- New York, N.Y. -- Science. 2007 Feb 9;315(5813):749.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17289948" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Disease Models, Animal ; Female ; *Genetic Therapy ; Humans ; Methyl-CpG-Binding Protein 2/*genetics/metabolism ; Mice ; Mutation ; Recombinant Fusion Proteins/metabolism ; Rett Syndrome/*genetics/*therapy
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  • 104
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-07-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lawrence, Toby -- Hageman, Thorsten -- Balkwill, Frances -- G0501974/Medical Research Council/United Kingdom -- G0601867/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2007 Jul 6;317(5834):51-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for Translational Oncology, Institute of Cancer, Barts and the London School of Medicine and Dentistry, Charterhouse Square, London EC1M 6BQ, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17615328" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Colonic Neoplasms/physiopathology ; Disease Progression ; Female ; Humans ; Immunity, Innate ; Interleukin-6/*metabolism ; Kupffer Cells/metabolism ; Liver Neoplasms, Experimental/immunology/physiopathology ; Male ; Mice ; Myeloid Differentiation Factor 88/*physiology ; NF-kappa B/metabolism ; Neoplasms/drug therapy/*physiopathology/prevention & control ; Sex Characteristics ; Signal Transduction
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  • 105
    Publication Date: 2007-08-11
    Description: Influenza virus entry is mediated by the receptor binding domain (RBD) of its spike, the hemagglutinin (HA). Adaptation of avian viruses to humans is associated with HA specificity for alpha2,6- rather than alpha2,3-linked sialic acid (SA) receptors. Here, we define mutations in influenza A subtype H5N1 (avian) HA that alter its specificity for SA either by decreasing alpha2,3- or increasing alpha2,6-SA recognition. RBD mutants were used to develop vaccines and monoclonal antibodies that neutralized new variants. Structure-based modification of HA specificity can guide the development of preemptive vaccines and therapeutic monoclonal antibodies that can be evaluated before the emergence of human-adapted H5N1 strains.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367145/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367145/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yang, Zhi-Yong -- Wei, Chih-Jen -- Kong, Wing-Pui -- Wu, Lan -- Xu, Ling -- Smith, David F -- Nabel, Gary J -- Z99 AI999999/Intramural NIH HHS/ -- New York, N.Y. -- Science. 2007 Aug 10;317(5839):825-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Vaccine Research Center, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Building 40, Room 4502, Mailstop Code MSC-3005, 40 Convent Drive, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17690300" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibodies, Monoclonal/immunology ; Antibodies, Viral/immunology ; Carbohydrate Conformation ; Cell Line ; Female ; Genes, Viral ; Hemagglutination Inhibition Tests ; Hemagglutinin Glycoproteins, Influenza Virus/*genetics/*immunology/metabolism ; Humans ; Influenza A Virus, H5N1 Subtype/*genetics/*immunology/metabolism ; Influenza Vaccines/immunology ; Mice ; Mice, Inbred BALB C ; Molecular Sequence Data ; *Mutation ; Neutralization Tests ; Receptors, Virus/*metabolism ; Sialic Acids/*metabolism ; Vaccination
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  • 106
    Publication Date: 2007-06-09
    Description: Allergic contact dermatitis affects about 5% of men and 11% of women in industrialized countries and is one of the leading causes for occupational diseases. In an animal model for cutaneous contact hypersensitivity, we show that mice lacking both known cannabinoid receptors display exacerbated allergic inflammation. In contrast, fatty acid amide hydrolase-deficient mice, which have increased levels of the endocannabinoid anandamide, displayed reduced allergic responses in the skin. Cannabinoid receptor antagonists exacerbated allergic inflammation, whereas receptor agonists attenuated inflammation. These results demonstrate a protective role of the endocannabinoid system in contact allergy in the skin and suggest a target for therapeutic intervention.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Karsak, Meliha -- Gaffal, Evelyn -- Date, Rahul -- Wang-Eckhardt, Lihua -- Rehnelt, Jennifer -- Petrosino, Stefania -- Starowicz, Katarzyna -- Steuder, Regina -- Schlicker, Eberhard -- Cravatt, Benjamin -- Mechoulam, Raphael -- Buettner, Reinhard -- Werner, Sabine -- Di Marzo, Vincenzo -- Tuting, Thomas -- Zimmer, Andreas -- New York, N.Y. -- Science. 2007 Jun 8;316(5830):1494-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Psychiatry, University of Bonn, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17556587" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arachidonic Acids/metabolism ; Bornanes/administration & dosage/pharmacology ; Cannabinoid Receptor Modulators/*physiology ; Cannabinoids/administration & dosage/pharmacology ; Chemokines/physiology ; Dermatitis, Allergic Contact/pathology/*physiopathology ; Dinitrofluorobenzene ; Disease Models, Animal ; Down-Regulation ; Dronabinol/administration & dosage/pharmacology ; *Endocannabinoids ; Female ; Glycerides/metabolism ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Oligonucleotide Array Sequence Analysis ; Piperidines/administration & dosage/pharmacology ; Polyunsaturated Alkamides/metabolism ; Pyrazoles/administration & dosage/pharmacology ; Receptor, Cannabinoid, CB1/agonists/antagonists & inhibitors/genetics/*physiology ; Receptor, Cannabinoid, CB2/agonists/antagonists & inhibitors/genetics/*physiology ; Skin/*metabolism/pathology ; Up-Regulation
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  • 107
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-12-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miller, Greg -- New York, N.Y. -- Science. 2007 Dec 14;318(5857):1710-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18079374" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Astrocytes/physiology ; Brain/*growth & development/metabolism ; Complement C1q/genetics/*metabolism ; Glaucoma/immunology/metabolism/pathology ; Mice ; Neurodegenerative Diseases/immunology/metabolism/pathology ; Neurons/*metabolism ; Retina/growth & development/metabolism ; Synapses/*physiology
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  • 108
    Publication Date: 2007-11-03
    Description: Hosts can in principle employ two different strategies to defend themselves against parasites: resistance and tolerance. Animals typically exhibit considerable genetic variation for resistance (the ability to limit parasite burden). However, little is known about whether animals can evolve tolerance (the ability to limit the damage caused by a given parasite burden). Using rodent malaria in laboratory mice as a model system and the statistical framework developed by plant-pathogen biologists, we demonstrated genetic variation for tolerance, as measured by the extent to which anemia and weight loss increased with increasing parasite burden. Moreover, resistance and tolerance were negatively genetically correlated. These results mean that animals, like plants, can evolve two conceptually different types of defense, a finding that has important implications for the understanding of the epidemiology and evolution of infectious diseases.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Raberg, Lars -- Sim, Derek -- Read, Andrew F -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2007 Nov 2;318(5851):812-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Evolutionary Biology and Institute of Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, West Mains Road, Edinburgh EH9 3JT, UK. lars.raberg@zooekol.lu.se〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17975068" target="_blank"〉PubMed〈/a〉
    Keywords: Anemia/genetics/physiopathology ; Animals ; Biological Evolution ; Disease Models, Animal ; Erythrocyte Count ; *Genetic Variation ; Host-Parasite Interactions ; Immunity, Innate/*genetics ; Malaria/*genetics/physiopathology ; Mice ; Mice, Inbred Strains ; *Plasmodium chabaudi ; Statistics as Topic
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  • 109
    Publication Date: 2007-11-17
    Description: The circadian clock temporally coordinates metabolic homeostasis in mammals. Central to this is heme, an iron-containing porphyrin that serves as prosthetic group for enzymes involved in oxidative metabolism as well as transcription factors that regulate circadian rhythmicity. The circadian factor that integrates this dual function of heme is not known. We show that heme binds reversibly to the orphan nuclear receptor Rev-erbalpha, a critical negative component of the circadian core clock, and regulates its interaction with a nuclear receptor corepressor complex. Furthermore, heme suppresses hepatic gluconeogenic gene expression and glucose output through Rev-erbalpha-mediated gene repression. Thus, Rev-erbalpha serves as a heme sensor that coordinates the cellular clock, glucose homeostasis, and energy metabolism.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yin, Lei -- Wu, Nan -- Curtin, Joshua C -- Qatanani, Mohammed -- Szwergold, Nava R -- Reid, Robert A -- Waitt, Gregory M -- Parks, Derek J -- Pearce, Kenneth H -- Wisely, G Bruce -- Lazar, Mitchell A -- R01 DK45586/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2007 Dec 14;318(5857):1786-9. Epub 2007 Nov 15.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18006707" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Clocks ; Cell Line ; Cell Line, Tumor ; *Circadian Rhythm/genetics ; DNA-Binding Proteins/*metabolism ; Energy Metabolism ; *Gene Expression Regulation ; Gluconeogenesis/genetics ; Glucose/*metabolism ; Glucose-6-Phosphatase/genetics/metabolism ; Heme/*metabolism ; Hemin/pharmacology ; Histone Deacetylases/metabolism ; Homeostasis ; Humans ; Male ; *Metabolic Networks and Pathways ; Mice ; Nuclear Proteins/metabolism ; Nuclear Receptor Co-Repressor 1 ; Nuclear Receptor Subfamily 1, Group D, Member 1 ; Receptors, Cytoplasmic and Nuclear/*metabolism ; Repressor Proteins/metabolism
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  • 110
    Publication Date: 2007-09-08
    Description: Mammalian spermatogenesis produces numerous sperm for a long period based on a highly potent stem cell system, which relies on a special microenvironment, or niche, that has not yet been identified. In this study, using time-lapse imaging of green fluorescent protein-labeled undifferentiated spermatogonia (A(undiff)) and three-dimensional reconstitution, we revealed a biased localization of A(undiff) to the vascular network and accompanying Leydig and other interstitial cells, in intact testes. Differentiating spermatogonia left these niche regions and dispersed throughout the basal compartment of the seminiferous epithelium. Moreover, rearrangement of A(undiff) accompanied the vasculature alteration. We propose that the mammalian germline niche is established as a consequence of vasculature pattern formation. This is different from what is observed in Drosophila or Caenorhabditis elegans, which display developmentally specified niche structures within polarized gonads.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yoshida, Shosei -- Sukeno, Mamiko -- Nabeshima, Yo-Ichi -- New York, N.Y. -- Science. 2007 Sep 21;317(5845):1722-6. Epub 2007 Sep 6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan. shosei@lmls.med.kyoto-u.ac.jp〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17823316" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Basic Helix-Loop-Helix Transcription Factors/genetics ; Blood Vessels/cytology ; Green Fluorescent Proteins ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Nerve Tissue Proteins/genetics ; Seminiferous Tubules/blood supply/cytology ; Spermatogenesis ; Spermatogonia/*cytology ; Testis/blood supply/*cytology
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  • 111
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-02-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Youle, Richard J -- New York, N.Y. -- Science. 2007 Feb 9;315(5813):776-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA. youler@ninds.nih.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17289967" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Apoptosis ; Apoptosis Regulatory Proteins/*metabolism ; BH3 Interacting Domain Death Agonist Protein/*metabolism ; Intracellular Membranes/metabolism ; Membrane Proteins/*metabolism ; Mice ; Mitochondria/metabolism ; Models, Biological ; Permeability ; Protein Conformation ; Protein Structure, Secondary ; Proto-Oncogene Proteins/*metabolism ; Proto-Oncogene Proteins c-bcl-2/chemistry/*metabolism ; bcl-2-Associated X Protein/chemistry/*metabolism
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  • 112
    Publication Date: 2007-11-22
    Description: Somatic cell nuclear transfer allows trans-acting factors present in the mammalian oocyte to reprogram somatic cell nuclei to an undifferentiated state. We show that four factors (OCT4, SOX2, NANOG, and LIN28) are sufficient to reprogram human somatic cells to pluripotent stem cells that exhibit the essential characteristics of embryonic stem (ES) cells. These induced pluripotent human stem cells have normal karyotypes, express telomerase activity, express cell surface markers and genes that characterize human ES cells, and maintain the developmental potential to differentiate into advanced derivatives of all three primary germ layers. Such induced pluripotent human cell lines should be useful in the production of new disease models and in drug development, as well as for applications in transplantation medicine, once technical limitations (for example, mutation through viral integration) are eliminated.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yu, Junying -- Vodyanik, Maxim A -- Smuga-Otto, Kim -- Antosiewicz-Bourget, Jessica -- Frane, Jennifer L -- Tian, Shulan -- Nie, Jeff -- Jonsdottir, Gudrun A -- Ruotti, Victor -- Stewart, Ron -- Slukvin, Igor I -- Thomson, James A -- P20 GM069981/GM/NIGMS NIH HHS/ -- P51 RR000167/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2007 Dec 21;318(5858):1917-20. Epub 2007 Nov 20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Genome Center of Wisconsin, Madison, WI 53706-1580, USA. jyu@primate.wisc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18029452" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; *Cell Line ; Cell Proliferation ; Cell Shape ; *Cellular Reprogramming ; DNA-Binding Proteins/genetics/physiology ; Embryonic Stem Cells/cytology ; Fetus ; Fibroblasts/*cytology ; HMGB Proteins/genetics/physiology ; Homeodomain Proteins/genetics/physiology ; Humans ; Infant, Newborn ; Karyotyping ; Mice ; Mice, SCID ; Octamer Transcription Factor-3/genetics/physiology ; Oligonucleotide Array Sequence Analysis ; Pluripotent Stem Cells/*cytology/physiology ; RNA-Binding Proteins/genetics/physiology ; SOXB1 Transcription Factors ; Stem Cell Transplantation ; Teratoma/pathology ; Transcription Factors/genetics/physiology ; Transduction, Genetic ; Transgenes
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  • 113
    Publication Date: 2007-09-01
    Description: Do learning and retrieval of a memory activate the same neurons? Does the number of reactivated neurons correlate with memory strength? We developed a transgenic mouse that enables the long-lasting genetic tagging of c-fos-active neurons. We found neurons in the basolateral amygdala that are activated during Pavlovian fear conditioning and are reactivated during memory retrieval. The number of reactivated neurons correlated positively with the behavioral expression of the fear memory, indicating a stable neural correlate of associative memory. The ability to manipulate these neurons genetically should allow a more precise dissection of the molecular mechanisms of memory encoding within a distributed neuronal network.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Reijmers, Leon G -- Perkins, Brian L -- Matsuo, Naoki -- Mayford, Mark -- 5-74653/PHS HHS/ -- 57368/PHS HHS/ -- New York, N.Y. -- Science. 2007 Aug 31;317(5842):1230-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cell Biology, Scripps Research Institute, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17761885" target="_blank"〉PubMed〈/a〉
    Keywords: Amygdala/cytology/*physiology ; Animals ; Brain Mapping ; Conditioning (Psychology) ; Extinction, Psychological ; Fear ; Genes, fos ; Learning ; *Memory ; *Mental Recall ; Mice ; Mice, Transgenic ; Nerve Net/*physiology ; Neuronal Plasticity ; Neurons/*physiology
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  • 114
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-04-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2007 Apr 27;316(5824):530.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17463259" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Gene Deletion ; Heart/*physiopathology ; Heart Diseases/*genetics ; Immune System/*physiology ; Mice ; Mice, Knockout ; MicroRNAs/*genetics/*physiology
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  • 115
    Publication Date: 2007-02-27
    Description: Primary transcripts of certain microRNA (miRNA) genes are subject to RNA editing that converts adenosine to inosine. However, the importance of miRNA editing remains largely undetermined. Here we report that tissue-specific adenosine-to-inosine editing of miR-376 cluster transcripts leads to predominant expression of edited miR-376 isoform RNAs. One highly edited site is positioned in the middle of the 5'-proximal half "seed" region critical for the hybridization of miRNAs to targets. We provide evidence that the edited miR-376 RNA silences specifically a different set of genes. Repression of phosphoribosyl pyrophosphate synthetase 1, a target of the edited miR-376 RNA and an enzyme involved in the uric-acid synthesis pathway, contributes to tight and tissue-specific regulation of uric-acid levels, revealing a previously unknown role for RNA editing in miRNA-mediated gene silencing.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953418/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953418/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kawahara, Yukio -- Zinshteyn, Boris -- Sethupathy, Praveen -- Iizasa, Hisashi -- Hatzigeorgiou, Artemis G -- Nishikura, Kazuko -- P01 CA072765/CA/NCI NIH HHS/ -- P01 CA072765-050002/CA/NCI NIH HHS/ -- R01 GM040536/GM/NIGMS NIH HHS/ -- R01 GM040536-16/GM/NIGMS NIH HHS/ -- R01 HL070045/HL/NHLBI NIH HHS/ -- R01 HL070045-04/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2007 Feb 23;315(5815):1137-40.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wistar Institute, 3601 Spruce Street, Philadelphia, PA 19104, USA. ykawahara@wistar.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17322061" target="_blank"〉PubMed〈/a〉
