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  • Articles  (610)
  • Animals  (547)
  • Male  (185)
  • Cell & Developmental Biology
  • American Association for the Advancement of Science (AAAS)  (610)
  • 1980-1984  (610)
Collection
  • Articles  (610)
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Keywords
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  • American Association for the Advancement of Science (AAAS)  (610)
  • Wiley-Blackwell  (218)
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  • 1
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    An about 50,000-dalton protein in adrenal medulla: a common precursor of [Met]- and [Leu]enkephalin (1980)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1980-06-27
    Description: A protein that may be an enkephalin precursor has been identified in extracts of bovine adrenal medulla. This protein (about 50,000 daltons) appears to contain seven copies of [Met]enkephalin and one copy of [Leu]enkephalin. Digestion with trypsin and carboxypeptidase B yields [Met]enkephalin and [Leu]enkephalin in a ratio of almost 7 to 1. The enkephalins were identified by chromatography and by their binding to opiate receptors. Some characteristics of several other adrenal peptides that may serve as intermediates in the biosynthesis of the enkephalins are presented.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lewis, R V -- Stern, A S -- Kimura, S -- Rossier, J -- Stein, S -- Udenfriend, S -- New York, N.Y. -- Science. 1980 Jun 27;208(4451):1459-61.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7384787" target="_blank"〉PubMed〈/a〉
    Keywords: Adrenal Medulla/*analysis ; Animals ; Cattle ; Chromaffin Granules/*analysis ; Chromaffin System/*analysis ; Endorphins/*biosynthesis ; Enkephalin, Leucine ; Enkephalin, Methionine ; Enkephalins/*biosynthesis ; Molecular Weight ; Oligopeptides/analysis ; Peptide Fragments/analysis ; Protein Precursors/*analysis ; Proteins/*analysis ; Trypsin
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 2
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    Multiple daily amphetamine administration: behavioral and neurochemical alterations (1980)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1980-02-15
    Description: In rats, multiple daily amphetamine injections (2.5 milligrams per kilogram of body weight, injected subcutaneously every 4 hours for 5 days) resulted in a progressive augmentation in response, characterized by a more rapid onset and an increased magnitude of stereotypy. By contrast, offset times of both the stereotypy and the poststereotypy hyperactivity periods were markedly shortened. When the animals were retested with the same dose of amphetamine 8 days after the long-term treatment was discontinued, the time of offset of the stereotypy and hyperactivity phases had recovered to values found with short-term amphetamine treatment, whereas the more rapid onset of stereotypy persisted. Brain monoamine and amphetamine concentrations and tyrosine hydroxylase activity were determined in comparably treated rats at times corresponding to the behavioral observations. The behavioral data indicate that enhanced responsiveness to amphetamine following its repeated administration may contribute to the development of amphetamine psychosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Segal, D S -- Weinberger, S B -- Cahill, J -- McCunney, S J -- New York, N.Y. -- Science. 1980 Feb 15;207(4433):905-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7188815" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior/*drug effects ; Behavior, Animal/*drug effects ; Brain/metabolism ; Brain Chemistry/drug effects ; Dextroamphetamine/administration & dosage/*pharmacology ; Dopamine/metabolism ; Dose-Response Relationship, Drug ; Humans ; Male ; Motor Activity/drug effects ; Norepinephrine/metabolism ; Rats ; Serotonin/metabolism ; Stereotyped Behavior/*drug effects ; Time Factors
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
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    Cell recognition during neuronal development (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-09-21
    Description: Insect embryos, with their relatively simple nervous systems, provide a model system with which to study the cellular and molecular mechanisms underlying cell recognition during neuronal development. Such an approach can take advantage of the accessible cells of the grasshopper embryo and the accessible genes of Drosophila. The growth cones of identified neurons express selective affinities for specific axonal surfaces; such specificities give rise to the stereotyped patterns of selective fasciculation common to both species. These and other results suggest that early in development cell lineage and cell interactions lead to the differential expression of cell recognition molecules on the surfaces of small subsets of embryonic neurons whose axons selectively fasciculate with one another. Monoclonal antibodies reveal surface molecules in the Drosophila embryo whose expression correlates with this prediction. It should now be possible to isolate the genes encoding these potential cell recognition molecules and to test their function through the use of molecular genetic approaches in Drosophila.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Goodman, C S -- Bastiani, M J -- Doe, C Q -- du Lac, S -- Helfand, S L -- Kuwada, J Y -- Thomas, J B -- NS 18366/NS/NINDS NIH HHS/ -- NS 20299/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1984 Sep 21;225(4668):1271-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6474176" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibodies, Monoclonal ; Antigens, Surface/analysis ; Axons/physiology ; *Cell Communication ; Drosophila/embryology ; Grasshoppers/embryology ; Insects/*embryology ; Models, Neurological ; Nervous System/*embryology ; Neurons/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
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    Adoptive immunotherapy of established pulmonary metastases with LAK cells and recombinant interleukin-2 (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-09-28
    Description: The activation of human peripheral blood leukocytes or murine splenocytes with interleukin-2 (IL-2) generated cells that were lytic in vitro for a variety of fresh tumor cells. The adoptive transfer of such lymphokine-activated killer (LAK) cells to mice with established pulmonary sarcoma metastases was highly effective in reducing the number (and size) of these tumor nodules when combined with repeated injections of recombinant IL-2. These findings provide a rationale for clinical trials of the infusion of human LAK cells generated with recombinant IL-2 as well as Phase I trials of the infusion of recombinant IL-2 systemically into humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mule, J J -- Shu, S -- Schwarz, S L -- Rosenberg, S A -- New York, N.Y. -- Science. 1984 Sep 28;225(4669):1487-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6332379" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; DNA, Recombinant ; *Immunization, Passive ; Interleukin-2/pharmacology/*therapeutic use ; Killer Cells, Natural/*immunology ; Lung Neoplasms/secondary/*therapy ; Lymphocyte Activation ; Mice ; Mice, Inbred C57BL ; Sarcoma, Experimental/secondary/*therapy ; Spleen/cytology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
