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  • United States  (1,318)
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  • American Association for the Advancement of Science (AAAS)  (2,360)
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  • 2000-2004  (2,360)
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  • American Association for the Advancement of Science (AAAS)  (2,360)
  • American Chemical Society (ACS)
  • Springer  (19)
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  • 1
    Publication Date: 2004-07-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bream, J H -- Young, H A -- Rice, N -- Martin, M P -- Smith, M W -- Carrington, M -- O'Brien, S J -- New York, N.Y. -- Science. 1999 Apr 9;284(5412):223.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Experimental Immunology, National Cancer Institute-Frederick Cancer, Research and Development Center (NCI-FCRDC), Frederick, MD 21702, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15224670" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/genetics/immunology/mortality/*physiopathology ; *Alleles ; Binding Sites ; Cell Nucleus/metabolism ; DNA-Binding Proteins/*metabolism ; Disease Progression ; Electrophoretic Mobility Shift Assay ; Humans ; Nuclear Proteins/*metabolism ; Oligodeoxyribonucleotides/metabolism ; Polymorphism, Single Nucleotide ; *Promoter Regions, Genetic ; Receptors, CCR5/*genetics ; Survival Rate ; T-Lymphocytes ; Transcription Factors/metabolism
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    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2004-11-20
    Description: An autoregulatory transcription-translation feedback loop is thought to be essential in generating circadian rhythms in any model organism. In the cyanobacterium Synechococcus elongatus, the essential clock protein KaiC is proposed to form this type of transcriptional negative feedback. Nevertheless, we demonstrate here temperature-compensated, robust circadian cycling of KaiC phosphorylation even without kaiBC messenger RNA accumulation under continuous dark conditions. This rhythm persisted in the presence of a transcription or translation inhibitor. Moreover, kinetic profiles in the ratio of KaiC autophosphorylation-dephosphorylation were also temperature compensated in vitro. Thus, the cyanobacterial clock can keep time independent of de novo transcription and translation processes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tomita, Jun -- Nakajima, Masato -- Kondo, Takao -- Iwasaki, Hideo -- New York, N.Y. -- Science. 2005 Jan 14;307(5707):251-4. Epub 2004 Nov 18.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Biological Science, Graduate School of Science, Nagoya University, and Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Furo-cho, Chikusa-ku, Nagoya 464-8602, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15550625" target="_blank"〉PubMed〈/a〉
    Keywords: Bacterial Proteins/biosynthesis/*metabolism ; *Circadian Rhythm ; Circadian Rhythm Signaling Peptides and Proteins ; Darkness ; Feedback, Physiological ; Light ; Mutation ; Operon ; Phosphorylation ; Protein Biosynthesis ; RNA, Bacterial/metabolism ; RNA, Messenger/metabolism ; Recombinant Proteins/metabolism ; Synechococcus/*genetics/*metabolism ; Temperature ; Transcription, Genetic
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2004-06-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Beckman, Mary -- New York, N.Y. -- Science. 2004 Jun 25;304(5679):1888-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15218114" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Bedding and Linens ; *Behavior, Animal ; Female ; Male ; *Maternal Deprivation ; Mice ; *Mothers ; Mutation ; *Object Attachment ; Odors ; Receptors, Opioid, mu/genetics/*physiology ; Vocalization, Animal
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  • 4
    Publication Date: 2004-06-05
    Description: The mechanisms by which hydrophobic molecules, such as long-chain fatty acids, enter cells are poorly understood. In Gram-negative bacteria, the lipopolysaccharide layer in the outer membrane is an efficient barrier for fatty acids and aromatic hydrocarbons destined for biodegradation. We report crystal structures of the long-chain fatty acid transporter FadL from Escherichia coli at 2.6 and 2.8 angstrom resolution. FadL forms a 14-stranded beta barrel that is occluded by a central hatch domain. The structures suggest that hydrophobic compounds bind to multiple sites in FadL and use a transport mechanism that involves spontaneous conformational changes in the hatch.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉van den Berg, Bert -- Black, Paul N -- Clemons, William M Jr -- Rapoport, Tom A -- New York, N.Y. -- Science. 2004 Jun 4;304(5676):1506-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA. lvandenberg@hms.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15178802" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Bacterial Outer Membrane Proteins/*chemistry/metabolism ; Binding Sites ; Biological Transport ; Crystallization ; Crystallography, X-Ray ; Escherichia coli/chemistry/metabolism ; Escherichia coli Proteins/*chemistry/metabolism ; Fatty Acid Transport Proteins ; Fatty Acids/*metabolism ; Hydrogen Bonding ; Hydrophobic and Hydrophilic Interactions ; Models, Biological ; Models, Molecular ; Molecular Sequence Data ; Protein Conformation ; Protein Structure, Secondary ; Protein Structure, Tertiary
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  • 5
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bedalov, Antonio -- Simon, Julian A -- New York, N.Y. -- Science. 2004 Aug 13;305(5686):954-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Clinical Research Division and J. A. Simon is in the Clinical Research and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. abedalov@fhcrc.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15310883" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/*physiology ; Cell Nucleus/metabolism ; Cell Survival ; Cells, Cultured ; Ganglia, Spinal/cytology ; Mice ; Mutation ; NAD/biosynthesis/*metabolism ; Nerve Tissue Proteins/genetics/*metabolism ; Neurodegenerative Diseases/drug therapy/physiopathology ; Neuroprotective Agents/therapeutic use ; Nicotinamide-Nucleotide Adenylyltransferase/metabolism ; RNA, Small Interfering ; Sirtuin 1 ; Sirtuins/metabolism ; Ubiquitin-Protein Ligases/metabolism ; Wallerian Degeneration/metabolism/*physiopathology
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  • 6
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Korn, David -- New York, N.Y. -- Science. 2004 Apr 23;304(5670):516.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15105474" target="_blank"〉PubMed〈/a〉
    Keywords: *Biomedical Research ; *Career Mobility ; *Education, Graduate ; Faculty ; National Institutes of Health (U.S.) ; *Research Personnel ; Salaries and Fringe Benefits ; United States ; Universities
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  • 7
    Publication Date: 2004-05-08
    Description: There are 481 segments longer than 200 base pairs (bp) that are absolutely conserved (100% identity with no insertions or deletions) between orthologous regions of the human, rat, and mouse genomes. Nearly all of these segments are also conserved in the chicken and dog genomes, with an average of 95 and 99% identity, respectively. Many are also significantly conserved in fish. These ultraconserved elements of the human genome are most often located either overlapping exons in genes involved in RNA processing or in introns or nearby genes involved in the regulation of transcription and development. Along with more than 5000 sequences of over 100 bp that are absolutely conserved among the three sequenced mammals, these represent a class of genetic elements whose functions and evolutionary origins are yet to be determined, but which are more highly conserved between these species than are proteins and appear to be essential for the ontogeny of mammals and other vertebrates.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bejerano, Gill -- Pheasant, Michael -- Makunin, Igor -- Stephen, Stuart -- Kent, W James -- Mattick, John S -- Haussler, David -- 1P41HG02371/HG/NHGRI NIH HHS/ -- New York, N.Y. -- Science. 2004 May 28;304(5675):1321-5. Epub 2004 May 6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz, CA 95064, USA. jill@soe.ucsc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15131266" target="_blank"〉PubMed〈/a〉
    Keywords: Alternative Splicing ; Animals ; Base Sequence ; Chickens/genetics ; Computational Biology ; *Conserved Sequence ; DNA, Intergenic ; Dogs/genetics ; Evolution, Molecular ; Exons ; Gene Expression Regulation ; Genes ; Genome ; *Genome, Human ; Humans ; Introns ; Mice/genetics ; Molecular Sequence Data ; Mutation ; Nucleic Acid Conformation ; RNA/chemistry/genetics/metabolism ; Rats/genetics ; Takifugu/genetics
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  • 8
    Publication Date: 2004-01-06
    Description: Pairing, synapsis, and recombination are prerequisites for accurate chromosome segregation in meiosis. The phs1 gene in maize is required for pairing to occur between homologous chromosomes. In the phs1 mutant, homologous chromosome synapsis is completely replaced by synapsis between nonhomologous partners. The phs1 gene is also required for installation of the meiotic recombination machinery on chromosomes, as the mutant almost completely lacks chromosomal foci of the recombination protein RAD51. Thus, in the phs1 mutant, synapsis is uncoupled from recombination and pairing. The protein encoded by the phs1 gene likely acts in a multistep process to coordinate pairing, recombination, and synapsis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pawlowski, Wojciech P -- Golubovskaya, Inna N -- Timofejeva, Ljudmilla -- Meeley, Robert B -- Sheridan, William F -- Cande, W Zacheus -- New York, N.Y. -- Science. 2004 Jan 2;303(5654):89-92.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA. wpawlows@nature.berkeley.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704428" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Cell Nucleus/metabolism ; *Chromosome Pairing ; Chromosomes, Plant/*physiology ; Cloning, Molecular ; Conserved Sequence ; DNA, Plant/metabolism ; DNA-Binding Proteins ; Genes, Plant ; In Situ Hybridization, Fluorescence ; In Situ Nick-End Labeling/methods ; *Meiosis ; Molecular Sequence Data ; Mutation ; Phenotype ; Plant Proteins/chemistry/genetics/*physiology ; RNA, Ribosomal, 5S/genetics ; Rad51 Recombinase ; *Recombination, Genetic ; Sequence Alignment ; Synaptonemal Complex/metabolism/ultrastructure ; Telomere/physiology ; Zea mays/*genetics/physiology
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  • 9
    Publication Date: 2004-01-06
