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  • Cells, Cultured  (48)
  • American Association for the Advancement of Science (AAAS)  (48)
  • American Meteorological Society
  • PANGAEA
  • 1995-1999  (48)
  • 1995  (48)
Collection
Publisher
  • American Association for the Advancement of Science (AAAS)  (48)
  • American Meteorological Society
  • PANGAEA
Years
  • 1995-1999  (48)
Year
  • 1
    Publication Date: 1995-07-07
    Description: Human T cell lymphotropic virus I (HTLV-I) is the etiological agent for adult T cell leukemia and tropical spastic paraparesis (also termed HTLV-I-associated myelopathy). HTLV-I-infected peripheral blood T cells exhibit an initial phase of interleukin-2 (IL-2)-dependent growth; over time, by an unknown mechanism, the cells become IL-2-independent. Whereas the Jak kinases Jak1 and Jak3 and the signal transducer and activator of transcription proteins Stat3 and Stat5 are activated in normal T cells in response to IL-2, this signaling pathway was constitutively activated in HTLV-I-transformed cells. In HTLV-I-infected cord blood lymphocytes, the transition from IL-2-dependent to IL-2-independent growth correlated with the acquisition of a constitutively activated Jak-STAT pathway, which suggests that this pathway participates in HTLV-I-mediated T cell transformation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Migone, T S -- Lin, J X -- Cereseto, A -- Mulloy, J C -- O'Shea, J J -- Franchini, G -- Leonard, W J -- New York, N.Y. -- Science. 1995 Jul 7;269(5220):79-81.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7604283" target="_blank"〉PubMed〈/a〉
    Keywords: Base Sequence ; Cell Line, Transformed ; *Cell Transformation, Viral ; Cells, Cultured ; DNA-Binding Proteins/*metabolism ; Enzyme Activation ; Fetal Blood/cytology ; Human T-lymphotropic virus 1/*physiology ; Humans ; Interleukin-2/pharmacology ; Janus Kinase 1 ; Janus Kinase 3 ; *Milk Proteins ; Molecular Sequence Data ; Phosphorylation ; Protein-Tyrosine Kinases/*metabolism ; Receptors, Interleukin-2/metabolism ; STAT3 Transcription Factor ; STAT5 Transcription Factor ; Signal Transduction ; T-Lymphocytes/metabolism/*virology ; Trans-Activators/*metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
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  • 2
    Publication Date: 1995-12-15
    Description: Immune responses dominated by interleukin-4 (IL-4)-producing T helper type 2 (TH2) cells or by interferon gamma (IFN-gamma)-producing T helper type 1 (TH1) cells express distinctive protection against infection with different pathogens. Interleukin-4 promotes the differentiation of naive CD4+ T cells into IL-4 producers and suppresses their development into IFN-gamma producers. CD1-specific splenic CD4+NK1.1+ T cells, a numerically minor population, produced IL-4 promptly on in vivo stimulation. This T cell population was essential for the induction of IL-4-producing cells and for switching to immunoglobulin E, an IL-4-dependent event, in response to injection of antibodies to immunoglobulin D.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yoshimoto, T -- Bendelac, A -- Watson, C -- Hu-Li, J -- Paul, W E -- New York, N.Y. -- Science. 1995 Dec 15;270(5243):1845-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institute of Health, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8525383" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; CD4-Positive T-Lymphocytes/*immunology ; Cells, Cultured ; Immunoglobulin E/*biosynthesis ; Interleukin-4/biosynthesis ; Killer Cells, Natural ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Spleen/cytology ; Th2 Cells/*immunology ; Thymus Gland/cytology
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  • 3
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-12-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fernandez-Sanchez, M T -- Novelli, A -- New York, N.Y. -- Science. 1995 Dec 22;270(5244):2019.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8533100" target="_blank"〉PubMed〈/a〉
    Keywords: Brain-Derived Neurotrophic Factor ; Cell Death/drug effects ; Cells, Cultured ; Cerebellum/cytology/drug effects ; Glutamic Acid/*toxicity ; Nerve Growth Factors/*pharmacology ; Nerve Tissue Proteins/*pharmacology ; Neurons/cytology/*drug effects ; Neurotrophin 3 ; Receptors, N-Methyl-D-Aspartate/physiology
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  • 4
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-01-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Montaner, L J -- Gordon, S -- New York, N.Y. -- Science. 1995 Jan 27;267(5197):538-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7824955" target="_blank"〉PubMed〈/a〉
    Keywords: Cells, Cultured ; Down-Regulation ; HIV-1/*physiology ; Humans ; Interleukins/biosynthesis/*immunology ; Macrophages/*virology ; T-Lymphocytes, Helper-Inducer/*immunology/virology ; Virus Replication
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  • 5
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-02-03
    Description: Neurotrophic factors participate in the development and maintenance of the nervous system. Application of ciliary neurotrophic factor (CNTF), a protein that promotes survival of motor neurons, resulted in an immediate potentiation of spontaneous and impulse-evoked transmitter release at developing neuromuscular synapses in Xenopus cell cultures. When CNTF was applied at the synapse, the onset of the potentiation was slower than that produced by application at the cell body of the presynaptic neuron. The potentiation effect was abolished when the neurite shaft was severed from the cell body. Thus, transmitter secretion from the nerve terminals is under immediate somatic control and can be regulated by CNTF.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stoop, R -- Poo, M M -- New York, N.Y. -- Science. 1995 Feb 3;267(5198):695-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences, Columbia University, New York, NY 10027.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7839148" target="_blank"〉PubMed〈/a〉
    Keywords: Acetylcholine/*metabolism ; Action Potentials/drug effects ; Animals ; Brain-Derived Neurotrophic Factor ; Calcium/metabolism ; Cells, Cultured ; Ciliary Neurotrophic Factor ; Cycloheximide/pharmacology ; Dactinomycin/pharmacology ; Nerve Tissue Proteins/metabolism/*pharmacology ; Neurites/physiology ; Neuromuscular Junction/drug effects/*metabolism ; Patch-Clamp Techniques ; Receptor, Ciliary Neurotrophic Factor ; Receptors, Nerve Growth Factor/metabolism ; *Signal Transduction ; Synapses/drug effects/*metabolism ; Synaptic Transmission ; Xenopus
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  • 6
    Publication Date: 1995-06-30
    Description: CD25 expression occurs early in thymocyte differentiation. The mechanism of induction of CD25 before T cell receptor rearrangement and the importance of this mechanism for T cell development are unknown. In a thymus reconstitution assay, tumor necrosis factor alpha (TNF-alpha) and interleukin-1 alpha (IL-1 alpha), two cytokines produced within the thymic microenvironment, induced CD25 expression on early immature thymocytes. Either TNF-alpha or IL-1 alpha was necessary for further thymocyte maturation and CD4+CD8+ differentiation. In irradiated mice reconstituted with CD117+CD25+ thymocytes, commitment to the T cell lineage was marked by the loss of precursor multipotency.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zuniga-Pflucker, J C -- Jiang, D -- Lenardo, M J -- New York, N.Y. -- Science. 1995 Jun 30;268(5219):1906-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7541554" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cells, Cultured ; Hematopoietic Stem Cells/*cytology/immunology ; Interleukin-1/pharmacology/*physiology ; Interleukin-7/pharmacology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, SCID ; Organ Culture Techniques ; Proto-Oncogene Proteins/biosynthesis ; Proto-Oncogene Proteins c-kit ; Receptor Protein-Tyrosine Kinases/biosynthesis ; Receptors, Colony-Stimulating Factor/biosynthesis ; Receptors, Interleukin-2/*biosynthesis ; Stromal Cells/physiology ; T-Lymphocyte Subsets/cytology/immunology ; T-Lymphocytes/*cytology/immunology ; Thymus Gland/cytology/*embryology/immunology ; Tumor Necrosis Factor-alpha/pharmacology/*physiology
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  • 7
    Publication Date: 1995-01-27
    Description: Lamellar ichthyosis is a severe congenital skin disorder characterized by generalized large scales and variable redness. Affected individuals in three families exhibited drastically reduced keratinocyte transglutaminase (TGK) activity. In two of these families, expression of TGK transcripts was diminished or abnormal and no TGK protein was detected. Homozygous or compound heterozygous mutations of the TGK gene were identified in all families. These data suggest that defects in TGK cause lamellar ichthyosis and that intact cross-linkage of cornified cell envelopes is required for epidermal tissue homeostasis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Huber, M -- Rettler, I -- Bernasconi, K -- Frenk, E -- Lavrijsen, S P -- Ponec, M -- Bon, A -- Lautenschlager, S -- Schorderet, D F -- Hohl, D -- New York, N.Y. -- Science. 1995 Jan 27;267(5197):525-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Dermatology, Centre Hospitalier Universitaire Vandois (CHUV), Hopital de Beaumont, Lausanne, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7824952" target="_blank"〉PubMed〈/a〉