    Keywords: 3' Untranslated Regions ; Adenosine/*metabolism ; Adenosine Deaminase/genetics/metabolism ; Animals ; Base Sequence ; Brain/metabolism ; HeLa Cells ; Humans ; Inosine/*metabolism ; Liver/metabolism ; Mice ; MicroRNAs/chemistry/genetics/*metabolism ; Molecular Sequence Data ; Nucleic Acid Conformation ; Organ Specificity ; Protein-Serine-Threonine Kinases/genetics/metabolism ; *RNA Editing ; *RNA Interference ; RNA-Binding Proteins ; Ribose-Phosphate Pyrophosphokinase/genetics/metabolism ; Uric Acid/metabolism
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  • 116
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-05-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miller, Greg -- New York, N.Y. -- Science. 2007 May 11;316(5826):826-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17495152" target="_blank"〉PubMed〈/a〉
    Keywords: Abnormalities, Drug-Induced/etiology ; Abortifacient Agents, Nonsteroidal/adverse effects ; Animals ; Autistic Disorder/etiology ; Brain Stem/abnormalities/embryology ; Databases, Factual ; Databases, Nucleic Acid ; *Facial Expression ; Female ; Genes, Homeobox ; Humans ; Male ; Mice ; Misoprostol/adverse effects ; *Mobius Syndrome/complications/etiology/genetics/surgery ; Placental Circulation ; Pregnancy
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  • 117
    Publication Date: 2007-06-16
    Description: Multiple signaling pathways, including Wnt signaling, participate in animal development, stem cell biology, and human cancer. Although many components of the Wnt pathway have been identified, unresolved questions remain as to the mechanism by which Wnt binding to its receptors Frizzled and Low-density lipoprotein receptor-related protein 6 (LRP6) triggers downstream signaling events. With live imaging of vertebrate cells, we show that Wnt treatment quickly induces plasma membrane-associated LRP6 aggregates. LRP6 aggregates are phosphorylated and can be detergent-solubilized as ribosome-sized multiprotein complexes. Phospho-LRP6 aggregates contain Wnt-pathway components but no common vesicular traffic markers except caveolin. The scaffold protein Dishevelled (Dvl) is required for LRP6 phosphorylation and aggregation. We propose that Wnts induce coclustering of receptors and Dvl in LRP6-signalosomes, which in turn triggers LRP6 phosphorylation to promote Axin recruitment and beta-catenin stabilization.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bilic, Josipa -- Huang, Ya-Lin -- Davidson, Gary -- Zimmermann, Timo -- Cruciat, Cristina-Maria -- Bienz, Mariann -- Niehrs, Christof -- MC_U105192713/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2007 Jun 15;316(5831):1619-22.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Molecular Embryology, Deutsches Krebsforschungszentrum, Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17569865" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing/*metabolism ; Animals ; Axin Protein ; Cell Line ; Cell Line, Tumor ; Cell Membrane/metabolism ; Centrifugation, Density Gradient ; Cytoplasm/metabolism ; Drosophila ; Glycogen Synthase Kinase 3/analysis/metabolism ; HeLa Cells ; Humans ; LDL-Receptor Related Proteins/analysis/genetics/*metabolism ; Low Density Lipoprotein Receptor-Related Protein-6 ; Mice ; Models, Biological ; Phosphoproteins/*metabolism ; Phosphorylation ; Repressor Proteins/analysis/metabolism ; *Signal Transduction ; Transfection ; Wnt Proteins/*metabolism ; Wnt3 Protein ; beta Catenin/metabolism
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  • 118
    Publication Date: 2007-07-21
    Description: The cancer stem cell hypothesis postulates that tumor growth is driven by a rare subpopulation of tumor cells. Much of the supporting evidence for this intriguing idea is derived from xenotransplantation experiments in which human leukemia cells are grown in immunocompromised mice. We show that, when lymphomas and leukemias of mouse origin are transplanted into histocompatible mice, a very high frequency (at least 1 in 10) of the tumor cells can seed tumor growth. We suggest that the low frequency of tumor-sustaining cells observed in xenotransplantation studies may reflect the limited ability of human tumor cells to adapt to growth in a foreign (mouse) milieu.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kelly, Priscilla N -- Dakic, Aleksandar -- Adams, Jerry M -- Nutt, Stephen L -- Strasser, Andreas -- New York, N.Y. -- Science. 2007 Jul 20;317(5836):337.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Walter and Eliza Hall Institute of Medical Research, Melbourne 3050, Australia.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17641192" target="_blank"〉PubMed〈/a〉
    Keywords: Acute Disease ; Animals ; Humans ; Leukemia, Myeloid/*pathology ; Lymphoma/*pathology ; Lymphoma, B-Cell/*pathology ; Mice ; Mice, Transgenic ; Neoplasm Transplantation ; Neoplastic Stem Cells/pathology/*physiology ; Thymus Neoplasms/*pathology ; Transplantation, Heterologous
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  • 119
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-06-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moore, David D -- New York, N.Y. -- Science. 2007 Jun 8;316(5830):1436-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA. moore@bcm.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17556573" target="_blank"〉PubMed〈/a〉
    Keywords: Acetyl Coenzyme A/metabolism ; Adenosine Monophosphate/metabolism ; Animals ; Body Temperature ; Energy Metabolism ; Fasting ; Fatty Acids/*metabolism ; Fibroblast Growth Factors/genetics/*metabolism/pharmacology ; Glucuronidase/metabolism ; Glycoside Hydrolases/metabolism ; Homeostasis ; Humans ; Ketone Bodies/metabolism ; Lipase/metabolism ; Liver/*metabolism ; Membrane Proteins/*metabolism ; Mice ; Mice, Transgenic ; Motor Activity ; Oxidation-Reduction ; PPAR alpha/*metabolism ; Signal Transduction
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  • 120
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-08-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stone, Richard -- New York, N.Y. -- Science. 2007 Aug 24;317(5841):1022-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17717162" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anti-Bacterial Agents/pharmacology/therapeutic use ; Bioterrorism ; *Burkholderia pseudomallei/cytology/genetics/pathogenicity/physiology ; Clinical Trials as Topic ; Endemic Diseases ; Humans ; *Melioidosis/diagnosis/drug therapy/epidemiology/microbiology ; Mice ; Prevalence ; Thailand/epidemiology ; Toll-Like Receptor 2/genetics/physiology
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  • 121
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-08-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Crabbe, John C -- Cunningham, Christopher L -- New York, N.Y. -- Science. 2007 Aug 24;317(5841):1033-5; author reply 1033-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17717168" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cocaine/*administration & dosage ; Genotype ; *Impulsive Behavior/genetics ; Mice ; Nucleus Accumbens/metabolism ; Rats ; Receptors, Dopamine D2/metabolism ; Receptors, Dopamine D3/metabolism ; Self Administration
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  • 122
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-08-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Leslie, Mitch -- New York, N.Y. -- Science. 2007 Aug 3;317(5838):614-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17673649" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autoimmune Diseases/*immunology/pathology ; Cell Degranulation ; Heart Diseases/*immunology/pathology ; Humans ; Immune Tolerance ; *Immunity, Innate ; Infection/*immunology ; Mast Cells/*immunology ; Mice ; Neoplasms/*immunology/pathology ; T-Lymphocytes/immunology
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  • 123
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-10-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Crawley, Jacqueline N -- New York, N.Y. -- Science. 2007 Oct 5;318(5847):56-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Intramural Research Program, National Institute of Mental Health, Bethesda, MD 20892-3730, USA. crawleyj@intra.nimh.nih.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17916718" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Animals ; Autistic Disorder/*genetics ; Brain/anatomy & histology/*physiology ; Cell Adhesion Molecules, Neuronal ; *Disease Models, Animal ; Humans ; Male ; Maze Learning ; Membrane Proteins/*genetics/metabolism ; Memory ; Mice ; *Mutation ; Nerve Tissue Proteins/*genetics/metabolism ; Neural Inhibition ; Social Behavior ; Synapses/*physiology ; *Synaptic Transmission
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  • 124
    Publication Date: 2007-01-06
    Description: Wilms tumor is a pediatric kidney cancer associated with inactivation of the WT1 tumor-suppressor gene in 5 to 10% of cases. Using a high-resolution screen for DNA copy-number alterations in Wilms tumor, we identified somatic deletions targeting a previously uncharacterized gene on the X chromosome. This gene, which we call WTX, is inactivated in approximately one-third of Wilms tumors (15 of 51 tumors). Tumors with mutations in WTX lack WT1 mutations, and both genes share a restricted temporal and spatial expression pattern in normal renal precursors. In contrast to biallelic inactivation of autosomal tumor-suppressor genes, WTX is inactivated by a monoallelic "single-hit" event targeting the single X chromosome in tumors from males and the active X chromosome in tumors from females.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rivera, Miguel N -- Kim, Woo Jae -- Wells, Julie -- Driscoll, David R -- Brannigan, Brian W -- Han, Moonjoo -- Kim, James C -- Feinberg, Andrew P -- Gerald, William L -- Vargas, Sara O -- Chin, Lynda -- Iafrate, A John -- Bell, Daphne W -- Haber, Daniel A -- P01-CA101942/CA/NCI NIH HHS/ -- R37 CA054358/CA/NCI NIH HHS/ -- R37 CA054358-17/CA/NCI NIH HHS/ -- R37-CA058596/CA/NCI NIH HHS/ -- T32-CA009216/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2007 Feb 2;315(5812):642-5. Epub 2007 Jan 4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Massachusetts General Hospital Cancer Center, Harvard Medical Center, Boston, MA 02114, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17204608" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing ; Alleles ; Amino Acid Sequence ; Animals ; Cell Line ; Chromosome Deletion ; Chromosomes, Human, X/*genetics ; Female ; Gene Expression ; *Gene Silencing ; *Genes, Wilms Tumor ; Heterozygote ; Humans ; In Situ Hybridization, Fluorescence ; Kidney/embryology/metabolism ; Kidney Neoplasms/*genetics ; Male ; Mice ; Mice, Inbred C57BL ; Molecular Sequence Data ; Mutation ; Point Mutation ; Tumor Suppressor Proteins/chemistry/*genetics/physiology ; Wilms Tumor/*genetics ; beta Catenin/genetics
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  • 125
    Publication Date: 2007-05-05
    Description: Many potential treatments for Alzheimer's disease target amyloid-beta peptides (Abeta), which are widely presumed to cause the disease. The microtubule-associated protein tau is also involved in the disease, but it is unclear whether treatments aimed at tau could block Abeta-induced cognitive impairments. Here, we found that reducing endogenous tau levels prevented behavioral deficits in transgenic mice expressing human amyloid precursor protein, without altering their high Abeta levels. Tau reduction also protected both transgenic and nontransgenic mice against excitotoxicity. Thus, tau reduction can block Abeta- and excitotoxin-induced neuronal dysfunction and may represent an effective strategy for treating Alzheimer's disease and related conditions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roberson, Erik D -- Scearce-Levie, Kimberly -- Palop, Jorge J -- Yan, Fengrong -- Cheng, Irene H -- Wu, Tiffany -- Gerstein, Hilary -- Yu, Gui-Qiu -- Mucke, Lennart -- AG011385/AG/NIA NIH HHS/ -- AG022074/AG/NIA NIH HHS/ -- K08 NS054811/NS/NINDS NIH HHS/ -- K08 NS054811-02/NS/NINDS NIH HHS/ -- MH070588/MH/NIMH NIH HHS/ -- NS054811/NS/NINDS NIH HHS/ -- RR18928-01/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2007 May 4;316(5825):750-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Gladstone Institute of Neurological Disease, San Francisco, CA 94158, USA. eroberson@gladstone.ucsf.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17478722" target="_blank"〉PubMed〈/a〉
    Keywords: Alzheimer Disease/*metabolism/pathology/physiopathology/*therapy ; Amyloid beta-Peptides/metabolism ; Amyloid beta-Protein Precursor/genetics/metabolism ; Animals ; Axons/ultrastructure ; Convulsants/pharmacology ; *Disease Models, Animal ; Excitatory Amino Acid Agonists/pharmacology ; Exploratory Behavior ; Hippocampus/pathology ; Humans ; Kainic Acid/pharmacology ; Maze Learning ; Memory ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Motor Activity ; Pentylenetetrazole/pharmacology ; Phosphorylation ; Seizures/prevention & control ; tau Proteins/genetics/*metabolism
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  • 126
    Publication Date: 2007-06-16
    Description: The cytokine transforming growth factor-beta (TGF-beta) converts naive T cells into regulatory T (Treg) cells that prevent autoimmunity. However, in the presence of interleukin-6 (IL-6), TGF-beta has also been found to promote the differentiation of naive T lymphocytes into proinflammatory IL-17 cytokine-producing T helper 17 (T(H)17) cells, which promote autoimmunity and inflammation. This raises the question of how TGF-beta can generate such distinct outcomes. We identified the vitamin A metabolite retinoic acid as a key regulator of TGF-beta-dependent immune responses, capable of inhibiting the IL-6-driven induction of proinflammatory T(H)17 cells and promoting anti-inflammatory Treg cell differentiation. These findings indicate that a common metabolite can regulate the balance between pro- and anti-inflammatory immunity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mucida, Daniel -- Park, Yunji -- Kim, Gisen -- Turovskaya, Olga -- Scott, Iain -- Kronenberg, Mitchell -- Cheroutre, Hilde -- R01 AI050265-06/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2007 Jul 13;317(5835):256-60. Epub 2007 Jun 14.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17569825" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cells, Cultured ; Colitis/immunology ; Dendritic Cells/immunology ; Dibenzazepines/pharmacology ; Forkhead Transcription Factors/biosynthesis ; Interleukin-17/*biosynthesis ; Interleukin-2/immunology ; Interleukin-6/immunology ; Intestinal Mucosa/cytology/immunology ; Listeriosis/immunology ; Lymphocyte Activation ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Spleen/cytology/immunology ; T-Lymphocyte Subsets/cytology/*immunology ; T-Lymphocytes, Helper-Inducer/cytology/*immunology ; T-Lymphocytes, Regulatory/cytology/*immunology ; Transforming Growth Factor beta/metabolism/pharmacology ; Tretinoin/pharmacology/*physiology
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  • 127
    Publication Date: 2007-08-04
    Description: Epigenetic inheritance in mammals relies in part on robust propagation of DNA methylation patterns throughout development. We show that the protein UHRF1 (ubiquitin-like, containing PHD and RING finger domains 1), also known as NP95 in mouse and ICBP90 in human, is required for maintaining DNA methylation. UHRF1 colocalizes with the maintenance DNA methyltransferase protein DNMT1 throughout S phase. UHRF1 appears to tether DNMT1 to chromatin through its direct interaction with DNMT1. Furthermore UHRF1 contains a methyl DNA binding domain, the SRA (SET and RING associated) domain, that shows strong preferential binding to hemimethylated CG sites, the physiological substrate for DNMT1. These data suggest that UHRF1 may help recruit DNMT1 to hemimethylated DNA to facilitate faithful maintenance of DNA methylation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bostick, Magnolia -- Kim, Jong Kyong -- Esteve, Pierre-Olivier -- Clark, Amander -- Pradhan, Sriharsa -- Jacobsen, Steven E -- GM060398/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2007 Sep 21;317(5845):1760-4. Epub 2007 Aug 2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17673620" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; CCAAT-Enhancer-Binding Proteins/*metabolism ; COS Cells ; Cell Line ; Cercopithecus aethiops ; Chromatin/metabolism ; DNA (Cytosine-5-)-Methyltransferase/*metabolism ; *DNA Methylation ; HeLa Cells ; Humans ; Mice ; Nuclear Proteins/*metabolism ; Protein Binding ; Protein Structure, Tertiary
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  • 128
    Publication Date: 2007-08-04
    Description: The chemokines CCL21 and CXCL13 are immune factors that dictate homing and motility of lymphocytes and dendritic cells in lymphoid tissues. However, the means by which these chemokines are regulated and how they influence cell trafficking during immune responses remain unclear. We show that CCL21 and CXCL13 are transiently down-regulated within lymphoid tissues during immune responses by a mechanism controlled by the cytokine interferon-gamma. This modulation was found to alter the localization of lymphocytes and dendritic cells within responding lymphoid tissues. As a consequence, priming of T cell responses to a second distinct pathogen after chemokine modulation became impaired. We propose that this transient chemokine modulation may help orchestrate local cellularity, thus minimizing competition for space and resources in activated lymphoid tissues.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mueller, Scott N -- Hosiawa-Meagher, Karoline A -- Konieczny, Bogumila T -- Sullivan, Brandon M -- Bachmann, Martin F -- Locksley, Richard M -- Ahmed, Rafi -- Matloubian, Mehrdad -- AI30048/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2007 Aug 3;317(5838):670-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Emory Vaccine Center and Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322, USA. mueller@microbio.emory.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17673664" target="_blank"〉PubMed〈/a〉