    Description: MDM2 binds the p53 tumor suppressor protein with high affinity and negatively modulates its transcriptional activity and stability. Overexpression of MDM2, found in many human tumors, effectively impairs p53 function. Inhibition of MDM2-p53 interaction can stabilize p53 and may offer a novel strategy for cancer therapy. Here, we identify potent and selective small-molecule antagonists of MDM2 and confirm their mode of action through the crystal structures of complexes. These compounds bind MDM2 in the p53-binding pocket and activate the p53 pathway in cancer cells, leading to cell cycle arrest, apoptosis, and growth inhibition of human tumor xenografts in nude mice.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vassilev, Lyubomir T -- Vu, Binh T -- Graves, Bradford -- Carvajal, Daisy -- Podlaski, Frank -- Filipovic, Zoran -- Kong, Norman -- Kammlott, Ursula -- Lukacs, Christine -- Klein, Christian -- Fotouhi, Nader -- Liu, Emily A -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):844-8. Epub 2004 Jan 2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Discovery Oncology, Roche Research Center, Hoffmann-La Roche, Inc., Nutley, NJ 07110, USA. lyubomir.vassilev@roche.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704432" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis/*drug effects ; Binding Sites ; Cell Cycle/drug effects ; Cell Division/*drug effects ; Cell Line ; Cell Line, Tumor ; Cell Survival/drug effects ; Crystallization ; Crystallography, X-Ray ; Cyclin-Dependent Kinase Inhibitor p21 ; Cyclins/metabolism ; Dose-Response Relationship, Drug ; Gene Expression ; Genes, p53 ; Humans ; Hydrophobic and Hydrophilic Interactions ; Imidazoles/chemistry/metabolism/*pharmacology ; Mice ; Mice, Nude ; Models, Molecular ; Molecular Weight ; NIH 3T3 Cells ; Neoplasm Transplantation ; Neoplasms, Experimental/drug therapy/metabolism/*pathology ; *Nuclear Proteins ; Phosphorylation ; Piperazines/chemistry/metabolism/*pharmacology ; Protein Conformation ; Proto-Oncogene Proteins/*antagonists & inhibitors/chemistry/metabolism ; Proto-Oncogene Proteins c-mdm2 ; Stereoisomerism ; Transplantation, Heterologous ; Tumor Suppressor Protein p53/*metabolism
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  • 10
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-03-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Krajick, Kevin -- New York, N.Y. -- Science. 2004 Mar 5;303(5663):1457.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15001752" target="_blank"〉PubMed〈/a〉
    Keywords: Academies and Institutes ; Animals ; Desert Climate ; *Ecology ; *Ecosystem ; Financial Support ; Genome ; *Genomics ; *International Cooperation ; Israel ; Jordan ; Sequence Analysis, DNA ; United States ; Universities
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  • 11
    Publication Date: 2004-01-06
    Description: RNA interference (RNAi) is a widespread silencing mechanism that acts at both the posttranscriptional and transcriptional levels. Here, we describe the purification of an RNAi effector complex termed RITS (RNA-induced initiation of transcriptional gene silencing) that is required for heterochromatin assembly in fission yeast. The RITS complex contains Ago1 (the fission yeast Argonaute homolog), Chp1 (a heterochromatin-associated chromodomain protein), and Tas3 (a novel protein). In addition, the complex contains small RNAs that require the Dicer ribonuclease for their production. These small RNAs are homologous to centromeric repeats and are required for the localization of RITS to heterochromatic domains. The results suggest a mechanism for the role of the RNAi machinery and small RNAs in targeting of heterochromatin complexes and epigenetic gene silencing at specific chromosomal loci.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3244756/" 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/PMC3244756/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Verdel, Andre -- Jia, Songtao -- Gerber, Scott -- Sugiyama, Tomoyasu -- Gygi, Steven -- Grewal, Shiv I S -- Moazed, Danesh -- R01 GM072805/GM/NIGMS NIH HHS/ -- R01 GM072805-01/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2004 Jan 30;303(5658):672-6. Epub 2004 Jan 2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cell Biology, Harvard Medical School, Boston, MA02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704433" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Argonaute Proteins ; Cell Cycle Proteins/chemistry/genetics/isolation & purification/*metabolism ; Centromere/metabolism ; Chromosomes, Fungal/metabolism ; Endoribonucleases/chemistry/genetics/isolation & purification/metabolism ; Genes, Reporter ; Heterochromatin/*metabolism ; Mass Spectrometry ; Models, Genetic ; Molecular Sequence Data ; Mutation ; Precipitin Tests ; Protein Binding ; *RNA Interference ; RNA, Fungal/metabolism ; RNA, Small Interfering/metabolism ; RNA-Binding Proteins ; Ribonuclease III/metabolism ; Schizosaccharomyces/*genetics/metabolism ; Schizosaccharomyces pombe Proteins/chemistry/genetics/isolation & ; purification/*metabolism
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  • 12
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-11-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Service, Robert F -- New York, N.Y. -- Science. 2004 Nov 5;306(5698):955.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15528413" target="_blank"〉PubMed〈/a〉
    Keywords: Environment ; *Nanotechnology/legislation & jurisprudence/organization & administration ; Public Policy ; Terminology as Topic ; United States
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  • 13
    Publication Date: 2004-02-21
    Description: We have engineered a pathway for the formation of disulfide bonds. By imposing evolutionary pressure, we isolated mutations that changed thioredoxin, which is a monomeric disulfide reductase, into a [2Fe-2S] bridged dimer capable of catalyzing O2-dependent sulfhydryl oxidation in vitro. Expression of the mutant protein in Escherichia coli with oxidizing cytoplasm and secretion via the Tat pathway restored disulfide bond formation in strains that lacked the complete periplasmic oxidative machinery (DsbA and DsbB). The evolution of [2Fe-2S] thioredoxin illustrates how mutations within an existing scaffold can add a cofactor and markedly change protein function.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Masip, Lluis -- Pan, Jonathan L -- Haldar, Suranjana -- Penner-Hahn, James E -- DeLisa, Matthew P -- Georgiou, George -- Bardwell, James C A -- Collet, Jean-Francois -- GM-38047/GM/NIGMS NIH HHS/ -- GM-55090/GM/NIGMS NIH HHS/ -- GM-57039/GM/NIGMS NIH HHS/ -- GM-64662/GM/NIGMS NIH HHS/ -- P41-RR01633/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 20;303(5661):1185-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemical Engineering and Institute for Cell and Molecular Biology, University of Texas, Austin, TX 78712, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976313" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Motifs ; Amino Acid Sequence ; Amino Acid Substitution ; Bacterial Proteins/genetics/metabolism ; Cell Membrane/metabolism ; Cysteine/analysis ; Cytoplasm/metabolism ; Dimerization ; Directed Molecular Evolution ; Disulfides/chemistry/*metabolism ; Escherichia coli/genetics/*metabolism/physiology ; Hirudins/chemistry/metabolism ; Iron/analysis ; Membrane Proteins/genetics/metabolism ; Movement ; Mutation ; Oxidation-Reduction ; Oxygen/metabolism ; Protein Disulfide-Isomerases/genetics/metabolism ; *Protein Engineering ; Protein Folding ; Proteins/chemistry/*metabolism ; Sulfides/analysis ; Thioredoxins/*chemistry/genetics/*metabolism
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  • 14
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-01-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Berger, Frederic -- New York, N.Y. -- Science. 2004 Jan 23;303(5657):483-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ecole Normale Superieure de Lyon, Laboratoire RDP UMR 5667, F-69364 Lyon Cedex 07, France. frederic.berger@ens-lyon.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14739448" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Arabidopsis/*genetics/growth & development/metabolism ; Arabidopsis Proteins/*genetics/metabolism ; DNA (Cytosine-5-)-Methyltransferase/genetics/metabolism ; DNA Methylation ; *Gene Expression Regulation, Plant ; Gene Silencing ; *Genomic Imprinting ; Homeodomain Proteins/*genetics/metabolism ; Mutation ; N-Glycosyl Hydrolases/genetics/metabolism ; Repetitive Sequences, Nucleic Acid ; Seeds/*genetics/metabolism ; Trans-Activators/genetics/metabolism ; Transcription Factors/*genetics/metabolism ; Transcription, Genetic
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  • 15
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fraser, Claire M -- New York, N.Y. -- Science. 2004 Apr 16;304(5669):359.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15087509" target="_blank"〉PubMed〈/a〉
    Keywords: *Anti-Infective Agents ; *Biomedical Research ; Bioterrorism/*prevention & control ; Communicable Disease Control ; Drug Evaluation, Preclinical ; *Drug Industry ; Global Health ; Government Programs ; Humans ; Infection/drug therapy ; United States ; *Vaccines
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  • 16
    Publication Date: 2004-10-30
    Description: Polar transport-dependent local accumulation of auxin provides positional cues for multiple plant patterning processes. This directional auxin flow depends on the polar subcellular localization of the PIN auxin efflux regulators. Overexpression of the PINOID protein kinase induces a basal-to-apical shift in PIN localization, resulting in the loss of auxin gradients and strong defects in embryo and seedling roots. Conversely, pid loss of function induces an apical-to-basal shift in PIN1 polar targeting at the inflorescence apex, accompanied by defective organogenesis. Our results show that a PINOID-dependent binary switch controls PIN polarity and mediates changes in auxin flow to create local gradients for patterning processes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Friml, Jiri -- Yang, Xiong -- Michniewicz, Marta -- Weijers, Dolf -- Quint, Ab -- Tietz, Olaf -- Benjamins, Rene -- Ouwerkerk, Pieter B F -- Ljung, Karin -- Sandberg, Goran -- Hooykaas, Paul J J -- Palme, Klaus -- Offringa, Remko -- New York, N.Y. -- Science. 2004 Oct 29;306(5697):862-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Developmental Genetics, Center for Molecular Biology of Plants, University Tubingen, Auf der Morgenstelle 3, D-72076 Tubingen, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15514156" target="_blank"〉PubMed〈/a〉
    Keywords: Arabidopsis/cytology/genetics/growth & development/*metabolism ; Arabidopsis Proteins/genetics/*metabolism ; Biological Transport ; Gene Expression Regulation, Plant ; Indoleacetic Acids/*metabolism ; Membrane Transport Proteins/genetics/*metabolism ; Meristem/metabolism ; Mutation ; Plant Epidermis/cytology/metabolism ; Plant Roots/metabolism ; Plant Shoots/metabolism ; Plants, Genetically Modified ; Protein-Serine-Threonine Kinases/genetics/*metabolism ; Recombinant Fusion Proteins/metabolism ; Seeds/metabolism
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Beutler, Ernest -- New York, N.Y. -- Science. 2004 Dec 17;306(5704):2051-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, CA 92037, USA. beutler@scripps.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15604397" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antimicrobial Cationic Peptides/*metabolism ; Biological Transport ; Cation Transport Proteins/genetics/*metabolism ; Enterocytes/metabolism ; Erythropoiesis ; Erythropoietin/genetics/metabolism ; Gene Expression Regulation ; Hemochromatosis/genetics ; Hepatocytes/metabolism ; Hepcidins ; Histocompatibility Antigens Class I/genetics ; Homeostasis ; Iron/*metabolism ; Iron Regulatory Protein 1/*metabolism ; Iron Regulatory Protein 2/*metabolism ; Membrane Proteins/genetics ; Mice ; Models, Biological ; Mutation ; Nitric Oxide/metabolism ; Oxygen/physiology ; Response Elements ; Signal Transduction ; Transcription, Genetic
