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  • Cell & Developmental Biology  (1,006)
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  • 201
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-06-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J L -- New York, N.Y. -- Science. 1986 Jun 13;232(4756):1341-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2940683" target="_blank"〉PubMed〈/a〉
    Keywords: Alzheimer Disease/physiopathology ; Animals ; Brain/*physiology ; Cell Survival ; Cholinergic Fibers/physiology ; Humans ; Huntington Disease/physiopathology ; Nerve Growth Factors/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
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  • 202
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-06-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J L -- New York, N.Y. -- Science. 1986 Jun 20;232(4757):1500-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2872725" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/physiology ; Cells, Cultured ; Neurons/cytology/*metabolism ; Neurotransmitter Agents/*biosynthesis ; Peripheral Nerves/physiology
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  • 203
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-02-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J L -- New York, N.Y. -- Science. 1986 Feb 21;231(4740):796-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3003911" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Membrane/physiology ; Cell Movement ; High Mobility Group Proteins/*physiology ; Humans ; Lymphocytes/physiology ; Membrane Proteins/physiology ; Ubiquitins/*physiology
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  • 204
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-06-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koshland, D E Jr -- New York, N.Y. -- Science. 1986 Jun 13;232(4756):1313.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3715450" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Humans ; Medical Laboratory Science/trends ; Research ; *Technology
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  • 205
    Publication Date: 1986-12-12
    Description: Hereditary hypogonadism in the hypogonadal (hpg) mouse is caused by a deletional mutation of at least 33.5 kilobases encompassing the distal half of the gene for the common biosynthetic precursor of gonadotropin-releasing hormone (GnRH) and GnRH-associated peptide (GAP). The partially deleted gene is transcriptionally active as revealed by in situ hybridization histochemistry of hpg hypothalamic tissue sections, but immunocytochemical analysis failed to show the presence of antigen corresponding to any part of the precursor protein.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mason, A J -- Hayflick, J S -- Zoeller, R T -- Young, W S 3rd -- Phillips, H S -- Nikolics, K -- Seeburg, P H -- New York, N.Y. -- Science. 1986 Dec 12;234(4782):1366-71.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3024317" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Base Sequence ; Brain Chemistry ; Chromosome Deletion ; Chromosome Mapping ; DNA Restriction Enzymes/metabolism ; Gonadotropin-Releasing Hormone/*genetics ; Histocytochemistry ; Hypogonadism/*genetics ; Mice ; Nucleic Acid Hybridization ; Protein Precursors/*genetics ; Transcription, Genetic
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  • 206
    Publication Date: 1986-04-18
    Description: Suppressor cells specific for acetylcholine receptor (AChR) were induced in a population of lymphocytes previously sensitized to AChR, obtained from rats with experimental autoimmune myasthenia gravis (EAMG). The lymphocytes were cultured with the immunosuppressive drug cyclosporin A plus purified AChR for 7 days. These cells, when mixed with lymphocytes from rats with EAMG in vitro, strongly suppressed the antibody response to AChR. They did not inhibit antibody responses to an unrelated antigen, an indication that suppression was specific for AChR. This approach should be a useful way to induce specific suppressor cells from sensitized populations of lymphocytes and may be applicable in the treatment of autoimmune diseases such as myasthenia gravis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McIntosh, K R -- Drachman, D B -- 5RO1 HD04817-16/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1986 Apr 18;232(4748):401-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2938256" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cyclosporins/pharmacology ; Female ; Lymph Nodes/cytology ; Lymphocytes/drug effects ; Myasthenia Gravis/*immunology ; Rats ; Rats, Inbred Lew ; Receptors, Cholinergic/*immunology ; Spleen/cytology ; T-Lymphocytes, Regulatory/*immunology
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  • 207
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-07-11
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lewin, R -- New York, N.Y. -- Science. 1986 Jul 11;233(4760):160.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3460175" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Genetic Engineering ; Humans ; Mice ; Transfection
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  • 208
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-08-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lewin, R -- New York, N.Y. -- Science. 1986 Aug 15;233(4765):720-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3090683" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; *Fossils ; Haplorhini/*anatomy & histology ; Humans ; Kenya ; Models, Genetic ; *Paleontology ; Skull/*anatomy & histology
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  • 209
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-12-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lewin, R -- New York, N.Y. -- Science. 1986 Dec 12;234(4782):1326.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3097821" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Fossils ; Haplorhini/*anatomy & histology ; Humans ; Paleodontology ; *Paleontology ; Skull/*anatomy & histology
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  • 210
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-05-16
    Description: The activities of both chymotrypsin and amylase in individual zymogen granules of rat pancreas were measured by means of micromanipulation and microfluorometric methods. The enzyme content and the ratio of amylase to chymotrypsin varied widely among granules taken from the same animal. These results are compatible with short-term nonparallel bulk secretion of the two enzymes through exocytosis. The distribution of each enzyme activity in a population of granules suggests quantal packaging of amylase and chymotrypsinogen into the granules.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mroz, E A -- Lechene, C -- AM26488/AM/NIADDK NIH HHS/ -- New York, N.Y. -- Science. 1986 May 16;232(4752):871-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2422756" target="_blank"〉PubMed〈/a〉
    Keywords: Amylases/*analysis ; Animals ; Chymotrypsin/*analysis ; Cytoplasmic Granules/*analysis ; Exocytosis ; Female ; Pancreas/*secretion ; Rats ; Rats, Inbred Strains
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  • 211
    Publication Date: 1986-06-06
    Description: Caffeine was shown to induce mitotic events in mammalian cells before DNA replication (S phase) was completed. Synchronized BHK cells that were arrested in early S phase underwent premature chromosome condensation, nuclear envelope breakdown, morphological "rounding up," and mitosis-specific phosphoprotein synthesis when they were exposed to caffeine. These mitotic responses occurred only after the cells had entered S phase and only while DNA synthesis was inhibited by more than 70 percent. Inhibitors of protein synthesis blocked these caffeine-induced events, while inhibitors of RNA synthesis had little effect. These results suggest that caffeine induces the translation or stabilizes the protein product (or products) of mitosis-related RNA that accumulates in S-phase cells when DNA replication is suppressed. The ability to chemically manipulate the onset of mitosis should be useful for studying the regulation of this event in mammalian cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schlegel, R -- Pardee, A B -- CA 22427/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1986 Jun 6;232(4755):1264-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2422760" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Caffeine/*pharmacology ; Cells, Cultured ; Cricetinae ; Cycloheximide/pharmacology ; *DNA Replication ; Dactinomycin/pharmacology ; Interphase ; Mitosis/*drug effects ; RNA/metabolism
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  • 212
    Publication Date: 1986-04-18
    Description: Efforts to investigate the progression of events that lead human cells of epithelial origin to become neoplastic in response to carcinogenic agents have been aided by the development of tissue culture systems for propagation of epithelial cells. In the present study, nontumorigenic human epidermal keratinocytes immortalized by adenovirus 12 and simian virus 40 (Ad 12-SV40) were transformed by treatment with the chemical carcinogens N-methyl-N'-nitro-N-nitrosoguanidine or 4-nitroquinoline-1-oxide. Such transformants showed morphological alterations and induced carcinomas when transplanted into nude mice, whereas primary human epidermal keratinocytes treated with these chemical carcinogens failed to show any evidence of transformation. This in vitro system may be useful in assessing environmental carcinogens for human epithelial cells and in detecting new human oncogenes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rhim, J S -- Fujita, J -- Arnstein, P -- Aaronson, S A -- New York, N.Y. -- Science. 1986 Apr 18;232(4748):385-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2421406" target="_blank"〉PubMed〈/a〉
    Keywords: 4-Nitroquinoline-1-oxide/*pharmacology ; Adenoviruses, Human/*metabolism ; Animals ; Cell Line ; Cell Transformation, Neoplastic/*chemically induced/metabolism ; Cell Transformation, Viral ; Epidermis/*cytology ; Humans ; *Keratins ; Methylnitronitrosoguanidine/*pharmacology ; Mice ; Mice, Nude ; Neoplasm Transplantation ; Nitroquinolines/*pharmacology ; Oncogenes ; Simian virus 40/*metabolism ; Skin Neoplasms/chemically induced/*etiology/microbiology
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  • 213
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-10-10
    Description: The secretion of follicle-stimulating hormone (FSH) by the anterior pituitary gland is regulated by the interaction of hypothalamic and gonadal hormones. Recently, proteins termed inhibins that selectively suppress FSH secretion have been purified and characterized from the gonadal fluids of several species. Antibodies to a synthetic peptide encompassing the amino terminal 25 residues of the recently characterized porcine inhibin were used to develop a specific radioimmunoassay (RIA) for inhibin and to neutralize endogenous inhibin during the estrous cycle of the rat. The administration of 20 international units of pregnant mare serum gonadotropin (PMSG) stimulated the secretion of inhibin in intact immature female rats, whereas ovariectomy caused an abrupt decrease in plasma inhibin concentrations that were not prevented by the injection of PMSG. The infusion of a polyclonal antiserum to inhibin, from 12 noon on proestrus to 1 a.m. on the morning of estrus, as well as its acute intravenous injection during diestrus I or II, caused an increase in plasma FSH (but not luteinizing hormone) concentrations. These results support the hypothesis of a feedback loop between the release of ovarian inhibin and FSH in the female rat.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rivier, C -- Rivier, J -- Vale, W -- HD13527/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1986 Oct 10;234(4773):205-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3092356" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Estrus ; Female ; Follicle Stimulating Hormone/blood/*secretion ; Gonadotropins, Equine/pharmacology ; Immune Sera ; Inhibins/blood/immunology/*secretion ; Luteinizing Hormone/blood ; Ovariectomy ; Proestrus ; Rats ; Rats, Inbred Strains
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  • 214
    Publication Date: 1986-06-06
    Description: Transforming growth factor-alpha (TGF-alpha) and epidermal growth factor (EGF) are structurally related peptides. Purified human TGF-alpha produced in Escherichia coli and pure natural mouse EGF were compared for their ability to bind to target cells in vitro and to promote angiogenesis in the hamster cheek pouch bioassay. Both polypeptides were found to bind in vitro to several target cells, including endothelial cells, and to stimulate their DNA synthesis in an equipotent fashion. In vivo, however, TGF-alpha was more potent than EGF in promoting angiogenesis and, because TGF-alpha is known to be secreted by a variety of human tumors, it is suggested that this growth factor may contribute to tumor-induced angiogenesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schreiber, A B -- Winkler, M E -- Derynck, R -- New York, N.Y. -- Science. 1986 Jun 6;232(4755):1250-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2422759" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Assay ; Epidermal Growth Factor/pharmacology ; Humans ; Mice ; *Neovascularization, Pathologic ; Peptides/metabolism/*pharmacology ; Receptor, Epidermal Growth Factor ; Receptors, Cell Surface/metabolism ; Transforming Growth Factors
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  • 215
    Publication Date: 1986-11-21
    Description: Expression of the dopa decarboxylase gene (Ddc) is regulated in a tissue- and developmental stage-specific manner throughout the life cycle of the fruit fly, Drosophila melanogaster. Essential Ddc regulatory elements lie within 208 base pairs upstream from the RNA start point. Functional elements within this 5' flanking region were mapped by deletion analysis, which assayed expression in vivo after germline integration via P element vectors. One of the elements is essential for expression in both the larval and adult central nervous system, and at least two other elements are necessary for quantitatively normal expression in the hypoderm. Within each of the intervals that have regulatory effects are found sequence elements conserved between the Ddc genes of two distantly related species of flies. On the basis of this correlation, regulatory functions for these sequence elements can be postulated.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Scholnick, S B -- Bray, S J -- Morgan, B A -- McCormick, C A -- Hirsh, J -- New York, N.Y. -- Science. 1986 Nov 21;234(4779):998-1002.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3095924" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Aromatic-L-Amino-Acid Decarboxylases/*genetics ; Base Sequence ; Central Nervous System/physiology ; Dopa Decarboxylase/*genetics ; Drosophila melanogaster/*genetics/growth & development ; *Gene Expression Regulation ; Genes
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  • 216
    Publication Date: 1986-05-09
    Description: In multidrug resistance, which is observed clinically and in tissue culture, cells that are challenged with certain cytotoxic drugs develop resistance not only to the selective agent but also to other, seemingly unrelated, agents. The multidrug-resistant phenotype is associated with DNA sequence amplification and with the overproduction of a number of cytosolic and membrane glycoproteins. The differential amplification and altered expression of at least two related genes, termed multidrug-resistant associated genes has been shown in multidrug-resistant Chinese hamster cells. In multidrug-resistant mouse and human cells, genes homologous to those in Chinese hamster cells are also amplified. The level of expression of these genes varied and did not correlate with their copy number. Furthermore, in Chinese hamster cells, the development of resistance to a single drug and multidrug resistance were closely related, but uncoupled, events. The overexpression of the multidrug-resistant genes was better correlated with the degree of resistance to the selective agent than it was with the extent of multidrug resistance.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Scotto, K W -- Biedler, J L -- Melera, P W -- CA-08748/CA/NCI NIH HHS/ -- CA-09207/CA/NCI NIH HHS/ -- CA-28595/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1986 May 9;232(4751):751-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2421411" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Line ; Cloning, Molecular ; Colchicine/pharmacology ; Cricetinae ; Cricetulus ; DNA/genetics ; Dactinomycin/pharmacology ; Daunorubicin/pharmacology ; *Drug Resistance ; Gene Amplification/*drug effects ; Gene Expression Regulation/*drug effects ; Humans ; Lung/cytology/drug effects ; Mice ; Nucleic Acid Hybridization ; RNA/genetics ; Vincristine/pharmacology