    Keywords: Base Sequence ; Cell Membrane/metabolism ; Cells, Cultured ; Codon ; Female ; Gene Deletion ; Genetic Linkage ; Heterozygote ; Homozygote ; Humans ; Ichthyosis, Lamellar/enzymology/*genetics ; Introns ; Keratinocytes/*enzymology/ultrastructure ; Male ; Membrane Proteins/metabolism ; Molecular Sequence Data ; Mutation ; Pedigree ; Point Mutation ; Protein Precursors/metabolism ; Transglutaminases/*genetics/metabolism
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  • 8
    Publication Date: 1995-07-28
    Description: Human papillomaviruses (HPVs) are associated with the majority of cervical cancers and encode a transforming protein, E6, that interacts with the tumor suppressor protein p53. Because E6 has p53-independent transforming activity, the yeast two-hybrid system was used to search for other E6-binding proteins. One such protein, E6BP, interacted with cancer-associated HPV E6 and with bovine papillomavirus type 1 (BPV-1) E6. The transforming activity of BPV-1 E6 mutants correlated with their E6BP-binding ability. E6BP is identical to a putative calcium-binding protein, ERC-55, that appears to be localized in the endoplasmic reticulum.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chen, J J -- Reid, C E -- Band, V -- Androphy, E J -- R01CA44174/CA/NCI NIH HHS/ -- R29CA56803/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1995 Jul 28;269(5223):529-31.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Dermatology, New England Medical Center, Boston, MA, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7624774" target="_blank"〉PubMed〈/a〉
    Keywords: Bovine papillomavirus 1/physiology ; Calcium-Binding Proteins/analysis/*metabolism ; Cell Transformation, Viral ; Cells, Cultured ; Endoplasmic Reticulum/chemistry ; HeLa Cells ; Humans ; Oncogene Proteins, Viral/analysis/*metabolism ; *Papillomaviridae ; Recombinant Fusion Proteins/metabolism ; *Repressor Proteins ; Ubiquitin-Protein Ligases ; Viral Proteins/metabolism
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  • 9
    Publication Date: 1995-05-05
    Description: After germinal center B cells undergo somatic mutation and antigen selection, they become either memory B cells or plasma cells, but the signal requirements that control entry into either pathway have been unclear. When purified human germinal center cells were cultured with interleukin-2, interleukin-10, and cells expressing CD40 ligand, cells with characteristics of memory B cells were generated. Removal of CD40 ligand from the system resulted in terminal differentiation of germinal center B cells into cells with the characteristics of plasma cells. These results indicate that CD40 ligand directs the differentiation of germinal center B cells toward memory B cells rather than toward plasma cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Arpin, C -- Dechanet, J -- Van Kooten, C -- Merville, P -- Grouard, G -- Briere, F -- Banchereau, J -- Liu, Y J -- New York, N.Y. -- Science. 1995 May 5;268(5211):720-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Schering-Plough, Laboratory for Immunological Research, Dardilly, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7537388" target="_blank"〉PubMed〈/a〉
    Keywords: ADP-ribosyl Cyclase ; Antigens, CD/analysis ; Antigens, CD20 ; Antigens, CD38 ; Antigens, Differentiation/analysis ; Antigens, Differentiation, B-Lymphocyte/analysis ; B-Lymphocyte Subsets/*immunology ; CD40 Ligand ; Cell Differentiation/*immunology ; Cell Division/immunology ; Cells, Cultured ; Humans ; Immunoglobulin Isotypes/analysis ; Immunologic Memory/immunology ; Immunophenotyping ; Lymph Nodes/cytology ; Membrane Glycoproteins/immunology ; Plasma Cells/*immunology
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  • 10
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-07-28
    Description: Whether neurons express major histocompatibility complex (MHC) class I genes has not been firmly established. The techniques of confocal laser microscopy, patch clamp electrophysiology, and reverse transcriptase-polymerase chain reaction were combined here to directly examine the inducibility of MHC class I genes in individual cultured rat hippocampal neurons. Transcription of MHC class I genes was very rare in neurons with spontaneous action potentials. In electrically silent neurons, transcription was noted, with expression of beta 2-microglobulin under tighter control than in class I heavy chain molecules. Surface expression of class I molecules occurred only in electrically silent neurons treated with interferon gamma. Immunosurveillance by cytotoxic T cells may be focused on functionally impaired neurons.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Neumann, H -- Cavalie, A -- Jenne, D E -- Wekerle, H -- New York, N.Y. -- Science. 1995 Jul 28;269(5223):549-52.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neuroimmunology, Max Planck Institute for Psychiatry, Martinsried, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7624779" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials/drug effects ; Animals ; Base Sequence ; Cells, Cultured ; *Gene Expression Regulation ; *Genes, MHC Class I ; Hippocampus/cytology ; Histocompatibility Antigens Class I/biosynthesis/genetics ; Interferon-gamma/pharmacology ; Molecular Sequence Data ; Patch-Clamp Techniques ; Polymerase Chain Reaction ; Pyramidal Cells/cytology/*metabolism/physiology ; RNA, Messenger/genetics/metabolism ; Rats ; Rats, Inbred Lew ; Tetrodotoxin/pharmacology ; Transcription, Genetic ; beta 2-Microglobulin/biosynthesis/genetics
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  • 11
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-11-24
    Description: Opioid analgesia, the selective suppression of pain without effects on other sensations, also distinguishes between different types of pain: severe, persistent pain is potently inhibited by opioids, but they fail to cohceal the sensation of a pinprick. The cellular basis for this specificity was analyzed by means of patch-clamp experiments performed on fluorescently labeled nociceptive neurons (nociceptors) that innervate rat tooth pulp. Activation of the mu opioid receptor inhibited calcium channels on almost all small nociceptors but had minimal effect on large nociceptors. Somatostatin had the opposite specificity, preferentially inhibiting calcium channels on the large cells. Because persistent pain is mediated by slow-conducting, small nociceptors, opioids are thus likely to inhibit neurotransmitter release only at those primary synapses specialized for persistent pain.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Taddese, A -- Nah, S Y -- McCleskey, E W -- New York, N.Y. -- Science. 1995 Nov 24;270(5240):1366-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Vollum Institute, Oregon Health Sciences University, Portland 97201, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7481826" target="_blank"〉PubMed〈/a〉
    Keywords: Analgesics/*pharmacology ; Animals ; Calcium Channels/drug effects ; Cells, Cultured ; Dental Pulp/innervation ; Enkephalin, Ala(2)-MePhe(4)-Gly(5)- ; Enkephalins/*pharmacology ; Male ; Neurons, Afferent/*drug effects/physiology ; Neurotransmitter Agents/metabolism ; Nociceptors/*drug effects/physiology ; Patch-Clamp Techniques ; Presynaptic Terminals/drug effects/metabolism ; Rats ; Rats, Sprague-Dawley ; Receptors, Opioid, mu/*physiology ; Receptors, Somatostatin/physiology ; Sodium Channel Blockers ; Somatostatin/pharmacology
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  • 12
    Publication Date: 1995-01-06
    Description: Hematopoietic cells differentiate in steps marked by the acquisition or loss of specific phenotypic characteristics. Human bone marrow cells that were responsive to the early-acting cytokines Kit ligand and interleukin-3 were forced to a metabolic death. The subfraction remaining represented 1 in 10(5) bone marrow mononuclear cells, were determined to be quiescent by cell cycle analysis, and had a stem cell immunophenotype. The cells were highly enriched for long-term culture-initiating cells, were capable of secondary colony formation, and produced both myeloid and lymphoid progeny. Thus, this technically simple strategy led to the efficient purification of cells with characteristics of hematopoietic stem cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Berardi, A C -- Wang, A -- Levine, J D -- Lopez, P -- Scadden, D T -- R01-HL44851/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1995 Jan 6;267(5194):104-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Hematology/Oncology, Deaconess Hospital, Harvard Medical School, Boston, MA 02215.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7528940" target="_blank"〉PubMed〈/a〉
    Keywords: Antigens, CD/analysis ; Antigens, CD34 ; Base Sequence ; Cell Differentiation ; Cell Division ; Cell Separation/*methods ; Cells, Cultured ; Colony-Forming Units Assay ; DNA, Complementary/genetics ; Flow Cytometry ; Fluorouracil/pharmacology ; Hematopoietic Cell Growth Factors/pharmacology ; Hematopoietic Stem Cells/*cytology/drug effects ; Humans ; Immunophenotyping ; Interleukin-3/pharmacology ; Molecular Sequence Data ; Proto-Oncogene Proteins/analysis ; Proto-Oncogene Proteins c-kit ; Receptor Protein-Tyrosine Kinases/analysis ; Receptors, Colony-Stimulating Factor/analysis ; Stem Cell Factor
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  • 13
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-03-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉O'Brien, C -- New York, N.Y. -- Science. 1995 Mar 3;267(5202):1263-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7871418" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Adhesion ; Cell Adhesion Molecules, Neuronal/chemistry/*physiology ; Cells, Cultured ; Neurites/*physiology ; Neurons/*cytology ; Receptors, Fibroblast Growth Factor/chemistry/*physiology ; *Signal Transduction