    Keywords: Adoptive Transfer ; Animals ; Arenaviridae Infections/immunology ; B-Lymphocytes/immunology ; CD4-Positive T-Lymphocytes/immunology ; CD8-Positive T-Lymphocytes/immunology ; Cell Movement ; Chemokine CCL19 ; Chemokine CCL21 ; Chemokine CXCL13 ; Chemokines, CC/genetics/*metabolism ; Chemokines, CXC/genetics/*metabolism ; Cytokines/immunology/metabolism ; Dendritic Cells/immunology ; Down-Regulation ; Female ; Homeostasis ; Interferon-gamma/immunology/metabolism ; Listeriosis/*immunology ; Lymph Nodes/*immunology ; Lymphocytic choriomeningitis virus ; Male ; Mice ; Mice, Inbred Strains ; Mice, Transgenic ; RNA, Messenger/genetics/metabolism ; Spleen/*immunology ; Virus Diseases/*immunology
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  • 129
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-04-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Robinson, Phillip J -- New York, N.Y. -- Science. 2007 Apr 27;316(5824):551-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cell Signalling Unit, Children's Medical Research Institute, Sydney, Australia. probinson@cmri.com.au〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17463275" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Calcium/metabolism ; Clathrin-Coated Vesicles/metabolism ; Dynamin I/genetics/physiology ; Dynamin II/physiology ; Dynamin III/physiology ; Electric Stimulation ; *Endocytosis ; Exocytosis ; Mice ; Mice, Knockout ; Models, Neurological ; Neurons/*physiology/ultrastructure ; Phosphorylation ; Presynaptic Terminals/physiology/ultrastructure ; Synapses/*physiology/ultrastructure ; Synaptic Transmission ; Synaptic Vesicles/*physiology/ultrastructure
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 130
    Publication Date: 2007-08-11
    Description: The regenerative potential of skeletal muscle declines with age, and this impairment is associated with an increase in tissue fibrosis. We show that muscle stem cells (satellite cells) from aged mice tend to convert from a myogenic to a fibrogenic lineage as they begin to proliferate and that this conversion is mediated by factors in the systemic environment of the old animals. We also show that this lineage conversion is associated with an activation of the canonical Wnt signaling pathway in aged myogenic progenitors and can be suppressed by Wnt inhibitors. Furthermore, components of serum from aged mice that bind to the Frizzled family of proteins, which are Wnt receptors, may account for the elevated Wnt signaling in aged cells. These results indicate that the Wnt signaling pathway may play a critical role in tissue-specific stem cell aging and an increase in tissue fibrosis with age.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brack, Andrew S -- Conboy, Michael J -- Roy, Sudeep -- Lee, Mark -- Kuo, Calvin J -- Keller, Charles -- Rando, Thomas A -- AG23806/AG/NIA NIH HHS/ -- DK069989/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2007 Aug 10;317(5839):807-10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17690295" target="_blank"〉PubMed〈/a〉
    Keywords: Aging/*physiology ; Animals ; Cell Aging/*physiology ; Cell Lineage ; Cell Proliferation ; Fibroblasts/cytology/physiology ; Fibrosis/*pathology ; Frizzled Receptors/metabolism ; Mice ; Mice, Inbred C57BL ; Muscle, Skeletal/cytology/metabolism/*pathology ; Parabiosis ; Regeneration ; Satellite Cells, Skeletal Muscle/cytology/*physiology ; *Signal Transduction ; Wnt Proteins/*metabolism
    Print ISSN: 0036-8075
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  • 131
    Publication Date: 2007-12-15
    Description: Kelly et al. (Brevia, 20 July 2007, p. 337) questioned xenotransplant experiments supporting the cancer stem cell (CSC) hypothesis because they found a high frequency of leukemia-initiating cells (L-IC) in some transgenic mouse models. However, the CSC hypothesis depends on prospective purification of cells with tumor-initiating capacity, irrespective of frequency. Moreover, we found similar L-IC frequencies in genetically comparable leukemias using syngeneic or xenogeneic models.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kennedy, James A -- Barabe, Frederic -- Poeppl, Armando G -- Wang, Jean C Y -- Dick, John E -- New York, N.Y. -- Science. 2007 Dec 14;318(5857):1722; author reply 1722.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Cell and Molecular Biology, University Health Network, Toronto, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18079385" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bone Marrow Cells/pathology ; Bone Marrow Transplantation ; Cell Separation ; Disease Models, Animal ; Humans ; Leukemia/*pathology/physiopathology ; Leukemia, Myeloid, Acute/pathology/physiopathology ; Mice ; Mice, Transgenic ; Neoplasm Transplantation ; Neoplastic Stem Cells/pathology/*physiology ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology/physiopathology ; Transplantation, Heterologous
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 132
    Publication Date: 2007-11-24
    Description: Upon intravenous transplantation, hematopoietic stem cells (HSCs) can home to specialized niches, yet most HSCs fail to engraft unless recipients are subjected to toxic preconditioning. We provide evidence that, aside from immune barriers, donor HSC engraftment is restricted by occupancy of appropriate niches by host HSCs. Administration of ACK2, an antibody that blocks c-kit function, led to the transient removal of 〉98% of endogenous HSCs in immunodeficient mice. Subsequent transplantation of these mice with donor HSCs led to chimerism levels of up to 90%. Extrapolation of these methods to humans may enable mild but effective conditioning regimens for transplantation.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527021/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527021/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Czechowicz, Agnieszka -- Kraft, Daniel -- Weissman, Irving L -- Bhattacharya, Deepta -- 5K01DK078318/DK/NIDDK NIH HHS/ -- 5K08HL076335/HL/NHLBI NIH HHS/ -- 5R01CA086065/CA/NCI NIH HHS/ -- 5R01HL058770/HL/NHLBI NIH HHS/ -- K01 DK078318/DK/NIDDK NIH HHS/ -- K01 DK078318-01/DK/NIDDK NIH HHS/ -- K08 HL076335-01A2/HL/NHLBI NIH HHS/ -- K08 HL076335-02/HL/NHLBI NIH HHS/ -- K08 HL076335-03/HL/NHLBI NIH HHS/ -- R01 CA086065/CA/NCI NIH HHS/ -- R01 CA086065-06/CA/NCI NIH HHS/ -- R01 CA086065-07/CA/NCI NIH HHS/ -- R01 CA086065-08/CA/NCI NIH HHS/ -- R01 HL058770/HL/NHLBI NIH HHS/ -- R01 HL058770-06/HL/NHLBI NIH HHS/ -- R01 HL058770-07/HL/NHLBI NIH HHS/ -- R01 HL058770-08/HL/NHLBI NIH HHS/ -- T32 AI007290/AI/NIAID NIH HHS/ -- T32AI0729022/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2007 Nov 23;318(5854):1296-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Stem Cell Biology and Regenerative Medicine, Departments of Pathology and Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18033883" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Antibodies, Monoclonal/administration & dosage/blood/immunology ; Bone Marrow Cells/cytology ; Bone Marrow Transplantation ; Cell Proliferation ; *Hematopoietic Stem Cell Transplantation ; Hematopoietic Stem Cells/cytology/*physiology ; Mice ; Proto-Oncogene Proteins c-kit/immunology ; Spleen/cytology ; Time Factors ; Transplantation Chimera ; Transplantation Conditioning/*methods
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  • 133
    Publication Date: 2007-04-28
    Description: MicroRNAs are a class of small RNAs that are increasingly being recognized as important regulators of gene expression. Although hundreds of microRNAs are present in the mammalian genome, genetic studies addressing their physiological roles are at an early stage. We have shown that mice deficient for bic/microRNA-155 are immunodeficient and display increased lung airway remodeling. We demonstrate a requirement of bic/microRNA-155 for the function of B and T lymphocytes and dendritic cells. Transcriptome analysis of bic/microRNA-155-deficient CD4+ T cells identified a wide spectrum of microRNA-155-regulated genes, including cytokines, chemokines, and transcription factors. Our work suggests that bic/microRNA-155 plays a key role in the homeostasis and function of the immune system.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2610435/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2610435/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rodriguez, Antony -- Vigorito, Elena -- Clare, Simon -- Warren, Madhuri V -- Couttet, Philippe -- Soond, Dalya R -- van Dongen, Stijn -- Grocock, Russell J -- Das, Partha P -- Miska, Eric A -- Vetrie, David -- Okkenhaug, Klaus -- Enright, Anton J -- Dougan, Gordon -- Turner, Martin -- Bradley, Allan -- 077187/Wellcome Trust/United Kingdom -- G117/424/Medical Research Council/United Kingdom -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2007 Apr 27;316(5824):608-11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17463290" target="_blank"〉PubMed〈/a〉
    Keywords: 3' Untranslated Regions ; Animals ; B-Lymphocytes/*immunology ; Cytokines/biosynthesis ; Dendritic Cells/*immunology ; Gene Expression Regulation ; Gene Targeting ; Homeostasis ; Immune System/*physiology ; Immunoglobulin G/biosynthesis ; Lung/pathology ; Lung Diseases/immunology/pathology ; Lymphocyte Activation ; Mice ; MicroRNAs/genetics/*physiology ; Oligonucleotide Array Sequence Analysis ; Proto-Oncogene Proteins c-maf/genetics/physiology ; Salmonella Infections, Animal/immunology ; T-Lymphocytes/*immunology ; Th1 Cells/immunology ; Th2 Cells/immunology ; Vaccination
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 134
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-04-21
    Description: Small noncoding RNAs have emerged as potent regulators of gene expression at both transcriptional and posttranscriptional levels. Recently, a class of small RNAs that interact with Piwi proteins has been discovered in the mammalian germ line and Drosophila. These Piwi-interacting RNAs (piRNAs) represent a distinct small RNA pathway.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lin, Haifan -- New York, N.Y. -- Science. 2007 Apr 20;316(5823):397.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Yale Stem Cell Center, Yale University School of Medicine, New Haven, CT 06510, USA. haifan.lin@yale.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17446387" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Argonaute Proteins ; Drosophila ; Drosophila Proteins/metabolism ; Epigenesis, Genetic ; Gene Expression Regulation, Developmental ; Germ Cells/cytology/*metabolism ; Mice ; Peptide Initiation Factors/metabolism ; Protein Biosynthesis ; Proteins/*metabolism ; RNA Stability ; RNA, Untranslated/genetics/*metabolism ; RNA-Induced Silencing Complex
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  • 135
    Publication Date: 2007-11-10
    Description: Endoplasmic reticulum (ER) stress activates a set of signaling pathways, collectively termed the unfolded protein response (UPR). The three UPR branches (IRE1, PERK, and ATF6) promote cell survival by reducing misfolded protein levels. UPR signaling also promotes apoptotic cell death if ER stress is not alleviated. How the UPR integrates its cytoprotective and proapoptotic outputs to select between life or death cell fates is unknown. We found that IRE1 and ATF6 activities were attenuated by persistent ER stress in human cells. By contrast, PERK signaling, including translational inhibition and proapoptotic transcription regulator Chop induction, was maintained. When IRE1 activity was sustained artificially, cell survival was enhanced, suggesting a causal link between the duration of UPR branch signaling and life or death cell fate after ER stress. Key findings from our studies in cell culture were recapitulated in photoreceptors expressing mutant rhodopsin in animal models of retinitis pigmentosa.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670588/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670588/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lin, Jonathan H -- Li, Han -- Yasumura, Douglas -- Cohen, Hannah R -- Zhang, Chao -- Panning, Barbara -- Shokat, Kevan M -- Lavail, Matthew M -- Walter, Peter -- K08 EY018313/EY/NEI NIH HHS/ -- K08 EY018313-01/EY/NEI NIH HHS/ -- R01 EY020846/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 2007 Nov 9;318(5852):944-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, University of California at San Francisco, San Francisco, CA 94158, USA. Jonathan.Lin@ucsf.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17991856" target="_blank"〉PubMed〈/a〉
    Keywords: Activating Transcription Factor 6/metabolism ; Animals ; Animals, Genetically Modified ; *Apoptosis ; Cell Line ; *Cell Survival ; Disease Models, Animal ; Endoplasmic Reticulum/*metabolism ; Endoribonucleases/genetics/*metabolism ; Humans ; Kinetics ; Membrane Proteins/genetics/*metabolism ; Mice ; Mutation ; *Protein Folding ; Protein-Serine-Threonine Kinases/genetics/*metabolism ; Proteins/chemistry/*metabolism ; Rats ; Retina/metabolism ; Retinitis Pigmentosa/metabolism ; Rhodopsin/chemistry/metabolism ; *Signal Transduction ; eIF-2 Kinase/metabolism
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  • 136
    Publication Date: 2007-07-21
    Description: Primary cilia are essential for transduction of the Hedgehog (Hh) signal in mammals. We investigated the role of primary cilia in regulation of Patched1 (Ptc1), the receptor for Sonic Hedgehog (Shh). Ptc1 localized to cilia and inhibited Smoothened (Smo) by preventing its accumulation within cilia. When Shh bound to Ptc1, Ptc1 left the cilia, leading to accumulation of Smo and activation of signaling. Thus, primary cilia sense Shh and transduce signals that play critical roles in development, carcinogenesis, and stem cell function.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rohatgi, Rajat -- Milenkovic, Ljiljana -- Scott, Matthew P -- R01 CA088060/CA/NCI NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2007 Jul 20;317(5836):372-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Departments of Developmental Biology, Genetics, and Bioengineering and Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17641202" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Membrane/metabolism ; Cells, Cultured ; Cilia/*metabolism ; Cyclohexylamines/pharmacology ; Embryo, Mammalian/metabolism ; Hedgehog Proteins/agonists/*metabolism ; Hydroxycholesterols/pharmacology ; Mesoderm/metabolism ; Mice ; NIH 3T3 Cells ; Protein Binding ; Receptors, Cell Surface/genetics/*metabolism ; Receptors, G-Protein-Coupled/metabolism ; *Signal Transduction ; Thiophenes/pharmacology ; Transcription, Genetic ; Transfection
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  • 137
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-04-21
    Description: The production of functional male gametes is dependent on the continuous activity of germline stem cells. The availability of a transplantation assay system to unequivocally identify male germline stem cells has allowed their in vitro culture, cryopreservation, and genetic modification. Moreover, the system has enabled the identification of conditions and factors involved in stem cell self-renewal, the foundation of spermatogenesis, and the production of spermatozoa. The increased knowledge about these cells is also of great potential practical value, for example, for the possible cryopreservation of stem cells from boys undergoing treatment for cancer to safeguard their germ line.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brinster, Ralph L -- HDO44445/PHS HHS/ -- New York, N.Y. -- Science. 2007 Apr 20;316(5823):404-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17446391" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Culture Techniques ; Cryopreservation ; Gene Expression Regulation, Developmental ; Germ Cells/*cytology/physiology ; Glial Cell Line-Derived Neurotrophic Factor/physiology ; Humans ; Male ; Mice ; Sertoli Cells/cytology/physiology ; Signal Transduction ; Spermatogenesis ; Spermatogonia/*cytology/physiology ; Stem Cell Transplantation ; Stem Cells/*cytology/physiology
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  • 138
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-03-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Littman, Dan R -- Singh, Harinder -- New York, N.Y. -- Science. 2007 Mar 23;315(5819):1673-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA. littman@saturn.med.nyu.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17379796" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigen Presentation ; Antigens, CD8/analysis ; CD8-Positive T-Lymphocytes/*cytology/*immunology ; Cell Differentiation ; *Cell Division ; Cell Lineage ; Cell Polarity ; Cytoplasm/physiology ; Dendritic Cells/immunology ; *Immunologic Memory ; Listeria monocytogenes/immunology ; Listeriosis/immunology ; Lymphocyte Activation ; Mice ; Mitosis ; Protein Kinase C/analysis ; Receptors, Antigen, T-Cell/immunology ; T-Lymphocyte Subsets/*cytology/*immunology ; T-Lymphocytes, Cytotoxic/cytology/immunology
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  • 139
    Publication Date: 2007-04-28