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  • 217
    Publication Date: 1986-05-23
    Description: Two metabolites of the steroid hormones progesterone and deoxycorticosterone, 3 alpha-hydroxy-5 alpha-dihydroprogesterone and 3 alpha, 5 alpha-tetrahydrodeoxycorticosterone, are potent barbiturate-like ligands of the gamma-aminobutyric acid (GABA) receptor-chloride ion channel complex. At concentrations between 10(-7) and 10(-5)M both steroids inhibited binding of the convulsant t-butylbicyclophosphorothionate to the GABA-receptor complex and increased the binding of the benzodiazepine flunitrazepam; they also stimulated chloride uptake (as measured by uptake of 36Cl-) into isolated brain vesicles, and potentiated the inhibitory actions of GABA in cultured rat hippocampal and spinal cord neurons. These data may explain the ability of certain steroid hormones to rapidly alter neuronal excitability and may provide a mechanism for the anesthetic and hypnotic actions of naturally occurring and synthetic anesthetic steroids.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Majewska, M D -- Harrison, N L -- Schwartz, R D -- Barker, J L -- Paul, S M -- New York, N.Y. -- Science. 1986 May 23;232(4753):1004-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2422758" target="_blank"〉PubMed〈/a〉
    Keywords: 20-alpha-Dihydroprogesterone/*analogs & derivatives/metabolism/pharmacology ; Animals ; Bicyclo Compounds/metabolism ; *Bicyclo Compounds, Heterocyclic ; Binding, Competitive ; Brain/metabolism ; Cells, Cultured ; Chlorides/metabolism ; Desoxycorticosterone/*analogs & derivatives/metabolism/pharmacology ; Drug Synergism ; Flunitrazepam/metabolism ; Hippocampus/metabolism ; In Vitro Techniques ; Ion Channels/metabolism ; Progesterone/*analogs & derivatives/metabolism/pharmacology ; Rats ; Receptors, GABA-A/*drug effects/metabolism ; Spinal Cord/metabolism
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  • 218
    Publication Date: 1986-08-15
    Description: Growth cones are specialized structures that form the distal tips of growing axons. During both normal development of the nervous system and regeneration of injured nerves, growth cones are essential for elongation and guidance of growing axons. Developmental and regenerative axon growth is frequently accompanied by elevated synthesis of a protein designated GAP-43. GAP-43 has now been found to be a major component of growth-cone membranes in developing rat brains. Relative to total protein, GAP-43 is approximately 12 times as abundant in growth-cone membranes as in synaptic membranes from adult brains. Immunohistochemical localization of GAP-43 in frozen sections of developing brain indicates that the protein is specifically associated with neuropil areas containing growth cones and immature synaptic terminals. The results support the proposal that GAP-43 plays a role in axon growth.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Skene, J H -- Jacobson, R D -- Snipes, G J -- McGuire, C B -- Norden, J J -- Freeman, J A -- EY01117/EY/NEI NIH HHS/ -- EY03718/EY/NEI NIH HHS/ -- NS18103/NS/NINDS NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1986 Aug 15;233(4765):783-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3738509" target="_blank"〉PubMed〈/a〉
    Keywords: Aging ; Animals ; Animals, Newborn ; Anura ; Axons/physiology ; Brain/growth & development/*physiology ; Cell Membrane/metabolism ; Fetus ; GAP-43 Protein ; Growth Substances/*biosynthesis/isolation & purification ; Membrane Proteins/*biosynthesis/isolation & purification ; *Nerve Regeneration ; Nerve Tissue Proteins/*biosynthesis/isolation & purification ; Optic Nerve/cytology/*physiology ; Rats ; Synaptic Membranes/metabolism
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  • 219
    Publication Date: 1986-03-14
    Description: Hemoparasitic diseases are endemic in half the world's livestock production areas and are the greatest obstacle to improved meat, milk, and fiber production in the Third World. The most prevalent of these diseases, anaplasmosis, occurs throughout tropical and subtropical regions and is responsible for 50,000 to 100,000 cattle deaths annually in the United States alone. Despite its prevalence and the severity of the losses, an effective immunoprophylaxis for anaplasmosis has not been developed. A neutralization-sensitive epitope on a surface protein with a molecular weight of 105,000 (Am 105) of the causative rickettsia Anaplasma marginale was identified by monoclonal antibody inhibition of infectivity. This epitope was determined to be common to eight isolates with antigenic, morphologic, and protein structural differences. Cattle immunized with Am 105 purified by immunoaffinity chromatography were protected against challenge with virulent Anaplasma marginale. The identification of Am 105 as bearing isolate-common epitopes capable of inducing protection in immunized cattle provides the basis for the development of an effective subunit vaccine for bovine anaplasmosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Palmer, G H -- Barbet, A F -- Davis, W C -- McGuire, T C -- GM 07853/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1986 Mar 14;231(4743):1299-302.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3945825" target="_blank"〉PubMed〈/a〉
    Keywords: Anaplasma/immunology ; Anaplasmosis/immunology/*prevention & control ; Animals ; Antibodies, Monoclonal ; Antigens, Surface/*immunology/isolation & purification ; Cattle ; Cattle Diseases/immunology/parasitology/*prevention & control ; Chromatography, Affinity ; Electrophoresis, Polyacrylamide Gel ; Immunization/*veterinary ; Plasmodium/immunology
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  • 220
    Publication Date: 1986-08-22
    Description: Protein kinase C, the major phorbol ester receptor, was purified from bovine brain and through the use of oligonucleotide probes based on partial amino acid sequence, complementary DNA clones were derived from bovine brain complementary DNA libraries. Thus, the complete amino acid sequence of bovine protein kinase C was determined, revealing a domain structure. At the amino terminal is a cysteine-rich domain with an internal duplication; a putative calcium-binding domain follows, and there is at the carboxyl terminal a domain that shows substantial homology, but not identity, to sequences of other protein kinase.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Parker, P J -- Coussens, L -- Totty, N -- Rhee, L -- Young, S -- Chen, E -- Stabel, S -- Waterfield, M D -- Ullrich, A -- New York, N.Y. -- Science. 1986 Aug 22;233(4766):853-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3755547" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Brain/metabolism ; *Caenorhabditis elegans Proteins ; Carrier Proteins ; Cattle ; Dna ; Models, Chemical ; Protein Biosynthesis ; *Protein Kinase C/isolation & purification ; RNA, Messenger/metabolism ; *Receptors, Drug ; *Receptors, Immunologic
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  • 221
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-06-13
    Description: Genetic diseases can be treated by transplantation of either normal allogeneic bone marrow or, potentially, autologous bone marrow into which the normal gene has been inserted in vitro (gene therapy). Histocompatible allogeneic bone marrow transplantation is used for the treatment of genetic diseases whose clinical expression is restricted to lymphoid or hematopoietic cells. The therapeutic role of bone marrow transplantation in the treatment of generalized genetic diseases, especially those affecting the central nervous system, is under investigation. The response of a generalized genetic disease to allogeneic bone marrow transplantation may be predicted by experiments in vitro. Gene therapy can be used only when the gene responsible for the disease has been characterized. Success of gene therapy for a specific genetic disease may be predicted by its clinical response to allogeneic bone marrow transplantation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Parkman, R -- New York, N.Y. -- Science. 1986 Jun 13;232(4756):1373-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3520819" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Bone Marrow Transplantation ; Enzymes/deficiency/genetics ; Genetic Diseases, Inborn/*therapy ; Genetic Engineering ; Humans ; Mice ; Transfection
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  • 222
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-03-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Milstein, C -- New York, N.Y. -- Science. 1986 Mar 14;231(4743):1261-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3080810" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibodies/immunology/*physiology ; Antibodies, Monoclonal/genetics ; *Antibody Diversity ; *Antibody Formation ; DNA, Recombinant/metabolism ; Genes, MHC Class II ; Genetic Engineering ; Humans ; Hybridomas/metabolism ; Immunoglobulin Heavy Chains/genetics ; Immunoglobulin Light Chains/genetics ; Immunoglobulins/physiology ; Mice ; Multiple Myeloma/genetics ; Mutation ; Myeloma Proteins/genetics ; RNA, Messenger/genetics
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  • 223
    Publication Date: 1986-09-19
    Description: The adoptive transfer of tumor-infiltrating lymphocytes (TIL) expanded in interleukin-2 (IL-2) to mice bearing micrometastases from various types of tumors showed that TIL are 50 to 100 times more effective in their therapeutic potency than are lymphokine-activated killer (LAK) cells. Therefore the use of TIL was explored for the treatment of mice with large pulmonary and hepatic metastatic tumors that do not respond to LAK cell therapy. Although treatment of animals with TIL alone or cyclophosphamide alone had little impact, these two modalities together mediated the elimination of large metastatic cancer deposits in the liver and lung. The combination of TIL and cyclophosphamide was further potentiated by the simultaneous administration of IL-2. With the combination of cyclophosphamide, TIL, and IL-2, 100% of mice (n = 12) bearing the MC-38 colon adenocarcinoma were cured of advanced hepatic metastases, and up to 50% of mice were cured of advanced pulmonary metastases. Techniques have been developed to isolate TIL from human tumors. These experiments provide a rationale for the use of TIL in the treatment of humans with advanced cancer.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rosenberg, S A -- Spiess, P -- Lafreniere, R -- New York, N.Y. -- Science. 1986 Sep 19;233(4770):1318-21.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3489291" target="_blank"〉PubMed〈/a〉
    Keywords: Adenocarcinoma/secondary/therapy ; Animals ; Colonic Neoplasms/therapy ; Combined Modality Therapy ; Cyclophosphamide/therapeutic use ; Humans ; *Immunotherapy ; Interleukin-2/pharmacology ; Liver Neoplasms/secondary ; Lung Neoplasms/secondary ; Lymphocyte Activation/drug effects ; Lymphocytes/immunology/*physiology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Neoplasms, Experimental/*therapy ; Sarcoma, Experimental/secondary/therapy
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  • 224
    Publication Date: 1986-01-24
    Description: A semisterile male translocation heterozygote [t(2; 14) 1Gso] that exhibited neurological symptoms and an inability to swim (diver) was found among the offspring of male mice treated with triethylenemelamine. All breeding and cytogenetic data showed a complete concordance between translocation heterozygosity and the neurological disorders. Homozygosity for the translocation seemed to be lethal at an early embryonic stage. Despite the distinctive neurologic symptoms, no anatomic or histological defects in either the ear or in the central nervous system were observed. Thus, a balanced chromosomal translocation can produce disease with an inheritance pattern that mimics a single dominant gene defect.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rutledge, J C -- Cain, K T -- Cacheiro, N L -- Cornett, C V -- Wright, C G -- Generoso, W M -- New York, N.Y. -- Science. 1986 Jan 24;231(4736):395-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3941902" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chromosome Mapping ; Female ; Heterozygote ; Humans ; Male ; Mice ; Mice, Inbred C3H ; Mice, Inbred C57BL ; Mice, Neurologic Mutants/*genetics ; Muscular Dystrophies/genetics ; *Translocation, Genetic ; Triethylenemelamine/pharmacology
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  • 225
    Publication Date: 1986-08-15
    Description: An esterase gene from the mosquito Culex quinquefasciatus that is responsible for resistance to a variety of organophosphorus (OP) insecticides was cloned in lambda gt11 phage. This gene was used to investigate the genetic mechanism of the high production of the esterase B1 it encodes in OP-resistant Culex quinquefasciatus Say (Tem-R strain) from California. Adults of the Tem-R strain were found to possess at least 250 times more copies of the gene than adults of a susceptible strain (S-Lab). The finding that selection by pesticides may result in the amplification of genes encoding detoxifying enzymes in whole, normally developed, reproducing insects emphasizes the biological importance of this mechanism and opens new areas of investigation in pesticide resistance management.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mouches, C -- Pasteur, N -- Berge, J B -- Hyrien, O -- Raymond, M -- de Saint Vincent, B R -- de Silvestri, M -- Georghiou, G P -- New York, N.Y. -- Science. 1986 Aug 15;233(4765):778-80.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3755546" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Culex/drug effects/enzymology/*genetics ; DNA/analysis ; Drug Resistance ; Esterases/*genetics ; *Gene Amplification ; *Genes ; Insecticides/*pharmacology ; Nucleic Acid Hybridization ; *Organophosphorus Compounds
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  • 226
    Publication Date: 1986-08-01
    Description: Whether growth hormone stimulates longitudinal bone growth by a direct effect at the site of the growth plate or indirectly by increasing the concentration of circulating somatomedins (insulin-like growth factors) has been the subject of controversy. Immunohistochemical methods were used to explore the localization and distribution of insulin-like growth factor I (IGF-I) immunoreactivity in the epiphyseal growth plate of the proximal tibia of male rats. Cells in the proliferative zone of the growth plate of normal rats exhibited a bright immunofluorescence, whereas cells in the germinal and hypertrophic zones stained only weakly. In rats subjected to hypophysectomy, the number of fluorescent cells was markedly reduced. When the hypophysectomized rats were treated with growth hormone, either systemically or at the site of the growth plate, the number of IGF-I-immunoreactive cells in the proliferative zone was increased. The results show that IGF-I is produced in proliferative chondrocytes in the growth plate and that the number of IGF-I-containing cells is directly regulated by growth hormone. These findings suggest that IGF-I has a specific role in the clonal expansion of differentiated chondrocytes and exerts its function locally through autocrine or paracrine mechanisms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nilsson, A -- Isgaard, J -- Lindahl, A -- Dahlstrom, A -- Skottner, A -- Isaksson, O G -- New York, N.Y. -- Science. 1986 Aug 1;233(4763):571-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3523759" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Fluorescent Antibody Technique ; Growth Hormone/pharmacology/*physiology ; Growth Plate/*cytology/drug effects/growth & development ; Hypophysectomy ; Insulin-Like Growth Factor I/pharmacology/*physiology ; Male ; Rats ; Rats, Inbred Strains ; Somatomedins/*physiology ; Tibia