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  • 14
    Publication Date: 1995-10-20
    Description: Adenosine deaminase (ADA) deficiency results in severe combined immunodeficiency, the first genetic disorder treated by gene therapy. Two different retroviral vectors were used to transfer ex vivo the human ADA minigene into bone marrow cells and peripheral blood lymphocytes from two patients undergoing exogenous enzyme replacement therapy. After 2 years of treatment, long-term survival of T and B lymphocytes, marrow cells, and granulocytes expressing the transferred ADA gene was demonstrated and resulted in normalization of the immune repertoire and restoration of cellular and humoral immunity. After discontinuation of treatment, T lymphocytes, derived from transduced peripheral blood lymphocytes, were progressively replaced by marrow-derived T cells in both patients. These results indicate successful gene transfer into long-lasting progenitor cells, producing a functional multilineage progeny.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bordignon, C -- Notarangelo, L D -- Nobili, N -- Ferrari, G -- Casorati, G -- Panina, P -- Mazzolari, E -- Maggioni, D -- Rossi, C -- Servida, P -- Ugazio, A G -- Mavilio, F -- B.36/Telethon/Italy -- New York, N.Y. -- Science. 1995 Oct 20;270(5235):470-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Telethon Gene Therapy Program for Genetic Diseases, DIBIT, Istituto Scientifico H. S. Raffaele, Milan, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7570000" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Deaminase/administration & ; dosage/blood/*deficiency/*genetics/therapeutic use ; Antibody Formation ; Base Sequence ; Bone Marrow Cells ; Cells, Cultured ; Child, Preschool ; *Gene Transfer Techniques ; *Genetic Therapy ; Genetic Vectors ; Hematopoietic Stem Cell Transplantation ; *Hematopoietic Stem Cells/enzymology ; Humans ; Immunity, Cellular ; Lymphocyte Transfusion ; *Lymphocytes/enzymology/immunology ; Molecular Sequence Data ; Severe Combined Immunodeficiency/enzymology/genetics/immunology/*therapy ; T-Lymphocytes/enzymology/immunology
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  • 15
    Publication Date: 1995-09-15
    Description: Before the fusion of synaptic vesicles with the plasma membrane, a protein complex is thought to form between VAMP--an integral membrane protein of the vesicle--and two proteins associated with the plasma membrane, SNAP-25 and syntaxin. The yeast two-hybrid interaction cloning system has now been used to identify additional proteins from Aplysia that interact directly with VAMP. A 33-kilodalton membrane protein, termed VAP-33 (VAMP-associated protein of 33 kilodaltons), was identified whose corresponding messenger RNA was detected only in the central nervous system and the gill of Aplysia. Presynaptic injection of antibodies specific for VAP-33 inhibited synaptic transmission, which suggests that VAP-33 is required for the exocytosis of neurotransmitter.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Skehel, P A -- Martin, K C -- Kandel, E R -- Bartsch, D -- R37 MH45923-06/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1995 Sep 15;269(5230):1580-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, College of Physicians and Surgeons of Columbia University, New York, NY 10032, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7667638" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Aplysia ; Base Sequence ; Carrier Proteins/chemistry/genetics/*physiology ; Cells, Cultured ; Central Nervous System/chemistry ; Cloning, Molecular ; Exocytosis ; Gills/innervation ; Membrane Proteins/chemistry/genetics/*metabolism/*physiology ; Molecular Sequence Data ; Molecular Weight ; Motor Neurons/physiology ; Nerve Tissue Proteins/*metabolism ; Neurons/*physiology ; Neurons, Afferent/physiology ; Neurotransmitter Agents/*metabolism ; R-SNARE Proteins ; *Synaptic Transmission ; Synaptic Vesicles/physiology ; *Vesicular Transport Proteins
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  • 16
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-02-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J -- New York, N.Y. -- Science. 1995 Feb 17;267(5200):963-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7863339" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Cell Cycle ; *Cell Differentiation ; Cells, Cultured ; Cyclin-Dependent Kinase Inhibitor p21 ; Cyclin-Dependent Kinases/antagonists & inhibitors ; Cyclins/genetics/*physiology ; Gene Expression Regulation, Developmental ; Mice ; Muscle, Skeletal/*cytology/embryology/metabolism
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  • 17
    Publication Date: 1995-09-22
    Description: The N-methyl-D-aspartate (NMDA) receptor subserves synaptic glutamate-induced transmission and plasticity in central neurons. The yeast two-hybrid system was used to show that the cytoplasmic tails of NMDA receptor subunits interact with a prominent postsynaptic density protein PSD-95. The second PDZ domain in PSD-95 binds to the seven-amino acid, COOH-terminal domain containing the terminal tSXV motif (where S is serine, X is any amino acid, and V is valine) common to NR2 subunits and certain NR1 splice forms. Transcripts encoding PSD-95 are expressed in a pattern similar to that of NMDA receptors, and the NR2B subunit co-localizes with PSD-95 in cultured rat hippocampal neurons. The interaction of these proteins may affect the plasticity of excitatory synapses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kornau, H C -- Schenker, L T -- Kennedy, M B -- Seeburg, P H -- NS-28710/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1995 Sep 22;269(5231):1737-40.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Molecular Biology (ZMBH), University of Heidelberg, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7569905" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Base Sequence ; Cells, Cultured ; Cytoplasm/chemistry ; Genes, Reporter ; Hippocampus/*metabolism ; Intracellular Signaling Peptides and Proteins ; Membrane Proteins ; Molecular Sequence Data ; Nerve Tissue Proteins/chemistry/genetics/*metabolism ; Neuronal Plasticity ; Neurons/*metabolism ; RNA Splicing ; Rats ; Receptors, N-Methyl-D-Aspartate/chemistry/genetics/*metabolism ; Recombinant Fusion Proteins/metabolism ; Signal Transduction
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  • 18
    Publication Date: 1995-02-10
    Description: Integrin receptors mediate cell adhesion, signal transduction, and cytoskeletal organization. How a single transmembrane receptor can fulfill multiple functions was clarified by comparing roles of receptor occupancy and aggregation. Integrin occupancy by monovalent ligand induced receptor redistribution, but minimal tyrosine phosphorylation signaling or cytoskeletal protein redistribution. Aggregation of integrins by noninhibitory monoclonal antibodies on beads induced intracellular accumulations of pp125FAK and tensin, as well as phosphorylation, but no accumulation of other cytoskeletal proteins such as talin. Combining antibody-mediated clustering with monovalent ligand occupancy induced accumulation of seven cytoskeletal proteins, including alpha-actinin, talin, and F-actin, thereby mimicking multivalent interactions with fibronectin or polyvalent peptides. Integrins therefore mediate a complex repertoire of functions through the distinct effects of receptor aggregation, receptor occupancy, or both together.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miyamoto, S -- Akiyama, S K -- Yamada, K M -- New York, N.Y. -- Science. 1995 Feb 10;267(5199):883-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Developmental Biology, National Institute of Dental Research, National Institutes of Health, Bethesda, MD 20892-4370.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7846531" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Antibodies, Monoclonal ; Cell Adhesion Molecules/metabolism ; Cell Membrane/*metabolism ; Cells, Cultured ; Cytoskeletal Proteins/*metabolism ; Focal Adhesion Kinase 1 ; Focal Adhesion Protein-Tyrosine Kinases ; Humans ; Integrins/*physiology ; Ligands ; Microfilament Proteins/metabolism ; Molecular Sequence Data ; Oligopeptides/metabolism ; Phosphorylation ; Protein-Tyrosine Kinases/metabolism ; Signal Transduction ; Tyrosine/metabolism
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  • 19
    Publication Date: 1995-06-09
    Description: Fluorescent probes offer insight into the highly localized and rapid molecular events that underlie cell function. However, methods are required that can efficiently transform the limited signals from such probes into high-resolution images. An algorithm has now been developed that produces highly accurate images of fluorescent probe distribution inside cells with minimal light exposure and a conventional light microscope. This method provides resolution nearly four times greater than that currently available from any fluorescence microscope and was used to study several biological problems.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Carrington, W A -- Lynch, R M -- Moore, E D -- Isenberg, G -- Fogarty, K E -- Fay, F S -- New York, N.Y. -- Science. 1995 Jun 9;268(5216):1483-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Program in Molecular Medicine, University of Massachusetts Medical School, Worcester 01605, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7770772" target="_blank"〉PubMed〈/a〉