    Description: Clinically successful hematopoietic cell transplantation is dependent on hematopoietic stem and progenitor cells. Here we identify the matricellular protein Nephroblastoma Overexpressed (Nov, CCN3) as being essential for their functional integrity. Nov expression is restricted to the primitive (CD34) compartments of umbilical vein cord blood, and its knockdown in these cells by lentivirus-mediated RNA interference abrogates their function in vitro and in vivo. Conversely, forced expression of Nov and addition of recombinant Nov protein both enhance primitive stem and/or progenitor activity. Taken together, our results identify Nov (CCN3) as a regulator of human hematopoietic stem or progenitor cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gupta, Rajeev -- Hong, Dengli -- Iborra, Francisco -- Sarno, Samantha -- Enver, Tariq -- MC_U137961143/Medical Research Council/United Kingdom -- MC_U137973816/Medical Research Council/United Kingdom -- MC_U137973817/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2007 Apr 27;316(5824):590-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Medical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Headington, OX3 9DS, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17463287" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens, CD34/analysis ; Cell Line ; Cells, Cultured ; Colony-Forming Units Assay ; Connective Tissue Growth Factor ; Genetic Vectors ; Hematopoiesis ; Hematopoietic Stem Cell Transplantation ; Hematopoietic Stem Cells/cytology/*physiology ; Humans ; Immediate-Early Proteins/genetics/*physiology ; Intercellular Signaling Peptides and Proteins/genetics/*physiology ; Lentivirus/genetics ; Mice ; Mice, Inbred NOD ; Mice, SCID ; Nephroblastoma Overexpressed Protein ; RNA Interference ; Recombinant Proteins/metabolism ; Transfection ; Transplantation, Heterologous
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  • 140
    Publication Date: 2007-08-11
    Description: The contribution of stem and progenitor cell dysfunction and depletion in normal aging remains incompletely understood. We explored this concept in the Klotho mouse model of accelerated aging. Analysis of various tissues and organs from young Klotho mice revealed a decrease in stem cell number and an increase in progenitor cell senescence. Because klotho is a secreted protein, we postulated that klotho might interact with other soluble mediators of stem cells. We found that klotho bound to various Wnt family members. In a cell culture model, the Wnt-klotho interaction resulted in the suppression of Wnt biological activity. Tissues and organs from klotho-deficient animals showed evidence of increased Wnt signaling, and ectopic expression of klotho antagonized the activity of endogenous and exogenous Wnt. Both in vitro and in vivo, continuous Wnt exposure triggered accelerated cellular senescence. Thus, klotho appears to be a secreted Wnt antagonist and Wnt proteins have an unexpected role in mammalian aging.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Liu, Hongjun -- Fergusson, Maria M -- Castilho, Rogerio M -- Liu, Jie -- Cao, Liu -- Chen, Jichun -- Malide, Daniela -- Rovira, Ilsa I -- Schimel, Daniel -- Kuo, Calvin J -- Gutkind, J Silvio -- Hwang, Paul M -- Finkel, Toren -- 1 R01 DK069989-01/DK/NIDDK NIH HHS/ -- Intramural NIH HHS/ -- New York, N.Y. -- Science. 2007 Aug 10;317(5839):803-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cardiology Branch, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17690294" target="_blank"〉PubMed〈/a〉
    Keywords: Aging/*physiology ; Animals ; Apoptosis ; Bone Density ; Bone and Bones/metabolism ; Cell Aging/*physiology ; Cell Count ; Cell Line ; Cell Shape ; Glucuronidase/chemistry/genetics/*metabolism ; Humans ; Mice ; Mice, Transgenic ; Protein Structure, Tertiary ; *Signal Transduction ; Stem Cells/cytology/*physiology ; Wnt Proteins/antagonists & inhibitors/*metabolism ; Wnt1 Protein/metabolism ; Wnt3 Protein
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  • 141
    Publication Date: 2007-04-28
    Description: The mechanisms that allow antigen-presenting cells (APCs) to selectively present extracellular antigen to CD8+ effector T cells (cross-presentation) or to CD4+ T helper cells are not fully resolved. We demonstrated that APCs use distinct endocytosis mechanisms to simultaneously introduce soluble antigen into separate intracellular compartments, which were dedicated to presentation to CD8+ or CD4+ T cells. Specifically, the mannose receptor supplied an early endosomal compartment distinct from lysosomes, which was committed to cross-presentation. These findings imply that antigen does not require intracellular diversion to access the cross-presentation pathway, because it can enter the pathway already during endocytosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Burgdorf, Sven -- Kautz, Andreas -- Bohnert, Volker -- Knolle, Percy A -- Kurts, Christian -- New York, N.Y. -- Science. 2007 Apr 27;316(5824):612-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Molecular Medicine and Experimental Immunology, Friedrich-Wilhelms-Universitat, Bonn, Germany. sven.burgdorf@ukb.uni-bonn.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17463291" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Antigen Presentation ; Antigens/*immunology ; CD4-Positive T-Lymphocytes/*immunology ; CD8-Positive T-Lymphocytes/*immunology ; Dendritic Cells/immunology ; Endocytosis ; Endosomes/immunology/metabolism ; Histocompatibility Antigens Class II/immunology ; Lectins, C-Type/metabolism ; *Lymphocyte Activation ; Lysosomes/immunology/metabolism ; Macrophages/immunology ; Mannose-Binding Lectins/metabolism ; Mice ; Mice, Inbred C57BL ; Models, Immunological ; Ovalbumin/immunology ; Pinocytosis ; Receptors, Cell Surface/metabolism ; Receptors, Scavenger/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 142
    Publication Date: 2007-08-25
    Description: Histidine kinases, used for environmental sensing by bacterial two-component systems, are involved in regulation of bacterial gene expression, chemotaxis, phototaxis, and virulence. Flavin-containing domains function as light-sensory modules in plant and algal phototropins and in fungal blue-light receptors. We have discovered that the prokaryotes Brucella melitensis, Brucella abortus, Erythrobacter litoralis, and Pseudomonas syringae contain light-activated histidine kinases that bind a flavin chromophore and undergo photochemistry indicative of cysteinyl-flavin adduct formation. Infection of macrophages by B. abortus was stimulated by light in the wild type but was limited in photochemically inactive and null mutants, indicating that the flavin-containing histidine kinase functions as a photoreceptor regulating B. abortus virulence.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Swartz, Trevor E -- Tseng, Tong-Seung -- Frederickson, Marcus A -- Paris, Gaston -- Comerci, Diego J -- Rajashekara, Gireesh -- Kim, Jung-Gun -- Mudgett, Mary Beth -- Splitter, Gary A -- Ugalde, Rodolfo A -- Goldbaum, Fernando A -- Briggs, Winslow R -- Bogomolni, Roberto A -- 1.U54-AI-057153/AI/NIAID NIH HHS/ -- R01 GM068886/GM/NIGMS NIH HHS/ -- R01-GM068886/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2007 Aug 24;317(5841):1090-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry and Biochemistry, University of California, Santa Cruz, Santa Cruz, CA, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17717187" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Triphosphate/metabolism ; Animals ; Brucella abortus/*enzymology/growth & development/pathogenicity ; Brucella melitensis/*enzymology ; Cell Line ; Cloning, Molecular ; Enzyme Activation ; Flavin Mononucleotide/metabolism ; *Light ; Macrophages/*microbiology ; Mice ; Molecular Sequence Data ; Mutation ; Phosphorylation ; Photochemistry ; Protein Kinases/chemistry/genetics/*metabolism ; Protein Structure, Tertiary ; Pseudomonas syringae/*enzymology ; Signal Transduction ; Sphingomonadaceae/*enzymology ; Virulence
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  • 143
    Publication Date: 2007-09-08
    Description: Autism spectrum disorders (ASDs) are characterized by impairments in social behaviors that are sometimes coupled to specialized cognitive abilities. A small percentage of ASD patients carry mutations in genes encoding neuroligins, which are postsynaptic cell-adhesion molecules. We introduced one of these mutations into mice: the Arg451--〉Cys451 (R451C) substitution in neuroligin-3. R451C mutant mice showed impaired social interactions but enhanced spatial learning abilities. Unexpectedly, these behavioral changes were accompanied by an increase in inhibitory synaptic transmission with no apparent effect on excitatory synapses. Deletion of neuroligin-3, in contrast, did not cause such changes, indicating that the R451C substitution represents a gain-of-function mutation. These data suggest that increased inhibitory synaptic transmission may contribute to human ASDs and that the R451C knockin mice may be a useful model for studying autism-related behaviors.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235367/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235367/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tabuchi, Katsuhiko -- Blundell, Jacqueline -- Etherton, Mark R -- Hammer, Robert E -- Liu, Xinran -- Powell, Craig M -- Sudhof, Thomas C -- AS1264/Autism Speaks/ -- K08 MH065975/MH/NIMH NIH HHS/ -- K08 MH065975-04/MH/NIMH NIH HHS/ -- K08 MH065975-05/MH/NIMH NIH HHS/ -- R01 MH081164/MH/NIMH NIH HHS/ -- R37 MH52804-08/MH/NIMH NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2007 Oct 5;318(5847):71-6. Epub 2007 Sep 6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17823315" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Animals ; Autistic Disorder/*genetics ; Brain/anatomy & histology/metabolism/*physiology ; Cell Adhesion Molecules, Neuronal ; *Disease Models, Animal ; Female ; Gene Targeting ; Hippocampus/physiology ; Humans ; Male ; Maze Learning ; Membrane Proteins/*genetics/metabolism ; Memory ; Mice ; Mice, Knockout ; *Mutation ; Nerve Tissue Proteins/*genetics/metabolism ; Social Behavior ; Somatosensory Cortex/physiology ; Synapses/*physiology ; *Synaptic Transmission ; Vesicular Glutamate Transport Protein 1/metabolism ; Vesicular Inhibitory Amino Acid Transport Proteins/metabolism
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  • 144
    Publication Date: 2007-07-21
    Description: Reduced insulin-like signaling extends the life span of Caenorhabditis elegans and Drosophila. Here, we show that, in mice, less insulin receptor substrate-2 (Irs2) signaling throughout the body or just in the brain extended life span up to 18%. At 22 months of age, brain-specific Irs2 knockout mice were overweight, hyperinsulinemic, and glucose intolerant; however, compared with control mice, they were more active and displayed greater glucose oxidation, and during meals they displayed stable superoxide dismutase-2 concentrations in the hypothalamus. Thus, less Irs2 signaling in aging brains can promote healthy metabolism, attenuate meal-induced oxidative stress, and extend the life span of overweight and insulin-resistant mice.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Taguchi, Akiko -- Wartschow, Lynn M -- White, Morris F -- DK38712/DK/NIDDK NIH HHS/ -- DK55326/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2007 Jul 20;317(5836):369-72.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Division of Endocrinology, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17641201" target="_blank"〉PubMed〈/a〉
    Keywords: Aging ; Animals ; Brain/*metabolism ; Circadian Rhythm ; Crosses, Genetic ; Diet ; Female ; Glucose/*metabolism ; *Homeostasis ; Insulin Receptor Substrate Proteins ; Insulin Resistance ; Intracellular Signaling Peptides and Proteins/*metabolism ; *Longevity ; Male ; Mice ; Mice, Knockout ; Mice, Transgenic ; Overweight ; Oxidation-Reduction ; Oxygen Consumption ; Phosphoproteins/*metabolism ; Respiration ; *Signal Transduction ; Superoxide Dismutase/metabolism
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 145
    Publication Date: 2007-04-14
    Description: Hyperlipidemia, one of the most important risk factors for coronary heart disease, is often associated with inflammation. We identified lymphotoxin (LT) and LIGHT, tumor necrosis factor cytokine family members that are primarily expressed on lymphocytes, as critical regulators of key enzymes that control lipid metabolism. Dysregulation of LIGHT expression on T cells resulted in hypertriglyceridemia and hypercholesterolemia. In low-density lipoprotein receptor-deficient mice, which lack the ability to control lipid levels in the blood, inhibition of LT and LIGHT signaling with a soluble lymphotoxin beta receptor decoy protein attenuated the dyslipidemia. These results suggest that the immune system directly influences lipid metabolism and that LT modulating agents may represent a novel therapeutic route for the treatment of dyslipidemia.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lo, James C -- Wang, Yugang -- Tumanov, Alexei V -- Bamji, Michelle -- Yao, Zemin -- Reardon, Catherine A -- Getz, Godfrey S -- Fu, Yang-Xin -- 5 T32 GM07281/GM/NIGMS NIH HHS/ -- AI062026/AI/NIAID NIH HHS/ -- CA097296/CA/NCI NIH HHS/ -- DK58891/DK/NIDDK NIH HHS/ -- HL 85516/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2007 Apr 13;316(5822):285-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Committee on Immunology, University of Chicago, Chicago, IL 60637, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17431181" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cells, Cultured ; Dyslipidemias/drug therapy/etiology/metabolism ; Female ; Homeostasis ; Humans ; Hypercholesterolemia/etiology ; *Lipid Metabolism ; Lipids/blood ; Liver/*metabolism ; Lymphotoxin beta Receptor/*metabolism/therapeutic use ; Lymphotoxin-alpha/metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Signal Transduction ; T-Lymphocytes/metabolism ; Tumor Necrosis Factor Ligand Superfamily Member ; 14/genetics/*metabolism/therapeutic use
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 146
    Publication Date: 2007-06-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2007 Jun 22;316(5832):1681.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17588905" target="_blank"〉PubMed〈/a〉
    Keywords: Adipocytes/secretion ; Animals ; *Cytokines/metabolism/secretion ; Female ; Humans ; Male ; Mice ; Nicotinamide Phosphoribosyltransferase ; Obesity/metabolism ; Publishing ; *Retraction of Publication as Topic ; Schools, Medical ; Universities
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  • 147
    Publication Date: 2007-07-28
    Description: Adeno-associated viruses (AAV) are promising gene therapy vectors that have little or no acute toxicity. We show that normal mice and mice with mucopolysaccharidosis VII (MPS VII) develop hepatocellular carcinoma (HCC) after neonatal injection of an AAV vector expressing b-glucuronidase. AAV proviruses were isolated from four tumors and were all located within a 6-kilobase region of chromosome 12. This locus encodes several imprinted transcripts, small nucleolar RNAs (snoRNAs), and microRNAs. Transcripts from adjacent genes encoding snoRNAs and microRNAs were overexpressed in tumors. Our findings implicate this locus in the development of HCC and raise concerns over the clinical use of AAV vectors.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Donsante, Anthony -- Miller, Daniel G -- Li, Yi -- Vogler, Carole -- Brunt, Elizabeth M -- Russell, David W -- Sands, Mark S -- R01 DK071657/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2007 Jul 27;317(5837):477.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Internal Medicine, Washington University School of Medicine, Box 8007, 660 South Euclid Avenue, St. Louis, MO 63110, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17656716" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carcinoma, Hepatocellular/*genetics/virology ; Cell Transformation, Viral ; Dependovirus/*genetics ; *Genetic Vectors ; Glucuronidase/genetics ; Liver/*virology ; Liver Neoplasms/*genetics/virology ; Mice ; Mice, Transgenic ; MicroRNAs/genetics ; *Mutagenesis, Insertional ; Oligonucleotide Array Sequence Analysis ; Proviruses/genetics ; RNA, Small Nucleolar/genetics ; Terminal Repeat Sequences ; *Virus Integration
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 148
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-04-21
    Description: Specification of germ cells in mice occurs relatively late in embryonic development. It is initiated by signals that induce expression of Blimp1, a key regulator of the germ cell, in a few epiblast cells of early postimplantation embryos. Blimp1 represses the incipient somatic program in these cells and promotes progression toward the germ cell fate. Blimp1 may also have a role in the maintenance of early germ cell characteristics by ensuring their escape from the somatic fate as well as possible reversion to pluripotent stem cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hayashi, Katsuhiko -- de Sousa Lopes, Susana M Chuva -- Surani, M Azim -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2007 Apr 20;316(5823):394-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Trust Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17446386" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cell Lineage ; Embryo, Mammalian/*cytology/physiology ; Embryonic Development ; Epigenesis, Genetic ; Gene Expression Regulation, Developmental ; Germ Cells/*cytology ; Mice ; Phenotype ; Pluripotent Stem Cells/cytology ; Protein Methyltransferases/genetics/physiology ; Repressor Proteins/physiology ; Transcription Factors/physiology ; Transcription, Genetic
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  • 149
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-12-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dorin, Julia R -- Jackson, Ian J -- MC_U127527200/Medical Research Council/United Kingdom -- MC_U127527201/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2007 Nov 30;318(5855):1395.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK. ian.jackson@hgu.mrc.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18048676" target="_blank"〉PubMed〈/a〉
    Keywords: Agouti Signaling Protein/genetics/metabolism ; Animals ; Dogs/*genetics/metabolism ; Female ; Hair Color/*genetics ; Haplotypes ; Humans ; Male ; Mice ; Mice, Transgenic ; Mutation ; Polymorphism, Genetic ; Receptor, Melanocortin, Type 1/*metabolism ; Sequence Deletion ; Signal Transduction ; Skin/metabolism ; beta-Defensins/chemistry/*genetics/*metabolism
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  • 150
    Publication Date: 2007-10-20