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, Elizabeth -- New York, N.Y. -- Science. 2004 Jul 2;305(5680):37.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15232086" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Awards and Prizes ; Berlin ; *Biological Evolution ; Biology/history ; Birds ; History, 20th Century ; History, 21st Century ; Museums/*history ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vogel, Gretchen -- New York, N.Y. -- Science. 2004 Oct 15;306(5695):400-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15486272" target="_blank"〉PubMed〈/a〉
    Keywords: Cysteine Endopeptidases/metabolism ; History, 20th Century ; History, 21st Century ; Israel ; Multienzyme Complexes/metabolism ; *Nobel Prize ; Proteasome Endopeptidase Complex ; Proteins/*metabolism ; Ubiquitin/*metabolism ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McManamon, Francis P -- New York, N.Y. -- Science. 2004 Oct 22;306(5696):612-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15498995" target="_blank"〉PubMed〈/a〉
    Keywords: *Bone and Bones ; Humans ; *Paleontology ; *Research Design ; Skeleton ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-03-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Service, Robert F -- New York, N.Y. -- Science. 2004 Mar 19;303(5665):1798.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15031491" target="_blank"〉PubMed〈/a〉
    Keywords: *Anti-Bacterial Agents ; *Biomedical Research ; Drug Approval ; *Drug Industry/economics ; Economics, Pharmaceutical ; Patents as Topic ; United States ; United States Food and Drug Administration
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-01-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Irion, Robert -- New York, N.Y. -- Science. 2004 Jan 2;303(5654):30-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704407" target="_blank"〉PubMed〈/a〉
    Keywords: Astronomical Phenomena ; *Astronomy ; Atmosphere ; Europe ; Exobiology ; Extraterrestrial Environment ; Financing, Government ; Interferometry ; Optics and Photonics ; *Planets ; *Spacecraft ; United States ; United States National Aeronautics and Space Administration
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, Elizabeth -- New York, N.Y. -- Science. 2004 Jun 18;304(5678):1736.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15205506" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Biological ; Alleles ; Animals ; *Biological Evolution ; Breeding ; Crosses, Genetic ; Environment ; Extremities/growth & development ; Fresh Water ; Gene Expression Regulation ; Genes ; Genome ; Homeodomain Proteins/*genetics/metabolism ; Mutation ; Paired Box Transcription Factors ; Seawater ; Selection, Genetic ; Smegmamorpha/*anatomy & histology/*genetics ; Transcription Factors/*genetics/metabolism
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  • 24
    Publication Date: 2004-02-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McNeil, John G -- Johnston, Margaret I -- Birx, Deborah L -- Tramont, Edmund C -- New York, N.Y. -- Science. 2004 Feb 13;303(5660):961.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, and 2Walter Reed Army Institute of Research, Washington, DC 20307, USA. jomcneil@mail.nih.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14963313" target="_blank"〉PubMed〈/a〉
    Keywords: *AIDS Vaccines/administration & dosage/*immunology ; CD4-Positive T-Lymphocytes/immunology ; CD8-Positive T-Lymphocytes/immunology ; *Clinical Trials, Phase III as Topic ; HIV Antibodies/biosynthesis/immunology ; HIV Infections/*immunology/prevention & control/therapy ; Humans ; Immunization Schedule ; Immunization, Secondary ; National Institutes of Health (U.S.) ; Thailand ; United States ; Vaccines, Synthetic/administration & dosage/immunology
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  • 25
    Publication Date: 2004-02-07
    Description: The 1918 influenza pandemic resulted in about 20 million deaths. This enormous impact, coupled with renewed interest in emerging infections, makes characterization of the virus involved a priority. Receptor binding, the initial event in virus infection, is a major determinant of virus transmissibility that, for influenza viruses, is mediated by the hemagglutinin (HA) membrane glycoprotein. We have determined the crystal structures of the HA from the 1918 virus and two closely related HAs in complex with receptor analogs. They explain how the 1918 HA, while retaining receptor binding site amino acids characteristic of an avian precursor HA, is able to bind human receptors and how, as a consequence, the virus was able to spread in the human population.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gamblin, S J -- Haire, L F -- Russell, R J -- Stevens, D J -- Xiao, B -- Ha, Y -- Vasisht, N -- Steinhauer, D A -- Daniels, R S -- Elliot, A -- Wiley, D C -- Skehel, J J -- AI-13654/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Mar 19;303(5665):1838-42. Epub 2004 Feb 5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Medical Research Council (MRC) National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764886" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Binding Sites ; Birds ; Crystallography, X-Ray ; Hemagglutinin Glycoproteins, Influenza Virus/*chemistry/*metabolism ; History, 20th Century ; Humans ; Hydrogen Bonding ; Influenza A virus/*immunology/metabolism/pathogenicity ; Influenza, Human/epidemiology/history/*virology ; Membrane Glycoproteins/chemistry/metabolism ; Models, Molecular ; Molecular Sequence Data ; Protein Conformation ; Protein Structure, Tertiary ; Receptors, Virus/*metabolism ; Sequence Alignment ; Sialic Acids/metabolism ; Species Specificity ; Swine
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-11-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2004 Nov 12;306(5699):1119.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15539576" target="_blank"〉PubMed〈/a〉
    Keywords: *Biomarkers/analysis ; Controlled Clinical Trials as Topic ; *Drug Approval ; Humans ; Treatment Outcome ; United States ; *United States Food and Drug Administration
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bhattacharjee, Yudhijit -- New York, N.Y. -- Science. 2004 Oct 1;306(5693):30.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15459355" target="_blank"〉PubMed〈/a〉
    Keywords: Commerce/*legislation & jurisprudence ; *Government Regulation ; Publishing/*legislation & jurisprudence ; United States ; United States Government Agencies
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  • 28
    Publication Date: 2004-12-04
    Description: DNA photolyases use light energy to repair DNA that comprises ultraviolet-induced lesions such as the cis-syn cyclobutane pyrimidine dimers (CPDs). Here we report the crystal structure of a DNA photolyase bound to duplex DNA that is bent by 50 degrees and comprises a synthetic CPD lesion. This CPD lesion is flipped into the active site and split there into two thymines by synchrotron radiation at 100 K. Although photolyases catalyze blue light-driven CPD cleavage only above 200 K, this structure apparently mimics a structural substate during light-driven DNA repair in which back-flipping of the thymines into duplex DNA has not yet taken place.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mees, Alexandra -- Klar, Tobias -- Gnau, Petra -- Hennecke, Ulrich -- Eker, Andre P M -- Carell, Thomas -- Essen, Lars-Oliver -- New York, N.Y. -- Science. 2004 Dec 3;306(5702):1789-93.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry and Biochemistry, Butenandt-Strasse 5-13, Ludwig Maximilians University, D-81377 Munich, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15576622" target="_blank"〉PubMed〈/a〉
    Keywords: Base Pairing ; Binding Sites ; Crystallization ; Crystallography, X-Ray ; DNA/*chemistry/metabolism ; *DNA Damage ; *DNA Repair ; DNA, Single-Stranded/chemistry/metabolism ; Deoxyribodipyrimidine Photo-Lyase/*chemistry/metabolism ; Flavin-Adenine Dinucleotide/metabolism ; Hydrogen Bonding ; Nucleic Acid Conformation ; Protein Conformation ; Pyrimidine Dimers/*chemistry/metabolism ; Synechococcus/*enzymology ; Thymine/chemistry
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mendoza-Londono, Roberto -- New York, N.Y. -- Science. 2004 Jul 30;305(5684):609.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15286346" target="_blank"〉PubMed〈/a〉
    Keywords: *Career Mobility ; Developing Countries ; *Education, Graduate ; *Emigration and Immigration ; *Foreign Medical Graduates ; Humans ; *Internship and Residency ; National Institutes of Health (U.S.) ; United States
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  • 30
    Publication Date: 2004-04-24
    Description: The mechanisms controlling axon guidance are of fundamental importance in understanding brain development. Growing corticospinal and somatosensory axons cross the midline in the medulla to reach their targets and thus form the basis of contralateral motor control and sensory input. The motor and sensory projections appeared uncrossed in patients with horizontal gaze palsy with progressive scoliosis (HGPPS). In patients affected with HGPPS, we identified mutations in the ROBO3 gene, which shares homology with roundabout genes important in axon guidance in developing Drosophila, zebrafish, and mouse. Like its murine homolog Rig1/Robo3, but unlike other Robo proteins, ROBO3 is required for hindbrain axon midline crossing.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1618874/" 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/PMC1618874/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jen, Joanna C -- Chan, Wai-Man -- Bosley, Thomas M -- Wan, Jijun -- Carr, Janai R -- Rub, Udo -- Shattuck, David -- Salamon, Georges -- Kudo, Lili C -- Ou, Jing -- Lin, Doris D M -- Salih, Mustafa A M -- Kansu, Tulay -- Al Dhalaan, Hesham -- Al Zayed, Zayed -- MacDonald, David B -- Stigsby, Bent -- Plaitakis, Andreas -- Dretakis, Emmanuel K -- Gottlob, Irene -- Pieh, Christina -- Traboulsi, Elias I -- Wang, Qing -- Wang, Lejin -- Andrews, Caroline -- Yamada, Koki -- Demer, Joseph L -- Karim, Shaheen -- Alger, Jeffry R -- Geschwind, Daniel H -- Deller, Thomas -- Sicotte, Nancy L -- Nelson, Stanley F -- Baloh, Robert W -- Engle, Elizabeth C -- DC00162/DC/NIDCD NIH HHS/ -- DC05524/DC/NIDCD NIH HHS/ -- EY12498/EY/NEI NIH HHS/ -- EY13583/EY/NEI NIH HHS/ -- EY15298/EY/NEI NIH HHS/ -- EY15311/EY/NEI NIH HHS/ -- MH60233/MH/NIMH NIH HHS/ -- P30 HD 18655/HD/NICHD NIH HHS/ -- R01 EY008313/EY/NEI NIH HHS/ -- R01 EY008313-14/EY/NEI NIH HHS/ -- R01 HL066251/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2004 Jun 4;304(5676):1509-13. Epub 2004 Apr 22.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurology, University of California, Los Angeles, CA 90095, USA. jjen@ucla.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15105459" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Alternative Splicing ; Amino Acid Motifs ; Amino Acid Sequence ; Axons/*physiology ; Evoked Potentials, Motor ; Evoked Potentials, Somatosensory ; Female ; Functional Laterality ; Genetic Linkage ; Humans ; In Situ Hybridization ; Magnetic Resonance Imaging ; Male ; Medulla Oblongata/growth & development/pathology ; Microsatellite Repeats ; Molecular Sequence Data ; Morphogenesis ; Mutation ; Neural Pathways ; Ophthalmoplegia/*genetics/pathology/physiopathology ; Pedigree ; Protein Structure, Tertiary ; Receptors, Immunologic/chemistry/*genetics/*metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Rhombencephalon/*growth & development/pathology ; Scoliosis/*genetics/pathology/physiopathology ; Sequence Analysis, DNA ; Syndrome