    Keywords: Algorithms ; Animals ; Calcium Channels/analysis ; Cell Line ; Cell Physiological Phenomena ; Cells/*chemistry/*ultrastructure ; Cells, Cultured ; Fluorescence ; *Fluorescent Dyes ; Guinea Pigs ; Hexokinase/analysis ; *Image Processing, Computer-Assisted ; Light ; Microscopy, Fluorescence ; Microtubules/ultrastructure ; Muscle Proteins/analysis ; Muscle, Smooth/cytology/enzymology ; Rats ; Ryanodine Receptor Calcium Release Channel
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 20
    Publication Date: 1995-12-15
    Description: The relative locations of several chromosomes within wheel-shaped prometaphase chromosome rosettes of human fibroblasts and HeLa cells were determined with fluorescence hybridization. Homologs were consistently positioned on opposite sides of the rosette, which suggests that chromosomes are separated into two haploid sets, each derived from one parent. The relative locations of chromosomes on the rosette were mapped by dual hybridizations. The data suggest that the chromosome orders within the two haploid sets are antiparallel. This chromosome arrangement in human cells appears to be both independent of cell type- and species-specific and may influence chromosome topology throughout the cell cycle.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nagele, R -- Freeman, T -- McMorrow, L -- Lee, H Y -- New York, N.Y. -- Science. 1995 Dec 15;270(5243):1831-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, University of Medicine and Dentistry of New Jersey, School of Osteopathic Medicine, Stratford 08084, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8525379" target="_blank"〉PubMed〈/a〉
    Keywords: Cells, Cultured ; Chromosomes/*physiology/ultrastructure ; DNA Probes ; Fibroblasts/ultrastructure ; HeLa Cells ; Humans ; In Situ Hybridization, Fluorescence ; Metaphase/genetics/*physiology
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  • 21
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-09-15
    Description: Endogenously synthesized antigenic determinants are generally presented on major histocompatibility complex (MHC) class I molecules, whereas exogenous determinants are presented by MHC class II molecules. Here, it is shown that exogenous antigens chaperoned by a heat shock protein can be channeled into the endogenous pathway, presented by MHC class I molecules, and recognized by CD8+ T lymphocytes. This pathway is functional only in a subset of macrophages among the cell types tested. These observations provide a basis for the tumor-specific and virus-specific immunogenicity of cognate heat shock protein preparations and offer a mechanism for the classical phenomenon of cross-priming.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Suto, R -- Srivastava, P K -- CA44786/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1995 Sep 15;269(5230):1585-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences, Fordham University, Bronx, NY 10458, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7545313" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Antigen Presentation ; Antigens, Neoplasm/*immunology ; Antigens, Viral/*immunology ; Cells, Cultured ; Chaperonins/*immunology ; Cytotoxicity, Immunologic ; Epitopes ; Histocompatibility Antigens Class I/immunology ; Macrophages/*immunology ; Macrophages, Peritoneal/immunology ; Mice ; Mice, Inbred C57BL ; Molecular Sequence Data ; Peptides/immunology ; T-Lymphocytes, Cytotoxic/*immunology ; Transfection ; Tumor Necrosis Factor-alpha/metabolism ; Vesicular stomatitis Indiana virus/*immunology
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  • 22
    Publication Date: 1995-07-28
    Description: T cell hybridomas require the immediate-early gene NGFI-B (nur77) for T cell receptor (TCR)-mediated apoptosis, a model for negative selection of self-reactive T cells. TCR-mediated death was examined in mice bearing an NGFI-B loss-of-function mutation, either by administration of antibodies to CD3 (anti-CD3) or in two well-characterized transgenic models expressing self-reactive TCRs. Both the extent and the rate of thymocyte death were unimpaired. Anti-CD3-induced death was normal in CD4+ peripheral T cells, in which death is mediated predominantly by the Fas signaling pathway. Thus, no unique requirement for NGFI-B is observed for thymic or peripheral T cell death.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lee, S L -- Wesselschmidt, R L -- Linette, G P -- Kanagawa, O -- Russell, J H -- Milbrandt, J -- P01 CA49712/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1995 Jul 28;269(5223):532-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7624775" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibodies ; Antigens, CD3/immunology/physiology ; *Apoptosis ; Cells, Cultured ; Clonal Deletion ; Crosses, Genetic ; DNA-Binding Proteins/genetics/*physiology ; Female ; Gene Targeting ; Hybridomas ; Male ; Mice ; Mice, Transgenic ; Nuclear Receptor Subfamily 4, Group A, Member 1 ; Receptors, Antigen, T-Cell, alpha-beta/*physiology ; Receptors, Cytoplasmic and Nuclear ; Receptors, Steroid/genetics/*physiology ; Stem Cells ; T-Lymphocyte Subsets/cytology ; T-Lymphocytes/*cytology/immunology ; Thymus Gland/cytology ; Transcription Factors/genetics/*physiology
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  • 23
    Publication Date: 1995-09-15
    Description: Cyclin-dependent kinases (CDKs) are activated by CDC25 phosphatases, which remove inhibitory phosphate from tyrosine and threonine residues. In human cells, CDC25 proteins are encoded by a multigene family, consisting of CDC25A, CDC25B, and CDC25C. In rodent cells, human CDC25A or CDC25B but not CDC25C phosphatases cooperate with either Ha-RASG12V or loss of RB1 in oncogenic focus formation. Such transformants were highly aneuploid, grew in soft agar, and formed high-grade tumors in nude mice. Overexpression of CDC25B was detected in 32 percent of human primary breast cancers tested. The CDC25 phosphatases may contribute to the development of human cancer.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Galaktionov, K -- Lee, A K -- Eckstein, J -- Draetta, G -- Meckler, J -- Loda, M -- Beach, D -- New York, N.Y. -- Science. 1995 Sep 15;269(5230):1575-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Cold Spring Harbor Laboratory, NY 11724, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7667636" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Breast Neoplasms/genetics ; Cell Cycle Proteins/*genetics ; Cell Division ; *Cell Transformation, Neoplastic ; Cells, Cultured ; Gene Expression ; Genes, Retinoblastoma ; Genes, p53 ; Genes, ras ; Humans ; In Situ Hybridization ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; *Multigene Family ; Neoplasm Transplantation ; *Oncogenes ; Phosphoprotein Phosphatases/*genetics ; Prognosis ; Transfection ; Tumor Cells, Cultured ; cdc25 Phosphatases
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  • 24
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-01-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Linskens, M H -- Harley, C B -- West, M D -- Campisi, J -- Hayflick, L -- New York, N.Y. -- Science. 1995 Jan 6;267(5194):17.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7848496" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Apoptosis ; *Cell Aging ; Cell Division ; Cells, Cultured ; Humans ; Telomere/physiology
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  • 25
    Publication Date: 1995-01-06
    Description: Specificity of protein kinases and phosphatases may be achieved through compartmentalization with preferred substrates. In neurons, adenosine 3', 5'-monophosphate (cAMP)-dependent protein kinase (PKA) is localized at postsynaptic densities by association of its regulatory subunit with an A kinase anchor protein, AKAP79. Interaction cloning experiments demonstrated that AKAP79 also binds protein phosphatase 2B, or calcineurin (CaN). A ternary complex of PKA, AKAP, and CaN was isolated from bovine brain, and colocalization of the kinase and the phosphatase was established in neurites of cultured hippocampal neurons. The putative CaN-binding domain of AKAP79 is similar to that of the immunophilin FKBP-12, and AKAP79 inhibited CaN phosphatase activity. These results suggest that both PKA and CaN are targeted to subcellular sites by association with a common anchor protein and thereby regulate the phosphorylation state of key neuronal substrates.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Coghlan, V M -- Perrino, B A -- Howard, M -- Langeberg, L K -- Hicks, J B -- Gallatin, W M -- Scott, J D -- DK09059/DK/NIDDK NIH HHS/ -- GM48231/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1995 Jan 6;267(5194):108-11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Vollum Institute, Oregon Health Sciences University, Portland 97201.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7528941" target="_blank"〉PubMed〈/a〉
    Keywords: A Kinase Anchor Proteins ; *Adaptor Proteins, Signal Transducing ; Amino Acid Sequence ; Animals ; Binding Sites ; *Brain Chemistry ; Calcineurin ; Calmodulin-Binding Proteins/analysis/antagonists & inhibitors/*metabolism ; Carrier Proteins/analysis ; Cattle ; Cells, Cultured ; Cyclic AMP-Dependent Protein Kinases/analysis/*metabolism ; Hippocampus/chemistry ; Molecular Sequence Data ; Neurites/chemistry ; Phosphoprotein Phosphatases/analysis/antagonists & inhibitors/*metabolism ; Phosphorylation ; Proteins/*metabolism/pharmacology ; Rats ; Recombinant Proteins/pharmacology ; Tacrolimus/pharmacology
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  • 26
    Publication Date: 1995-03-03