    Description: Genetic analysis of mammalian color variation has provided fundamental insight into human biology and disease. In most vertebrates, two key genes, Agouti and Melanocortin 1 receptor (Mc1r), encode a ligand-receptor system that controls pigment type-switching, but in domestic dogs, a third gene is implicated, the K locus, whose genetic characteristics predict a previously unrecognized component of the melanocortin pathway. We identify the K locus as beta-defensin 103 (CBD103) and show that its protein product binds with high affinity to the Mc1r and has a simple and strong effect on pigment type-switching in domestic dogs and transgenic mice. These results expand the functional role of beta-defensins, a protein family previously implicated in innate immunity, and identify an additional class of ligands for signaling through melanocortin receptors.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2906624/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2906624/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Candille, Sophie I -- Kaelin, Christopher B -- Cattanach, Bruce M -- Yu, Bin -- Thompson, Darren A -- Nix, Matthew A -- Kerns, Julie A -- Schmutz, Sheila M -- Millhauser, Glenn L -- Barsh, Gregory S -- R01 DK064265/DK/NIDDK NIH HHS/ -- R01 DK064265-08/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2007 Nov 30;318(5855):1418-23. Epub 2007 Oct 18.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Departments of Genetics and Pediatrics, Stanford University, Stanford, CA, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17947548" target="_blank"〉PubMed〈/a〉
    Keywords: Agouti Signaling Protein/genetics/metabolism ; Amino Acid Sequence ; Animals ; Cell Line ; Chromosome Mapping ; Dogs/*genetics/metabolism ; Female ; Hair Color/*genetics ; Haplotypes ; Humans ; Keratinocytes/metabolism ; Male ; Mice ; Mice, Transgenic ; Molecular Sequence Data ; Mutation ; Polymorphism, Genetic ; Receptor, Melanocortin, Type 1/*metabolism ; Sequence Analysis, DNA ; Sequence Deletion ; Signal Transduction ; Skin/metabolism ; beta-Defensins/chemistry/*genetics/*metabolism
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  • 151
    Publication Date: 2007-01-06
    Description: During cell division, copies of mouse chromosome 7 are segregated selectively or randomly to daughter cells depending on the cell type. The mechanism for differential segregation is unknown. Because mouse left-right dynein (LRD) gene mutations result in randomization of visceral organs' laterality, we hypothesized that LRD may also function in selective chromatid segregation. Indeed, upon knock-down by RNA interference methods, LRD depletion disrupts biased segregation. LRD messenger RNA presence or absence correlates with the observed segregation patterns. This work supports the claim that LRD functions in a mechanism for selective chromatid segregation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Armakolas, Athanasios -- Klar, Amar J S -- Intramural NIH HHS/ -- New York, N.Y. -- Science. 2007 Jan 5;315(5808):100-1.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research, National Cancer Institute at Frederick, Post Office Box B, Frederick, MD 21702-1201, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17204651" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axonemal Dyneins ; Body Patterning ; Cell Line ; Cell Lineage ; Chromatids/*physiology ; *Chromosome Segregation ; DNA Replication ; Dyneins/*genetics/*physiology ; Ectoderm/*cytology ; Embryonic Stem Cells/*cytology ; Endoderm/*cytology ; Interphase ; Mice ; Mitosis ; Mutation ; RNA Interference ; Recombination, Genetic
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  • 152
    Publication Date: 2007-09-01
    Description: Somatic hypermutation (SHM) is a major means by which diversity is achieved in antibody genes, and it is initiated by the deamination of cytosines to uracils in DNA by activation-induced deaminase (AID). However, the process that leads from these initiating deamination events to mutations at other residues remains poorly understood. We demonstrate that a single cytosine on the top (nontemplate) strand is sufficient to recruit AID and lead to mutations of upstream and downstream A/T residues. In contrast, the targeting of cytosines on the bottom strand by AID does not lead to substantial mutation of neighboring residues. This strand asymmetry is eliminated in mice deficient in mismatch repair, indicating that the error-prone mismatch repair machinery preferentially targets top-strand uracils in a way that promotes SHM during the antibody response.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Unniraman, Shyam -- Schatz, David G -- New York, N.Y. -- Science. 2007 Aug 31;317(5842):1227-30.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06511, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17761884" target="_blank"〉PubMed〈/a〉
    Keywords: Adenine/metabolism ; Animals ; B-Lymphocytes ; Base Sequence ; Cytidine Deaminase/*metabolism ; Cytosine/*metabolism ; DNA Mismatch Repair ; Deamination ; *Genes, Immunoglobulin ; Immunoglobulin Variable Region/genetics ; Immunoglobulin kappa-Chains/genetics ; Mice ; Mice, Transgenic ; Molecular Sequence Data ; *Somatic Hypermutation, Immunoglobulin ; Thymine/metabolism ; Transgenes ; Uracil/metabolism
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  • 153
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-06-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, Constance -- New York, N.Y. -- Science. 2007 Jun 29;316(5833):1825.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17600188" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Line ; Cloning, Organism ; Embryo Implantation ; Embryo Research/ethics/legislation & jurisprudence ; Embryo, Mammalian ; Embryonic Development ; *Embryonic Stem Cells/cytology/physiology ; Humans ; Mice ; *Pluripotent Stem Cells/cytology ; Politics ; Rats
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 154
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-06-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, Constance -- New York, N.Y. -- Science. 2007 Jun 8;316(5830):1404.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17556554" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Line ; *Cellular Reprogramming ; Cloning, Organism ; *Embryonic Stem Cells ; Mice ; *Nuclear Transfer Techniques ; *Zygote
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  • 155
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-06-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, Constance -- New York, N.Y. -- Science. 2007 Jun 8;316(5830):1404-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17556553" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Cellular Reprogramming ; Embryo Research ; Embryo, Mammalian ; Embryonic Stem Cells/cytology ; Epigenesis, Genetic ; Fetus/cytology ; Fibroblasts/*cytology ; Genetic Vectors ; Germ Cells/cytology ; Mice ; *Pluripotent Stem Cells/cytology/physiology ; Stem Cell Transplantation ; Transcription Factors/genetics
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  • 156
    Publication Date: 2007-12-08
    Description: Mammalian dosage compensation involves silencing of one of the two X chromosomes in females and is controlled by the X-inactivation center (Xic). The Xic, which includes Xist and its antisense transcription unit Tsix/Xite, somehow senses the number of X chromosomes and triggers Xist up-regulation from one of the two X chromosomes in females. We found that a segment of the mouse Xic lying several hundred kilobases upstream of Xist brings the two Xics together before the onset of X inactivation. This region can autonomously drive Xic trans-interactions even as an ectopic single-copy transgene. Its introduction into male embryonic stem cells is strongly selected against, consistent with a possible role in trans-activating Xist. We propose that homologous associations driven by this novel X-pairing region (Xpr) of the Xic enable a cell to sense that more than one X chromosome is present and coordinate reciprocal Xist/Tsix expression.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Augui, S -- Filion, G J -- Huart, S -- Nora, E -- Guggiari, M -- Maresca, M -- Stewart, A F -- Heard, E -- New York, N.Y. -- Science. 2007 Dec 7;318(5856):1632-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉CNRS UMR218, Curie Institute, 26 rue d'Ulm, Paris 75005, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18063799" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Cell Differentiation ; Cell Line ; *Chromosome Pairing ; Chromosomes, Artificial, Bacterial ; Down-Regulation ; Embryonic Stem Cells ; Female ; Mice ; Mice, Transgenic ; RNA, Long Noncoding ; RNA, Untranslated/genetics/metabolism ; S Phase ; Transfection ; Transgenes ; Up-Regulation ; X Chromosome/*genetics/physiology ; *X Chromosome Inactivation
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 157
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-02-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chatterjee, Rhitu -- New York, N.Y. -- Science. 2007 Feb 16;315(5814):928-31.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17303729" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Specimen Banks/standards ; Biomedical Research/standards ; Cell Culture Techniques/standards ; *Cell Line/chemistry ; Cell Line, Tumor/chemistry ; DNA Fingerprinting ; Humans ; Mice ; Periodicals as Topic/standards ; Retraction of Publication as Topic
    Print ISSN: 0036-8075
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  • 158
    Publication Date: 2007-01-06
    Description: Dendritic cells (DCs) process and present self and foreign antigens to induce tolerance or immunity. In vitro models suggest that induction of immunity is controlled by regulating the presentation of antigen, but little is known about how DCs control antigen presentation in vivo. To examine antigen processing and presentation in vivo, we specifically targeted antigens to two major subsets of DCs by using chimeric monoclonal antibodies. Unlike CD8+ DCs that express the cell surface protein CD205, CD8- DCs, which are positive for the 33D1 antigen, are specialized for presentation on major histocompatibility complex (MHC) class II. This difference in antigen processing is intrinsic to the DC subsets and is associated with increased expression of proteins involved in MHC processing.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dudziak, Diana -- Kamphorst, Alice O -- Heidkamp, Gordon F -- Buchholz, Veit R -- Trumpfheller, Christine -- Yamazaki, Sayuri -- Cheong, Cheolho -- Liu, Kang -- Lee, Han-Woong -- Park, Chae Gyu -- Steinman, Ralph M -- Nussenzweig, Michel C -- New York, N.Y. -- Science. 2007 Jan 5;315(5808):107-11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10021, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17204652" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Antibodies, Monoclonal/immunology ; *Antigen Presentation ; Antigens, CD/analysis/immunology ; Antigens, CD8/analysis/immunology ; Base Sequence ; Dendritic Cells/*immunology ; Histocompatibility Antigens Class I/immunology ; Histocompatibility Antigens Class II/immunology ; Lectins, C-Type/analysis/immunology ; Lymphocyte Activation ; Mice ; Mice, Inbred C3H ; Mice, Inbred C57BL ; Mice, Transgenic ; Molecular Sequence Data ; Oligonucleotide Array Sequence Analysis ; Receptors, Cell Surface/analysis/immunology ; T-Lymphocytes/immunology
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  • 159
    Publication Date: 2007-07-28
    Description: The activation of metabotropic glutamate receptors (mGluRs) leads to long-term depression (mGluR-LTD) at many synapses of the brain. The induction of mGluR-LTD is well characterized, whereas the mechanisms underlying its expression remain largely elusive. mGluR-LTD in the ventral tegmental area (VTA) efficiently reverses cocaine-induced strengthening of excitatory inputs onto dopamine neurons. We show that mGluR-LTD is expressed by an exchange of GluR2-lacking AMPA receptors for GluR2-containing receptors with a lower single-channel conductance. The synaptic insertion of GluR2 depends on de novo protein synthesis via rapid messenger RNA translation of GluR2. Regulated synthesis of GluR2 in the VTA is therefore required to reverse cocaine-induced synaptic plasticity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mameli, Manuel -- Balland, Benedicte -- Lujan, Rafael -- Luscher, Christian -- New York, N.Y. -- Science. 2007 Jul 27;317(5837):530-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Basic Neuroscience, Medical Faculty, University of Geneva, CH-1211 Geneva, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17656725" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cocaine/administration & dosage/pharmacology ; Dopamine/metabolism ; Excitatory Postsynaptic Potentials ; *Long-Term Synaptic Depression ; Methoxyhydroxyphenylglycol/analogs & derivatives/pharmacology ; Mice ; Mice, Inbred C57BL ; Neurons/metabolism ; Protein Biosynthesis ; Protein Kinases/metabolism ; RNA, Messenger/genetics/metabolism ; Receptors, AMPA/biosynthesis/*metabolism ; Receptors, Metabotropic Glutamate/*metabolism ; Synapses/*metabolism ; TOR Serine-Threonine Kinases ; Ventral Tegmental Area/cytology/drug effects/*metabolism
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  • 160
    Publication Date: 2007-09-18
    Description: Antibodies play a central role in immunity by forming an interface with the innate immune system and, typically, mediate proinflammatory activity. We describe a novel posttranslational modification that leads to anti-inflammatory activity of antibodies of immunoglobulin G, isotype 4 (IgG4). IgG4 antibodies are dynamic molecules that exchange Fab arms by swapping a heavy chain and attached light chain (half-molecule) with a heavy-light chain pair from another molecule, which results in bispecific antibodies. Mutagenesis studies revealed that the third constant domain is critical for this activity. The impact of IgG4 Fab arm exchange was confirmed in vivo in a rhesus monkey model with experimental autoimmune myasthenia gravis. IgG4 Fab arm exchange is suggested to be an important biological mechanism that provides the basis for the anti-inflammatory activity attributed to IgG4 antibodies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉van der Neut Kolfschoten, Marijn -- Schuurman, Janine -- Losen, Mario -- Bleeker, Wim K -- Martinez-Martinez, Pilar -- Vermeulen, Ellen -- den Bleker, Tamara H -- Wiegman, Luus -- Vink, Tom -- Aarden, Lucien A -- De Baets, Marc H -- van de Winkel, Jan G J -- Aalberse, Rob C -- Parren, Paul W H I -- New York, N.Y. -- Science. 2007 Sep 14;317(5844):1554-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Sanquin Research-AMC Landsteiner Laboratory, Department of Immunopathology, Plesmanlaan 125, 1066 CX Amsterdam, the Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17872445" target="_blank"〉PubMed〈/a〉
    Keywords: Allergens/immunology ; Animals ; Antibodies, Bispecific/immunology ; Antibodies, Monoclonal/immunology ; Antigens, CD20/immunology ; Antigens, Plant ; Autoantibodies/immunology ; Glycoproteins/immunology ; Humans ; Immunoglobulin Constant Regions/chemistry ; Immunoglobulin Fab Fragments/*chemistry/*immunology/metabolism ; Immunoglobulin G/*chemistry/*immunology/metabolism ; Immunoglobulin Heavy Chains ; Macaca mulatta ; Mice ; Mutation ; Myasthenia Gravis, Autoimmune, Experimental/immunology/prevention & control ; Protein Processing, Post-Translational ; Receptor, Epidermal Growth Factor/immunology ; Receptors, Cholinergic/immunology
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  • 161
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-04-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, Constance -- New York, N.Y. -- Science. 2007 Apr 20;316(5823):353.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17446359" target="_blank"〉PubMed〈/a〉
    Keywords: Amyotrophic Lateral Sclerosis/genetics/metabolism/*pathology ; Animals ; Astrocytes/*metabolism ; Cell Death ; Cell Line ; Cells, Cultured ; Embryonic Stem Cells/cytology ; Glutamic Acid/metabolism ; Humans ; Mice ; Motor Neurons/*pathology ; Mutation ; Superoxide Dismutase/*genetics/metabolism
    Print ISSN: 0036-8075
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  • 162
    Publication Date: 2007-11-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉van der Windt, Dirk J -- Kok, Niels F M -- Ijzermans, Jan -- New York, N.Y. -- Science. 2007 Nov 23;318(5854):1239-40; author reply 1239-40.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18033865" target="_blank"〉PubMed〈/a〉
    Keywords: Adenoma, Liver Cell/etiology/physiopathology ; Animals ; Carcinoma, Hepatocellular/*etiology ; Contraceptives, Oral, Hormonal/administration & dosage/adverse effects ; Disease Progression ; Estrogens/*administration & dosage/adverse effects ; Female ; Liver Diseases/complications ; Liver Neoplasms/etiology/*physiopathology ; Liver Neoplasms, Experimental/chemically induced/physiopathology ; Male ; Mice ; Risk Factors ; *Sex Characteristics
    Print ISSN: 0036-8075
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  • 163
    Publication Date: 2007-11-10
    Description: The identification of neural stem and progenitor cells (NPCs) by in vivo brain imaging could have important implications for diagnostic, prognostic, and therapeutic purposes. We describe a metabolic biomarker for the detection and quantification of NPCs in the human brain in vivo. We used proton nuclear magnetic resonance spectroscopy to identify and characterize a biomarker in which NPCs are enriched and demonstrated its use as a reference for monitoring neurogenesis. To detect low concentrations of NPCs in vivo, we developed a signal processing method that enabled the use of magnetic resonance spectroscopy for the analysis of the NPC biomarker in both the rodent brain and the hippocampus of live humans. Our findings thus open the possibility of investigating the role of NPCs and neurogenesis in a wide variety of human brain disorders.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039561/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039561/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Manganas, Louis N -- Zhang, Xueying -- Li, Yao -- Hazel, Raphael D -- Smith, S David -- Wagshul, Mark E -- Henn, Fritz -- Benveniste, Helene -- Djuric, Petar M -- Enikolopov, Grigori -- Maletic-Savatic, Mirjana -- 5K08 NS044276/NS/NINDS NIH HHS/ -- K08 NS044276/NS/NINDS NIH HHS/ -- K08 NS044276-01/NS/NINDS NIH HHS/ -- R01 NS032764/NS/NINDS NIH HHS/ -- R01-NS32764/NS/NINDS NIH HHS/ -- R21 NS053875/NS/NINDS NIH HHS/ -- R21 NS053875-01A1/NS/NINDS NIH HHS/ -- R21NS05875-1/NS/NINDS NIH HHS/ -- T32DK07521-16/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2007 Nov 9;318(5852):980-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉SUNY Stony Brook, Stony Brook, NY 11794, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17991865" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Adult Stem Cells/chemistry/*cytology ; Algorithms ; Animals ; Biomarkers/analysis/chemistry ; Brain/cytology/embryology ; Brain Chemistry ; Cell Differentiation ; Child ; Embryonic Stem Cells/chemistry/cytology ; Fatty Acids/*analysis/chemistry ; Female ; Hippocampus/chemistry/*cytology ; Humans ; Magnetic Resonance Spectroscopy/*methods ; Male ; Mice ; Neurons/chemistry/*cytology ; Protons ; Rats ; Signal Processing, Computer-Assisted ; Stem Cells/chemistry/*cytology