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  • 227
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-01-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sun, M -- New York, N.Y. -- Science. 1986 Jan 31;231(4737):448.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3941909" target="_blank"〉PubMed〈/a〉
    Keywords: Air Pollutants, Occupational/*toxicity ; Animals ; Ethylene Oxide/*toxicity ; Female ; Humans ; Male ; Mice ; Pregnancy ; Risk ; *Teratogens ; United States ; United States Occupational Safety and Health Administration
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  • 228
    Publication Date: 1986-12-05
    Description: Transient stimulation of target tissues by sex steroids can cause long-lasting changes that may facilitate or alter responses to subsequent hormonal treatment. How these altered characteristics are propagated during cell division in the absence of the stimulating hormone is unknown. The human hepatocarcinoma cell line HepG2 was used as a model to examine the effects of estrogen on the synthesis of serum apolipoproteins in vitro. Treatment with low concentrations of estrogen for 24 to 48 hours resulted in long-lasting alterations in the kinetics with which the cells responded to subsequent stimulation with estrogen. Manifestation of this memory effect was correlated quantitatively with the induction and propagation of a moderate-affinity, nuclear, estrogen-binding protein with the characteristics of a type II estrogen receptor. The data indicate that transient exposure of these cells to estrogen can induce changes in their response characteristics and composition of nuclear proteins that are inherited by daughter cells grown in the absence of hormone for more than ten generations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tam, S P -- Hache, R J -- Deeley, R G -- New York, N.Y. -- Science. 1986 Dec 5;234(4781):1234-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3022381" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apolipoproteins B/pharmacology ; Apolipoproteins E/pharmacology ; Carcinoma, Hepatocellular/metabolism ; Cell Division ; Cell Line ; Chick Embryo ; Estradiol/pharmacology ; Estrogens/*pharmacology ; Humans ; Liver/*cytology/drug effects ; Liver Neoplasms/metabolism ; Receptors, Estrogen/drug effects
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  • 229
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-08-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Walsh, J -- New York, N.Y. -- Science. 1986 Aug 15;233(4765):718-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3738504" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Cetacea ; *Conservation of Natural Resources ; *Industry ; Japan ; Research ; United States ; *Whales
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  • 230
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-07-11
    Description: When a male Sierra dome spider (Linyphia litigiosa) encounters a virgin female that has been sexually mature for 7 to 10 days, he rapidly packs the silk of her web into a tight mass. This behavior hinders evaporation of a male-attractant chemical that such highly receptive females apply to their webs. The male thereby reduces the likelihood that his mating partner will attract rival males.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Watson, P J -- 5T32MH15793/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1986 Jul 11;233(4760):219-21.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3726530" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Copulation/physiology ; Female ; Male ; Pheromones/*physiology ; Sex Attractants/*physiology ; Spiders/*physiology
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  • 231
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-09-12
    Description: Can animal mating systems result in the choice of mates carrying genotypes that are otherwise favored by natural selection? This question is addressed by studying, in natural populations of Colias butterflies, how the phosphoglucose isomerase (PGI) enzyme genotype of males mating Colias females varies with degree of female mate discrimination. Certain PGI genotypes (as predicted from their biochemical properties) have been found previously to have an advantage in diverse fitness-related properties: flight capacity, survivorship, and overall mating success. It is shown here that males of these same genotypes have even greater advantage in remating older, more discriminating females than they do in mating previously unmated, less discriminating females. Assortative mating is not found and thus cannot explain this effect. The mating system of these insects does, at least in this case, result in active female choice of generally favorable male genotypes as mates.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Watt, W B -- Carter, P A -- Donohue, K -- GM 26758/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1986 Sep 12;233(4769):1187-90.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3738528" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Butterflies/genetics/*physiology ; Courtship ; Female ; Genotype ; Glucose-6-Phosphate Isomerase/physiology ; Lepidoptera/*physiology ; Male ; Sexual Behavior, Animal/*physiology
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  • 232
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-08-15
    Description: In the membrane of the flight muscle cells of developing Drosophila a large calcium-sensitive potassium current, IKc, was found. It was present before the development of voltage-activated potassium channels and seems to be the first potassium current to develop in the membrane. Also present in these early cells were large numbers of occult (hidden) calcium channels, which remained inactive until the end of pupal development. These inactive calcium channels could be made to function by injecting adenosine triphosphate or ethyleneglycol tetraacetic acid into the early cells. IKc has kinetic properties resembling the later developing voltage-sensitive current IKv, and is distinct from the fast, transient calcium-dependent outward current IAc, which appears much later in development. IAc closely resembles the voltage-sensitive current IAv, also present in these cells. Thus, both of the voltage-sensitive potassium channel types, IAv and IKv, have similar calcium-sensitive counterparts, IAc and IKc, that are present in the same cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wei, A -- Salkoff, L -- 5-T32-NS07057-08/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1986 Aug 15;233(4765):780-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2426780" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials/drug effects ; Adenosine Triphosphate/pharmacology ; Alleles ; Animals ; Calcium/*metabolism/pharmacology ; Drosophila/genetics/*growth & development/physiology ; Egtazic Acid/pharmacology ; Ion Channels/drug effects/*physiology ; Mutation ; Potassium/*metabolism ; Pupa
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  • 233
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-08-29
    Description: Study of the neurobiology of learning and memory is in a most exciting phase. Behavioral studies in animals are characterizing the categories and properties of learning and memory; essential memory trace circuits in the brain are being defined and localized in mammalian models; work on human memory and the brain is identifying neuronal systems involved in memory; the neuronal, neurochemical, molecular, and biophysical substrates of memory are beginning to be understood in both invertebrate and vertebrate systems; and theoretical and mathematical analysis of basic associative learning and of neuronal networks in proceeding apace. Likely applications of this new understanding of the neural bases of learning and memory range from education to the treatment of learning disabilities to the design of new artificial intelligence systems.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Thompson, R F -- New York, N.Y. -- Science. 1986 Aug 29;233(4767):941-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3738519" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Aplysia/physiology ; Brain/physiology ; Cerebellum/physiology ; Cerebral Cortex/physiology ; Conditioning, Classical/physiology ; Hippocampus/physiology ; Humans ; Learning/*physiology ; Memory/*physiology ; Neural Pathways/physiology ; Neurons/physiology ; Primates ; Rats ; Synapses/physiology
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  • 234
    Publication Date: 1986-07-11
    Description: Carbon-13 nuclear magnetic resonance spectroscopy has been used in the study of glucose metabolism, specifically aldose reductase inhibition, in intact rabbit lenses maintained in organ culture. This technique provides an effective method of screening potential inhibitors of aldose reductase under conditions that more closely approximate in vivo conditions than do earlier methods. The aspirin substitutes acetaminophen and ibuprofen were studied as aldose reductase inhibitors and were found to be effective in reducing sorbitol accumulation in lenses exposed to high glucose stress. Results of this work with various inhibitors of aldose reductase are discussed in terms of lens metabolism and implications regarding diabetic complications such as cataract formation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Williams, W F -- Odom, J D -- New York, N.Y. -- Science. 1986 Jul 11;233(4760):223-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3088727" target="_blank"〉PubMed〈/a〉
    Keywords: Acetaminophen/pharmacology ; Aldehyde Reductase/*antagonists & inhibitors ; Animals ; Ibuprofen/pharmacology ; Imidazoles/pharmacology ; *Imidazolidines ; Lens, Crystalline/*enzymology ; *Magnetic Resonance Spectroscopy ; Naphthalenes/pharmacology ; Organ Culture Techniques ; Rabbits ; Sorbitol/metabolism ; Sugar Alcohol Dehydrogenases/*antagonists & inhibitors
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  • 235
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-11-21
    Description: Long-term potentiation (LTP), a long-lasting enhancement of synaptic efficacy, is considered a model for learning and memory. In anesthetized rats, activation of dentate granule cells by stimulating either the medial or lateral perforant pathway at frequencies of 100 to 400 Hz produced LTP of the stimulated pathway preferentially at 400 Hz. However, hippocampal pathways do not normally fire at this high rate. Stimuli at 200 Hz were then applied to either the medial or lateral pathway separately, to both pathways simultaneously, or to the two pathways asynchronously so that the composite stimulus applied to the granule cell dendrite was 400 Hz. LTP was produced preferentially in the asynchronous condition. Thus, lower frequency, physiological input volleys arriving asynchronously at medial and lateral synapses can induce LTP by activating a 400-Hz sensitive mechanism capable of integrating spatially separated granule cell inputs. This may reflect how LTP is normally produced in the dentate gyrus.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Winson, J -- Dahl, D -- 5-K02-MH00232/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1986 Nov 21;234(4779):985-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3775372" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Electric Stimulation ; Evoked Potentials ; Hippocampus/*physiology ; Neurons, Afferent/physiology ; Rats
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  • 236
    Publication Date: 1986-02-07
    Description: A monoclonal antibody (Epi 1) has been produced that recognizes an antigen expressed in epidermal cells of Xenopus laevis embryos. The Epi 1 antigen appears in embryonic epidermis at the end of gastrulation and is not expressed in nonepidermal structures derived from ectoderm (for example, neural tube or cement gland). The capacity to express the Epi 1 antigen is restricted to cells of the animal hemisphere prior to the midblastula stage of development (stage 8), and tissue interactions during gastrulation inhibit the expression of the Epi 1 antigen in neural ectoderm. This epidermal antigen will be a valuable marker for studies of ectodermal commitment.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Akers, R M -- Phillips, C R -- Wessells, N K -- HD 04708/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1986 Feb 7;231(4738):613-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3945801" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens/*immunology ; Blastocyst/immunology ; *Cell Differentiation ; Ectoderm/immunology ; Embryo, Nonmammalian/immunology ; *Embryonic Induction ; Epidermis/immunology/*physiology ; Xenopus laevis/*embryology/immunology
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  • 237
    Publication Date: 1986-02-07
    Description: Protein kinase C activity in rat hippocampal membranes and cytosol was determined 1 minute and 1 hour after induction of the synaptic plasticity of long-term potentiation. At 1 hour after long-term potentiation, but not at 1 minute, protein kinase C activity was increased twofold in membranes and decreased proportionately in cytosol, suggesting translocation of the activity. This time-dependent redistribution of enzyme activity was directly related to the persistence of synaptic plasticity, suggesting a novel mechanism regulating the strength of synaptic transmission.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Akers, R F -- Lovinger, D M -- Colley, P A -- Linden, D J -- Routtenberg, A -- MH25281/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1986 Feb 7;231(4738):587-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3003904" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Membrane/enzymology ; Cytosol/enzymology ; Enzyme Activation ; Hippocampus/*enzymology/physiology ; Male ; Neuronal Plasticity ; Protein Kinase C/metabolism/*physiology ; Rats ; Synaptic Membranes/enzymology ; Synaptic Transmission
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  • 238
    Publication Date: 1986-11-07
    Description: Dense, focal injections of wheat germ agglutinin conjugated-horseradish peroxidase in the locus coeruleus of rats labeled afferent neurons in unexpectedly few brain regions. Major inputs emanate from only two nuclei--the paragigantocellularis and the prepositus hypoglossi, both in the rostral medulla. The dorsal cap of the paraventricular hypothalamic nucleus and the spinal intermediate gray are possible minor afferents to locus coeruleus. Other areas reported to project to locus coeruleus (for example, amygdala, nucleus tractus solitarius, and spinal dorsal horn) did not exhibit consistent retrograde labeling. Anterograde tracing and electrophysiologic experiments confirmed the absence of input to locus coeruleus from these areas, which instead terminate in targets adjacent to locus coeruleus. These findings redefine the anatomic organization of the locus coeruleus, and have implications for hypotheses concerning the functions of this noradrenergic brain nucleus.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Aston-Jones, G -- Ennis, M -- Pieribone, V A -- Nickell, W T -- Shipley, M T -- NS20643/NS/NINDS NIH HHS/ -- NS22320/NS/NINDS NIH HHS/ -- NS23348/NS/NINDS NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1986 Nov 7;234(4777):734-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3775363" target="_blank"〉PubMed〈/a〉
    Keywords: Afferent Pathways ; Animals ; Efferent Pathways ; Electric Stimulation ; Locus Coeruleus/anatomy & histology/*physiology ; Male ; Medulla Oblongata/cytology ; Paraventricular Hypothalamic Nucleus/cytology ; Rats ; Spinal Cord/cytology ; Wheat Germ Agglutinins