    Description: Cell cycle checkpoints enhance genetic fidelity by causing arrest at specific stages of the cell cycle when previous events have not been completed. The tumor suppressor p53 has been implicated in a G1 checkpoint. To investigate whether p53 also participates in a mitotic checkpoint, cultured fibroblasts from p53-deficient mouse embryos were exposed to spindle inhibitors. The fibroblasts underwent multiple rounds of DNA synthesis without completing chromosome segregation, thus forming tetraploid and octaploid cells. Deficiency of p53 was also associated with the development of tetraploidy in vivo. These results suggest that murine p53 is a component of a spindle checkpoint that ensures the maintenance of diploidy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cross, S M -- Sanchez, C A -- Morgan, C A -- Schimke, M K -- Ramel, S -- Idzerda, R L -- Raskind, W H -- Reid, B J -- R01CA55814/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1995 Mar 3;267(5202):1353-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, University of Washington, Seattle 98195.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7871434" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Cycle ; Cells, Cultured ; DNA/biosynthesis ; Demecolcine/pharmacology ; Diploidy ; Female ; Genes, p53 ; Male ; Mice ; *Mitosis ; Nocodazole/pharmacology ; Ploidies ; Spindle Apparatus/*physiology ; Tumor Suppressor Protein p53/*physiology
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  • 27
    Publication Date: 1995-06-16
    Description: Long-term potentiation has previously been studied with electrophysiological techniques that do not readily separate presynaptic and postsynaptic contributions. Changes in exocytotic-endocytotic cycling have now been monitored at synapses between cultured rat hippocampal neurons by measuring the differential uptake of antibodies that recognize the intraluminal domain of the synaptic vesicle protein synaptotagmin. Vesicular cycling increased markedly during glutamate-induced long-term potentiation. The degree of potentiation was heterogeneous, appearing greater at synapses at which the initial extent of vesicular turnover was low. Thus, changes in presynaptic activity were visualized directly and the spatial distribution of potentiation could be determined at the level of single synaptic boutons.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Malgaroli, A -- Ting, A E -- Wendland, B -- Bergamaschi, A -- Villa, A -- Tsien, R W -- Scheller, R H -- D.016/Telethon/Italy -- New York, N.Y. -- Science. 1995 Jun 16;268(5217):1624-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Scientific Institute San Raffaele, Milan, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7777862" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; *Calcium-Binding Proteins ; Cells, Cultured ; Glutamic Acid/pharmacology ; Hippocampus/*cytology/physiology ; Long-Term Potentiation/drug effects/*physiology ; Membrane Glycoproteins/analysis/immunology ; Molecular Sequence Data ; Nerve Tissue Proteins/analysis/immunology ; Neurons/*physiology ; Patch-Clamp Techniques ; Potassium/pharmacology ; Presynaptic Terminals/drug effects/*physiology ; Pyrroles/pharmacology ; Rats ; Receptors, N-Methyl-D-Aspartate/physiology ; *Synaptic Transmission/drug effects ; Synaptic Vesicles/chemistry/metabolism ; Synaptotagmins
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  • 28
    Publication Date: 1995-07-14
    Description: CD22 is a membrane immunoglobulin (mIg)-associated protein of B cells. CD22 is tyrosine-phosphorylated when mIg is ligated. Tyrosine-phosphorylated CD22 binds and activates SHP, a protein tyrosine phosphatase known to negatively regulate signaling through mIg. Ligation of CD22 to prevent its coaggregation with mIg lowers the threshold at which mIg activates the B cell by a factor of 100. In secondary lymphoid organs, CD22 may be sequestered away from mIg through interactions with counterreceptors on T cells. Thus, CD22 is a molecular switch for SHP that may bias mIg signaling to anatomic sites rich in T cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Doody, G M -- Justement, L B -- Delibrias, C C -- Matthews, R J -- Lin, J -- Thomas, M L -- Fearon, D T -- GM-46524/GM/NIGMS NIH HHS/ -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 1995 Jul 14;269(5221):242-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Trust Immunology Unit, Department of Medicine, University of Cambridge, School of Clinical Medicine, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7618087" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Antigens, CD/*immunology/metabolism ; Antigens, Differentiation, B-Lymphocyte/*immunology/metabolism ; B-Lymphocytes/*immunology ; *Cell Adhesion Molecules ; Cells, Cultured ; Humans ; Immunoglobulin M/immunology ; Intracellular Signaling Peptides and Proteins ; *Lectins ; *Lymphocyte Activation ; Mice ; Molecular Sequence Data ; Phosphorylation ; Protein Tyrosine Phosphatase, Non-Receptor Type 11 ; Protein Tyrosine Phosphatase, Non-Receptor Type 6 ; Protein Tyrosine Phosphatases/*metabolism ; Recombinant Proteins/metabolism ; Sialic Acid Binding Ig-like Lectin 2 ; Signal Transduction ; Tumor Cells, Cultured
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  • 29
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-04-28
    Description: The effects of neurotrophins on several forms of neuronal degeneration in murine cortical cell cultures were examined. Consistent with other studies, brain-derived neurotrophic factor, neurotrophin-3, and neurotrophin-4/5 all attenuated the apoptotic death induced by serum deprivation or exposure to the calcium channel antagonist nimodipine. Unexpectedly, however, 24-hour pretreatment with these same neurotrophins markedly potentiated the necrotic death induced by exposure to oxygen-glucose deprivation or N-methyl-D-aspartate. Thus, certain neurotrophins may have opposing effects on different types of death in the same neurons.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koh, J Y -- Gwag, B J -- Lobner, D -- Choi, D W -- NS 30337/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1995 Apr 28;268(5210):573-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for the Study of Nervous System Injury, Washington University School of Medicine, St. Louis, MO 63110, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7725105" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis/drug effects ; Brain-Derived Neurotrophic Factor ; Calcium/metabolism ; Cell Death/drug effects ; Cells, Cultured ; Cerebral Cortex/cytology ; Dizocilpine Maleate/pharmacology ; Mice ; N-Methylaspartate/pharmacology ; Necrosis ; Nerve Degeneration/*drug effects ; Nerve Growth Factors/*pharmacology ; Nerve Tissue Proteins/pharmacology ; Neurons/*cytology/drug effects/pathology ; Neurotrophin 3 ; Quinoxalines/pharmacology ; Receptors, AMPA/antagonists & inhibitors
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  • 30
    Publication Date: 1995-10-13
    Description: Stimulation of rat vascular smooth muscle cells (VSMCs) by platelet-derived growth factor (PDGF) transiently increased the intracellular concentration of hydrogen peroxide (H2O2). This increase could be blunted by increasing the intracellular concentration of the scavenging enzyme catalase or by the chemical antioxidant N-acetylcysteine. The response of VSMCs to PDGF, which includes tyrosine phosphorylation, mitogen-activated protein kinase stimulation, DNA synthesis, and chemotaxis, was inhibited when the growth factor-stimulated rise in H2O2 concentration was blocked. These results suggest that H2O2 may act as a signal-transducing molecule, and they suggest a potential mechanism for the cardioprotective effects of antioxidants.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sundaresan, M -- Yu, Z X -- Ferrans, V J -- Irani, K -- Finkel, T -- New York, N.Y. -- Science. 1995 Oct 13;270(5234):296-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cardiology Branch, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, MD 20892-1650, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7569979" target="_blank"〉PubMed〈/a〉
    Keywords: Acetylcysteine/pharmacology ; Adenoviridae/genetics/physiology ; Animals ; Calcium-Calmodulin-Dependent Protein Kinases/metabolism ; Catalase/metabolism ; Cell Line ; Cells, Cultured ; Chemotaxis/drug effects ; Endopeptidase K ; Free Radical Scavengers/pharmacology ; Humans ; Hydrogen Peroxide/*metabolism ; Mitogen-Activated Protein Kinase 1 ; Mitogen-Activated Protein Kinase 3 ; *Mitogen-Activated Protein Kinases ; Muscle, Smooth, Vascular/cytology/drug effects/*metabolism/virology ; Phosphorylation ; Phosphotyrosine/metabolism ; Platelet-Derived Growth Factor/*pharmacology ; Protein-Tyrosine Kinases/metabolism ; Rats ; Serine Endopeptidases/metabolism ; *Signal Transduction
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 31
    Publication Date: 1995-12-15