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  • 164
    Publication Date: 2007-03-24
    Description: The heart responds to diverse forms of stress by hypertrophic growth accompanied by fibrosis and eventual diminution of contractility, which results from down-regulation of alpha-myosin heavy chain (alphaMHC) and up-regulation of betaMHC, the primary contractile proteins of the heart. We found that a cardiac-specific microRNA (miR-208) encoded by an intron of the alphaMHC gene is required for cardiomyocyte hypertrophy, fibrosis, and expression of betaMHC in response to stress and hypothyroidism. Thus, the alphaMHC gene, in addition to encoding a major cardiac contractile protein, regulates cardiac growth and gene expression in response to stress and hormonal signaling through miR-208.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉van Rooij, Eva -- Sutherland, Lillian B -- Qi, Xiaoxia -- Richardson, James A -- Hill, Joseph -- Olson, Eric N -- New York, N.Y. -- Science. 2007 Apr 27;316(5824):575-9. Epub 2007 Mar 22.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17379774" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cardiac Myosins/genetics/metabolism ; Cardiomegaly/pathology/physiopathology ; Fibrosis ; Gene Deletion ; *Gene Expression Regulation ; Heart/physiopathology ; Heart Diseases/*genetics/pathology/physiopathology ; Hypothyroidism/physiopathology ; Introns ; Mediator Complex ; Mice ; Mice, Transgenic ; MicroRNAs/genetics/*physiology ; Myocardial Contraction ; Myocardium/*metabolism/*pathology ; Myocytes, Cardiac/pathology ; Myosin Heavy Chains/*genetics ; Oligonucleotide Array Sequence Analysis ; Rats ; Signal Transduction ; Stress, Physiological/physiopathology ; Transcription Factors/genetics/metabolism ; Triiodothyronine/metabolism ; Up-Regulation ; Ventricular Myosins/*genetics/metabolism
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  • 165
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-08-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, Jean -- New York, N.Y. -- Science. 2007 Aug 24;317(5841):1029-31.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17717165" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antineoplastic Agents/pharmacology/therapeutic use ; Cell Differentiation ; DNA Repair ; Female ; Humans ; Male ; Mice ; Neoplasm Metastasis ; Neoplasm Transplantation ; Neoplasms/*pathology/therapy ; Neoplastic Stem Cells/cytology/drug effects/*physiology ; Neovascularization, Pathologic ; Signal Transduction
    Print ISSN: 0036-8075
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  • 166
    Publication Date: 2007-12-01
    Description: JAM-C is an adhesion molecule that is expressed on cells within the vascular compartment and epithelial cells and, to date, has been largely studied in the context of inflammatory events. Using immunolabeling procedures in conjunction with confocal and electron microscopy, we show here that JAM-C is also expressed in peripheral nerves and that this expression is localized to Schwann cells at junctions between adjoining myelin end loops. Sciatic nerves from JAM-C-deficient [having the JAM-C gene knocked out (KO)] mice exhibited loss of integrity of the myelin sheath and defective nerve conduction as indicated by morphological and electrophysiological studies, respectively. In addition, behavioral tests showed motor abnormalities in the KO animals. JAM-C was also expressed in human sural nerves with an expression profile similar to that seen in mice. These results demonstrate that JAM-C is a component of the autotypic junctional attachments of Schwann cells and plays an important role in maintaining the integrity and function of myelinated peripheral nerves.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299566/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299566/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Scheiermann, Christoph -- Meda, Paolo -- Aurrand-Lions, Michel -- Madani, Rime -- Yiangou, Yiangos -- Coffey, Peter -- Salt, Thomas E -- Ducrest-Gay, Dominique -- Caille, Dorothee -- Howell, Owain -- Reynolds, Richard -- Lobrinus, Alexander -- Adams, Ralf H -- Yu, Alan S L -- Anand, Praveen -- Imhof, Beat A -- Nourshargh, Sussan -- 064920/Wellcome Trust/United Kingdom -- PG/03/123/16102/British Heart Foundation/United Kingdom -- R01 DK062283/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2007 Nov 30;318(5855):1472-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉National Heart and Lung Institute, Imperial College London, London, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18048693" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Cell Adhesion Molecules/*metabolism ; Humans ; Immunoglobulins/*metabolism ; Intercellular Junctions/metabolism ; Membrane Proteins/*metabolism ; Mice ; Mice, Knockout ; Myelin Sheath/metabolism/*physiology/ultrastructure ; Nerve Fibers, Myelinated/metabolism/*physiology/ultrastructure ; Neural Conduction ; Peripheral Nerves/*metabolism/physiology ; Peripheral Nervous System Diseases/metabolism/pathology/physiopathology ; Schwann Cells/*metabolism ; Sciatic Nerve/metabolism/physiology/ultrastructure ; Sural Nerve/metabolism/physiology
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  • 167
    Publication Date: 2007-03-17
    Description: Lymphocytes require sphingosine-1-phosphate (S1P) receptor-1 to exit lymphoid organs, but the source(s) of extracellular S1P and whether S1P directly promotes egress are unknown. By using mice in which the two kinases that generate S1P were conditionally ablated, we find that plasma S1P is mainly hematopoietic in origin, with erythrocytes a major contributor, whereas lymph S1P is from a distinct radiation-resistant source. Lymphocyte egress from thymus and secondary lymphoid organs was markedly reduced in kinase-deficient mice. Restoration of S1P to plasma rescued egress to blood but not lymph, and the rescue required lymphocyte expression of S1P-receptor-1. Thus, separate sources provide S1P to plasma and lymph to help lymphocytes exit the low-S1P environment of lymphoid organs. Disruption of compartmentalized S1P signaling is a plausible mechanism by which S1P-receptor-1 agonists function as immunosuppressives.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pappu, Rajita -- Schwab, Susan R -- Cornelissen, Ivo -- Pereira, Joao P -- Regard, Jean B -- Xu, Ying -- Camerer, Eric -- Zheng, Yao-Wu -- Huang, Yong -- Cyster, Jason G -- Coughlin, Shaun R -- HL07731/HL/NHLBI NIH HHS/ -- R01 HL065590/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2007 Apr 13;316(5822):295-8. Epub 2007 Mar 15.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cardiovascular Research Institute, University of California, San Francisco, 600 16th Street S472D, San Francisco, CA 94143-2240, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17363629" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bone Marrow/*metabolism ; Chemotaxis, Leukocyte/physiology ; Chromatography, Liquid ; Endothelium, Vascular ; Female ; Hematopoietic Stem Cells/metabolism ; Lymphocytes/metabolism/*physiology ; Lysophospholipids/*biosynthesis/blood/deficiency/*physiology ; Male ; Mice ; Mice, Inbred C57BL ; Phosphotransferases (Alcohol Group Acceptor)/genetics/metabolism ; Receptors, Lysosphingolipid/physiology ; Sphingosine/*analogs & derivatives/biosynthesis/blood/deficiency/physiology ; Tandem Mass Spectrometry
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  • 168
    Publication Date: 2007-06-26
    Description: Actin, which is best known as a cytoskeletal component, also participates in the control of gene expression. We report a function of nuclear actin in the regulation of MAL, a coactivator of the transcription factor serum response factor (SRF). MAL, which binds monomeric actin, is cytoplasmic in many cells but accumulates in the nucleus upon serum-induced actin polymerization. MAL rapidly shuttles between cytoplasm and nucleus in unstimulated cells. Serum stimulation effectively blocks MAL nuclear export, which requires MAL-actin interaction. Nuclear MAL binds SRF target genes but remains inactive unless actin binding is disrupted. Fluorescence resonance energy transfer analysis demonstrates that the MAL-actin interaction responds to extracellular signals. Serum-induced signaling is thus communicated to nuclear actin to control a transcriptional regulator.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vartiainen, Maria K -- Guettler, Sebastian -- Larijani, Banafshe -- Treisman, Richard -- New York, N.Y. -- Science. 2007 Jun 22;316(5832):1749-52.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Transcription Laboratory, Cancer Research UK, London Research Institute, Lincoln's Inn Fields Laboratories, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17588931" target="_blank"〉PubMed〈/a〉
    Keywords: 3T3 Cells ; Actins/*physiology ; *Active Transport, Cell Nucleus ; Animals ; Cell Nucleus/*metabolism ; Cytoplasm/metabolism ; Fluorescence Resonance Energy Transfer ; Gene Expression Regulation ; Green Fluorescent Proteins ; Mice ; Protein Binding ; Trans-Activators/*metabolism
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  • 169
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2007-06-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, Jean -- New York, N.Y. -- Science. 2007 Jun 8;316(5830):1416-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17556561" target="_blank"〉PubMed〈/a〉
    Keywords: Alzheimer Disease/*drug therapy/*metabolism/pathology ; Amyloid beta-Peptides/metabolism ; Amyloid beta-Protein Precursor/genetics ; Animals ; Anti-Inflammatory Agents/therapeutic use ; Brain/metabolism/pathology ; Disease Models, Animal ; Humans ; Mice ; Microtubules/metabolism ; Mutation ; Nerve Degeneration ; Neurofibrillary Tangles/pathology ; Neurons/pathology ; Phosphorylation ; Protein Kinase Inhibitors/therapeutic use ; Tubulin Modulators/therapeutic use ; tau Proteins/genetics/*metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 170
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    Publication Date: 2011-08-24
    Description: The NASA STARDUST mission collected thousands of particles from Comet Wild 2 that are now being studied by two hundred scientists around the world. The spacecraft captured the samples during a close flyby of the comet in 2004 and returned them to Earth with a dramatic entry into the atmosphere early in 2006. The precious cargo of comet dust is being studied to determine new information about the origin of the Sun and planets. The comet formed at the edge of the solar system, beyond the orbit of Neptune, and is a sample of the material from which the solar system was formed. One of the most dramatic early findings from the mission was that a comet that formed in the coldest place in the solar system contained minerals that formed in the hottest place in the solar system. The comet samples are telling stories of fire and ice and they providing fascinating and unexpected information about our origins.
    Keywords: Lunar and Planetary Science and Exploration
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  • 171
    Publication Date: 2019-04-04
    Description: The lunar surface is covered with a thick layer of sub-micron/micron size dust grains formed by meteoritic impact over billions of years. The fine dust grains are levitated and transported on the lunar surface, as indicated by the transient dust clouds observed over the lunar horizon during the Apollo 17 mission. Theoretical models suggest that the dust grains on the lunar surface are charged by the solar UV radiation as well as the solar wind. Even without any physical activity, the dust grains are levitated by electrostatic fields and transported away from the surface in the near vacuum environment of the Moon. The current dust charging and levitation models, however, do not fully explain the observed phenomena. Since the abundance of dust on the Moon s surface with its observed adhesive characteristics has the potential of severe impact on human habitat and operations and lifetime of a variety of equipment, it is necessary to investigate the charging properties and the lunar dust phenomena in order to develop appropriate mitigating strategies. Photoelectric emission induced by the solar UV radiation with photon energies higher than the work function of the grain materials is recognized to be the dominant process for charging of the lunar dust, and requires measurements of the photoelectric yields to determine the charging and equilibrium potentials of individual dust grains. In this paper, we present the first laboratory measurements of the photoelectric efficiencies and yields of individual sub-micron/micron size dust grains selected from sample returns of Apollo 17, and Luna 24 missions, as well as similar size dust grains from the JSC-1 simulants. The measurements were made on a laboratory facility based on an electrodynamic balance that permits a variety of experiments to be conducted on individual sub-micron/micron size dust grains in simulated space environments. The photoelectric emission measurements indicate grain size dependence with the yield increasing by an order of magnitude for grains of sub-micron to several micron size radii, at which it reaches asymptotic values. The yield for large size grains is found to be more than an order of magnitude higher than the bulk measurements on lunar fines reported in the literature.
    Keywords: Lunar and Planetary Science and Exploration
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  • 172
    Publication Date: 2018-06-11
    Description: The Martian ionosphere's local total electron content (TEC) and the neutral atmosphere scale height can be derived from radar echoes reflected from the surface of the planet. We report the global distribution of the TEC by analyzing more than 750,000 echoes of the Mars Advanced Radar for Subsurface and Ionospheric Sounding (MARSIS). This is the first direct measurement of the TEC of the Martian ionosphere. The technique used in this paper is a novel 'transmission-mode' sounding of the ionosphere of Mars in contrast to the Active Ionospheric Sounding experiment (AIS) on MARSIS, which generally operates in the reflection mode. This technique yields a global map of the TEC for the Martian ionosphere. The radar transmits a wideband chirp signal that travels through the ionosphere before and after being reflected from the surface. The received waves are attenuated, delayed and dispersed, depending on the electron density in the column directly below the spacecraft. In the process of correcting the radar signal, we are able to estimate the TEC and its global distribution with an unprecedented resolution of about 0.1 deg in latitude (5 km footprint). The mapping of the relative geographical variations in the estimated nightside TEC data reveals an intricate web of high electron density regions that correspond to regions where crustal magnetic field lines are connected to the solar wind. Our data demonstrates that these regions are generally but not exclusively associated with areas that have magnetic field lines perpendicular to the surface of Mars. As a result, the global TEC map provides a high-resolution view of where the Martian crustal magnetic field is connected to the solar wind. We also provide an estimate of the neutral atmospheric scale height near the ionospheric peak and observe temporal fluctuations in peak electron density related to solar activity.
    Keywords: Lunar and Planetary Science and Exploration
    Type: Geophysical Research Letters; Volume 34; 2007
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  • 173
    Publication Date: 2018-06-11
    Description: Iapetus has preserved evidence that constrains the modeling of its geophysical history from the time of its accretion until now. The evidence is (a) its present 79.33-day rotation or spin rate, (b) its shape that corresponds to the equilibrium figure for a hydrostatic body rotating with a period of approximately 16 h, and (c) its high, equatorial ridge, which is unique in the Solar System. This paper reports the results of an investigation into the coupling between Iapetus' thermal and orbital evolution for a wide range of conditions including the spatial distributions with time of composition, porosity, short-lived radioactive isotopes (SLRI), and temperature. The thermal model uses conductive heat transfer with temperature-dependent conductivity. Only models with a thick lithosphere and an interior viscosity in the range of about the water ice melting point can explain the observed shape. Short-lived radioactive isotopes provide the heat needed to decrease porosity in Iapetus? early history. This increases thermal conductivity and allows the development of the strong lithosphere that is required to preserve the 16-h rotational shape and the high vertical relief of the topography. Long-lived radioactive isotopes and SLRI raise internal temperatures high enough that significant tidal dissipation can start, and despin Iapetus to synchronous rotation. This occurred several hundred million years after Iapetus formed. The models also constrain the time when Iapetus formed because the successful models are critically dependent upon having just the right amount of heat added by SLRI decay in this early period. The amount of heat available from short-lived radioactivity is not a free parameter but is fixed by the time when Iapetus accreted, by the canonical concentration of Al-26, and, to a lesser extent, by the concentration of Fe-60. The needed amount of heat is available only if Iapetus accreted between 2.5 and 5.0Myr after the formation of the calcium aluminum inclusions as found in meteorites. Models with these features allow us to explain Iapetus? present synchronous rotation, its fossil 16-h shape, and the context within which the equatorial ridge arose.