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vogel, Gretchen -- New York, N.Y. -- Science. 2004 Apr 23;304(5670):501-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15105467" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; *Embryonic and Fetal Development ; Female ; Gene Expression Regulation, Developmental ; *Genomic Imprinting ; Insulin-Like Growth Factor II/genetics/physiology ; Japan ; Mice ; Mutation ; Oocytes/*physiology ; *Parthenogenesis ; RNA, Long Noncoding ; RNA, Untranslated/genetics/physiology
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, Elizabeth -- New York, N.Y. -- Science. 2004 Apr 2;304(5667):27.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15060291" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Conservation of Natural Resources ; Ecosystem ; Environment ; Food Chain ; *Invertebrates ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-05-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bhattacharjee, Yudhijit -- New York, N.Y. -- Science. 2004 May 28;304(5675):1282-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15166362" target="_blank"〉PubMed〈/a〉
    Keywords: Culture ; *Education, Graduate ; *Faculty ; *Foreign Professional Personnel ; Internationality ; Language ; Research ; *Research Personnel ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bhattacharjee, Yudhijit -- New York, N.Y. -- Science. 2004 Apr 9;304(5668):187.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15073341" target="_blank"〉PubMed〈/a〉
    Keywords: *Authorship ; Commerce/*legislation & jurisprudence ; International Cooperation/legislation & jurisprudence ; Peer Review, Research/*legislation & jurisprudence ; Publishing/*legislation & jurisprudence ; Societies, Scientific ; United States ; *United States Government Agencies
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2004 Jul 23;305(5683):468-70.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15273374" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Antidepressive Agents, Second-Generation/adverse ; effects/pharmacokinetics/pharmacology/therapeutic use ; Brain/metabolism ; Child ; Clinical Trials as Topic ; Depressive Disorder/*drug therapy ; Emotions ; Humans ; Risk Factors ; Self-Injurious Behavior ; Serotonin/metabolism ; Serotonin Uptake Inhibitors/*adverse ; effects/pharmacokinetics/pharmacology/*therapeutic use ; Suicide ; United States ; United States Food and Drug Administration
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  • 36
    Publication Date: 2004-11-06
    Description: In RNA interference (RNAi), double-stranded RNA (dsRNA) triggers degradation of homologous messenger RNA. In many organisms, RNA-dependent RNA polymerase (RdRp) is required to initiate or amplify RNAi, but the substrate for dsRNA synthesis in vivo is not known. Here, we show that RdRp-dependent transgene silencing in Arabidopsis was caused by mutation of XRN4, which is a ribonuclease (RNase) implicated in mRNA turnover by means of decapping and 5'-3' exonucleolysis. When both XRN4 and the RdRp were mutated, the plants accumulated decapped transgene mRNA. We propose that mRNAs lacking a cap structure become exposed to RdRp to initiate or maintain RNAi.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gazzani, S -- Lawrenson, T -- Woodward, C -- Headon, D -- Sablowski, R -- BBS/E/J/00000594/Biotechnology and Biological Sciences Research Council/United Kingdom -- New York, N.Y. -- Science. 2004 Nov 5;306(5698):1046-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cell and Developmental Biology, John Innes Centre, Norwich NR4 7UH, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15528448" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arabidopsis/*genetics ; Arabidopsis Proteins/genetics ; Exoribonucleases/genetics ; Gene Silencing ; Homeodomain Proteins/genetics ; Mutation ; Plant Proteins/genetics ; Plants, Genetically Modified ; RNA Caps ; *RNA Interference ; RNA Replicase/metabolism ; RNA, Messenger/*metabolism ; RNA, Plant/*metabolism ; Rats ; Recombinant Fusion Proteins/genetics
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gazzaniga, Michael S -- New York, N.Y. -- Science. 2004 Apr 16;304(5669):388-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15087527" target="_blank"〉PubMed〈/a〉
    Keywords: Beginning of Human Life ; *Cloning, Organism/ethics/legislation & jurisprudence ; *Embryo Research/ethics ; Embryonic and Fetal Development ; Humans ; Korea ; Personhood ; Stem Cells ; United States ; Value of Life
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  • 38
    Publication Date: 2004-05-25
    Description: The protein-remodeling factor Hsp104 governs inheritance of [PSI+], a yeast prion formed by self-perpetuating amyloid conformers of the translation termination factor Sup35. Perplexingly, either excess or insufficient Hsp104 eliminates [PSI+]. In vitro, at low concentrations, Hsp104 catalyzed the formation of oligomeric intermediates that proved critical for the nucleation of Sup 35 fibrillization de novo and displayed a conformation common among amyloidogenic polypeptides. At higher Hsp104 concentrations, amyloidogenic oligomerization and contingent fibrillization were abolished. Hsp104 also disassembled mature fibers in a manner that initially exposed new surfaces for conformational replication but eventually exterminated prion conformers. These Hsp104 activities differed in their reaction mechanism and can explain [PSI+] inheritance patterns.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shorter, James -- Lindquist, Susan -- GM25874/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Jun 18;304(5678):1793-7. Epub 2004 May 20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA 02142, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15155912" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Triphosphatases/metabolism ; Adenosine Triphosphate/metabolism ; Amyloid/chemistry ; Amyloid beta-Peptides/chemistry/immunology ; Antibodies/immunology ; Biopolymers ; Catalysis ; Heat-Shock Proteins/chemistry/genetics/*metabolism ; Hydrolysis ; Mutation ; Peptide Fragments/chemistry/immunology ; Peptide Termination Factors ; Prions/*chemistry/*metabolism ; Protein Conformation ; Protein Structure, Tertiary ; Saccharomyces cerevisiae Proteins/*chemistry/genetics/*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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  • 39
    Publication Date: 2004-03-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bidoia, C -- Misgeld, T -- Weinzierl, E -- Buffelli, M -- Feng, G -- Cangiano, A -- Lichtman, J W -- Sanes, J R -- New York, N.Y. -- Science. 2004 Mar 26;303(5666):1977; author reply 1977.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Dipartimento di Scienze Neurologiche e della Visione, Universita' di Verona, Strada Le Grazie 8, Verona, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15044788" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/physiology/ultrastructure ; Cell Adhesion Molecules, Neuronal/genetics/*physiology ; Crosses, Genetic ; Diaphragm/innervation ; Extracellular Matrix Proteins/genetics/*physiology ; Mice ; Mice, Neurologic Mutants ; Mice, Transgenic ; Motor Endplate/ultrastructure ; Muscle, Skeletal/innervation ; Mutation ; Nerve Tissue Proteins ; Neuromuscular Junction/*growth & development/physiology/ultrastructure ; Phenotype ; Serine Endopeptidases ; Synapses/*physiology/ultrastructure
    Print ISSN: 0036-8075
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  • 40
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jordan, Frank -- GM-50380/GM/NIGMS NIH HHS/ -- GM-62330/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Oct 29;306(5697):818-20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, Rutgers University, Newark, NJ 07102, USA. frjordan@newark.rutgers.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15514144" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Binding Sites ; Dihydrolipoyllysine-Residue Acetyltransferase ; Dimerization ; Geobacillus stearothermophilus/*enzymology ; Glutamic Acid/chemistry ; Hydrogen Bonding ; Hydrogen-Ion Concentration ; Kinetics ; Protein Structure, Quaternary ; Protein Structure, Tertiary ; Protein Subunits ; Protons ; Pyruvate Dehydrogenase (Lipoamide)/*chemistry/*metabolism ; Pyruvate Dehydrogenase Complex/*chemistry/*metabolism ; Thiamine Pyrophosphate/chemistry/*metabolism
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  • 41
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):159.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247442" target="_blank"〉PubMed〈/a〉
    Keywords: *Bacillus ; *Faculty ; Fraud/*legislation & jurisprudence ; Postal Service/legislation & jurisprudence ; *Serratia marcescens ; United States ; Universities
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  • 42
    Publication Date: 2004-08-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Geeta, R -- Levy, Andre -- Hoch, J Matt -- Mark, Melissa -- New York, N.Y. -- Science. 2004 Aug 20;305(5687):1105-6; author reply 1105-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15326334" target="_blank"〉PubMed〈/a〉
    Keywords: *Biodiversity ; *Classification ; Developing Countries ; United States
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 43
    Publication Date: 2004-05-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gaudioso, Jennifer -- Salerno, Reynolds M -- New York, N.Y. -- Science. 2004 Apr 30;304(5671):687.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Sandia National Laboratories, Albuquerque, NM 87185, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15118148" target="_blank"〉PubMed〈/a〉
    Keywords: Biological Warfare/*prevention & control ; *Biomedical Research ; Bioterrorism/legislation & jurisprudence/*prevention & control ; Federal Government ; Government Regulation ; *Microbiology ; Research Personnel ; Risk Assessment ; *Security Measures/legislation & jurisprudence ; United States
    Print ISSN: 0036-8075
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  • 44
    Publication Date: 2004-12-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bhattacharjee, Yudhijit -- Holden, Constance -- Seife, Charles -- Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Dec 3;306(5702):1663.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15576576" target="_blank"〉PubMed〈/a〉
    Keywords: Censuses ; National Institutes of Health (U.S.)/*legislation & jurisprudence ; Nuclear Warfare/legislation & jurisprudence ; *Science ; Travel/legislation & jurisprudence ; United States
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  • 45
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mervis, Jeffrey -- New York, N.Y. -- Science. 2004 Oct 8;306(5694):220-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15472055" target="_blank"〉PubMed〈/a〉
    Keywords: Biomedical Research/*economics ; Financing, Government ; *National Institutes of Health (U.S.)/economics ; Peer Review, Research ; Public Policy ; *Research Support as Topic ; Risk ; United States ; *United States Government Agencies
    Print ISSN: 0036-8075
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  • 46
    Publication Date: 2004-09-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mervis, Jeffrey -- New York, N.Y. -- Science. 2004 Sep 24;305(5692):1883.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15448230" target="_blank"〉PubMed〈/a〉
    Keywords: *Administrative Personnel ; History, 21st Century ; Politics ; *Science/history ; United States ; *United States Government Agencies
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 47
    Publication Date: 2004-08-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mervis, Jeffrey -- New York, N.Y. -- Science. 2004 Jul 30;305(5684):587.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15286332" target="_blank"〉PubMed〈/a〉