    Description: Evidence suggests that CD8+ T lymphocytes are involved in the control of human immunodeficiency virus (HIV) infection in vivo, either by cytolytic mechanisms or by the release of HIV-suppressive factors (HIV-SF). The chemokines RANTES, MIP-1 alpha, and MIP-1 beta were identified as the major HIV-SF produced by CD8+ T cells. Two active proteins purified from the culture supernatant of an immortalized CD8+ T cell clone revealed sequence identity with human RANTES and MIP-1 alpha. RANTES, MIP-1 alpha, and MIP-1 beta were released by both immortalized and primary CD8+ T cells. HIV-SF activity produced by these cells was completely blocked by a combination of neutralizing antibodies against RANTES, MIP-1 alpha, and MIP-1 beta. Recombinant human RANTES, MIP-1 alpha, and MIP-1 beta induced a dose-dependent inhibition of different strains of HIV-1, HIV-2, and simian immunodeficiency virus (SIV). These data may have relevance for the prevention and therapy of AIDS.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cocchi, F -- DeVico, A L -- Garzino-Demo, A -- Arya, S K -- Gallo, R C -- Lusso, P -- New York, N.Y. -- Science. 1995 Dec 15;270(5243):1811-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Tumor Cell Biology, National Cancer Institute, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8525373" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Amino Acid Sequence ; Animals ; Antiviral Agents/*physiology ; CD8-Positive T-Lymphocytes/*immunology ; Cell Division/physiology ; Cell Line ; Cells, Cultured ; Chemokine CCL4 ; Chemokine CCL5/antagonists & inhibitors/*immunology ; Culture Media, Conditioned ; Cytokines/antagonists & inhibitors/*immunology ; Dose-Response Relationship, Immunologic ; Escherichia coli ; HIV Infections/immunology ; HIV-1/*immunology ; HIV-2/immunology ; Herpesvirus 6, Human/immunology ; Herpesvirus 7, Human/immunology ; Human T-lymphotropic virus 1/immunology ; Humans ; Immunoglobulin G/immunology ; Lymphocyte Activation ; Macaca nemestrina ; Macrophage Inflammatory Proteins ; Molecular Sequence Data ; Monokines/antagonists & inhibitors/*immunology ; Recombinant Proteins/immunology ; Simian Immunodeficiency Virus/immunology
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  • 32
    Publication Date: 1995-11-24
    Description: Development of the mammalian nervous system is regulated by neural impulse activity, but the molecular mechanisms are not well understood. If cell recognition molecules [for example, L1 and the neural cell adhesion molecule (NCAM)] were influenced by specific patterns of impulse activity, cell-cell interactions controlling nervous system structure could be regulated by nervous system function at critical stages of development. Low-frequency electrical pulses delivered to mouse sensory neurons in culture (0.1 hertz for 5 days) down-regulated expression of L1 messenger RNA and protein (but not NCAM). Fasciculation of neurites, adhesion of neuroblastoma cells, and the number of Schwann cells on neurites was reduced after 0.1-hertz stimulation, but higher frequencies or stimulation after synaptogenesis were without effect.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Itoh, K -- Stevens, B -- Schachner, M -- Fields, R D -- New York, N.Y. -- Science. 1995 Nov 24;270(5240):1369-72.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉National Institutes of Health, National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7481827" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/physiology ; Cell Adhesion ; Cells, Cultured ; Down-Regulation ; Electric Stimulation ; Ganglia, Spinal/cytology ; Leukocyte L1 Antigen Complex ; Mice ; Nerve Growth Factors/pharmacology ; Neural Cell Adhesion Molecules/*biosynthesis/genetics ; Neurites/physiology ; Neurons, Afferent/*metabolism/physiology ; RNA, Messenger/genetics/metabolism ; Schwann Cells/physiology ; Spinal Cord/cytology/physiology ; Tumor Cells, Cultured
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  • 33
    Publication Date: 1995-09-22
    Description: Activation of early response genes by interferons (IFNs) requires tyrosine phosphorylation of STAT (signal transducers and activators of transcription) proteins. It was found that the serine-threonine kinase mitogen-activated protein kinase (MAPK) [specifically, the 42-kilodalton MAPK or extracellular signal-regulated kinase 2 (ERK2)] interacted with the alpha subunit of IFN-alpha/beta receptor in vitro and in vivo. Treatment of cells with IFN-beta induced tyrosine phosphorylation and activation of MAPK and caused MAPK and Stat1 alpha to coimmunoprecipitate. Furthermore, expression of dominant negative MAPK inhibited IFN-beta-induced transcription. Therefore, MAPK appears to regulate IFN-alpha and IFN-beta activation of early response genes by modifying the Jak-STAT signaling cascade.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉David, M -- Petricoin, E 3rd -- Benjamin, C -- Pine, R -- Weber, M J -- Larner, A C -- GM47332/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1995 Sep 22;269(5231):1721-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Cytokine Biology, Center for Biologics Evaluation and Research, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7569900" target="_blank"〉PubMed〈/a〉
    Keywords: Binding Sites ; Calcium-Calmodulin-Dependent Protein Kinases/*metabolism ; Cells, Cultured ; DNA-Binding Proteins/*metabolism ; Enzyme Activation ; *Gene Expression Regulation ; Humans ; Interferon-alpha/pharmacology ; Interferon-beta/*pharmacology ; Membrane Proteins ; Mitogen-Activated Protein Kinase 1 ; Phosphorylation ; Receptor, Interferon alpha-beta ; Receptors, Interferon/*metabolism ; Recombinant Fusion Proteins/metabolism ; STAT1 Transcription Factor ; *Signal Transduction ; Trans-Activators/*metabolism ; Transcription, Genetic ; Transfection ; Tumor Cells, Cultured ; Tyrosine/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 34
    Publication Date: 1995-11-10
    Description: The role of the cell-surface molecule CTLA-4 in the regulation of T cell activation has been controversial. Here, lymph nodes and spleens of CTLA-4-deficient mice accumulated T cell blasts with up-regulated activation markers. These blast cells also infiltrated liver, heart, lung, and pancreas tissue, and amounts of serum immunoglobulin were elevated. The mice invariably became moribund by 3 to 4 weeks of age. Although CTLA-4-deficient T cells proliferated spontaneously and strongly when stimulated through the T cell receptor, they were sensitive to cell death induced by cross-linking of the Fas receptor and by gamma irradiation. Thus, CTLA-4 acts as a negative regulator of T cell activation and is vital for the control of lymphocyte homeostasis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Waterhouse, P -- Penninger, J M -- Timms, E -- Wakeham, A -- Shahinian, A -- Lee, K P -- Thompson, C B -- Griesser, H -- Mak, T W -- New York, N.Y. -- Science. 1995 Nov 10;270(5238):985-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Immunology, University of Toronto, Ontario, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7481803" target="_blank"〉PubMed〈/a〉
    Keywords: Abatacept ; Animals ; Antigens, CD/analysis ; Antigens, CD95/metabolism ; Antigens, Differentiation/genetics/*physiology ; Apoptosis ; B-Lymphocytes/immunology ; CTLA-4 Antigen ; Cells, Cultured ; Concanavalin A/pharmacology ; Female ; Gamma Rays ; Gene Targeting ; Homeostasis ; *Immunoconjugates ; Immunoglobulins/blood ; Immunophenotyping ; Lymph Nodes/immunology/pathology ; *Lymphocyte Activation ; Lymphoproliferative Disorders/*immunology/pathology ; Male ; Mice ; Mice, Inbred C57BL ; Spleen/immunology/pathology ; T-Lymphocytes/*immunology
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  • 35
    Publication Date: 1995-04-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Watson, C A -- Camera-Benson, L -- Palmer-Crocker, R -- Pober, J S -- New York, N.Y. -- Science. 1995 Apr 21;268(5209):447-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7716553" target="_blank"〉PubMed〈/a〉
    Keywords: Cell Division/drug effects ; Cell Separation ; Cells, Cultured ; Culture Media ; Endothelium, Vascular/*cytology/drug effects ; Humans ; Interleukin-8/*pharmacology ; Umbilical Veins/cytology/drug effects
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  • 36
    Publication Date: 1995-06-16
    Description: Gonadal steroidogenesis is regulated by pituitary gonadotropins and a locally produced, unidentified factor. A 70-kilodalton (kD) protein complex secreted from rat Sertoli cells was isolated. The complex, composed of 28- and 38-kD proteins, stimulated steroidogenesis by Leydig cells and ovarian granulosa cells in a dose-dependent and adenosine 3',5'-monophosphate-independent manner. The follicle-stimulating hormone-induced 28-kD protein appeared to be responsible for the bioactivity, but the 38-kD protein was indispensable for maximal activity. The 28- and 38-kD proteins were shown to be identical to the tissue inhibitor of metalloproteinase-1 (TIMP-1) and the proenzyme form of cathepsin L, respectively. Thus, a TIMP-1-procathepsin L complex is a potent activator of steroidogenesis and may regulate steroid concentrations and, thus, germ cell development in both males and females.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Boujrad, N -- Ogwuegbu, S O -- Garnier, M -- Lee, C H -- Martin, B M -- Papadopoulos, V -- HD01031/HD/NICHD NIH HHS/ -- HD24633/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1995 Jun 16;268(5217):1609-12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cell Biology, Georgetown University Medical Center, Washington, DC 20007, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7777858" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Cathepsin L ; Cathepsins/chemistry/*isolation & purification/pharmacology/physiology ; Cells, Cultured ; Culture Media, Conditioned ; Cyclic AMP/metabolism ; Enzyme Precursors/chemistry/*isolation & purification/pharmacology/physiology ; Female ; Follicle Stimulating Hormone/pharmacology ; Glycoproteins/chemistry/genetics/*isolation & ; purification/pharmacology/physiology ; Granulosa Cells/drug effects/metabolism ; Leydig Cells/drug effects/metabolism ; Male ; Molecular Sequence Data ; Molecular Weight ; Pregnenolone/*biosynthesis ; Progesterone/*biosynthesis ; Rats ; Rats, Sprague-Dawley ; Sertoli Cells/*chemistry ; Tissue Inhibitor of Metalloproteinases ; Transfection