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  • 239
    Publication Date: 1986-02-28
    Description: Differentiation of lymphoid precursor cells in a variety of species is induced by polypeptide hormones such as thymopoietin for T cells and bursin for B cells. In the present experiments, bursin isolated from the bursa of Fabricius of chicken was found to induce the phenotypic differentiation of mammalian and avian B precursor cells but not of T precursor cells in vitro. Similarly, bursin increased cyclic guanosine monophosphate in cells of the human B-cell line Daudi but not in cells of the human T-cell line CEM. These inducing properties of bursin are the reverse of the inducing properties of thymopoietin produced by the thymus and are appropriate to a physiological B-cell-inducing hormone. A tripeptide sequence (lysyl-histidyl-glycyl-amide) was determined for bursin and confirmed by synthesizing this proposed structure and demonstrating chemical identity of the natural and synthetic peptides. Similarity of biological action was indicated in induction assays by elevation of cyclic adenosine monophosphate and guanosine monophosphate in Daudi B cells but not in CEM T cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Audhya, T -- Kroon, D -- Heavner, G -- Viamontes, G -- Goldstein, G -- New York, N.Y. -- Science. 1986 Feb 28;231(4741):997-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3484838" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; B-Lymphocytes/*physiology ; Bursa of Fabricius/*physiology ; Cell Line ; Chickens ; Chromatography, High Pressure Liquid ; Chromatography, Thin Layer ; Humans ; Mass Spectrometry ; Oligopeptides/*isolation & purification/pharmacology/physiology ; Rats ; T-Lymphocytes/drug effects
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  • 240
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-03-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barnes, B M -- New York, N.Y. -- Science. 1986 Mar 28;231(4745):1505.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3952493" target="_blank"〉PubMed〈/a〉
    Keywords: Aging ; Animals ; Brain/cytology/*embryology ; Cell Differentiation ; Nerve Tissue/transplantation ; Peripheral Nerves/*cytology ; Rats
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  • 241
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-09-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barnes, D M -- New York, N.Y. -- Science. 1986 Sep 12;233(4769):1149-53.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3016904" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/immunology/*prevention & control ; Animals ; Antibodies, Viral/immunology ; Deltaretrovirus/immunology ; Genetic Engineering ; HIV Antibodies ; Pan troglodytes ; *Vaccines/immunology
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  • 242
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-11-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barnes, D M -- New York, N.Y. -- Science. 1986 Nov 21;234(4779):938-40.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3022378" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/physiopathology ; Disease Models, Animal ; Epilepsy/*physiopathology ; Humans ; Kindling, Neurologic ; Neural Inhibition ; Rats ; *Synaptic Transmission
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  • 243
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-04-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barnes, D M -- New York, N.Y. -- Science. 1986 Apr 18;232(4748):309-11.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3961483" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Laboratory ; Cats ; *Disease Models, Animal ; Dogs ; Horses ; National Institutes of Health (U.S.) ; Pan troglodytes ; Primates ; Research Support as Topic/*economics ; United States
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  • 244
    Publication Date: 1986-01-10
    Description: In rats infected with the parasite Schistosoma mansoni, the concentration of C-reactive protein in the serum increases after the lung stage of infection and is at its highest at the time of terminal worm rejection. The peak of platelet-mediated cytotoxicity induced by infected serum that has been heated (and is free of immunoglobulin E) as well as the time course for the development of platelet cytotoxic activity in infected rats was found to be correlated with the concentration of C-reactive protein. Rat and human platelets treated with homologous serum obtained during an acute phase of inflammation or with purified C-reactive protein were able to kill the immature forms of the worm in vitro. Platelets treated with C-reactive protein were furthermore capable of conferring significant protection against schistosomiasis in transfer experiments. Collectively these data indicate that a system that includes C-reactive protein and platelets participates in the natural resistance of the rat to schistosomal infection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bout, D -- Joseph, M -- Pontet, M -- Vorng, H -- Deslee, D -- Capron, A -- New York, N.Y. -- Science. 1986 Jan 10;231(4734):153-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3079916" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood Platelets/*drug effects/immunology ; C-Reactive Protein/blood/immunology/*pharmacology ; Cytotoxicity, Immunologic/*drug effects ; Dose-Response Relationship, Drug ; Immunity, Innate/drug effects ; Rats ; Schistosomiasis mansoni/*immunology ; Turpentine/pharmacology
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  • 245
    Publication Date: 1986-08-15
    Description: Predictions of the structures of the antigen-binding domains of an antibody, recorded before its experimental structure determination and tested subsequently, were based on comparative analysis of known antibody structures or on conformational energy calculations. The framework, the relative positions of the hypervariable regions, and the folds of four of the hypervariable loops were predicted correctly. This portion includes all residues in contact with the antigen, in this case hen egg white lysozyme, implying that the main chain conformation of the antibody combining site does not change upon ligation. The conformations of three residues in each of the other two hypervariable loops are different in the predicted models and the experimental structure.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chothia, C -- Lesk, A M -- Levitt, M -- Amit, A G -- Mariuzza, R A -- Phillips, S E -- Poljak, R J -- GM25435/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1986 Aug 15;233(4765):755-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3090684" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Antibodies, Monoclonal ; *Antigen-Antibody Complex ; Chickens ; Egg White ; Female ; Immunoglobulin Fab Fragments ; *Immunoglobulin G ; Immunoglobulin Heavy Chains ; Immunoglobulin Light Chains ; Immunoglobulin Variable Region ; Models, Molecular ; Muramidase/immunology ; Protein Conformation
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  • 246
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-02-28
    Description: gamma-Aminobutyric acid (GABA) is one of the major inhibitory neurotransmitters in the central nervous system. In the cerebral cortex, GABA-containing cells represent a subpopulation of interneurons. With semithin frozen sections, it is possible to demonstrate that most GABA neurons in the rat somatosensory cortex contain the calcium-binding protein parvalbumin and that parvalbumin is found virtually only in GABA neurons. Parvalbumin seems to influence the electrical properties and enzymatic machinery to modulate neuronal excitability and activity. The specific role of parvalbumin in GABA-containing cortical cells may be related to controlling the effectiveness of their inhibitory action.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Celio, M R -- New York, N.Y. -- Science. 1986 Feb 28;231(4741):995-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3945815" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cerebral Cortex/analysis/*cytology ; Electrophysiology ; Male ; Muscle Proteins/*analysis ; Neurons/*analysis/physiology ; Parvalbumins/*analysis ; Rats ; gamma-Aminobutyric Acid/*physiology
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  • 247
    Publication Date: 1986-09-12
    Description: The observation that voltage-dependent K+ channels are required for activation of human T lymphocytes suggests that pathological conditions involving abnormal mitogen responses might be reflected in ion channel abnormalities. Gigaohm seal techniques were used to study T cells from MRL/MpJ-lpr/lpr mice; these mice develop generalized lymphoproliferation of functionally and phenotypically abnormal T cells and a disease resembling human systemic lupus erythematosus. The number and predominant type of K+ channels in T cells from these mice differ dramatically from those in T cells from control strains and a congenic strain lacking the lpr gene locus. Thus an abnormal pattern of ion channel expression has now been associated with a genetic defect in cells of the immune system.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chandy, K G -- DeCoursey, T E -- Fischbach, M -- Talal, N -- Cahalan, M D -- Gupta, S -- AI-20717/AI/NIAID NIH HHS/ -- AI-21808/AI/NIAID NIH HHS/ -- NS-14609/NS/NINDS NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1986 Sep 12;233(4769):1197-200.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2426784" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Drosophila ; Humans ; Ion Channels/*metabolism/physiology ; Lymphocyte Activation ; Membrane Potentials ; Mice ; Mice, Inbred Strains ; Mice, Mutant Strains ; *Mutation ; Potassium/*metabolism ; T-Lymphocytes/abnormalities/*metabolism/physiology
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  • 248
    Publication Date: 1986-08-15
    Description: To define the functional domains of the progesterone receptor required for gene regulation, complementary DNA (cDNA) clones encoding the chicken progesterone receptor have been isolated from a chicken oviduct lambda gt11 cDNA expression library. Positive clones expressed antigenic determinants that cross-reacted with six monospecific antibodies derived from two independent sources. A 36-amino acid peptide sequence obtained by microsequencing of purified progesterone receptor was encoded by nucleotide sequences in the longest cDNA clone. Analysis of the amino acid sequence of the progesterone receptor deduced from the cDNA clones revealed a cysteine-rich region that was homologous to a region found in the estrogen and glucocorticoid receptors and to the avian erythroblastosis virus gag-erb-A fusion protein. Northern blot analysis with chicken progesterone receptor cDNA's indicated the existence of at least three messenger RNA species. These messages were found only in oviduct and could be induced by estrogens.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Conneely, O M -- Sullivan, W P -- Toft, D O -- Birnbaumer, M -- Cook, R G -- Maxwell, B L -- Zarucki-Schulz, T -- Greene, G L -- Schrader, W T -- O'Malley, B W -- New York, N.Y. -- Science. 1986 Aug 15;233(4765):767-70.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2426779" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Antibodies, Monoclonal ; Base Sequence ; Chickens ; *Cloning, Molecular ; Cross Reactions ; DNA/*metabolism ; Epitopes/analysis ; Female ; *Genes ; Humans ; Nucleic Acid Hybridization ; Oviducts/metabolism ; RNA, Messenger/genetics ; Receptors, Progesterone/*genetics ; Species Specificity
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  • 249
    Publication Date: 1986-08-22
    Description: A new family of protein kinase C-related genes has been identified in bovine, human, and rat genomes. The alpha-, beta-, and gamma-type protein kinase sequences are highly homologous, include a kinase domain, and potential calcium-binding sites, and they contain interspersed variable regions. The corresponding genes are located on distinct human chromosomes; the possibility of even greater genetic complexity of this gene family is suggested by Northern and Southern hybridization analyses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Coussens, L -- Parker, P J -- Rhee, L -- Yang-Feng, T L -- Chen, E -- Waterfield, M D -- Francke, U -- Ullrich, A -- New York, N.Y. -- Science. 1986 Aug 22;233(4766):859-66.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3755548" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Base Sequence ; Cattle ; Chromosome Mapping ; Chromosomes, Human, 16-18 ; Dna ; Genes ; Humans ; Nucleic Acid Hybridization ; Protein Kinase C/*genetics ; Rats
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  • 250
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-10-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Crawford, M -- New York, N.Y. -- Science. 1986 Oct 24;234(4775):422.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3764419" target="_blank"〉PubMed〈/a〉
    Keywords: *2,4-Dinitrophenol/*analogs & derivatives ; Acetamides/toxicity ; Animals ; Dinitrophenols/*toxicity ; Herbicides/*toxicity ; Rabbits ; United States ; United States Environmental Protection Agency
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  • 251
    Publication Date: 1986-04-04
    Description: The pathophysiology of anaphylaxis is very complex, and the sequelae of events are not fully explained in terms of the effects of histamine and peptide leukotrienes alone. Platelet-activating factor (1-O-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine, PAF-acether) has been detected in animals undergoing anaphylaxis. Injection of synthetic PAF-acether induces similar effects, including bronchoconstriction, respiratory arrest, systemic hypotension, neutropenia, and thrombocytopenia. The results reported here demonstrate that the histamine- and leukotriene-independent component of guinea pig anaphylaxis in vivo and in isolated lung parenchymal strips in vitro is mediated by PAF-acether. However, PAF-acether is not responsible for the anaphylaxis-induced thrombocytopenia.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Darius, H -- Lefer, D J -- Smith, J B -- Lefer, A M -- HL-25575/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1986 Apr 4;232(4746):58-60.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3082008" target="_blank"〉PubMed〈/a〉
    Keywords: 4,5-Dihydro-1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amine ; Alprazolam ; *Anaphylaxis ; Animals ; Anti-Inflammatory Agents/pharmacology ; Benzodiazepines/pharmacology ; Blood Pressure ; Diphenhydramine/pharmacology ; Guinea Pigs ; In Vitro Techniques ; Kinetics ; Lung/drug effects/*immunology ; Male ; Ovalbumin ; Platelet Activating Factor/*immunology ; Platelet Count/drug effects ; Pyrazoles/pharmacology
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  • 252
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-12-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dickson, D -- New York, N.Y. -- Science. 1986 Dec 19;234(4783):1494.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3787257" target="_blank"〉PubMed〈/a〉
    Keywords: *Animal Welfare ; Animals ; Europe
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  • 253
    Publication Date: 1986-11-07