    Keywords: *Budgets ; Military Personnel ; National Institutes of Health (U.S.)/economics ; *Science ; United States ; United States Department of Veterans Affairs/economics ; United States Government Agencies ; United States National Aeronautics and Space Administration/economics
    Print ISSN: 0036-8075
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  • 48
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lawler, Andrew -- New York, N.Y. -- Science. 2004 Jun 25;304(5679):1888.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15218115" target="_blank"〉PubMed〈/a〉
    Keywords: *Biomedical Research ; Cell Line ; Humans ; *Politics ; *Research Support as Topic ; *Science ; Stem Cells ; United States
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  • 49
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- Vogel, Gretchen -- New York, N.Y. -- Science. 2004 Apr 9;304(5668):192-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15073347" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arrhythmias, Cardiac ; *Bone Marrow Transplantation/adverse effects ; Cardiac Output, Low/therapy ; Clinical Trials as Topic ; Europe ; Granulocyte Colony-Stimulating Factor/adverse effects ; *Heart/physiology ; Heart Diseases/pathology/physiopathology/*therapy ; Humans ; Myoblasts/*transplantation ; Myocardial Infarction/therapy ; Myocardium/pathology ; Myocytes, Cardiac/physiology ; *Stem Cell Transplantation/adverse effects ; United States ; United States Food and Drug Administration
    Print ISSN: 0036-8075
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  • 50
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-05-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mervis, Jeffrey -- New York, N.Y. -- Science. 2004 May 28;304(5675):1280.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15166360" target="_blank"〉PubMed〈/a〉
    Keywords: Education, Graduate/*standards ; Emigration and Immigration ; *Students ; United States
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  • 51
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pickrell, John -- New York, N.Y. -- Science. 2004 Jul 16;305(5682):332-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15256653" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anthozoa/growth & development ; Diving ; Ecosystem ; France ; History, 20th Century ; History, 21st Century ; *Marine Biology/history ; Organizations, Nonprofit ; Societies, Scientific/*organization & administration ; United States
    Print ISSN: 0036-8075
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  • 52
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-02-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):784-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764863" target="_blank"〉PubMed〈/a〉
    Keywords: Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; *Bayes Theorem ; Breast Neoplasms/drug therapy ; Clinical Protocols ; *Clinical Trials as Topic/methods/statistics & numerical data ; History, 20th Century ; History, 21st Century ; Humans ; Mammography ; Research Design ; United States
    Print ISSN: 0036-8075
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-05-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mervis, Jeffrey -- New York, N.Y. -- Science. 2004 May 7;304(5672):808.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15131276" target="_blank"〉PubMed〈/a〉
    Keywords: Asia ; Europe ; *Publishing ; *Research ; *Science ; Technology ; United States ; United States Government Agencies
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  • 54
    Publication Date: 2004-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Oct 15;306(5695):394-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15486267" target="_blank"〉PubMed〈/a〉
    Keywords: Adjuvants, Immunologic ; Antiviral Agents/supply & distribution/*therapeutic use ; Clinical Trials as Topic ; Developed Countries ; Developing Countries ; Disease Outbreaks/*prevention & control ; *Global Health ; Humans ; Influenza A virus/immunology/pathogenicity ; *Influenza Vaccines/supply & distribution ; Influenza, Human/epidemiology/*prevention & control ; Orthomyxoviridae/immunology/pathogenicity ; Patents as Topic ; United States ; Vaccines, Synthetic
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  • 55
    Publication Date: 2004-08-17
    Description: The SOS response aids bacterial propagation by inhibiting cell division during repair of DNA damage. We report that inactivation of the ftsI gene product, penicillin binding protein 3, by either beta-lactam antibiotics or genetic mutation induces SOS in Escherichia coli through the DpiBA two-component signal transduction system. This event, which requires the SOS-promoting recA and lexA genes as well as dpiA, transiently halts bacterial cell division, enabling survival to otherwise lethal antibiotic exposure. Our findings reveal defective cell wall synthesis as an unexpected initiator of the bacterial SOS response, indicate that beta-lactam antibiotics are extracellular stimuli of this response, and demonstrate a novel mechanism for mitigation of antimicrobial lethality.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miller, Christine -- Thomsen, Line Elnif -- Gaggero, Carina -- Mosseri, Ronen -- Ingmer, Hanne -- Cohen, Stanley N -- R01 AI08619/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Sep 10;305(5690):1629-31. Epub 2004 Aug 12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, Stanford University, Stanford, CA 94305, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15308764" target="_blank"〉PubMed〈/a〉
    Keywords: Ampicillin/*pharmacology ; Anti-Bacterial Agents/metabolism/*pharmacology ; Bacterial Proteins/genetics/metabolism ; Carrier Proteins/genetics/metabolism ; Cell Division ; Cell Wall/metabolism ; Escherichia coli/*drug effects/genetics/*metabolism ; Escherichia coli Proteins/genetics/metabolism ; Hexosyltransferases/genetics/metabolism ; Lac Operon ; Muramoylpentapeptide Carboxypeptidase/genetics/metabolism ; Mutation ; Operon ; Penicillin-Binding Proteins ; *Peptidoglycan Glycosyltransferase ; Peptidyl Transferases/genetics/metabolism ; Protein Kinases/genetics/metabolism ; *SOS Response (Genetics) ; Signal Transduction ; Temperature ; Transcription Factors/genetics/metabolism ; beta-Galactosidase/biosynthesis ; beta-Lactams/metabolism/*pharmacology
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Aug 6;305(5685):764.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15297639" target="_blank"〉PubMed〈/a〉
    Keywords: *Access to Information ; Authorship ; Financing, Government ; *Information Dissemination ; *Internet ; Medline ; *National Institutes of Health (U.S.) ; Periodicals as Topic ; *Publishing ; Research Support as Topic ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Jul 23;305(5683):462.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15273370" target="_blank"〉PubMed〈/a〉
    Keywords: Budgets ; *Congresses as Topic ; *Internationality ; *National Institutes of Health (U.S.) ; *Research Personnel ; *Travel ; United States ; United States Dept. of Health and Human Services
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Sep 10;305(5690):1552-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15361597" target="_blank"〉PubMed〈/a〉
    Keywords: *Global Health ; History, 21st Century ; International Cooperation ; Politics ; *Public Policy ; Travel ; United States ; United States Dept. of Health and Human Services/*organization & administration ; World Health Organization
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Aug 20;305(5687):1090.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15326321" target="_blank"〉PubMed〈/a〉
    Keywords: *Conflict of Interest ; *Consultants ; *Drug Industry ; Ethics, Professional ; National Institutes of Health (U.S.)/*ethics ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Sep 10;305(5690):1548.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15361594" target="_blank"〉PubMed〈/a〉
    Keywords: *Access to Information ; Financing, Government ; Information Dissemination ; *Internet ; *National Institutes of Health (U.S.) ; *Publishing ; Research Support as Topic ; Societies, Scientific ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Michalakis, Yannis -- Roze, Denis -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1492-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Genetique et Evolution des Maladies Infectieuses, UMR CNRS IRD 2724, Montpellier Cedex 5, France. yannis.michalakis@mpl.ird.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567846" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; *Epistasis, Genetic ; *Evolution, Molecular ; Genes, Viral ; HIV Infections/drug therapy/virology ; HIV Protease/chemistry/genetics ; HIV Reverse Transcriptase/chemistry/genetics ; HIV-1/*genetics/physiology ; Humans ; Models, Genetic ; Mutation ; *Recombination, Genetic ; Reproduction ; Selection, Genetic ; Vesicular stomatitis Indiana virus/*genetics/physiology
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  • 62
    Publication Date: 2004-11-30
    Description: Reproductive strategies such as sexual reproduction and recombination that involve the shuffling of parental genomes for the production of offspring are ubiquitous in nature. However, their evolutionary benefit remains unclear. Many theories have identified potential benefits, but progress is hampered by the scarcity of relevant data. One class of theories is based on the assumption that mutations affecting fitness exhibit negative epistasis. Retroviruses recombine frequently and thus provide a unique opportunity to test these theories. Using amino acid sequence data and fitness values from 9466 human immunodeficiency virus 1 (HIV-1) isolates, we find in contrast to these theories strong statistical evidence for a predominance of positive epistasis in HIV-1.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bonhoeffer, Sebastian -- Chappey, Colombe -- Parkin, Neil T -- Whitcomb, Jeanette M -- Petropoulos, Christos J -- R43 AI050321/AI/NIAID NIH HHS/ -- R43 AI057068/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1547-50.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ecology and Evolution, ETH Zurich, ETH Zentrum NW, CH-8092 Zurich, Switzerland. seb@env.ethz.ch〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567861" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Amino Acids ; Anti-HIV Agents/pharmacology ; Drug Resistance, Viral ; *Epistasis, Genetic ; *Evolution, Molecular ; Genotype ; HIV Infections/drug therapy/virology ; HIV Protease/chemistry/genetics/metabolism ; HIV Reverse Transcriptase/chemistry/genetics/metabolism ; HIV-1/drug effects/*genetics/physiology ; Humans ; Mutation ; *Recombination, Genetic ; Software ; Virus Replication
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 63
    Publication Date: 2004-12-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lawler, Andrew -- Mervis, Jeffrey -- New York, N.Y. -- Science. 2004 Dec 3;306(5702):1662-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15576575" target="_blank"〉PubMed〈/a〉
    Keywords: *Budgets ; Financing, Government ; National Institutes of Health (U.S.)/*economics ; Politics ; *Research Support as Topic ; *Science ; Security Measures ; United States ; *United States Government Agencies ; United States National Aeronautics and Space Administration/economics
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  • 64
    Publication Date: 2004-02-21