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  • 37
    Publication Date: 1995-03-31
    Description: The interleukin-1 beta (IL-1 beta) converting enzyme (ICE) processes the inactive IL-1 beta precursor to the proinflammatory cytokine. Adherent monocytes from mice harboring a disrupted ICE gene (ICE-/-) did not export IL-1 beta or interleukin-1 alpha (IL-1 alpha) after stimulation with lipopolysaccharide. Export of tumor necrosis factor-alpha and interleukin-6 (IL-6) from these cells was also diminished. Thymocytes from ICE-/- mice were sensitive to apoptosis induced by dexamethasone or ionizing radiation, but were resistant to apoptosis induced by Fas antibody. Despite this defect in apoptosis, ICE-/- mice proceed normally through development.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kuida, K -- Lippke, J A -- Ku, G -- Harding, M W -- Livingston, D J -- Su, M S -- Flavell, R A -- New York, N.Y. -- Science. 1995 Mar 31;267(5206):2000-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7535475" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Antibodies, Monoclonal/immunology ; Antigens, CD95 ; Antigens, Surface/immunology ; *Apoptosis/drug effects/radiation effects ; Base Sequence ; Caspase 1 ; Cells, Cultured ; Chimera ; Cysteine Endopeptidases/deficiency/*metabolism ; Cytokines/*metabolism ; Dexamethasone/pharmacology ; Female ; Interleukin-1/metabolism ; Lipopolysaccharides/pharmacology ; Male ; Mice ; Mice, Inbred C57BL ; Molecular Sequence Data ; Monocytes/*immunology ; Nigericin/pharmacology ; T-Lymphocytes/*cytology
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  • 38
    Publication Date: 1995-03-10
    Description: bcl-x is a member of the bcl-2 gene family, which may regulate programmed cell death. Mice were generated that lacked Bcl-x. The Bcl-x-deficient mice died around embryonic day 13. Extensive apoptotic cell death was evident in postmitotic immature neurons of the developing brain, spinal cord, and dorsal root ganglia. Hematopoietic cells in the liver were also apoptotic. Analyses of bcl-x double-knockout chimeric mice showed that the maturation of Bcl-x-deficient lymphocytes was diminished. The life-span of immature lymphocytes, but not mature lymphocytes, was shortened. Thus, Bcl-x functions to support the viability of immature cells during the development of the nervous and hematopoietic systems.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Motoyama, N -- Wang, F -- Roth, K A -- Sawa, H -- Nakayama, K -- Negishi, I -- Senju, S -- Zhang, Q -- Fujii, S -- New York, N.Y. -- Science. 1995 Mar 10;267(5203):1506-10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, MO 63110.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7878471" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Apoptosis ; Bone Marrow Cells ; Brain/cytology/embryology ; Cell Differentiation ; Cell Survival ; Cells, Cultured ; Ganglia, Spinal/cytology/embryology ; Hematopoietic Stem Cells/*cytology ; Liver/cytology/embryology ; Lymphocytes/*cytology ; Mice ; Mice, Knockout ; Nerve Degeneration ; Neurons/*cytology ; Proto-Oncogene Proteins/deficiency/*physiology ; *Proto-Oncogene Proteins c-bcl-2 ; Spinal Cord/cytology/embryology ; Transfection ; bcl-X Protein
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  • 39
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-10-27
    Description: There is increasing evidence that neurotrophins (NTs) are involved in processes of neuronal plasticity besides their well-established actions in regulating the survival, differentiation, and maintenance of functions of specific populations of neurons. Nerve growth factor, brain-derived neurotrophic factor, NT-4/5, and corresponding antibodies dramatically modify the development of the visual cortex. Although the neuronal elements involved have not yet been identified, complementary studies of other systems have demonstrated that NT synthesis is rapidly regulated by neuronal activity and that NTs are released in an activity-dependent manner from neuronal dendrites. These data, together with the observation that NTs enhance transmitter release from neurons that express the corresponding signal-transducing Trk receptors, suggest a role for NTs as selective retrograde messengers that regulate synaptic efficacy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Thoenen, H -- New York, N.Y. -- Science. 1995 Oct 27;270(5236):593-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurochemistry, Max Planck Institute for Psychiatry, Martinsried, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7570017" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain-Derived Neurotrophic Factor ; Cells, Cultured ; Central Nervous System/cytology/metabolism ; Culture Techniques ; Long-Term Potentiation ; Nerve Growth Factors/metabolism/pharmacology/*physiology ; Nerve Tissue Proteins/metabolism/pharmacology/*physiology ; *Neuronal Plasticity ; Neurons/metabolism/*physiology ; Neurotransmitter Agents/metabolism ; Receptor Protein-Tyrosine Kinases/metabolism ; Synaptic Transmission/drug effects ; Visual Cortex/cytology/physiology
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  • 40
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-03-10
    Description: Desensitization is a phenomenon that is common to many ligand-gated ion channels but has been demonstrated only rarely with physiological stimulation. Numerous studies describe desensitization of the N-methyl-D-aspartate (NMDA) subtype of glutamate receptor by exogenous agonists, but whether synaptic stimulation causes desensitization has been unknown. Synaptic stimulation of NMDA receptors on rat hippocampal neurons resulted in desensitization that was prevented by intracellular 1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (BAPTA), adenosine-5'-O-(3-thiotriphosphate) (ATP-gamma-S), or inhibitors of phosphatase 2B (calcineurin), but not by inhibitors of phosphatases 1 and 2A or of tyrosine phosphatases. Synaptic NMDA receptors may fluctuate between phosphorylated and dephosphorylated forms, depending on the rate of synaptic stimulation and the magnitude of the associated influx of calcium through NMDA receptors.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tong, G -- Shepherd, D -- Jahr, C E -- NS21419/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1995 Mar 10;267(5203):1510-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Vollum Institute, Oregon Health Sciences University, Portland 97201-3098.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7878472" target="_blank"〉PubMed〈/a〉
    Keywords: 2-Amino-5-phosphonovalerate/pharmacology ; Adenosine Triphosphate/analogs & derivatives/pharmacology ; Animals ; Calcineurin ; Calcium/metabolism ; Calmodulin-Binding Proteins/*pharmacology ; Cells, Cultured ; Egtazic Acid/analogs & derivatives/pharmacology ; Electric Stimulation ; Glycine/pharmacology ; Hippocampus ; Membrane Potentials ; Neurons/physiology ; Patch-Clamp Techniques ; Phosphoprotein Phosphatases/*pharmacology ; Phosphorylation ; Rats ; Receptors, N-Methyl-D-Aspartate/*drug effects/physiology ; Synapses/*physiology
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  • 41
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-10-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barinaga, M -- New York, N.Y. -- Science. 1995 Oct 27;270(5236):581.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7570014" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/*cytology ; Brain-Derived Neurotrophic Factor ; Cell Communication ; Cell Survival ; Cells, Cultured ; Models, Neurological ; Nerve Growth Factors/pharmacology/*physiology ; Nerve Tissue Proteins/pharmacology/physiology ; Neural Pathways ; Neurons/*cytology/*physiology ; Rats
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  • 42
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-05-26
    Description: It has been proposed that the development of insulin-dependent diabetes is controlled by the T helper 1 (TH1) versus TH2 phenotype of autoreactive TH cells: TH1 cells would promote diabetes, whereas TH2 cells would actually protect from disease. This proposition was tested by establishing cultures of TH1 and TH2 cells that express an identical diabetogenic T cell receptor and comparing their ability to initiate disease in neonatal nonobese diabetic mice. TH1-like cells actively promoted diabetes; TH2-like cells invaded the islets but did not provoke disease--neither did they provide substantial protection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Katz, J D -- Benoist, C -- Mathis, D -- New York, N.Y. -- Science. 1995 May 26;268(5214):1185-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institut de Genetique et de Biologie Moleculaire et Cellulaire, INSERM-CNRS-Universite Louis Pasteur, Illkirch, CU de Strasbourg, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7761837" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Autoimmunity/immunology ; Cell Movement/immunology ; Cells, Cultured ; Diabetes Mellitus, Type 1/*immunology ; Islets of Langerhans/immunology ; Lymphocyte Activation/immunology ; Mice ; Mice, Inbred NOD ; Mice, Transgenic ; Receptors, Antigen, T-Cell, alpha-beta/genetics/immunology ; Spleen/cytology ; Th1 Cells/*immunology/transplantation ; Th2 Cells/*immunology/transplantation
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  • 43
    Publication Date: 1995-11-17