    Keywords: Lunar and Planetary Science and Exploration
    Type: Icarus; Volume 190; 179-202
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  • 174
    Publication Date: 2018-06-11
    Description: Shock recovery experiments to determine whether magnetite could be produced by the decomposition of iron-carbonate were initiated. Naturally occurring siderite was first characterized by electron microprobe (EMP), transmission electron microscopy (TEM), Mossbauer spectroscopy, and magnetic susceptibility measurements to be sure that the starting material did not contain detectable magnetite. Samples were shocked in tungsten-alloy holders (W=90%, Ni=6%, Cu=4%) to further insure that any iron phases in the shock products were contributed by the siderite rather than the sample holder. Each sample was shocked to a specific pressure between 30 to 49 GPa. Previously reported results of TEM analyses on 49 GPa experiments indicated the presence of nano-phase spinel-structured iron oxide. Transformation of siderite to magnetite as characterized by TEM was found in the 49 GPa shock experiment. Compositions of most magnetites are greater than 50% Fe sup(+2) in the octahedral site of the inverse spinel structure. Magnetites produced in shock experiments display the same range of single-domain, superparamagnetic sizes (approx. 50 100 nm), compositions (100% magnetite to 80% magnetite-20% magnesioferrite), and morphologies (equant, elongated, euhedral to subhedral) as magnetites synthesized by Golden et al. (2001) or magnetites grown naturally by MV1 magnetotactic bacteria, and as the magnetites in Martian meteorite ALH84001. Fritz et al. (2005) previously concluded that ALH84001 experienced approx. 32 GPa pressure and a resultant thermal pulse of approx. 100 - 110 C. However, ALH84001 contains evidence of local temperature excursions high enough to 1 melt feldspar, pyroxene, and a silica-rich phase. This 49 GPa experiment demonstrates that magnetite can be produced by the shock decomposition of siderite as a result of local heating to greater than 470 C. Therefore, magnetite in the rims of carbonates in Martian meteorite ALH84001 could be a product of shock devolatilization of siderite as well.
    Keywords: Lunar and Planetary Science and Exploration
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  • 175
    Publication Date: 2018-06-11
    Description: The Imager for Mars Pathfinder (IMP) was a mast-mounted instrument on the Mars Pathfinder lander which landed on Mars Ares Vallis floodplain on July 4, 1997. During the 83 sols of Mars Pathfinders landed operations, the IMP collected over 16,600 images. Multispectral images were collected using twelve narrowband filters at wavelengths between 400 and 1000 nm in the visible and near infrared (VNIR) range. The IMP provided VNIR spectra of the materials surrounding the lander including rocks, bright soils, dark soils, and atmospheric observations. During the primary mission, only a single primary rock spectral class, Gray Rock, was recognized; since then, Black Rock, has been identified. The Black Rock spectra have a stronger absorption at longer wavelengths than do Gray Rock spectra. A number of coated rocks have also been described, the Red and Maroon Rock classes, and perhaps indurated soils in the form of the Pink Rock class. A number of different soil types were also recognized with the primary ones being Bright Red Drift, Dark Soil, Brown Soil, and Disturbed Soil. Examination of spectral parameter plots indicated two trends which were interpreted as representing alteration products formed in at least two different environmental epochs of the Ares Vallis area. Subsequent analysis of the data and comparison with terrestrial analogs have supported the interpretation that the rock coatings provide evidence of earlier martian environments. However, the presence of relatively uncoated examples of the Gray and Black rock classes indicate that relatively unweathered materials can persist on the martian surface.
    Keywords: Lunar and Planetary Science and Exploration
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  • 176
    Publication Date: 2018-06-11
    Description: Multispectral imaging from the Panoramic Camera (Pancam) instruments on the Mars Exploration Rovers Spirit and Opportunity has provided important new insights about the geology and geologic history of the rover landing sites and traverse locations in Gusev crater and Meridiani Planum. Pancam observations from near-UV to near-IR wavelengths provide limited compositional and mineralogic constraints on the presence abundance, and physical properties of ferric- and ferrous-iron bearing minerals in rocks, soils, and dust at both sites. High resolution and stereo morphologic observations have also helped to infer some aspects of the composition of these materials at both sites. Perhaps most importantly, Pancam observations were often efficiently and effectively used to discover and select the relatively small number of places where in situ measurements were performed by the rover instruments, thus supporting and enabling the much more quantitative mineralogic discoveries made using elemental chemistry and mineralogy data. This chapter summarizes the major compositionally- and mineralogically-relevant results at Gusev and Meridiani derived from Pancam observations. Classes of materials encountered in Gusev crater include outcrop rocks, float rocks, cobbles, clasts, soils, dust, rock grindings, rock coatings, windblown drift deposits, and exhumed whitish/yellowish salty soils. Materials studied in Meridiani Planum include sedimentary outcrop rocks, rock rinds, fracture fills, hematite spherules, cobbles, rock fragments, meteorites, soils, and windblown drift deposits. This chapter also previews the results of a number of coordinated observations between Pancam and other rover-based and Mars-orbital instruments that were designed to provide complementary new information and constraints on the mineralogy and physical properties of martian surface materials.
    Keywords: Lunar and Planetary Science and Exploration
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  • 177
    Publication Date: 2018-06-11
    Description: Home Plate is a layered plateau in Gusev crater on Mars. It is composed of clastic rocks of moderately altered alkali basalt composition, enriched in some highly volatile elements. A coarse-grained lower unit is overlain by a finer-grained upper unit. Textural observations indicate that the lower strata were emplaced in an explosive event, and geochemical considerations favor an explosive volcanic origin over an impact origin. The lower unit likely represents accumulation of pyroclastic materials, while the upper unit may represent eolian reworking of the same pyroclastic materials.
    Keywords: Lunar and Planetary Science and Exploration
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  • 178
    Publication Date: 2018-06-11
    Description: Aluminium foils were used on Stardust to stabilize the aerogel specimens in the modular collector tray. Part of these foils were fully exposed to the flux of cometary grains emanating from Wild 2. Because the exposed part of these foils had to be harvested before extraction of the aerogel, numerous foil strips some 1.7 mm wide and 13 or 33 mm long were generated during Stardusts's Preliminary Examination (PE). These strips are readily accommodated in their entirety in the sample chambers of modern SEMs, thus providing the opportunity to characterize in situ the size distribution and residue composition - employing EDS methods - of statistically more significant numbers of cometary dust particles compared to aerogel, the latter mandating extensive sample preparation. We describe here the analysis of nearly 300 impact craters and their implications for Wild 2 dust.
    Keywords: Lunar and Planetary Science and Exploration
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  • 179
    Publication Date: 2018-06-11
    Description: This paper describes our flight aboard NASA's C9 Weightless Wonder, more affectionately known as The Vomit Comet. The C9 is NASA's aircraft that creates multiple periods of microgravity by conducting a series of parabolic maneuvers over the Gulf of Mexico.
    Keywords: Lunar and Planetary Science and Exploration
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  • 180
    Publication Date: 2018-06-11
    Description: Recent chondritic meteorite finds in Antarctica have included CB, CH, CK and R chondrites, the latter two of which are among the most oxidized materials found in meteorite collections. In this study we present petrographic and mineralogic data for a suite of CK and R chondrites, and compare to previous studies of CK and R, as well as some CV chondrites. In particular we focus on the opaque minerals magnetite, chromite, sulfides, and metal as well as unusual silicates hornblende, biotite, and plagioclase. Several mineral thermometers and oxy-barometers are utilized to calculate temperatures and oxygen fugacities for these unusual meteorites compared to other more common chondrite groups. R and CK chondrites show lower equilibrium temperatures than ordinary chondrites, even though they are at similar petrologic grades (e.g., thermal type 6). Oxygen fugacity calculated for CV and R chondrites ranges from values near the iron-wustite (IW) oxygen buffer to near the fayalite-magnetite-quartz (FMQ) buffer. In comparison, the fO2 recorded by ilmenite-magnetite pairs from CK chondrites are much higher, from FMQ+3.1 to FMQ+5.2. The latter values are the highest recorded for materials in meteorites, and place some constraints on the formation conditions of these magnetite-bearing chondrites. Differences between mineralogic and O isotopic compositions of CK and R chondrites suggest two different oxidation mechanisms, which may be due to high and low water: rock ratios during metamorphism, or to different fluid compositions, or both.
    Keywords: Lunar and Planetary Science and Exploration
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  • 181
    Publication Date: 2018-06-11
    Description: SIMS U-Pb analyses show that zircons from breccias from Apollo 14 and Apollo 17 have essentially identical age distributions in the range 4350 to 4200 Ma but, whereas Apollo 14 zircons additionally show ages from 4200 to 3900 Ma, the Apollo 17 samples have no zircons with ages 〈4200 Ma. The zircon results also show an uneven distribution with distinct peaks of magmatic activity. In explaining these observations we propose that periodic episodes of KREEP magmatism were generated from a primary reservoir of KREEP magma, which contracted over time towards the centre of Procellarum KREEP terrane.
    Keywords: Lunar and Planetary Science and Exploration
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  • 182
    Publication Date: 2018-06-11
    Description: A viewgraph describing the food system that NASA is developing for Manned Mars Missions is shown. The topics include: 1) The President's Vision for U.S. Space Exploration -January 14, 2004; 2) Introducing Orion (and Ares); 3) Mercury (1961-1963); 4) Gemini (1965-1966); 5) Apollo (1968-1972); 6) Skylab (1973-1974); 7) Shuttle/Mir (1995-1998); 8) Shuttle (1981-present) International Space Station (2000-present); 9) NASA Stored Food System; 10) Advanced Food Technology; 11) Orion Missions; 12) Orion Challenges; 13) Food Packaging; 14) Mars Mission Assumptions; 15) Planetary Food System Selected Crops; 16) Food Processing Equipment Constraints; 17) Crew Involvement Constraints; 18) Advanced Food Technology Integration; 19) Research Highlights Internal; and 20) Research Highlights External.
    Keywords: Lunar and Planetary Science and Exploration
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  • 183
    Publication Date: 2018-06-11
    Description: Systematic in-situ FTIR heating experiments of Tagish Lake meteorite grains have been performed in order to study thermal stability of chondritic organics. Some aliphatic model organic substances have also been used to elucidate effects of hydrous phyllosilicate minerals on the thermal stability of organics. The experimental results indicated that organic matter in the Tagish Lake meteorite might contain oxygenated aliphatic hydrocarbons which are thermally stable carbonyls such as ester and/or C=O in ring compounds. The presence of hydrous phyllosilicate minerals has a pronounced effect on the increase of the thermal stability of aliphatic and oxygenated functions. These oxygenated aliphatic organics in Tagish Lake can be formed during the aqueous alteration in the parent body and the formation temperature condition might be less than 200 C, based especially on the thermal stability of C-O components. The hydrous phyllosilicates might provide sites for organic globule formation and protected some organic decomposition
    Keywords: Lunar and Planetary Science and Exploration
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  • 184
    Publication Date: 2018-06-11
    Description: CR carbonaceous chondrites are of the major interest since they contain one of the most primitive organic matters. However, aqueous alteration has more or less overprinted their original features in a way that needed to be assessed. That was done in the present study by comparing the mineralogy of the most altered CR1 chondrite, GRO 95577, to a less altered CR2, Renazzo. Their modal analyses were achieved thanks to a new method, based on X-ray elemental maps acquired on electron microprobe, and on IDL image treatment. It allowed the collection of new data on the composition of Renazzo and confirmed the classification of GRO 95577 as a CR1. New alteration products for CRs, vermiculite and clinochlore, were observed. The homogeneity of the Fe-poor clays in the CR1 and the distinctive matrix composition in the two chondrites suggest a wide-range of aqueous alteration on CRs. The preservation of the outlines of the chondrules in GRO 95577 and the elemental transfers of Al, Fe and Ca throughout the chondrule and of Fe and S from the matrix to the chondrule favor the idea of an asteroidal location of the aqueous alteration. From their mineralogical descriptions and modal abundances, the element repartitions in Renazzo and GRO 95577 were computed. It indicates a possible relationship between these two chondrites via an isochemical alteration process. Knowing the chemical reactions that occurred during the alteration, it was thus possible to decipher the mineralogical modal abundances in the unaltered CR body.
    Keywords: Lunar and Planetary Science and Exploration
    Type: Meteoritics and Planetary Science, projected release date Jan. 1, 2007
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  • 185
    Publication Date: 2018-06-12
    Description: The lunar surface is covered with a thick layer of sub-micron/micron size dust grains formed by meteoritic impact over billions of years. The fine dust grains are levitated and transported on the lunar surface, as indicated by the transient dust clouds observed over the lunar horizon during the Apollo 17 mission. Theoretical models suggest that the dust grains on the lunar surface are charged by the solar ultraviolet (UV) radiation as well as the solar wind. Even without any physical activity, the dust grains are levitated by electrostatic fields and transported away from the surface in the near vacuum environment of the Moon. The current dust charging and levitation models, however, do not fully explain the observed phenomena. Since the abundance of dust on the Moon's surface with its observed adhesive characteristics has the potential of severe impact on human habitat and operations and lifetime of a variety of equipment, it is necessary to investigate the charging properties and the lunar dust phenomena in order to develop appropriate mitigating strategies. Photoelectric emission induced by the solar UV radiation with photon energies higher than the work function (WF) of the grain materials is recognized to be the dominant process for charging of the lunar dust, and requires measurements of the photoelectric yields to determine the charging and equilibrium potentials of individual dust grains. In this paper, we present the first laboratory measurements of the photoelectric efficiencies and yields of individual sub-micron/micron size dust grains selected from sample returns of Apollo 17 and Luna-24 missions as well as similar size dust grains from the JSC-1 simulants. The measurements were made on a laboratory facility based on an electrodynamic balance that permits a variety of experiments to be conducted on individual sub-micron/micron size dust grains in simulated space environments. The photoelectric emission measurements indicate grain size dependence with the yield increasing by an order of magnitude for grains of sub-micron to several micron size radii, at which it reaches asymptotic values. The yield for large size grains is found to be more than an order of magnitude higher than the bulk measurements on lunar fines reported in the literature.
    Keywords: Lunar and Planetary Science and Exploration
    Type: Planetary and Space Science; Volume 55; No. 7-8; 953-965
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  • 186
    facet.materialart.
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    In:  Other Sources
    Publication Date: 2018-06-12
    Description: Presents a supplemental video supporting the original conference presentation under the same title. The conference presentation discussed NASA's preparation for its return to the moon with the Lunar CRater Observation and Sensing Satellite (LCROSS) mission which will robotically seek to determine the presence of water ice at the Moon's South Pole. This secondary payload spacecraft will travel with the Lunar Reconnaissance Orbiter (LRO) satellite to the Moon on the same Atlas-V 401 Centaur rocket launched from Cape Canaveral Air Force Station, Florida. The 1000kg Secondary Payload budget is efficiently used to provide a highly modular and reconfigurable LCROSS Spacecraft with extensive heritage to accurately guide the expended Centaur into the crater. Upon separation, LCROSS flies through the impact plume, telemetering real-time images and characterizing water ice in the plume with infrared cameras and spectrometers. LCROSS then becomes a 700kg impactor itself, to provide a second opportunity to study the nature of the Lunar Regolith. LCROSS provides a critical ground-truth for Lunar Prospector and LRO neutron and radar maps, making it possible to assess the total lunar water inventory. The video contains an animated simulation of the Centaur launch, LRO separation, LRO high resolution lunar survey, LCROSS mission elements and LCROSS impactor separation and impact observations.
    Keywords: Lunar and Planetary Science and Exploration
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  • 187
    facet.materialart.
    Unknown
    In:  CASI
    Publication Date: 2018-06-06
    Description: Vision tasks include: a) Complete the International Space Station; b) Safely fly the Space Shuttle until 2010; c) Develop and fly the Crew Exploration Vehicle (by 2014); d) Return to the moon (by 2020); e) Sustained and affordable human and robotic program; f) Develop innovative technologies, knowledge, and infrastructures; and g) Promote international and commercial participation.
    Keywords: Lunar and Planetary Science and Exploration
    Type: 2006 NASA Seal/Secondary Air System Workshop; Volume 1; 39-57; NASA/CP-2007-214995/VOL1
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  • 188
    facet.materialart.