    Description: To achieve X-chromosome dosage compensation, organisms must distinguish X chromosomes from autosomes. We identified multiple, cis-acting regions that recruit the Caenorhabditis elegans dosage compensation complex (DCC) through a search for regions of X that bind the complex when detached from X. The DCC normally assembles along the entire X chromosome, but not all detached regions recruit the complex, despite having genes known to be dosage compensated on the native X. Thus, the DCC binds first to recruitment sites, then spreads to neighboring X regions to accomplish chromosome-wide gene repression. From a large chromosomal domain, we defined a 793-base pair fragment that functions in vivo as an X-recognition element to recruit the DCC.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Csankovszki, Gyorgyi -- McDonel, Patrick -- Meyer, Barbara J -- F32-GM065007/GM/NIGMS NIH HHS/ -- R37-GM30702/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 20;303(5661):1182-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720-3204, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976312" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Genetically Modified ; Base Sequence ; Binding Sites ; Caenorhabditis elegans/*genetics/metabolism ; Caenorhabditis elegans Proteins/*metabolism ; Carrier Proteins/metabolism ; Chromosomes/metabolism ; Cosmids ; DNA-Binding Proteins/metabolism ; Disorders of Sex Development ; *Dosage Compensation, Genetic ; Female ; In Situ Hybridization, Fluorescence ; Male ; Models, Genetic ; Molecular Sequence Data ; Nuclear Proteins/metabolism ; Repetitive Sequences, Nucleic Acid ; X Chromosome/*metabolism
    Print ISSN: 0036-8075
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  • 65
    Publication Date: 2004-02-07
    Description: Theory on the evolution of virulence generally predicts selection for an optimal level of virulence determined by trade-offs with transmission and/or recovery. Here we consider the evolution of pathogen virulence in hosts who acquire long-lived immunity and live in a spatially structured population. We show theoretically that large shifts in virulence may occur in pathogen populations as a result of a bistability in evolutionary dynamics caused by the local contact or social population structure of the host. This model provides an explanation for the rapid emergence of the highly virulent strains of rabbit hemorrhagic disease virus.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Boots, M -- Hudson, P J -- Sasaki, A -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):842-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Animal and Plant Sciences, University of Sheffield, Western Bank, Sheffield S10 2TN, UK. m.boots@sheffield.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764881" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Caliciviridae Infections/epidemiology/*veterinary/virology ; *Communicable Diseases/epidemiology/immunology/transmission ; Disease Susceptibility ; Hemorrhagic Disease Virus, Rabbit/genetics/*pathogenicity ; Humans ; Immunity, Active ; Mathematics ; Models, Biological ; Molecular Epidemiology ; Mutation ; Recombination, Genetic ; *Virulence/genetics
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  • 66
    Publication Date: 2004-06-12
    Description: During embryogenesis, differentiation of skeletal muscle is regulated by transcription factors that include members of the Msx homeoprotein family. By investigating Msx1 function in repression of myogenic gene expression, we identified a physical interaction between Msx1 and H1b, a specific isoform of mouse histone H1. We found that Msx1 and H1b bind to a key regulatory element of MyoD, a central regulator of skeletal muscle differentiation, where they induce repressed chromatin. Moreover, Msx1 and H1b cooperate to inhibit muscle differentiation in cell culture and in Xenopus animal caps. Our findings define a previously unknown function for "linker" histones in gene-specific transcriptional regulation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lee, Hansol -- Habas, Raymond -- Abate-Shen, Cory -- HD29446/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2004 Jun 11;304(5677):1675-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Advanced Biotechnology and Medicine, University of Medicine and Dentistry of New Jersey (UMDNJ)-Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15192231" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cell Line ; Embryo, Nonmammalian/cytology/metabolism ; Enhancer Elements, Genetic ; *Gene Expression Regulation, Developmental ; Histones/genetics/*metabolism ; Homeodomain Proteins/chemistry/genetics/*metabolism ; MSX1 Transcription Factor ; Mice ; Models, Genetic ; *Muscle Development ; Muscle, Skeletal/*cytology/metabolism ; Mutation ; MyoD Protein/genetics ; Myoblasts/*cytology/metabolism ; Precipitin Tests ; Protein Binding ; RNA Interference ; Recombinant Proteins/metabolism ; Regulatory Sequences, Nucleic Acid ; Transcription Factors/chemistry/genetics/*metabolism ; *Transcription, Genetic ; Xenopus/embryology/metabolism ; Xenopus Proteins
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  • 67
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Webster, Paul -- New York, N.Y. -- Science. 2004 Jun 18;304(5678):1730.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15205501" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Canada ; *Environmental Exposure ; Environmental Pollutants/analysis/toxicity ; Flame Retardants/*analysis/*toxicity ; Humans ; Milk, Human/*chemistry ; Phenyl Ethers/*analysis/blood/*toxicity ; United States
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  • 68
    Publication Date: 2004-07-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):168-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247450" target="_blank"〉PubMed〈/a〉
    Keywords: Biomedical Research/*legislation & jurisprudence ; Databases, Factual ; Epidemiologic Studies ; Genetic Privacy ; Genetics, Population ; *Health Insurance Portability and Accountability Act ; Humans ; Informed Consent ; Medical Records/*legislation & jurisprudence ; *Privacy ; Treatment Outcome ; United States
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  • 69
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miller, Greg -- New York, N.Y. -- Science. 2004 Oct 8;306(5694):207.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15472044" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; History, 20th Century ; History, 21st Century ; Humans ; *Nobel Prize ; Olfactory Receptor Neurons/physiology ; Rats ; *Receptors, Odorant/genetics/physiology ; Smell/*physiology ; United States
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  • 70
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):162.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247445" target="_blank"〉PubMed〈/a〉
    Keywords: *Congresses as Topic ; Hungary ; *National Institutes of Health (U.S.) ; *Neurosciences ; Public Policy ; *Travel ; United States ; United States Dept. of Health and Human Services
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  • 71
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-05-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 May 7;304(5672):807.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15131275" target="_blank"〉PubMed〈/a〉
    Keywords: Advisory Committees ; Animals ; *Conservation of Natural Resources ; *Fisheries ; *Oncorhynchus mykiss ; Population Density ; Public Policy ; *Salmon ; United States
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  • 72
    Publication Date: 2004-07-13
    Description: Erythropoietin (EPO) is both hematopoietic and tissue protective, putatively through interaction with different receptors. We generated receptor subtype-selective ligands allowing the separation of EPO's bioactivities at the cellular level and in animals. Carbamylated EPO (CEPO) or certain EPO mutants did not bind to the classical EPO receptor (EPOR) and did not show any hematopoietic activity in human cell signaling assays or upon chronic dosing in different animal species. Nevertheless, CEPO and various nonhematopoietic mutants were cytoprotective in vitro and conferred neuroprotection against stroke, spinal cord compression, diabetic neuropathy, and experimental autoimmune encephalomyelitis at a potency and efficacy comparable to EPO.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Leist, Marcel -- Ghezzi, Pietro -- Grasso, Giovanni -- Bianchi, Roberto -- Villa, Pia -- Fratelli, Maddalena -- Savino, Costanza -- Bianchi, Marina -- Nielsen, Jacob -- Gerwien, Jens -- Kallunki, Pekka -- Larsen, Anna Kirstine -- Helboe, Lone -- Christensen, Soren -- Pedersen, Lars O -- Nielsen, Mette -- Torup, Lars -- Sager, Thomas -- Sfacteria, Alessandra -- Erbayraktar, Serhat -- Erbayraktar, Zubeyde -- Gokmen, Necati -- Yilmaz, Osman -- Cerami-Hand, Carla -- Xie, Qiao-Wen -- Coleman, Thomas -- Cerami, Anthony -- Brines, Michael -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):239-42.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉H. Lundbeck A/S, 2500 Valby, Denmark.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247477" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis ; Binding Sites ; Cells, Cultured ; Diabetic Neuropathies/drug therapy ; Drug Design ; Encephalomyelitis, Autoimmune, Experimental/drug therapy ; Erythropoiesis ; Erythropoietin/*analogs & ; derivatives/chemistry/genetics/metabolism/pharmacology/*therapeutic use ; Female ; Hematocrit ; Humans ; Ligands ; Mice ; Mice, Inbred C3H ; Mutagenesis ; Nervous System Diseases/*drug therapy ; Neurons/metabolism ; Neuroprotective Agents/chemistry/metabolism/pharmacology/*therapeutic use ; Rats ; Rats, Sprague-Dawley ; Receptors, Erythropoietin/metabolism ; Recombinant Proteins ; Signal Transduction ; Spinal Cord Compression/drug therapy ; Stroke/drug therapy ; Structure-Activity Relationship
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  • 73
    Publication Date: 2004-06-26
    Description: Endogenous opioid binding to micro receptors is hypothesized to mediate natural rewards and has been proposed to be the basis of infant attachment behavior. Here, we report that micro-opioid receptor knockout mouse pups emit fewer ultrasonic vocalizations when removed from their mothers but not when exposed to cold or male mice odors. Moreover these knockout pups do not show a preference toward their mothers' cues and do not show ultrasonic calls potentiation after brief maternal exposure. Results from this study may indicate a molecular mechanism for diseases characterized by deficits in attachment behavior, such as autism or reactive attachment disorder.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moles, Anna -- Kieffer, Brigitte L -- D'Amato, Francesca R -- New York, N.Y. -- Science. 2004 Jun 25;304(5679):1983-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Consiglio Nazionale delle Ricerche Institute of Neuroscience, Psychobiology and Psychopharmacology, Viale Marx 43, 00137 Roma, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15218152" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Bedding and Linens ; *Behavior, Animal ; Cold Temperature ; Cues ; Female ; Genotype ; Male ; Maternal Behavior ; *Maternal Deprivation ; Mice ; Mice, Knockout ; *Mothers ; Mutation ; *Object Attachment ; Odors ; Receptors, Opioid, mu/genetics/*physiology ; Reward ; Vocalization, Animal
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  • 74
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-02-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):741.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764836" target="_blank"〉PubMed〈/a〉