    Description: The current prevalence of the acquired immune deficiency syndrome in humans has provoked renewed interest in methods of protective immunization against retrovirus-induced diseases. In this study, a vaccinia-retrovirus recombinant vector was constructed to study mechanisms of immune protection against Friend virus leukemia in mice. The envelope (env) gene from Friend murine leukemia virus (F-MuLV) was inserted into the genome of a vaccinia virus expression vector. Infected cells synthesized gp85, the glycosylated primary product of the env gene. Processing to gp70 and p15E, and cell surface localization, were similar to that occurring in cells infected with F-MuLV. Mice inoculated with live recombinant vaccinia virus had an envelope-specific T-cell proliferative response and, after challenge with Friend virus complex, developed neutralizing antibody and cytotoxic T cells (CTL) and were protected against leukemia. In contrast, unimmunized and control groups developed a delayed neutralizing antibody response, but no detectable CTL, and succumbed to leukemia. Genes of the major histocompatibility complex influenced protection induced by the vaccinia recombinant but not that induced by attenuated N-tropic Friend virus.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Earl, P L -- Moss, B -- Morrison, R P -- Wehrly, K -- Nishio, J -- Chesebro, B -- New York, N.Y. -- Science. 1986 Nov 7;234(4777):728-31.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3490689" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibodies, Viral/immunology ; Antigens/*immunology ; DNA, Recombinant ; Female ; Friend murine leukemia virus/genetics/immunology ; *Genes, Viral ; Leukemia, Erythroblastic, Acute/prevention & control ; Leukemia, Experimental/*prevention & control ; Lymphocyte Activation ; Male ; Mice ; Mice, Inbred Strains ; Sex Factors ; Spleen/microbiology ; T-Lymphocytes/*immunology ; T-Lymphocytes, Cytotoxic/immunology ; Vaccines, Synthetic/*immunology ; Vaccinia virus/genetics/immunology ; Viral Envelope Proteins/genetics/*immunology ; Viral Vaccines/*immunology
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  • 254
    Publication Date: 1986-01-24
    Description: When platelets were incubated with prostacyclin, prostaglandin E1, or prostaglandin D2 at concentrations insufficient to increase the level of adenosine 3',5'-monophosphate (cyclic AMP), coagulation factor X was activated by a platelet cysteine protease. Prostacyclin or prostaglandin E1 at higher concentrations increased the cyclic AMP level and inhibited the activation of factor X by platelets. Inhibition of platelet adenylate cyclase by 2',5'-dideoxyadenosine allowed the activation of the protease at higher concentrations of the autocoids. Prostaglandins A1, A2, B1, B2, E2, F2 alpha, 6-keto-prostaglandin F1 alpha, and thromboxane B2, which do not affect platelet cyclic AMP level, did not stimulate the protease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dutta-Roy, A K -- Ray, T K -- Sinha, A K -- New York, N.Y. -- Science. 1986 Jan 24;231(4736):385-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3001935" target="_blank"〉PubMed〈/a〉
    Keywords: Adenylyl Cyclases/metabolism ; Alprostadil/pharmacology ; Animals ; Blood Platelets/*drug effects/metabolism/physiology ; Cattle ; Cyclic AMP/metabolism ; Deoxyadenosines/analogs & derivatives/pharmacology ; *Dideoxyadenosine/*analogs & derivatives ; Epoprostenol/*pharmacology ; Factor X/*physiology ; Humans ; Peptide Hydrolases/metabolism ; Prostaglandin D2 ; Prostaglandins/pharmacology ; Prostaglandins D/pharmacology
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  • 255
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-02-07
    Description: Measurements confirm the quantitative theoretical prediction that the autonomic nonendocrine abnormality of rapid daytime gastric emptying is the major primary cause of the obesity resulting from ventromedial hypothalamic lesions in rats. Therapy for obesity could include slowing of stomach emptying.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Duggan, J P -- Booth, D A -- New York, N.Y. -- Science. 1986 Feb 7;231(4738):609-11.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3511527" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Feeding and Eating Disorders/*physiopathology ; *Gastric Emptying/drug effects ; Humans ; Hyperphagia/etiology/*physiopathology ; Insulin/pharmacology ; Obesity/etiology/*physiopathology ; Rats ; Rats, Inbred Strains ; Time Factors ; Ventromedial Hypothalamic Nucleus/*physiology
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  • 256
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-01-31
    Description: Pineal melatonin may play an important role in regulation of vertebrate circadian rhythms and in human affective disorders. In some mammals, such as hamsters and sheep, melatonin is involved in photoperiodic time measurement and in control of reproduction. Although wild mice (Mus domesticus) and some wild-derived inbred strains of mice have melatonin in their pineal glands, several inbred strains of laboratory mice (for example, C57BL/6J) were found not to have detectable melatonin in their pineal glands. Genetic analysis suggests that melatonin deficiency in C57BL/6J mice results from mutations in two independently segregating, autosomal recessive genes. Synthesis of melatonin from serotonin in the pineal gland requires the enzymes N-acetyltransferase (NAT) and hydroxyindole-O-methyltransferase (HIOMT). Pineal glands from C57BL/6J mice have neither NAT nor HIOMT activity. These results suggest that the two genes involved in melatonin deficiency are responsible for the absence of normal NAT and HIOMT enzyme activity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ebihara, S -- Marks, T -- Hudson, D J -- Menaker, M -- 13162/PHS HHS/ -- FO5TW03377/TW/FIC NIH HHS/ -- New York, N.Y. -- Science. 1986 Jan 31;231(4737):491-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3941912" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chromatography, High Pressure Liquid ; Female ; Kinetics ; Male ; Melatonin/biosynthesis/deficiency/*genetics ; Mice ; Mice, Inbred C57BL ; Mice, Inbred Strains ; Pineal Gland/*metabolism ; Reference Values ; Species Specificity
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  • 257
    Publication Date: 1986-09-26
    Description: The potential utility of cultured neuroblastoma cells as donor tissue for neutral implants into the mammalian brain has been examined. Cells from a human neuroblastoma cell line, IMR-32, were labeled with [3H]thymidine and chemically rendered amitotic. These differentiated IMR-32 cells were grafted into the hippocampi of five adult African Green monkeys, and graft survival was evaluated for up to 270 days after transplantation. Autoradiographically labeled grafted cells were identified in four animals. Processes from grafted cells could be followed for distances of up to 150 micrometers into the host brain. No evidence for neoplastic growth of the transplant was found. Thus, grafted neuroblastoma cells can survive for prolonged periods in the primate brain and may serve as a practical source of donor tissue for neural implants.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gash, D M -- Notter, M F -- Okawara, S H -- Kraus, A L -- Joynt, R J -- New York, N.Y. -- Science. 1986 Sep 26;233(4771):1420-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3749886" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autoradiography ; Brain/*cytology ; Cell Line ; Cercopithecus aethiops ; DNA Replication ; Female ; Humans ; Male ; Neoplasm Transplantation ; Neuroblastoma/*pathology ; Neurons/*transplantation ; Thymidine/metabolism ; Tritium
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  • 258
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-09-26
    Description: Although individual neurons in the arm area of the primate motor cortex are only broadly tuned to a particular direction in three-dimensional space, the animal can very precisely control the movement of its arm. The direction of movement was found to be uniquely predicted by the action of a population of motor cortical neurons. When individual cells were represented as vectors that make weighted contributions along the axis of their preferred direction (according to changes in their activity during the movement under consideration) the resulting vector sum of all cell vectors (population vector) was in a direction congruent with the direction of movement. This population vector can be monitored during various tasks, and similar measures in other neuronal populations could be of heuristic value where there is a neural representation of variables with vectorial attributes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Georgopoulos, A P -- Schwartz, A B -- Kettner, R E -- NS07226/NS/NINDS NIH HHS/ -- NS17413/NS/NINDS NIH HHS/ -- NS20868/NS/NINDS NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1986 Sep 26;233(4771):1416-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3749885" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arm/innervation ; Macaca mulatta ; Mathematics ; Models, Neurological ; Motor Cortex/*physiology ; Motor Neurons/*physiology
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  • 259
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-05-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gershon, E S -- New York, N.Y. -- Science. 1986 May 23;232(4753):919.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3010457" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Humans ; National Institutes of Health (U.S.) ; *Research Support as Topic ; United States ; United States Substance Abuse and Mental Health Services Administration
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  • 260
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-10-03
    Description: Cholinergic agonists rapidly and transiently induced transcription of the c-fos protooncogene and one or more actin genes in neuronally differentiated PC12 cells. Transcription was activated within minutes after stimulation of the nicotinic acetylcholine receptor and required an influx of extracellular Ca2+ ions through voltage-sensitive calcium channels. Nicotine activation proceeded by a different pathway from activation by nerve growth factor, whose stimulation of these genes is independent of extracellular Ca2+ ions. These findings suggest that neurotransmitters may rapidly activate specific gene transcription in nondividing neuronally differentiated cells. They also suggest a functional role for neurotransmitter induction of c-fos and actin expression in the nervous system.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Greenberg, M E -- Ziff, E B -- Greene, L A -- GM 30760/GM/NIGMS NIH HHS/ -- NS16036/NS/NINDS NIH HHS/ -- P30 CA 16087/CA/NCI NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1986 Oct 3;234(4772):80-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3749894" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials/drug effects ; Adrenal Gland Neoplasms/metabolism ; Animals ; Calcium/metabolism ; Cell Line ; Dose-Response Relationship, Drug ; Nerve Growth Factors/pharmacology ; Nicotine/pharmacology ; Pheochromocytoma/metabolism ; Rats ; Receptors, Cholinergic/*drug effects ; Transcription, Genetic/*drug effects
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  • 261
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-10-24
    Description: The Golgi complex is a series of membrane compartments through which proteins destined for the plasma membrane, secretory vesicles, and lysosomes move sequentially. A model is proposed whereby these three different classes of proteins are sorted into different vesicles in the last Golgi compartment, the trans Golgi network. This compartment corresponds to a tubular reticulum on the trans side of the Golgi stack, previously called Golgi endoplasmic reticulum lysosomes (GERL).〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Griffiths, G -- Simons, K -- New York, N.Y. -- Science. 1986 Oct 24;234(4775):438-43.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2945253" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carrier Proteins/physiology ; *Cell Compartmentation ; Endocytosis ; Exocytosis ; Glycosylation ; Golgi Apparatus/*physiology/ultrastructure ; Humans ; Hydrogen-Ion Concentration ; Intracellular Membranes/physiology ; Lysosomes/physiology ; Membrane Proteins/metabolism ; *Protein Processing, Post-Translational ; Proteins/secretion ; Receptor, IGF Type 2
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  • 262
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-01-17
    Description: Because aerobic metabolic rates decrease in hypoxia-sensitive cells under oxygen-limiting conditions, the demand for glucose or glycogen for anaerobic glycolysis may rise drastically as a means of making up for the energetic shortfall. However, ion and electrical potentials typically cannot be sustained because of energy insufficiency and high membrane permeabilities; therefore metabolic and membrane functions in effect become decoupled. In hypoxia-tolerant animals, these problems are resolved through a number of biochemical and physiological mechanisms; of these metabolic arrest and stabilized membrane functions are the most effective strategies for extending tolerance to hypoxia. Metabolic arrest is achieved by means of a reversed or negative Pasteur effect (reduced or unchanging glycolytic flux at reduced O2 availability); and coupling of metabolic and membrane function is achievable, in spite of the lower energy turnover rates, by maintaining membranes of low permeability (probably via reduced densities of ion-specific channels). The possibility of combining metabolic arrest with channel arrest has been recognized as an intervention strategy. To date, the success of this strategy has been minimal, mainly because depression of metabolism through cold is the usual arrest mechanism used, and hypothermia in itself perturbs controlled cell function in most endotherms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hochachka, P W -- New York, N.Y. -- Science. 1986 Jan 17;231(4735):234-41.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2417316" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Triphosphate/metabolism ; Animals ; Anoxia/*metabolism/physiopathology ; Artemia ; Bivalvia ; Brain Ischemia/metabolism ; Calcium/metabolism ; Cell Membrane/metabolism/physiology ; Cell Membrane Permeability ; Cricetinae ; Energy Metabolism ; Hibernation ; Hypothermia/*metabolism/physiopathology ; Ion Channels ; Mammals ; Potassium/metabolism ; Reptiles/metabolism ; Sodium/metabolism ; Sodium-Potassium-Exchanging ATPase/metabolism
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  • 263
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-10-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 1986 Oct 3;234(4772):21.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3092354" target="_blank"〉PubMed〈/a〉
    Keywords: *Animal Welfare ; Animals ; *Animals, Laboratory ; Haplorhini ; Jurisprudence ; *National Institutes of Health (U.S.) ; United States
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  • 264
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-12-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G -- New York, N.Y. -- Science. 1986 Dec 5;234(4781):1198-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3775379" target="_blank"〉PubMed〈/a〉
    Keywords: Alcoholic Intoxication/*drug therapy ; Animals ; Azides/*pharmacology/therapeutic use ; Benzodiazepines/*pharmacology/therapeutic use ; Ethanol/*antagonists & inhibitors ; Humans ; Rats
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  • 265
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-04-11
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 1986 Apr 11;232(4747):147-50.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3952503" target="_blank"〉PubMed〈/a〉
    Keywords: Animal Care Committees ; *Animal Experimentation ; Animal Testing Alternatives ; *Animal Welfare ; Animals ; *Animals, Laboratory ; Aplysia ; Birds ; Chick Embryo ; Decapodiformes ; Federal Government ; Government Regulation ; Horseshoe Crabs ; Macaca ; Mice ; National Institutes of Health (U.S.) ; Rabbits ; Rats ; United States ; are discussed. The enactment of amendments to the Animal Welfare Act of 1966 and ; revisions to the Public Health Service's animal care guidelines are described as ; major federal moves to tighten standards and to locate responsibility for proper ; animal care at the institutional level. These regulatory changes will have a ; significant economic impact on the cost of doing research, but are generally ; accepted by the scientific community as necessary. Although moderate animal ; welfare groups see signs of progress, there is a growing number of activists who ; see recent policy developments as only a step toward the real goal of total ; elimination of the use of animals in research. It is apparent that the ; combination of political pressure, financial stringency, and better experimental ; methodologies will result in a continued reduction in laboratory animal use.