    Unknown
    In:  CASI
    Publication Date: 2018-06-12
    Description: NASA is preparing for its return to the moon with the Lunar CRater Observation and Sensing Satellite (LCROSS) mission. This secondary payload spacecraft will travel with the Lunar Reconnaissance Orbiter (LRO) satellite to the Moon on the same Atlas-V 401 Centaur rocket launched from Cape Canaveral Air Force Station, Florida. The LCROSS mission will robotically seek to determine the presence of water ice at the Moon's South Pole. The 1000kg Secondary Payload budget is efficiently used to provide a highly modular and reconfigurable LCROSS Spacecraft with extensive heritage to accurately guide the expended Centaur into the crater. Upon separation, LCROSS flies through the impact plume, telemetering real-time images and characterizing water ice in the plume with infrared cameras and spectrometers. LCROSS then becomes a 700kg impactor itself, to provide a second opportunity to study the nature of the Lunar Regolith. LCROSS provides a critical ground-truth for Lunar Prospector and LRO neutron and radar maps, making it possible to assess the total lunar water inventory. This presentation contains a reference to video animation of the LCROSS mission that will be covered separately.
    Keywords: Lunar and Planetary Science and Exploration
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  • 189
    Publication Date: 2018-06-12
    Description: In January 2004, President Bush announced a new vision for space exploration. This included retirement of the current Space Shuttle fleet by 2010 and the development of new set of launch vehicles. The President's vision did not include significant increases in the NASA budget, so these development programs need to be cost conscious. Current trade study procedures address factors such as performance, reliability, safety, manufacturing, maintainability, operations, and costs. It would be desirable, however, to have increased insight into the cost factors behind each of the proposed system architectures. This paper reports on a set of component trade studies completed on the upper stage engine for the new launch vehicles. Increased insight into architecture costs was developed by including a Net Present Value (NPV) method and applying a set of associated risks to the base parametric cost data. The use of the NPV method along with the risks was found to add fidelity to the trade study and provide additional information to support the selection of a more robust design architecture.
    Keywords: Lunar and Planetary Science and Exploration
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  • 190
    Publication Date: 2018-06-06
    Description: In this chapter we examine what can be learned about extrasolar planet atmospheres by concentrating on a class of planets that transit their parent stars. As discussed in the previous chapter, one way of detecting an extrasolar planet is by observing the drop in stellar intensity as the planet passes in front of the star. A transit represents a special case in which the geometry of the planetary system is such that the planet s orbit is nearly edge-on as seen from Earth. As we will explore, the transiting planets provide opportunities for detailed follow-up observations that allow physical characterization of extrasolar planets, probing their bulk compositions and atmospheres.
    Keywords: Lunar and Planetary Science and Exploration
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  • 191
    Publication Date: 2018-06-11
    Description: The Mars Reconnaissance Orbiter (MRO) is the latest addition to the suite of missions on or orbiting Mars as part of the NASA Mars Exploration Program. Launched on 12 August 2005, the orbiter successfully entered Mars orbit on 10 March 2006 and finished aerobraking on 30 August 2006. Now in its near-polar, near-circular, low-altitude (approximately 300 km), 3 p.m. orbit, the spacecraft is operating its payload of six scientific instruments throughout a one-Mars-year Primary Science Phase (PSP) of global mapping, regional survey, and targeted observations. Eight scientific investigations were chosen for MRO, two of which use either the spacecraft accelerometers or tracking of the spacecraft telecom signal to acquire data needed for analysis. Six instruments, including three imaging systems, a visible-near infrared spectrometer, a shallow-probing subsurface radar, and a thermal-infrared profiler, were selected to complement and extend the capabilities of current working spacecraft at Mars. Whether observing the atmosphere, surface, or subsurface, the MRO instruments are designed to achieve significantly higher resolution while maintaining coverage comparable to the current best observations. The requirements to return higher-resolution data, to target routinely from a low-altitude orbit, and to operate a complex suite of instruments were major challenges successfully met in the design and build of the spacecraft, as well as by the mission design. Calibration activities during the seven-month cruise to Mars and limited payload operations during a three-day checkout prior to the start of aerobraking demonstrated, where possible, that the spacecraft and payload still had the functions critical to the science mission. Two critical events, the deployment of the SHARAD radar antenna and the opening of the CRISM telescope cover, were successfully accomplished in September 2006. Normal data collection began 7 November 2006 after solar conjunction. As part of its science mission, MRO will also aid identification and characterization of the most promising sites for future landed missions, both in terms of safety and in terms of the scientific potential for future discovery. Ultimately, MRO data will advance our understanding of how Mars has evolved and by which processes that change occurs, all within a framework of identifying the presence, extent, and role of water in shaping the planet s climate over time.
    Keywords: Lunar and Planetary Science and Exploration
    Type: Journal Of Geophysical Research; Volume 112
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  • 192
    Publication Date: 2018-06-11
    Description: The aeroheating environment of the Mars Reconnaissance Orbiter (MRO) has been analyzed using the direct simulation Monte Carlo and free-molecular techniques. The results of these analyses were used to develop an aeroheating database to be used for the preflight planning and the in-flight operations support for the aerobraking phase of the MRO mission. The aeroheating predictions calculated for the MRO include the heat transfer coefficient (CH) over a range of angles-of-attack, sideslip angles, and number densities. The effects of flow chemistry, surface temperature, and surface grid resolution were also investigated to determine the aeroheating database uncertainties. Flight heat flux data has been calculated from surface temperature sensor data returned to Earth from the MRO in orbit around Mars during the aerobraking phase of its mission. The heat flux data have been compared to the aeroheating database and agree favorably.
    Keywords: Lunar and Planetary Science and Exploration
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  • 193
    Publication Date: 2018-06-06
    Description: NASA is considering that its Mars Exploration Program (MEP) will launch an orbiter to Mars in the 2013 launch opportunity. To further explore this opportunity, NASA has formed a Science Definition Team (SDT) for this orbiter mission, provisionally called the Mars Science Orbiter (MSO). Membership and leadership of the SDT are given in Appendix 1. Dr. Michael D. Smith chaired the SDT. The purpose of the SDT was to define the: 1) Scientific objectives of an MSO mission to be launched to Mars no earlier than the 2013 launch opportunity, building on the findings for Plan A [Atmospheric Signatures and Near-Surface Change] of the Mars Exploration Program Analysis Group (MEPAG) Second Science Analysis Group (SAG-2); 2) Science requirements of instruments that are most likely to make high priority measurements from the MSO platform, giving due consideration to the likely mission, spacecraft and programmatic constraints. The possibilities and opportunities for international partners to provide the needed instrumentation should be considered; 3) Desired orbits and mission profile for optimal scientific return in support of the scientific objectives, and the likely practical capabilities and the potential constraints defined by the science requirements; and 4) Potential science synergies with, or support for, future missions, such as a Mars Sample Return. This shall include imaging for evaluation and certification of future landing sites. As a starting point, the SDT was charged to assume spacecraft capabilities similar to those of the Mars Reconnaissance Orbiter (MRO). The SDT was further charged to assume that MSO would be scoped to support telecommunications relay of data from, and commands to, landed assets, over a 10 Earth year period following orbit insertion. Missions supported by MSO may include planned international missions such as EXOMARS. The MSO SDT study was conducted during October - December 2007. The SDT was directed to complete its work by December 15, 2007. This rapid turn-around was required in order to allow time to prepare an Announcement of Opportunity (AO) for science investigations, to be released in early 2008.
    Keywords: Lunar and Planetary Science and Exploration
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  • 194
    Publication Date: 2018-06-06
    Description: Water ices in surface crusts of Europa, Enceladus, Saturn's main rings, and Kuiper Belt Objects can become heavily oxidized from radiolytic chemical alteration of near-surface water ice by space environment irradiation. Oxidant accumulations and gas production are manifested in part through observed H2O2 on Europa. tentatively also on Enceladus, and found elsewhere in gaseous or condensed phases at moons and rings of Jupiter and Saturn. On subsequent chemical contact in sub-surface environments with significant concentrations of primordially abundant reductants such as NH3 and CH4, oxidants of radiolytic origin can react exothermically to power gas-driven cryovolcanism. The gas-piston effect enormously amplifies the mass flow output in the case of gas formation at basal thermal margins of incompressible fluid reservoirs. Surface irradiation, H2O2 production, NH3 oxidation, and resultant heat, gas, and gas-driven mass flow rates are computed in the fluid reservoir case for selected bodies. At Enceladus the oxidant power inputs are comparable to limits on nonthermal kinetic power for the south polar plumes. Total heat output and plume gas abundance may be accounted for at Enceladus if plume activity is cyclic in high and low "Old Faithful" phases, so that oxidants can accumulate during low activity phases. Interior upwelling of primordially abundant NH3 and CH4 hydrates is assumed to resupply the reductant fuels. Much lower irradiation fluxes on Kuiper Belt Objects require correspondingly larger times for accumulation of oxidants to produce comparable resurfacing, but brightness and surface composition of some objects suggest that such activity may be ongoing.
    Keywords: Lunar and Planetary Science and Exploration
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  • 195
    Publication Date: 2018-06-11
    Description: North-West-Africa 3171 is a 506 g, relatively fresh appearing, basaltic shergottite with similarities to Zagami and Shergotty, but not obviously paired with any of the other known African basaltic shergottites. Its exposure age has the range of 2.5-3.1 Myr , similar to those of Zagami and Shergotty. We made AR-39-AR-40 analyses of a "plagioclase" (now shock-converted to maskelynite) separate and of a glass hand-picked from a vein connected to shock melt pockets.. Plagioclase was separated using its low magnetic susceptibility and then heavy liquid with density of 〈2.85 g/cm(exp 3). The AR-39-AR-40 age spectrum of NWA-317 1 plag displays a rise in age over 20-100% of the 39Ar release, from 0.24 Gyr to 0.27 Gy.
    Keywords: Lunar and Planetary Science and Exploration
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  • 196
    Publication Date: 2018-06-11
    Description: NASA Johnson Space Center (JSC) personnel assisted Kennedy Space Center (KSC) inspection teams in the identification of 41 micrometeoroid/orbital debris (MMOD) impact sites on the OV-103 vehicle (Discovery) during STS-114 postflight inspections. There were 14 MMOD impacts reported on the crew module windows (Figure 1). The largest impact feature, a 6.6 mm x 5.8 mm crater on window #4, was caused by a particle with an estimated diameter of 0.22 mm (Figure 2). This impact was among the largest ever recorded on a crew module window. The window was removed and replaced. Scanning Electron Microscope/Energy Dispersive X-ray (SEM/EDX) analysis of dental mold samples from the impact site to determine particle origin was inconclusive, possibly due to contamination picked up on the ferry flight from Edwards Air Force Base to KSC. The radiators on the inside of the payload bay doors sustained 19 impacts (Figure 3) with one of the impacts causing a face sheet perforation. The 0.61 mm diameter hole was produced by a particle with an estimated diameter of 0.4 mm, which approaches the 0.5-mm critical particle diameter of the wing leading edge reinforced carbon-carbon (RCC) panel high-temperature regions (Zone 3, Figure 4) that was established during Return to Flight testing of the RCC panels. An inspection of the payload bay door exterior insulation (FRSI) revealed a 5.8 mm x 4.5 mm defect that was caused by an MMOD particle with unknown composition, as the sample obtained was contaminated. Figure 5 provides a summary of the exterior surface survey that was conducted following the STS-114 mission. Two windows were removed and replaced due to hypervelocity impact. Nineteen impacts were recorded on the payload bay door radiators, with one face sheet penetration. Three impact sites were identified on the FRSI. There were four hypervelocity impact sites detected on the wing leading edge RCC panels. One impact was detected on the top cover of the TPS sample box (TSB) payload that was mounted on a carrier in the aft portion of the payload bay.
    Keywords: Lunar and Planetary Science and Exploration
    Type: Orbital Debris Quarterly News; 2-3
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  • 197
    facet.materialart.
    Unknown
    In:  Other Sources
    Publication Date: 2019-07-27
    Description: This paper will summarize the study that was conducted under the auspices of the National Aeronautics and Space Administration (NASA), lead by Johnson Space Center s Engineering Directorate in support of the Lunar Lander Preparatory Study (LLPS) as sponsored by the Constellation Program Office (CxPO), Advanced Projects Office (APO). The lunar lander conceptual design and analysis is intended to provide an understanding of requirements for human space exploration of the Moon using the Advanced Projects Office Pre-Lander Project Office selected "HabiTank" Lander concept. In addition, these analyses help identify system "drivers," or significant sources of cost, performance, risk, and schedule variation along with areas needing technology development. Recommendations, results, and conclusions in this paper do not reflect NASA policy or programmatic decisions. This paper is an executive summary of this study.
    Keywords: Lunar and Planetary Science and Exploration
    Type: Rept-2007-01-3058 , International Conference on Environmental Systems; 9-12, 2007; Chicago, Il; United States
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  • 198
    Publication Date: 2019-07-27
    Description: The near-Earth orbital debris population will continue to increase in the future due to ongoing space activities, on-orbit explosions, and accidental collisions among resident space objects. Commonly adopted mitigation measures, such as limiting postmission orbital lifetimes of satellites to less than 25 years, will slow down the population growth, but may be insufficient to stabilize the environment. The nature of the growth, in the low Earth orbit (LEO) region, is further demonstrated by a recent study where no future space launches were conducted in the environment projection simulations. The results indicate that, even with no new launches, the LEO debris population would remain relatively constant for only the next 50 years. Beyond that, the debris population would begin to increase noticeably, due to the production of collisional debris. Therefore, to better limit the growth of future debris population to protect the environment, remediation option, i.e., removing existing large and massive objects from orbit, needs to be considered. This paper does not intend to address the technical or economical issues for active debris removal. Rather, the objective is to provide a sensitivity study to quantify the effectiveness of various remediation options. A removal criterion based upon mass and collision probability is developed to rank objects at the beginning of each projection year. This study includes simulations with removal rates ranging from 2 to 20 objects per year, starting in the year 2020. The outcome of each simulation is analyzed, and compared with others. The summary of the study serves as a general guideline for future debris removal consideration.
    Keywords: Lunar and Planetary Science and Exploration
    Type: 58th International Astronautical Congress; 24-28 Sept. 2007; Hyderabad; India
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  • 199
    facet.materialart.
    Unknown
    In:  CASI
    Publication Date: 2019-07-27
    Description: A viewgraph presentation exploring Earth and its analogues is shown. The topics include: 1) ESMD Goals for the Use of Earth Analogues; 2) Stakeholders Summary; 3) Issues with Current Analogue Situation; 4) Current state of Analogues; 5) External Implementation Plan (Second Step); 6) Recent Progress in Utilizing Analogues; 7) Website Layout Example-Home Page; 8) Website Layout Example-Analogue Site; 9) Website Layout Example-Analogue Mission; 10) Objectives of ARDIG Analog Initiatives; 11) Future Plans; 12) Example: Cold-Trap Sample Return; 13) Example: Site Characterization Matrix; 14) Integrated Analogue Studies-Prerequisites for Human Exploration; and 15) Rating Scale Definitions.
    Keywords: Lunar and Planetary Science and Exploration
    Type: 2nd International WOrkshop: Exploring Mars and Its Earth Analogues; 1923 June 2007; Trento; Italy
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  • 200
    Publication Date: 2019-07-13
    Description: In-Situ Resource Utilization (ISRU) seeks to make human space exploration feasible; by using available resources from a planet or the moon to produce consumables, parts, and structures that otherwise would be brought from Earth. Producing these in situ reduces the mass of such that must be launched and doing so allows more payload mass' for each mission. The production of oxygen from lunar regolith, for life support and propellant, is one of the tasks being studied under ISRU. NASA is currently funding three processes that have shown technical merit for the production of oxygen from regolith: Molten Salt Electrolysis, Hydrogen Reduction of Ilmenite, and Carbothermal Reduction. The ISRU program is currently developing system models of, the , abovementioned processes to: (1) help NASA in the evaluation process to select the most cost-effective and efficient process for further prototype development, (2) identify key parameters, (3) optimize the oxygen production process, (4) provide estimates on energy and power requirements, mass and volume.of the system, oxygen production rate, mass of regolith required, mass of consumables, and other important parameters, and (5) integrate into the overall end-to-end ISRU system model, which could be integrated with mission architecture models. The oxygen production system model is divided into modules that represent unit operations (e.g., reactor, water electrolyzer, heat exchanger). Each module is modeled theoretically using Excel and Visual Basic for Applications (VBA), and will be validated using experimental data from on-going laboratory work. This modularity (plug-n-play) feature of each unit operation allows the use of the same model on different oxygen production systems simulations resulting in comparable results. In this presentation, preliminary results for mass, power, volume will be presented along with brief description of the oxygen production system model.
    Keywords: Lunar and Planetary Science and Exploration
    Type: KSC-2007-002 , Space Technology and Applications International Forum (STAIF); Feb 12, 2007 - Feb 15, 2007; Albuquerque, NM; United States
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