    Keywords: Financing, Government ; Humans ; *National Institutes of Health (U.S.) ; *Peer Review, Research ; Politics ; *Research Support as Topic ; *Sexuality ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Davis, Mark A -- New York, N.Y. -- Science. 2004 Dec 10;306(5703):1891.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15591186" target="_blank"〉PubMed〈/a〉
    Keywords: *Awards and Prizes ; Female ; Humans ; Male ; Men ; *National Institutes of Health (U.S.) ; *Prejudice ; United States ; *Women
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-05-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 May 21;304(5674):1091.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15155918" target="_blank"〉PubMed〈/a〉
    Keywords: Bioethical Issues ; Conflict of Interest ; *Consultants ; Income ; National Institutes of Health (U.S.)/*ethics/standards ; Private Sector ; *Research Personnel/economics/ethics/standards ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Leshner, Alan I -- New York, N.Y. -- Science. 2004 Dec 24;306(5705):2163.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15618489" target="_blank"〉PubMed〈/a〉
    Keywords: *Budgets ; *Financing, Government ; Politics ; Public Policy ; Research Personnel ; *Science/education ; United States ; United States Government Agencies
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-05-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Apr 30;304(5671):662-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15118131" target="_blank"〉PubMed〈/a〉
    Keywords: Centers for Disease Control and Prevention (U.S.)/*organization & administration ; Disease Outbreaks ; Health Promotion ; Preventive Medicine ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stein, Zena -- Susser, Mervyn -- New York, N.Y. -- Science. 2004 Dec 10;306(5703):1890; author reply 1890.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15597431" target="_blank"〉PubMed〈/a〉
    Keywords: Anti-HIV Agents/*administration & dosage/pharmacology/therapeutic use ; *Condoms ; Double-Blind Method ; Female ; HIV Infections/*prevention & control/*transmission ; Humans ; Male ; National Institutes of Health (U.S.) ; Patient Selection ; Placebos ; Randomized Controlled Trials as Topic/*ethics ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grimm, David -- New York, N.Y. -- Science. 2004 Sep 24;305(5692):1905.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15448247" target="_blank"〉PubMed〈/a〉
    Keywords: Aquaporins/*metabolism ; *Awards and Prizes ; Computer Simulation/history ; History, 21st Century ; *Models, Molecular ; United States ; Water/*metabolism
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-03-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Mar 19;303(5665):1749.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15031469" target="_blank"〉PubMed〈/a〉
    Keywords: Advisory Committees ; *Conflict of Interest ; *Consultants ; Fees and Charges ; *National Institutes of Health (U.S.)/organization & administration/standards ; Public Policy ; Research Support as Topic ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-02-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Feb 27;303(5662):1272-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14988526" target="_blank"〉PubMed〈/a〉
    Keywords: Advisory Committees ; Ethics Committees, Research ; *Ethics, Research ; Guidelines as Topic ; Humans ; Maximum Allowable Concentration ; National Academy of Sciences (U.S.) ; Nontherapeutic Human Experimentation/*ethics/standards ; Pesticides/*toxicity ; United States ; *United States Environmental Protection Agency
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  • 83
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉White, Alice -- New York, N.Y. -- Science. 2004 Jun 11;304(5677):1595.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15192200" target="_blank"〉PubMed〈/a〉
    Keywords: Air Microbiology ; *Animal Husbandry ; Animals ; Drug Resistance, Bacterial ; Politics ; Public Policy ; *Science ; *Swine ; United States
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  • 84
    Publication Date: 2004-04-06
    Description: Huntington's disease (HD) is characterized by the accumulation of a pathogenic protein, Huntingtin (Htt), that contains an abnormal polyglutamine expansion. Here, we report that a pathogenic fragment of Htt (Httex1p) can be modified either by small ubiquitin-like modifier (SUMO)-1 or by ubiquitin on identical lysine residues. In cultured cells, SUMOylation stabilizes Httex1p, reduces its ability to form aggregates, and promotes its capacity to repress transcription. In a Drosophila model of HD, SUMOylation of Httex1p exacerbates neurodegeneration, whereas ubiquitination of Httex1p abrogates neurodegeneration. Lysine mutations that prevent both SUMOylation and ubiquitination of Httex1p reduce HD pathology, indicating that the contribution of SUMOylation to HD pathology extends beyond preventing Htt ubiquitination and degradation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Steffan, Joan S -- Agrawal, Namita -- Pallos, Judit -- Rockabrand, Erica -- Trotman, Lloyd C -- Slepko, Natalia -- Illes, Katalin -- Lukacsovich, Tamas -- Zhu, Ya-Zhen -- Cattaneo, Elena -- Pandolfi, Pier Paolo -- Thompson, Leslie Michels -- Marsh, J Lawrence -- CA-62203/CA/NCI NIH HHS/ -- HD36049/HD/NICHD NIH HHS/ -- HD36081/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2004 Apr 2;304(5667):100-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychiatry and Human Behavior, Gillespie 2121, University of California, Irvine, CA 92697, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15064418" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Genetically Modified ; Cell Line ; Cell Nucleus/metabolism ; Corpus Striatum/cytology ; Cytoplasm/metabolism ; Drosophila ; Genes, MDR ; HeLa Cells ; Humans ; Huntington Disease/metabolism/*pathology ; Lysine/genetics/metabolism ; Mutation ; Nerve Degeneration ; Nerve Tissue Proteins/chemistry/genetics/*metabolism ; Neurons/metabolism ; Nuclear Proteins/chemistry/genetics/*metabolism ; Proline/genetics/metabolism ; Promoter Regions, Genetic ; Rats ; Recombinant Fusion Proteins/metabolism ; SUMO-1 Protein/genetics/*metabolism ; Transcription, Genetic ; Transfection ; Ubiquitin/metabolism
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  • 85
    Publication Date: 2004-01-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Jan 23;303(5657):451.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14739430" target="_blank"〉PubMed〈/a〉
    Keywords: *Continental Population Groups ; *Delivery of Health Care ; *Ethnic Groups ; *Health Services Accessibility ; Humans ; Minority Groups ; Politics ; *Socioeconomic Factors ; United States ; United States Dept. of Health and Human Services
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  • 86
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grimm, David -- New York, N.Y. -- Science. 2004 Oct 15;306(5695):389.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15486263" target="_blank"〉PubMed〈/a〉
    Keywords: *Aneuploidy ; Animals ; Cell Cycle Proteins ; Child ; *Chromosomal Instability ; *DNA Repair ; *Genetic Predisposition to Disease ; Genomic Instability ; Humans ; Mice ; Mosaicism ; Mutation ; Neoplasms/*genetics ; Protein Kinases/genetics ; Protein-Serine-Threonine Kinases
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  • 87
    Publication Date: 2004-01-06
    Description: Hsp70s are a ubiquitous family of molecular chaperones involved in many cellular processes. Two Hsp70s, Lhs1p and Kar2p, are required for protein biogenesis in the yeast endoplasmic reticulum. Here, we found that Lhs1p and Kar2p specifically interacted to couple, and coordinately regulate, their respective activities. Lhs1p stimulated Kar2p by providing a specific nucleotide exchange activity, whereas Kar2p reciprocally activated the Lhs1p adenosine triphosphatase (ATPase). The two ATPase activities are coupled, and their coordinated regulation is essential for normal function in vivo.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Steel, Gregor J -- Fullerton, Donna M -- Tyson, John R -- Stirling, Colin J -- New York, N.Y. -- Science. 2004 Jan 2;303(5654):98-101.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Biological Sciences, University of Manchester, Manchester M13 9PT, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704430" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Triphosphatases/metabolism ; Adenosine Triphosphate/metabolism ; Carrier Proteins/metabolism ; Endoplasmic Reticulum/metabolism ; *Guanine Nucleotide Exchange Factors ; HSP70 Heat-Shock Proteins/chemistry/genetics/*metabolism ; Heat-Shock Proteins/chemistry/metabolism ; Membrane Transport Proteins/chemistry/metabolism ; Molecular Chaperones/chemistry/genetics/*metabolism ; Mutation ; Protein Binding ; Protein Folding ; Protein Structure, Tertiary ; Saccharomyces cerevisiae/genetics/*metabolism ; Saccharomyces cerevisiae Proteins/chemistry/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 88
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Leshner, Alan I -- New York, N.Y. -- Science. 2004 Oct 8;306(5694):197.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15472042" target="_blank"〉PubMed〈/a〉
    Keywords: Internationality ; Public Policy ; Publishing ; Religion and Science ; Research Support as Topic ; *Science ; United States
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  • 89
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grimm, David -- New York, N.Y. -- Science. 2004 Sep 24;305(5692):1907.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15448250" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Awards and Prizes ; Chiroptera/*physiology ; *Echolocation ; History, 21st Century ; *Multimedia ; United States
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 90
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brown, Kathryn -- New York, N.Y. -- Science. 2004 Aug 27;305(5688):1228-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15333816" target="_blank"〉PubMed〈/a〉
    Keywords: Aerosols ; *Air Microbiology ; Biological Warfare ; *Bioterrorism ; Environmental Monitoring/*instrumentation ; Humans ; Immunoassay ; Mass Spectrometry ; Molecular Probe Techniques ; Polymerase Chain Reaction ; Population Surveillance ; *Security Measures ; United States
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  • 91
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Michel J -- New York, N.Y. -- Science. 2004 Jun 11;304(5677):1595.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15192198" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Anthozoa ; *Conservation of Natural Resources ; *Ecosystem ; Environment ; *Fishes ; Seawater ; United States
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  • 92
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Levitan, Irwin B -- New York, N.Y. -- Science. 2004 Apr 16;304(5669):394-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neuroscience, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA. levitani@mail.med.upenn.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15087533" target="_blank"〉PubMed〈/a〉
    Keywords: Calcium/*metabolism ; Calcium Channels, L-Type/chemistry/*metabolism ; Calcium Signaling ; Calmodulin/chemistry/genetics/*metabolism ; Cell Membrane/metabolism ; Cytoplasm/metabolism ; Mutation ; Peptides/chemistry/genetics ; Recombinant Fusion Proteins/metabolism
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  • 93