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  • 266
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-04-25
    Description: The genetic control of courtship song differences between Drosophila melanogaster and Drosophila simulans males was investigated by producing hybrids from reciprocal crosses. The song rhythm difference between the parental species appears to be due to sex-linked genes, whereas the basic interpulse-interval difference is autosomally inherited. Hybrid females show selective preferences for artificially generated songs carrying intermediate "hybrid" characteristics.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kyriacou, C P -- Hall, J C -- GM 21473/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1986 Apr 25;232(4749):494-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3083506" target="_blank"〉PubMed〈/a〉
    Keywords: *Animal Communication ; Animals ; *Courtship ; Drosophila/*genetics/physiology ; Drosophila melanogaster/genetics/physiology ; Female ; Male ; Species Specificity
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  • 267
    Publication Date: 1986-07-25
    Description: Adhesive interactions between cells and the extracellular matrix occur at several stages of metastasis. Such interactions might be inhibited by synthetic peptide probes derived from the cell-binding regions of matrix molecules. Gly-Arg-Gly-Asp-Ser (GRGDS) is a pentapeptide sequence that appears to be critical for cell interaction with fibronectin. Coinjection of GRGDS with B16-F10 murine melanoma cells dramatically inhibited the formation of lung colonies in C57BL/6 mice. Two closely related control peptides, in which specific amino acids within the GRGDS sequence were transposed or substituted, displayed little or no activity. Inhibition by GRGDS was dose-dependent, noncytotoxic, and did not result from an impairment of cellular tumorigenicity. GRGDS may function by inhibiting tumor cell retention in the lung since radiolabeled B16-F10 tumor cells injected with the peptide were lost at a substantially greater rate than control cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Humphries, M J -- Olden, K -- Yamada, K M -- CA-34918/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1986 Jul 25;233(4762):467-70.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3726541" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Fibronectins ; Lung Neoplasms/drug therapy/*secondary ; Melanoma/drug therapy/pathology/*secondary ; Mice ; Mice, Inbred C57BL ; *Neoplasm Metastasis ; Neoplasm Transplantation ; Oligopeptides/*therapeutic use
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  • 268
    Publication Date: 1986-01-24
    Description: A 70 percent reduction in the rate of blood flow through the common carotid artery in rabbits caused a 21 percent decrease in the diameter of this artery within 2 weeks. The smooth muscle relaxant papaverine did not attenuate the response; therefore, such reductions in diameter probably reflect a structural modification of the arterial wall rather than sustained contraction of smooth muscle. This arterial response to reduced blood flow was abolished when the endothelium was removed from the vessels. It appears that the endothelium is essential for the compensatory arterial response to long-term changes in luminal blood flow rates.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Langille, B L -- O'Donnell, F -- New York, N.Y. -- Science. 1986 Jan 24;231(4736):405-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3941904" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arteries/*pathology/physiopathology/ultrastructure ; *Blood Circulation ; Blood Platelets/physiopathology ; Carotid Arteries/pathology/physiopathology ; Endothelium/pathology/physiopathology ; Male ; Microscopy, Electron, Scanning ; Muscle, Smooth, Vascular/pathology/physiopathology ; Octoxynol ; Polyethylene Glycols ; Rabbits
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  • 269
    Publication Date: 1986-12-12
    Description: While much information exists about the structure and function of the clonally distributed T cell receptor (TCR) alpha beta heterodimer, little is known about the gamma protein, the product of a third rearranging TCR gene. An antiserum to a carboxyl-terminal peptide common to several of the murine gamma chain constant regions and a monoclonal antibody to the murine T3 complex were used to identify products of this TCR gene family in a subpopulation of Lyt2-, L3T4- thymocytes. This subpopulation does not express TCR alpha or full-length TCR beta messenger RNA. The gamma chain is a 35-kilodalton (kD) protein that is disulfide-bonded to a 45-kD partner and is associated with the T3 complex. Analysis of the glycosylation pattern of this thymic gamma chain revealed that the major variable region gamma (V gamma) gene transcribed in activated peripheral T cells is absent from this subpopulation. The cells that bear this second T cell receptor may therefore represent a distinct lineage differentiating within the thymus.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lew, A M -- Pardoll, D M -- Maloy, W L -- Fowlkes, B J -- Kruisbeek, A -- Cheng, S F -- Germain, R N -- Bluestone, J A -- Schwartz, R H -- Coligan, J E -- New York, N.Y. -- Science. 1986 Dec 12;234(4782):1401-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3787252" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Disulfides/analysis ; Electrophoresis, Polyacrylamide Gel ; Glycosylation ; Macromolecular Substances ; Mice ; Molecular Weight ; RNA, Messenger/metabolism ; Receptors, Antigen, T-Cell/*biosynthesis/genetics ; Structure-Activity Relationship ; Thymus Gland/*metabolism
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  • 270
    Publication Date: 1986-08-01
    Description: Basic and acidic fibroblast growth factors (FGF's) are potent mitogens for capillary endothelial cells in vitro, stimulate angiogenesis in vivo, and may participate in tissue repair. An oligonucleotide probe for bovine basic FGF was designed from the nucleotide sequence of the amino-terminal exon of bovine acidic FGF, taking into account the 55 percent amino acid sequence homology between the two factors. With this oligonucleotide probe, a full length complementary DNA for basic FGF was isolated from bovine pituitary. Basic FGF in bovine hypothalamus was shown to be encoded by a single 5.0-kilobase messenger RNA; in a human hepatoma cell line, both 4.6- and 2.2-kilobase basic FGF messenger RNA's were present. Both growth factors seem to be synthesized with short amino-terminal extensions that are not found on the isolated forms for which the amino acid sequences have been determined. Neither basic nor acidic FGF has a classic signal peptide.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Abraham, J A -- Mergia, A -- Whang, J L -- Tumolo, A -- Friedman, J -- Hjerrild, K A -- Gospodarowicz, D -- Fiddes, J C -- New York, N.Y. -- Science. 1986 Aug 1;233(4763):545-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2425435" target="_blank"〉PubMed〈/a〉
    Keywords: Angiogenesis Inducing Agents/*genetics ; Animals ; Base Sequence ; Cattle ; Cloning, Molecular ; Fibroblast Growth Factors/*genetics/pharmacology ; Growth Substances/*genetics ; Neovascularization, Pathologic
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  • 271
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-04-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Alpher, V S -- New York, N.Y. -- Science. 1986 Apr 18;232(4748):307.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3961482" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Humans ; Male ; *Psychosexual Development ; Rats ; Sexual Behavior
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  • 272
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-05-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Althuis, T H -- Ichinose, L Y -- New York, N.Y. -- Science. 1986 May 30;232(4754):1079-80.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3704636" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Animals, Laboratory ; Legislation as Topic ; Research ; United States
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  • 273
    Publication Date: 1986-07-11
    Description: Chronic myelogenous leukemia (CML) is a human disease associated with a consistent chromosomal translocation that results in sequences from the c-abl locus on chromosome 9 being fused to sequences in a breakpoint cluster region (bcr) on chromosome 22. CML cells have two novel products: an 8.5-kilobase RNA transcript containing both abl and bcr and a 210-kilodalton phosphoprotein (P210) recognized by v-abl-specific antisera. To test whether the P210 is the product of the novel 8.5-kilobase bcr/abl fusion transcript, antibodies were prepared against c-abl and bcr determinants. By using these reagents and v-abl-specific antisera, it was demonstrated that the P210 in CML cells is indeed the protein product of the 8.5-kilobase transcript. By analogy to the gag/abl fusion protein of Abelson murine leukemia virus, the replacement of amino terminal c-abl sequences by bcr sequences in P210 may create a transforming protein involved in CML. A 190-kilodalton phosphoprotein that is a candidate for the normal bcr protein was identified in both HeLa and K562 cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ben-Neriah, Y -- Daley, G Q -- Mes-Masson, A M -- Witte, O N -- Baltimore, D -- New York, N.Y. -- Science. 1986 Jul 11;233(4760):212-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3460176" target="_blank"〉PubMed〈/a〉
    Keywords: Abelson murine leukemia virus/genetics ; Animals ; Chromosomes, Human, 21-22 and Y ; Chromosomes, Human, 6-12 and X ; HeLa Cells/metabolism ; Humans ; Immune Sera/immunology ; Leukemia, Myeloid/*genetics ; Neoplasm Proteins/*genetics ; *Oncogenes ; Philadelphia Chromosome ; Protein-Tyrosine Kinases/genetics ; Rabbits/immunology
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  • 274
    Publication Date: 1986-07-18
    Description: Determination of the molecular structure and properties of allergens that elicit severe immediate-type hypersensitivity diseases in humans and a knowledge of the structure of their antibody-binding sites should provide new insight into the pathogenetic mechanisms of allergic diseases. Monomeric and homodimeric hemoglobins (CTT I to X) have been identified as potent allergenic components of Chironomidae, a family of Diptera. Immunologic investigations of peptides of three of these hemoglobins (CTT IV, CTT VI, and CTT VIII) showed that human antibodies of the E and G classes recognize at least two different sites within each molecule. Individual hemoglobin peptides were aligned with homologous regions of chironomid hemoglobin CTT III, whose tertiary structure has been determined by x-ray analysis at a resolution of 1.4 angstroms. The antigenic site CTT IV(91 to 101) showed the following characteristics: (i) seven polar or hydroxylated amino acids, from a total of eleven, occupying predominantly superficial regions; (ii) the property of linkage to other molecules by hydrogen bonds or solvent clusters; and (iii) high thermal mobility factors. In contrast, peptide CTT IV(102 to 108), which does not bind human antibodies, contained no polar amino acids and had low thermal mobility factors. These results support the idea that the antigenicity of clinically relevant proteins is related to regions with a predominance of polar amino acids and with low energy barriers between different conformations, which allow high flexibility, including site-specific adaptation in antibody binding.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Baur, X -- Aschauer, H -- Mazur, G -- Dewair, M -- Prelicz, H -- Steigemann, W -- New York, N.Y. -- Science. 1986 Jul 18;233(4761):351-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2425431" target="_blank"〉PubMed〈/a〉
    Keywords: Allergens/*immunology ; Amino Acid Sequence ; Animals ; Chironomidae/*immunology ; Diptera/*immunology ; Epitopes/*analysis ; Hemoglobins/analysis/*immunology ; Larva/analysis ; Molecular Conformation ; Peptide Fragments/analysis ; Temperature
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  • 275
    Publication Date: 1986-04-04
    Description: Platelet-derived growth factor (PDGF) is a potent mitogen for vascular smooth muscle cells that has been implicated in the pathogenesis of atherosclerosis. The potential role of PDGF in the altered vasoreactivity of atherosclerotic vessels has been studied through an examination of its effects on contractility in the rat aorta. PDGF caused a concentration-dependent contraction of aortic strips and was significantly more potent on a molar basis than the classic vasoconstrictor peptide angiotensin II. Furthermore, PDGF increased the cytosolic free calcium concentration in cultured rat aortic smooth muscle cells. These observations suggest a new biological activity for PDGF that may contribute to the enhanced vasoreactivity of certain atherosclerotic vessels.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Berk, B C -- Alexander, R W -- Brock, T A -- Gimbrone, M A Jr -- Webb, R C -- HL20054/HL/NHLBI NIH HHS/ -- HL22602/HL/NHLBI NIH HHS/ -- HL35013/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1986 Apr 4;232(4746):87-90.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3485309" target="_blank"〉PubMed〈/a〉
    Keywords: Aminoquinolines ; Angiotensin II/pharmacology ; Animals ; Aorta/*drug effects/metabolism/physiology ; Calcium/metabolism ; Cytosol/metabolism ; Dose-Response Relationship, Drug ; Epidermal Growth Factor/pharmacology ; Fluorescent Dyes ; Homeostasis/drug effects ; Humans ; In Vitro Techniques ; Kinetics ; Platelet-Derived Growth Factor/*pharmacology ; Rats ; Vasoconstriction/*drug effects
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  • 276
    Publication Date: 1986-06-20
    Description: Activated mononuclear cells appear to be important effector cells in autoimmune beta cell destruction leading to insulin-dependent (type 1) diabetes mellitus. Conditioned medium from activated mononuclear cells (from human blood) is cytotoxic to isolated rat and human islets of Langerhans. This cytotoxic activity was eliminated from crude cytokine preparations by adsorption with immobilized, purified antibody to interleukin-1 (IL-1). The islet-inhibitory activity and the IL-1 activity (determined by its comitogenic effect on thymocytes) were recovered by acid wash. Purified natural IL-1 and recombinant IL-1 derived from the predominant pI 7 form of human IL-1, consistently inhibited the insulin response. The pI 6 and pI 5 forms of natural IL-1 were ineffective. Natural and recombinant IL-1 exhibited similar dose responses in their islet-inhibitory effect and their thymocyte-stimulatory activity. Concentrations of IL-1 that inhibited islet activity were in the picomolar range. Hence, monocyte-derived pI 7 IL-1 may contribute to islet cell damage and therefore to the development of insulin-dependent diabetes mellitus.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bendtzen, K -- Mandrup-Poulsen, T -- Nerup, J -- Nielsen, J H -- Dinarello, C A -- Svenson, M -- AI-15614/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 1986 Jun 20;232(4757):1545-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3086977" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Survival ; Glucagon/secretion ; Humans ; Insulin/secretion ; Interferon-gamma/pharmacology ; Interleukin-1/*immunology ; Islets of Langerhans/*immunology/pathology/secretion ; Monocytes/immunology ; Rats ; Recombinant Proteins ; T-Lymphocytes/immunology
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  • 277
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-04-25
    Description: A systematic search for sequences that potentially could form metal-binding domains in proteins has been performed. Five classes of proteins involved in nucleic acid binding or gene regulation were found to contain such sequences. These observations suggest numerous experiments aimed at determining whether metal-binding domains are present in these proteins and, if present, what roles such domains play in the processes of nucleic acid binding and gene regulation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Berg, J M -- New York, N.Y. -- Science. 1986 Apr 25;232(4749):485-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2421409" target="_blank"〉PubMed〈/a〉