    Description: The efficacy of pre- and postexposure treatment with the antiviral compound (R)-9-(2-phosphonylmethoxypropyl)adenine (PMPA) was tested against simian immunodeficiency virus (SIV) in macaques as a model for human immunodeficiency virus (HIV). PMPA was administered subcutaneously once daily beginning either 48 hours before, 4 hours after, or 24 hours after virus inoculation. Treatment continued for 4 weeks and the virologic, immunologic, and clinical status of the macaques was monitored for up to 56 weeks. PMPA prevented SIV infection in all macaques without toxicity, whereas all control macaques became infected. These results suggest a potential role for PMPA prophylaxis against early HIV infection in cases of known exposure.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tsai, C C -- Follis, K E -- Sabo, A -- Beck, T W -- Grant, R F -- Bischofberger, N -- Benveniste, R E -- Black, R -- N01-AI-15120/AI/NIAID NIH HHS/ -- RR00166/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1995 Nov 17;270(5239):1197-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉University of Washington Regional Primate Research Center, Seattle 98195, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7502044" target="_blank"〉PubMed〈/a〉
    Keywords: Adenine/administration & dosage/*analogs & derivatives/pharmacology ; Animals ; Antibodies, Viral/blood ; Antiviral Agents/administration & dosage/*therapeutic use ; Base Sequence ; Cells, Cultured ; HIV Infections/drug therapy/*prevention & control ; Humans ; Injections, Subcutaneous ; Leukocytes, Mononuclear/virology ; Lymph Nodes/virology ; Macaca fascicularis ; Molecular Sequence Data ; *Organophosphonates ; Organophosphorus Compounds/administration & dosage/*pharmacology ; Simian Acquired Immunodeficiency Syndrome/drug therapy/*prevention & control ; Simian Immunodeficiency Virus/*drug effects/immunology/isolation & purification ; Tenofovir
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  • 44
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1995-09-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barinaga, M -- New York, N.Y. -- Science. 1995 Sep 22;269(5231):1668-70.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7569889" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Astrocytes ; Axons/*physiology ; Cell Movement ; Cells, Cultured ; Chickens ; Ephrin-A2 ; Glycosylphosphatidylinositols/physiology ; Ligands ; Nervous System Physiological Phenomena ; Proteins/metabolism/*physiology ; Rats ; Receptor Protein-Tyrosine Kinases/metabolism/*physiology ; Receptor, EphA8 ; Retina/*physiology ; Superior Colliculi/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 45
    Publication Date: 1995-04-28
    Description: B61, a cytokine-inducible endothelial gene product, is the ligand for the Eck receptor protein tyrosine kinase (RPTK). Expression of a B61-immunoglobulin chimera showed that B61 could act as an angiogenic factor in vivo and a chemoattractant for endothelial cells in vitro. The Eck RPTK was activated by tumor necrosis factor-alpha (TNF-alpha) through induction of B61, and an antibody to B61 attenuated angiogenesis induced by TNF-alpha but not by basic fibroblast growth factor. This finding suggests the existence of an autocrine or paracrine loop involving activation of the Eck RPTK by its inducible ligand B61 after an inflammatory stimulus, the net effect of which would be to promote angiogenesis, a hallmark of chronic inflammation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pandey, A -- Shao, H -- Marks, R M -- Polverini, P J -- Dixit, V M -- DK 39255/DK/NIDDK NIH HHS/ -- HL 39926/HL/NHLBI NIH HHS/ -- P0 1AI331890004/AI/NIAID NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1995 Apr 28;268(5210):567-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, University of Michigan Medical School, Ann Arbor 48109, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7536959" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Base Sequence ; Cattle ; Cells, Cultured ; Chemotaxis ; Endothelium, Vascular/cytology/*physiology ; Enzyme Activation ; Ephrin-A1 ; Female ; Humans ; Membrane Proteins/*metabolism ; Molecular Sequence Data ; Neovascularization, Pathologic/*etiology ; Phosphorylation ; Protein-Tyrosine Kinases/*metabolism ; Proteins/*physiology ; Rats ; Rats, Inbred F344 ; Receptor, EphA2 ; Recombinant Fusion Proteins ; Tumor Necrosis Factor-alpha/*pharmacology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 46
    Publication Date: 1995-01-13
    Description: The cyclin-dependent kinase 4 (CDK4) regulates progression through the G1 phase of the cell cycle. The activity of CDK4 is controlled by the opposing effects of the D-type cyclin, an activating subunit, and p16INK4, an inhibitory subunit. Ectopic expression of p16INK4 blocked entry into S phase of the cell cycle induced by oncogenic Ha-Ras, and this block was relieved by coexpression of a catalytically inactive CDK4 mutant. Expression of p16INK4 suppressed cellular transformation of primary rat embryo fibroblasts by oncogenic Ha-Ras and Myc, but not by Ha-Ras and E1a. Together, these observations provide direct evidence that p16INK4 can inhibit cell growth.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Serrano, M -- Gomez-Lahoz, E -- DePinho, R A -- Beach, D -- Bar-Sagi, D -- CA55360/CA/NCI NIH HHS/ -- EY09300-01/EY/NEI NIH HHS/ -- HD28317-02/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1995 Jan 13;267(5195):249-52.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Cold Spring Harbor Laboratory, NY 11724.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7809631" target="_blank"〉PubMed〈/a〉
    Keywords: Adenovirus E1A Proteins/genetics/physiology ; Animals ; Carrier Proteins/genetics/*physiology ; *Cell Division ; *Cell Transformation, Neoplastic ; Cells, Cultured ; Cyclin-Dependent Kinase 4 ; Cyclin-Dependent Kinase Inhibitor p16 ; *Cyclin-Dependent Kinases ; Genes, Reporter ; Genes, Retinoblastoma ; Genes, myc ; Genes, ras ; Plasmids ; Protein-Serine-Threonine Kinases/antagonists & inhibitors/metabolism ; *Proto-Oncogene Proteins ; Rats ; Retinoblastoma Protein/physiology ; S Phase ; Transcriptional Activation ; Transfection ; Tumor Cells, Cultured ; ras Proteins/genetics/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 47
    Publication Date: 1995-06-09
    Description: Progesterone is shown here to be produced from pregnenolone by Schwann cells in peripheral nerves. After cryolesion of the sciatic nerve in male mice, axons regenerate and become myelinated. Blocking either the local synthesis or the receptor-mediated action of progesterone impaired remyelination. Administration of progesterone or its precursor, pregnenolone, to the lesion site increased the extent of myelin sheath formation. Myelination of axons was also increased when progesterone was added to cultures of rat dorsal root ganglia. These observations indicate a role for locally produced progesterone in myelination, demonstrate that progesterone is not simply a sex steroid, and suggest a new therapeutic approach to promote myelin repair.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koenig, H L -- Schumacher, M -- Ferzaz, B -- Thi, A N -- Ressouches, A -- Guennoun, R -- Jung-Testas, I -- Robel, P -- Akwa, Y -- Baulieu, E E -- New York, N.Y. -- Science. 1995 Jun 9;268(5216):1500-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratoire Neurobiologie du Developpement, Universite Bordeaux I, Talence, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7770777" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/ultrastructure ; Cells, Cultured ; Dihydrotestosterone/analogs & derivatives/pharmacology ; Ganglia, Spinal ; Male ; Mice ; Mifepristone/pharmacology ; Myelin Sheath/*physiology/ultrastructure ; Nerve Regeneration ; Pregnenolone/metabolism/pharmacology ; Progesterone/*biosynthesis/pharmacology/physiology ; Schwann Cells/*metabolism ; Sciatic Nerve/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 48
    Publication Date: 1995-07-07
    Description: Many proteins are associated with the outer layer of the cell membrane through a posttranslationally added glycosyl phosphatidylinositol (GPI) anchor. The functional significance of this type of protein linkage is unclear, although it results in increased lateral mobility, sorting to the apical surface of the cell, reinsertion into cell membranes, and possibly cell signaling. Here evidence is presented that GPI-linked proteins can undergo intermembrane transfer in vivo. GPI-linked proteins expressed on the surface of transgenic mouse red blood cells were transferred in a functional form to endothelial cells in vivo. This feature of GPI linkage may be potentially useful for the delivery of therapeutic proteins to vascular endothelium.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kooyman, D L -- Byrne, G W -- McClellan, S -- Nielsen, D -- Tone, M -- Waldmann, H -- Coffman, T M -- McCurry, K R -- Platt, J L -- Logan, J S -- HL 46810/HL/NHLBI NIH HHS/ -- HL 50985/HL/NHLBI NIH HHS/ -- HL 52297/HL/NHLBI NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1995 Jul 7;269(5220):89-92.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Sir William Dunn School of Pathology, Oxford, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7541557" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens, CD/genetics/*metabolism ; Antigens, CD55 ; Antigens, CD59 ; Base Sequence ; Bone Marrow Transplantation ; Cell Membrane/metabolism ; Cells, Cultured ; Complement Inactivator Proteins/genetics/*metabolism ; Endothelium, Vascular/cytology/*metabolism ; Erythrocytes/*metabolism ; Globins/genetics ; Glycosylphosphatidylinositols/*metabolism ; Humans ; Membrane Glycoproteins/genetics/*metabolism ; Mice ; Mice, Transgenic ; Molecular Sequence Data ; Myocardium/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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