    Publication Date: 2004-02-21
    Description: PTEN is a tumor suppressor protein that dephosphorylates phosphatidylinositol 3,4,5 trisphosphate and antagonizes the phosphatidylinositol-3 kinase signaling pathway. We show here that PTEN can also inhibit cell migration through its C2 domain, independent of its lipid phosphatase activity. This activity depends on the protein phosphatase activity of PTEN and on dephosphorylation at a single residue, threonine(383). The ability of PTEN to control cell migration through its C2 domain is likely to be an important feature of its tumor suppressor activity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Raftopoulou, Myrto -- Etienne-Manneville, Sandrine -- Self, Annette -- Nicholls, Sarah -- Hall, Alan -- New York, N.Y. -- Science. 2004 Feb 20;303(5661):1179-81.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Medical Research Council Laboratory for Molecular Cell Biology and Cell Biology Unit, Cancer Research UK Oncogene and Signal Transduction Group, University College London, Gower Street, London WC1E 6BT, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976311" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; COS Cells ; Catalysis ; Catalytic Domain ; Cell Line, Tumor ; Cell Movement/*physiology ; Cercopithecus aethiops ; Glioma ; Humans ; Mutation ; PTEN Phosphohydrolase ; Phosphoprotein Phosphatases/chemistry/metabolism ; Phosphoric Monoester Hydrolases/*chemistry/genetics/metabolism/*physiology ; Phosphorylation ; Phosphothreonine/metabolism ; Precipitin Tests ; Protein Structure, Tertiary ; Recombinant Proteins/pharmacology ; Sequence Deletion ; Transfection ; Tumor Suppressor Proteins/*chemistry/genetics/metabolism/*physiology
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  • 94
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grimm, David -- New York, N.Y. -- Science. 2004 Aug 27;305(5688):1235.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15333821" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biodiversity ; *Ecosystem ; Fisheries ; *Fishes ; Humans ; Population Density ; *Recreation ; United States
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  • 95
    Publication Date: 2004-04-17
    Description: Calmodulin (CaM) interactions with Ca2+ channels mediate both Ca2+ regulation of channels and local Ca2+ triggering of transcription factors implicated in neuronal memory. Crucial to these functions are the number of CaM molecules (CaMs) regulating each channel, and the number of CaMs privy to the local Ca2+ signal from each channel. To resolve these parameters, we fused L-type Ca2+ channels to single CaM molecules. These chimeric molecules revealed that a single CaM directs L-type channel regulation. Similar fusion molecules were used to estimate the local CaM concentration near Ca2+ channels. This estimate indicates marked enrichment of local CaM, as if a "school" of nearby CaMs were poised to enhance the transduction of local Ca2+ entry into diverse signaling pathways.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mori, Masayuki X -- Erickson, Michael G -- Yue, David T -- New York, N.Y. -- Science. 2004 Apr 16;304(5669):432-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ca2+ Signals Laboratory, Department of Biomedical Engineering , Johns Hopkins University School of Medicine, 720 Rutland Avenue, Baltimore, MD 21205, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15087548" target="_blank"〉PubMed〈/a〉
    Keywords: Calcium/*metabolism ; Calcium Channels, L-Type/chemistry/*metabolism ; Calcium Signaling ; Calmodulin/chemistry/genetics/*metabolism ; Cell Line ; Cell Nucleus/metabolism ; Cyclic AMP Response Element-Binding Protein/metabolism ; Fluorescence Resonance Energy Transfer ; Humans ; Mathematics ; Mutation ; Patch-Clamp Techniques ; Peptides/chemistry/genetics ; Protein Structure, Tertiary ; Recombinant Fusion Proteins/chemistry/metabolism ; Transfection
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  • 96
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gropp, Robert E -- New York, N.Y. -- Science. 2004 Oct 29;306(5697):811-2; author reply 811-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15514134" target="_blank"〉PubMed〈/a〉
    Keywords: *Budgets ; *Financial Support ; *Museums ; *Natural History ; Research Support as Topic ; United States
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  • 97
    Publication Date: 2004-04-10
    Description: Directionality in intracellular trafficking is essential to ensure the correct localization of proteins along the secretory pathway. Here, we found evidence for an active mechanism that prohibited back-fusion of de novo-generated vesicles with their donor compartment. Tip20p is a peripheral membrane protein implicated in consumption of COPI vesicles at the endoplasmic reticulum. However, a specific mutant of TIP20 did not interfere with COPII vesicle generation but allowed these vesicles to fuse back to the endoplasmic reticulum, a process that does not occur normally in the cell.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kamena, Faustin -- Spang, Anne -- New York, N.Y. -- Science. 2004 Apr 9;304(5668):286-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Friedrich Miescher Laboratorium der Max Planck Gesellschaft, Spemannstrasse 39, D-72076 Tubingen, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15073376" target="_blank"〉PubMed〈/a〉
    Keywords: COP-Coated Vesicles/*physiology/ultrastructure ; Carrier Proteins/genetics/*physiology ; Endoplasmic Reticulum/metabolism/*physiology/ultrastructure ; Glycoproteins/genetics/*physiology ; Golgi Apparatus/metabolism ; Intracellular Membranes/physiology/ultrastructure ; *Membrane Fusion ; Mutation ; Peptides/metabolism ; Protein Transport ; Recombinant Fusion Proteins/metabolism ; Saccharomyces cerevisiae/genetics/*physiology/ultrastructure ; Saccharomyces cerevisiae Proteins/genetics/metabolism ; Vesicular Transport Proteins ; alpha-Glucosidases/genetics/metabolism
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  • 98
    Publication Date: 2004-02-07
    Description: The 1918 "Spanish" influenza pandemic represents the largest recorded outbreak of any infectious disease. The crystal structure of the uncleaved precursor of the major surface antigen of the extinct 1918 virus was determined at 3.0 angstrom resolution after reassembly of the hemagglutinin gene from viral RNA fragments preserved in 1918 formalin-fixed lung tissues. A narrow avian-like receptor-binding site, two previously unobserved histidine patches, and a less exposed surface loop at the cleavage site that activates viral membrane fusion reveal structural features primarily found in avian viruses, which may have contributed to the extraordinarily high infectivity and mortality rates observed during 1918.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stevens, James -- Corper, Adam L -- Basler, Christopher F -- Taubenberger, Jeffery K -- Palese, Peter -- Wilson, Ian A -- AI058113/AI/NIAID NIH HHS/ -- AI42266/AI/NIAID NIH HHS/ -- AI50619/AI/NIAID NIH HHS/ -- CA55896/CA/NCI NIH HHS/ -- P50-GM 62411/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Mar 19;303(5665):1866-70. Epub 2004 Feb 5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764887" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Binding Sites ; Carbohydrate Conformation ; Cloning, Molecular ; Crystallography, X-Ray ; Glycosylation ; Hemagglutinin Glycoproteins, Influenza Virus/*chemistry/metabolism ; Histidine/chemistry/metabolism ; History, 20th Century ; Humans ; Hydrogen Bonding ; Influenza A virus/classification/*immunology/pathogenicity ; Influenza, Human/epidemiology/history/virology ; Molecular Sequence Data ; Protein Conformation ; Protein Structure, Quaternary ; Protein Structure, Secondary ; Protein Structure, Tertiary ; Receptors, Virus/metabolism ; Sialic Acids/metabolism
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  • 99
    Publication Date: 2004-10-23
    Description: Computational tools can markedly accelerate the rate at which murine genetic models can be analyzed. We developed a computational method for mapping phenotypic traits that vary among inbred strains onto haplotypic blocks. This method correctly predicted the genetic basis for strain-specific differences in several biologically important traits. It was also used to identify an allele-specific functional genomic element regulating H2-Ealpha gene expression. This functional element, which contained the binding sites for YY1 and a second transcription factor that is probably serum response factor, is located within the first intron of the H2-Ealpha gene. This computational method will greatly improve our ability to identify the genetic basis for a variety of phenotypic traits, ranging from qualitative trait information to quantitative gene expression data, which vary among inbred mouse strains.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Liao, Guochun -- Wang, Jianmei -- Guo, Jingshu -- Allard, John -- Cheng, Janet -- Ng, Anh -- Shafer, Steve -- Puech, Anne -- McPherson, John D -- Foernzler, Dorothee -- Peltz, Gary -- Usuka, Jonathan -- 1 R01 HG02322-01/HG/NHGRI NIH HHS/ -- New York, N.Y. -- Science. 2004 Oct 22;306(5696):690-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics and Genomics, Roche Palo Alto, 3431 Hillview Avenue, Palo Alto, CA 94304-1397, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15499019" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Binding Sites ; *Computational Biology ; Electrophoretic Mobility Shift Assay ; Gene Expression Profiling ; *Gene Expression Regulation ; Genes, MHC Class II ; Genetic Variation ; H-2 Antigens/*genetics ; Haplotypes ; Hydrocarbons, Aromatic/pharmacology ; Introns ; Liver/metabolism ; Lung/metabolism ; Major Histocompatibility Complex ; Mice ; Mice, Inbred Strains ; Oligodeoxyribonucleotides/metabolism ; Oligonucleotide Array Sequence Analysis ; Phenotype ; Polymorphism, Single Nucleotide ; Receptors, Aryl Hydrocarbon/chemistry/genetics/metabolism ; Regulatory Sequences, Nucleic Acid ; Serum Response Factor/metabolism ; Transcription Factors/metabolism
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  • 100
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Guy-Grand, Delphine -- Vassalli, Pierre -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):185-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Unite de Recherche et d'Expertise Antivirale, INSERM U277, Institut Pasteur, 75724 Paris Cedex 15, France. guygrand@pasteur.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247461" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; CD4-Positive T-Lymphocytes/immunology ; CD8-Positive T-Lymphocytes/immunology ; Cell Lineage ; DNA-Binding Proteins/metabolism ; Female ; Hematopoietic Stem Cells/immunology/physiology ; Immunity, Innate ; Immunity, Mucosal ; Interleukins/biosynthesis ; Intestinal Mucosa/cytology/*immunology ; Killer Cells, Natural/immunology ; Ligands ; Lymphoid Tissue/embryology/immunology ; Lymphotoxin-alpha/analysis ; Male ; Mice ; Mice, Nude ; Mice, Transgenic ; Models, Immunological ; Mutation ; Nuclear Receptor Subfamily 1, Group F, Member 3 ; Receptors, Antigen, T-Cell, alpha-beta/analysis/genetics ; Receptors, Antigen, T-Cell, gamma-delta/analysis ; Receptors, Retinoic Acid/genetics/metabolism ; Receptors, Thyroid Hormone/genetics/metabolism ; T-Lymphocyte Subsets/immunology ; T-Lymphocytes/*immunology ; Thymus Gland/cytology/*immunology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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