    Keywords: Adenoviridae/genetics ; Amino Acyl-tRNA Synthetases/metabolism ; Animals ; Base Sequence ; DNA-Binding Proteins/genetics/metabolism ; Escherichia coli/genetics ; Geobacillus stearothermophilus/metabolism ; Metals/metabolism ; Nucleic Acids/*metabolism ; RNA/metabolism ; Retroviridae/genetics ; Xenopus laevis
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  • 278
    Publication Date: 1986-10-10
    Description: Vascular smooth muscle from different arteries of the rabbit varies in sensitivity to norepinephrine, even when factors known to contribute to this variation are excluded. Sensitivity to norepinephrine mediated through the alpha-adrenoceptor is linearly related to the agonist dissociation constant, but is not significantly related to receptor reserve. These results suggest that agonist affinity is the primary determinant of sensitivity to norepinephrine, at least in these arteries, and that this is a locally regulated characteristic which may account for regional sensitivity changes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bevan, J A -- Oriowo, M A -- Bevan, R D -- HL 32383/HL/NHLBI NIH HHS/ -- HL 32985/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1986 Oct 10;234(4773):196-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3018932" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arteries ; Muscle Contraction/drug effects ; Muscle, Smooth, Vascular/*drug effects/physiology ; Norepinephrine/*pharmacology ; Rabbits ; Receptors, Adrenergic, alpha/*metabolism
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  • 279
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-03-21
    Description: The mutation rates of DNA sequences during evolution can be estimated from interspecies DNA sequence differences by assaying changes that have little or no effect on the phenotype (neutral mutations). Examination of available measurements shows that rates of DNA change of different phylogenetic groups differ by a factor of 5. The slowest rates are observed for higher primates and some bird lineages, while faster rates are seen in rodents, sea urchins, and drosophila. The rate of DNA sequence change has decreased markedly during primate evolution. The contrast in rates of DNA sequence change is probably due to evolutionary variation and selection of biochemical mechanisms such as DNA replication or repair.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Britten, R J -- GM34031/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1986 Mar 21;231(4744):1393-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3082006" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Base Sequence ; *Biological Evolution ; Cricetinae ; DNA/*genetics ; DNA Repair ; DNA Replication ; Drosophila ; Gene Frequency ; Genes ; Genetics, Population ; Gorilla gorilla ; Haplorhini ; Humans ; Hylobates ; Mice ; Nucleic Acid Hybridization ; Pan troglodytes ; Phenotype ; Rabbits ; Rats ; Species Specificity
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  • 280
    Publication Date: 1986-08-01
    Description: The specific inhibitor of glutathione biosynthesis, L-buthionine sulfoximine (L-BSO), although relatively nontoxic in adult mice, induces severe glutathione depletion and age-specific pathological changes when repeatedly administered to male suckling mice. Dense cataracts developed when mice aged 9 to 12 days were given a series of injections of L-BSO, despite excellent survival and the absence of other significant long-term effects. By contrast, similar treatment of mice aged 14 to 17 days, although slightly less effective in reducing glutathione levels, resulted frequently in death, hind-leg paralysis, or impaired spermatogenesis, but did not produce cataracts. Administration of L-BSO to preweanling mice provides a novel model system for the induction of cataracts by depletion of lens glutathione and may enable the study of critical functions of glutathione in the lens and other growing tissues during early postnatal development.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Calvin, H I -- Medvedovsky, C -- Worgul, B V -- EY-02648/EY/NEI NIH HHS/ -- HD-17932/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1986 Aug 1;233(4763):553-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3726547" target="_blank"〉PubMed〈/a〉
    Keywords: Age Factors ; Animals ; Buthionine Sulfoximine ; Cataract/*chemically induced ; Disease Models, Animal ; Glutathione/analysis/*metabolism ; Humans ; Kidney/analysis ; Lens, Crystalline/analysis ; Liver/analysis ; Male ; Methionine Sulfoximine/*analogs & derivatives/pharmacology ; Mice ; Testis/analysis
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  • 281
    Publication Date: 1986-01-10
    Description: Interleukin-3 (IL-3), a protein of 140 amino acids, was chemically synthesized by means of an automated peptide synthesizer and was shown to have the biological activities attributed to native IL-3. Assays of synthetic analogues established that an amino terminal fragment has detectable IL-3 activity, but that the stable tertiary structure of the complete molecule was required for full activity. The results demonstrate that automated peptide synthesis can be applied to the study of the structure and function of proteins.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Clark-Lewis, I -- Aebersold, R -- Ziltener, H -- Schrader, J W -- Hood, L E -- Kent, S B -- R01-CA38684-01/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1986 Jan 10;231(4734):134-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3079915" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Cell Line ; Chromatography, High Pressure Liquid ; Electrophoresis, Polyacrylamide Gel ; Interleukin-3 ; Lymphokines/*chemical synthesis/pharmacology ; Mast Cells/drug effects ; Megakaryocytes/drug effects ; Mice ; Protein Conformation ; Structure-Activity Relationship
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  • 282
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-11-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Crawford, M -- New York, N.Y. -- Science. 1986 Nov 7;234(4777):667-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3022375" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Containment of Biohazards ; DNA, Recombinant ; Herpesvirus 1, Suid/genetics/*immunology ; Swine ; Viral Vaccines/*standards
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  • 283
    Publication Date: 1986-09-12
    Description: Isolated hepatocytes, harvested from normal rat livers by portal vein collagenase perfusion, can be attached to collagen-coated dextran microcarriers and transplanted by intraperitoneal injection into rats. Survival and function of the transplanted hepatocytes have been demonstrated in mutant rats lacking bilirubin-uridine diphosphate glucuronosyltransferase activity (Gunn strain) and rats with inherited lack of plasma albumin (Nagase analbuminemia rat strain). This simple technique promises to be useful in the treatment of acute liver failure in humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Demetriou, A A -- Whiting, J F -- Feldman, D -- Levenson, S M -- Chowdhury, N R -- Moscioni, A D -- Kram, M -- Chowdhury, J R -- 5-R01-GM19328/GM/NIGMS NIH HHS/ -- AM-17702/AM/NIADDK NIH HHS/ -- AM-34357/AM/NIADDK NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1986 Sep 12;233(4769):1190-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2426782" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bilirubin/blood ; Collagen ; Dextrans ; Injections, Intraperitoneal ; Liver/cytology ; *Liver Transplantation ; *Microspheres ; Rats ; Rats, Gunn ; Rats, Mutant Strains ; Transplantation, Homologous
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  • 284
    Publication Date: 1986-03-07
    Description: Calcium ions flow into cells through several distinct classes of voltage-dependent calcium-selective channels. Such fluxes play important roles in electrical signaling at the cell membrane and in chemical signaling within cells. Further information about calcium channels was obtained by injecting RNA isolated from rat brain, heart and skeletal muscle into Xenopus oocytes. Macroscopic currents through voltage-operated calcium channels were resolved when the endogenous calcium-dependent chloride current was blocked by replacing external calcium with barium and chloride with methanesulfonate. The resulting barium current was insensitive to tetrodotoxin but was completely blocked by cadmium or cobalt. With both heart and brain RNA at least two distinct types of calcium ion conductance were found, distinguishable by their time course and inactivation properties. In oocytes injected with heart RNA, the slowly inactivating component was selectively blocked by the calcium-channel antagonist nifedipine. Barium ion currents induced by heart RNA were modulated by isoproterenol, cyclic adenosine monophosphate, and acetylcholine.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dascal, N -- Snutch, T P -- Lubbert, H -- Davidson, N -- Lester, H A -- GM-10991/GM/NIGMS NIH HHS/ -- GM-29836/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1986 Mar 7;231(4742):1147-50.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2418503" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Barium/metabolism ; Cadmium/pharmacology ; Cobalt/pharmacology ; Electrophysiology ; Ion Channels/*metabolism ; Mesylates/metabolism ; Myocardium/metabolism ; Nifedipine/pharmacology ; Ovum/*metabolism ; RNA/*pharmacology ; Tetrodotoxin/pharmacology ; Xenopus
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  • 285
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-03-21
    Description: The bovine leukemia virus, like the human T-cell leukemia viruses (HTLV-I and HTLV-II), are unusual biologically in that viral transcripts are not detected in tumors or infected tissues. The bovine leukemia virus long terminal repeat (BLV LTR) functions as a transcriptional promoter only in cell lines productively infected with BLV. Deletion mapping indicated that at least two regions of the LTR, on the 5' and 3' sides of the RNA start site, influenced gene expression. An analysis has now been made of the effects of coupling sequences from these LTR regions to a heterologous core promoter derived from the SV40 early promoter unit. Through the use of the transient expression of the bacterial chloramphenicol acetyltransferase (CAT) gene to monitor transcriptional activity in vivo, two independent, regulatory elements were identified in the BLV LTR. One was present in a fragment of 75 base pairs derived from the U3 region of the LTR and behaved much like other enhancer elements. It may be a major determinant of BLV expression in productively infected cell lines, since it enhanced transcription controlled by the heterologous core promoter only in these cells. The second element was contained in a 250-bp fragment derived from LTR sequences in the R region, located downstream from the RNA start site. Its activation of CAT expression was not dependent on BLV infection and was evident only when the fragment was located immediately downstream from the RNA start site. BLV expression thus appears to be regulated in part by a cell-specific enhancer element upstream from the core promoter and a novel sequence downstream from the RNA initiation site in the viral LTR.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Derse, D -- Casey, J W -- CA07392/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1986 Mar 21;231(4744):1437-40.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3006241" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cattle ; Cell Line ; Cercopithecus aethiops ; DNA, Recombinant ; DNA, Viral/genetics ; Deltaretrovirus/genetics ; *Enhancer Elements, Genetic ; Gene Expression Regulation ; *Genes, Regulator ; Genes, Viral ; Humans ; Leukemia Virus, Bovine/*genetics ; Plasmids ; *Promoter Regions, Genetic ; RNA, Messenger/genetics ; *Repetitive Sequences, Nucleic Acid ; Retroviridae/*genetics ; Transcription, Genetic
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  • 286
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-03-28
    Description: Atrial natriuretic factor results in diuresis in animals and humans, perhaps because atrial natriuretic factor increases renal blood flow. The possibility that this diuresis is due to direct inhibition of renal tubular epithelial water transport was examined in rabbit collecting tubules perfused in vitro. Atriopeptin III inhibition of the hydraulic conductivity response to the hormone arginine vasopressin but not to either 3'5'-cyclic adenosine monophosphate or forskolin was found. These results suggest that atriopeptin III acts proximal to cyclic adenosine monophosphate formation to directly affect vasopressin-stimulated water transport in the mammalian nephron. They also suggest a potential role for inhibition by atrial natriuretic factor of the renal response to arginine vasopressin as a contributor to a diuretic state.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dillingham, M A -- Anderson, R J -- 1K08 AM-01245/AM/NIADDK NIH HHS/ -- AM-26111/AM/NIADDK NIH HHS/ -- AM-30448/AM/NIADDK NIH HHS/ -- New York, N.Y. -- Science. 1986 Mar 28;231(4745):1572-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3006248" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arginine Vasopressin/*antagonists & inhibitors ; Atrial Natriuretic Factor/*pharmacology ; Colforsin/pharmacology ; Cyclic AMP/physiology ; Cyclic GMP/physiology ; Diuresis/drug effects ; In Vitro Techniques ; Kidney Tubules/*drug effects ; Kidney Tubules, Collecting/*drug effects/physiology ; Rabbits
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  • 287
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-02-14
    Description: Because infant rats learn about odors that elicit suckling, and because certain chemosensory cues that help elicit mating behavior in adults are similar to those that elicit suckling, an experiment was undertaken to assess the influence of suckling-associated odors experienced during infancy on adult sexual behavior. Rat pups lived with and suckled dams whose nipple and vaginal odors were altered with citral, a lemon scent. The rats were weaned and never exposed again, until testing, to citral or females. At about 100 days of age, the males were paired in mating tests with a normal sexually receptive female or with a sexually receptive female that had been treated perivaginally with citral immediately before testing. The males ejaculated readily when paired with citral-treated females but were slow to achieve ejaculation when paired with normal females. These findings implicate an infantile experience as a determinant of adult sexual behavior in a mammal.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fillion, T J -- Blass, E M -- AM 18560/AM/NIADDK NIH HHS/ -- MH 00524/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1986 Feb 14;231(4739):729-31.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3945807" target="_blank"〉PubMed〈/a〉
    Keywords: Animal Population Groups/*physiology ; Animals ; Animals, Suckling/*physiology ; Learning/physiology ; Male ; Odors ; Pheromones/*physiology ; Rats ; Sexual Behavior, Animal/*physiology ; Smell/physiology
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  • 288
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-09-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fox, M W -- New York, N.Y. -- Science. 1986 Sep 19;233(4770):1247.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3749874" target="_blank"〉PubMed〈/a〉
    Keywords: Animal Husbandry ; Animals ; Cattle/*physiology ; Growth Hormone/biosynthesis/*pharmacology ; Milk ; Recombinant Proteins/biosynthesis
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  • 289
    Publication Date: 1986-01-17
    Description: D2 dopamine receptors in the putamen of living human subjects were characterized by using the selective, high-affinity D2 dopamine receptor antagonist carbon-11-labeled raclopride and positron emission tomography. Experiments in four healthy men demonstrated saturability of [11C]raclopride binding to an apparently homogeneous population of sites with Hill coefficients close to unity. In the normal putamen, maximum binding ranged from 12 to 17 picomoles per cubic centimeter and dissociation constants from 3.4 to 4.7 nanomolar. Maximum binding for human putamen at autopsy was 15 picomoles per cubic centimeter. Studies of [11C]raclopride binding indicate that clinically effective doses of chemically distinct neuroleptic drugs result in 85 to 90 percent occupancy of D2 dopamine receptors in the putamen of schizophrenic patients.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Farde, L -- Hall, H -- Ehrin, E -- Sedvall, G -- New York, N.Y. -- Science. 1986 Jan 17;231(4735):258-61.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2867601" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Antipsychotic Agents/metabolism ; Benzamides/metabolism ; Brain/*metabolism ; Cerebellum/metabolism ; Humans ; Male ; Middle Aged ; Putamen/metabolism ; Raclopride ; Receptors, Dopamine/*metabolism ; Receptors, Dopamine D2 ; Rodentia ; Schizophrenia/metabolism ; *Tomography, Emission-Computed
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  • 290
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-06-20
    Description: Light causes both depolarization and adaptation to light in Limulus ventral photoreceptors. Both visual excitation and adaptation were blocked by guanosine 5'-O-(2-thiodiphosphate) (GDP-beta-S), a metabolically stable analog of guanosine 5'-diphosphate (GDP). However, GDP-beta-S did not block the excitation caused by injection of inositol 1,4,5-trisphosphate into the cell. These results suggest a molecular cascade of visual excitation and adaptation: Light isomerizes the visual pigment rhodopsin, which in turn activates a guanyl nucleotide-binding protein. The binding protein then stimulates production of inositol 1,4,5-trisphosphate, which causes release of calcium from the endoplasmic reticulum.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fein, A -- EY 01362/EY/NEI NIH HHS/ -- EY 03793/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 1986 Jun 20;232(4757):1543-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3487116" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Ocular/drug effects ; Animals ; *Guanine Nucleotides ; Guanosine Diphosphate/*analogs & derivatives/pharmacology ; Horseshoe Crabs/*physiology ; Inositol 1,4,5-Trisphosphate ; Inositol Phosphates/pharmacology ; Photic Stimulation ; Photoreceptor Cells/drug effects/*physiology ; Thionucleotides/*pharmacology ; Vision, Ocular
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 291
    Publication Date: 1986-03-14
    Description: Yeast cells were transformed with a plasmid containing complementary DNA encoding the alpha subunit of the Torpedo californica acetylcholine receptor. These cells synthesized a protein that had the expected molecular weight, antigenic specificity, and ligand-binding properties of the alpha subunit. The subunit was inserted into the yeast plasma membrane, demonstrating that yeast has the apparatus to express a membrane-bound receptor protein and to insert such a foreign protein into its plasma membrane. The alpha subunit constituted approximately 1 percent of the total yeast membrane. The alpha subunit constituted approximately 1 percent of the total yeast membrane proteins, and its density was about the same in the plasma membrane of yeast and in the receptor-rich electric organ of Electrophorus electricus. In view of the available technology for obtaining large quantities of yeast proteins, it may now be possible to obtain amplified amounts of interesting membrane-bound proteins for physical and biochemical studies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fujita, N -- Nelson, N -- Fox, T D -- Claudio, T -- Lindstrom, J -- Riezman, H -- Hess, G P -- New York, N.Y. -- Science. 1986 Mar 14;231(4743):1284-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3511531" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; DNA/metabolism ; Electrophorus ; Plasmids ; Receptors, Cholinergic/*biosynthesis/genetics ; Recombinant Proteins/*biosynthesis/genetics ; Saccharomyces cerevisiae/genetics ; Torpedo
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  • 292
    Publication Date: 1986-02-14
    Description: The anomalous scattering data from five Cd in the native protein were used to determine the crystal structure of cadmium, zinc (Cd,Zn) metallothionein isoform II from rat liver. The structure of a 4-Cd cluster was solved by direct methods. A 2.3 A resolution electron density map was calculated by iterative single-wavelength anomalous scattering. The structure is folded into two domains. The amino terminal domain (beta) of residues 1 to 29 enfolds a three-metal cluster of one Cd and two Zn atoms coordinated by six terminal cysteine thiolate ligands and three bridging cysteine thiolates. The carboxyl terminal domain (alpha) of residues 30 to 61 enfolds a 4-Cd cluster coordinated by six terminal and five bridging cysteine thiolates. All seven metal sites have tetrahedral coordination geometry. The domains are roughly spherical, and the diameter is 15 to 20 A; there is limited contact between domains. The folding of alpha and beta is topologically similar but with opposite chirality. Redundant, short cysteine-containing sequences have similar roles in cluster formation in both alpha and beta.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Furey, W F -- Robbins, A H -- Clancy, L L -- Winge, D R -- Wang, B C -- Stout, C D -- GM-36535/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1986 Feb 14;231(4739):704-10.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3945804" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Binding Sites ; Cadmium ; Crystallography ; Cysteine ; *Metallothionein ; Models, Molecular ; Protein Conformation ; Rats ; Solutions ; X-Ray Diffraction ; Zinc
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  • 293
    Publication Date: 1986-10-31
    Description: Neuroleukin is a lymphokine product of lectin-stimulated T cells that induces immunoglobulin secretion by cultured human peripheral blood mononuclear cells. Neuroleukin acts early in the in vitro response that leads to formation of antibody-secreting cells, but continued production of immunoglobulin by differentiated antibody-secreting cells is neuroleukin-independent. Although the factor is not directly mitogenic, cellular proliferation is a late component of the response to neuroleukin. Neuroleukin does not have B-cell growth factor (BCGF) or B-cell differentiation factor (BCDF) activity in defined assays. Neuroleukin-evoked induction of immunoglobulin secretion is both monocyte- and T-cell-dependent.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gurney, M E -- Apatoff, B R -- Spear, G T -- Baumel, M J -- Antel, J P -- Bania, M B -- Reder, A T -- 5PO1 NS24412/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1986 Oct 31;234(4776):574-81.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3020690" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; B-Lymphocytes/drug effects/physiology ; Bone Marrow/metabolism ; Cell Line ; Cells, Cultured ; Deltaretrovirus/genetics ; Glucose-6-Phosphate Isomerase ; Growth Substances/genetics/pharmacology/*physiology ; Humans ; Immunity, Cellular/drug effects ; Immunoglobulins/biosynthesis ; Lectins/pharmacology ; Leukemia/metabolism ; Lymphokines/genetics/pharmacology/*physiology ; Lymphoma/metabolism ; Mice ; Pokeweed Mitogens/pharmacology ; Sequence Homology, Nucleic Acid ; T-Lymphocytes/drug effects/*physiology
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  • 294
    Publication Date: 1986-01-24
    Description: Retinal photoreceptor cell dystrophies have been widely observed in humans and in animals, but pathogenetic mechanisms are known in only a few such disorders, and successful therapeutic intervention has been reported in fewer still. Spontaneously hypertensive albino rats develop a retinal photoreceptor cell dystrophy with onset late in the first year or early in the second year of life. Between 60 and 70 percent of the animals are affected. A substantial reduction in the prevalence and severity of the dystrophy occurred in such animals whose diet contained 30 percent (by weight) D-galactose. Neither an inhibitor of the enzyme aldose reductase, present in the diet, nor diabetes mellitus, induced by streptozotocin, had any statistically significant influence on the dystrophy. Ambient light and systolic blood pressure levels also did not seem to influence the course of the disorder. The mechanism by which galactose exerts its effect is unknown, but a mutant enzyme with an elevated Michaelis constant (Km) for galactose is plausible.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Frank, R N -- Keirn, R J -- Keirn, G V -- Mancini, M A -- Khoury, J K -- EY-02566/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 1986 Jan 24;231(4736):376-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3941900" target="_blank"〉PubMed〈/a〉
    Keywords: Age Factors ; Animals ; Blood Pressure ; Diabetes Mellitus, Experimental/complications ; Female ; Galactose/*therapeutic use ; Humans ; Imidazoles/therapeutic use ; *Imidazolidines ; Rats ; *Rats, Inbred SHR ; *Rats, Inbred Strains ; Retina/pathology ; Retinal Degeneration/complications/*drug therapy/pathology
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  • 295
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-11-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Furano, A V -- New York, N.Y. -- Science. 1986 Nov 21;234(4779):1005-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3775369" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Base Sequence ; Brain/*metabolism ; Rats ; *Repetitive Sequences, Nucleic Acid
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  • 296
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-08-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hait, W N -- Harding, M W -- Handschumacher, R E -- New York, N.Y. -- Science. 1986 Aug 29;233(4767):987-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3016900" target="_blank"〉PubMed〈/a〉
    Keywords: 3',5'-Cyclic-AMP Phosphodiesterases/metabolism ; Animals ; Calmodulin/*metabolism ; Carrier Proteins/*metabolism ; Cattle ; Cyclosporins/*metabolism/pharmacology ; Humans ; Kinetics ; Peptidylprolyl Isomerase ; Rabbits
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  • 297
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-02-21
    Description: The distribution in chicken retina of the alpha subunit of transducin, the guanine nucleotide--binding protein that couples light-dependent activation of rhodopsin with activation of guanosine 3',5'-monophosphate phosphodiesterase, was determined with the aid of a specific antiserum. alpha-Transducin was found in rod photoreceptor cells but was not detected in cones. These results show that rods and cones differ with respect to alpha-transducin content and suggest that the processes of phototransduction may differ correspondingly in rods and cones.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grunwald, G B -- Gierschik, P -- Nirenberg, M -- Spiegel, A -- New York, N.Y. -- Science. 1986 Feb 21;231(4740):856-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3080807" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibody Specificity ; Cattle ; Chickens ; Fluorescent Antibody Technique ; GTP-Binding Proteins/*metabolism ; Humans ; Macaca mulatta ; Macromolecular Substances ; Membrane Proteins/immunology/*metabolism ; Photoreceptor Cells/*metabolism ; Retina/growth & development/metabolism ; Tissue Distribution ; Transducin
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  • 298
    Publication Date: 1986-10-31
    Description: A novel 56,000-dalton growth factor found in mouse salivary gland was purified, molecularly cloned, and expressed in monkey COS cells. The protein is a neurotrophic factor and also, surprisingly, a lymphokine product of lectin-stimulated T cells. The factor was therefore named neuroleukin. Neuroleukin promotes the survival in culture of a subpopulation of embryonic spinal neurons that probably includes skeletal motor neurons. Neuroleukin also supports the survival of cultured sensory neurons that are insensitive to nerve growth factor, but has no effect on sympathetic or parasympathetic neurons. The amino acid sequence of neuroleukin is partly homologous to a highly conserved region of the external envelope protein of HTLV-III/LAV, the retrovirus that causes acquired immune deficiency syndrome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gurney, M E -- Heinrich, S P -- Lee, M R -- Yin, H S -- 5PO1 NS-21442/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1986 Oct 31;234(4776):566-74.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3764429" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Cells, Cultured ; Chick Embryo ; Cloning, Molecular ; DNA/genetics ; Glucose-6-Phosphate Isomerase ; Growth Substances/genetics/*physiology ; Lymphokines/genetics/*physiology ; Male ; Mice ; Mice, Inbred BALB C ; Motor Neurons/drug effects ; Muscles/innervation ; Nerve Growth Factors/genetics/isolation & purification/*physiology ; Neurons/drug effects ; Neurons, Afferent/drug effects ; Salivary Glands/metabolism ; Spinal Cord/cytology
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  • 299
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-06-27
    Description: Two reovirus isolates (type 1 Lang and type 3 Dearing) differ in their transmissibility between littermates of newborn mice. They also differ in the amounts of virus excreted by the gastrointestinal tract. With the use of reassortant viruses, these properties were mapped to the L2 gene. Thus environmental spread of reovirus is a genetic property.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Keroack, M -- Fields, B N -- 5R01 AI13178/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 1986 Jun 27;232(4758):1635-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3012780" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn/microbiology ; Digestive System/microbiology ; *Genes, Viral ; Mammalian orthoreovirus 3/physiology ; Mice ; Reoviridae/physiology ; Reoviridae Infections/microbiology/*transmission
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  • 300
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-04-04
    Description: Contraction and myosin light-chain phosphorylation were measured in electrically stimulated tracheal smooth muscle. Latencies for the onset of force, stiffness, and light-chain phosphorylation were 500 milliseconds. Myosin light chain was phosphorylated from 0.04 to 0.80 mole of phosphate per mole of light chain with a pseudo-first-order rate of 1.1 per second with no evidence of an ordered or negatively cooperative process. Following the period of latency, stiffness increased with phosphorylation and both increased more rapidly than isometric force. The linear relation between stiffness and phosphorylation during activation suggests independent attachment of each myosin head upon phosphorylation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kamm, K E -- Stull, J T -- HL 26043/HL/NHLBI NIH HHS/ -- HL 32607/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1986 Apr 4;232(4746):80-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3754063" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carbachol/pharmacology ; Electric Stimulation ; In Vitro Techniques ; Kinetics ; *Muscle Contraction/drug effects ; Muscle, Smooth/*physiology ; Myosin-Light-Chain Kinase ; Myosins/*metabolism ; Phosphorylation ; Protein Kinases/metabolism ; Trachea/physiology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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