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    Separation of morphine analgesia from physical dependence (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-10-26
    Description: Intravenous infusion of morphine sulfate in rats for 24 hours produced marked opioid dependence, manifested by a series of well-documented signs appearing after injection of the opiate antagonist naloxone. Treatment of rats with naloxonazine significantly reduced the analgesia associated with the morphine infusions for more than 24 hours. Furthermore, 14 of 16 withdrawal signs observed in naloxonazine-treated rats were virtually identical to those in rats that received morphine alone. These results raise the possibility that different receptor mechanisms mediate morphine analgesia and many of the withdrawal signs associated with morphine dependence.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ling, G S -- MacLeod, J M -- Lee, S -- Lockhart, S H -- Pasternak, G W -- DA 002615/DA/NIDA NIH HHS/ -- NS 00415/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1984 Oct 26;226(4673):462-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6541807" target="_blank"〉PubMed〈/a〉
    Keywords: *Analgesia ; Animals ; Humans ; Male ; Morphine/*pharmacology ; Naloxone/*analogs & derivatives/pharmacology ; Rats ; Rats, Inbred Strains ; Substance Withdrawal Syndrome ; *Substance-Related Disorders
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
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    Sparing of the brain in neonatal undernutrition: amino acid transport and incorporation into brain and muscle (1980)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1980-02-22
    Description: Rates of tyrosine and lysine transport and incorporation into protein were measured in control and undernourished weanling rats. Undernutrition was induced by feeding lactating dams a low protein diet (12 percent casein) from birth to day 21. At weaning, body and brain weights of undernourished rats were 50 percent and 88 percent, respectively, of control values. Lysine and tyrosine transport rates into skeletal muscle were reduced by over 75 percent, more than twice the reduction seen in brain. Rates of amino acid incorporation into muscle protein were reduced by approximately 50 percent; the change in rate of incorporation into brain protein was not statistically significant. These data indicate that, in spite of marked retardation of amino acid transport into brain, the brain seems fully capable of maintaining normal rates of protein synthesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Freedman, L S -- Samuels, S -- Fish, I -- Schwartz, S A -- Lange, B -- Katz, M -- Morgano, L -- New York, N.Y. -- Science. 1980 Feb 22;207(4433):902-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6766565" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acids/*metabolism ; Animals ; Animals, Newborn/metabolism ; Biological Transport ; Body Weight ; Brain/growth & development/*metabolism ; Disease Models, Animal ; Female ; Lactation ; Male ; Muscles/*metabolism ; Pregnancy ; Protein-Energy Malnutrition/*metabolism ; Rats
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
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    Substance P analog, DiMe-C7: evidence for stability in rat brain and prolonged central actions (1982)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1982-01-08
    Description: A metabolically protected analog of substance P, [pGlu5-MePhe8-MeGly9]SP(5-11) (DiMe-C7), was approximately equipotent with substance P in causing increased locomotor activity after microinfusion into the ventral tegmental area of rat brain, but the effects of DiMe-C7 on behavior were considerably prolonged. There was little metabolic degradation of tritiated DiMe-C7 for up to 1 hour after infusion, whereas tritiated substance P was completely degraded within 10 minutes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Eison, A S -- Iversen, S D -- Sandberg, B E -- Watson, S P -- Hanley, M R -- Iversen, L L -- New York, N.Y. -- Science. 1982 Jan 8;215(4529):188-90.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6171884" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal/drug effects ; Brain/*metabolism ; Motor Activity/drug effects ; *Peptide Fragments ; Pyrrolidonecarboxylic Acid/analogs & derivatives ; Rats ; Substance P/*analogs & derivatives/metabolism/pharmacology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
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    Mass mortality of harbor seals: pneumonia associated with influenza A virus (1982)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1982-02-26
    Description: More than 400 harbor seals, most of them immature, died along the New England coast between December 1979 and October 1980 of acute pneumonia associated with influenza virus, A/Seal/Mass/1/180 (H7N7). The virus has avian characteristics, replicates principally in mammals, and causes mild respiratory disease in experimentally infected seals. Concurrent infection with a previously undescribed mycoplasma or adverse environmental conditions may have triggered the epizootic. The similarities between this epizootic and other seal mortalities in the past suggest that these events may be linked by common biological and environmental factors.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Geraci, J R -- St Aubin, D J -- Barker, I K -- Webster, R G -- Hinshaw, V S -- Bean, W J -- Ruhnke, H L -- Prescott, J H -- Early, G -- Baker, A S -- Madoff, S -- Schooley, R T -- AI02649/AI/NIAID NIH HHS/ -- AI16841/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 1982 Feb 26;215(4536):1129-31.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7063847" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Disease Outbreaks/*veterinary ; Influenza A virus/isolation & purification ; Orthomyxoviridae Infections/*veterinary ; Pinnipedia/*microbiology ; Pneumonia/*veterinary ; Seals, Earless/*microbiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
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    Expression of a platelet-derived growth factor-like protein in simian sarcoma virus transformed cells (1983)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1983-09-30
    Description: The near identity of the partial amino acid sequence of human platelet-derived growth factor (PDGF) and that predicted for p28sis, the putative transforming protein of the simian sarcoma virus (SSV), suggests expression of a growth factor activity may be central for transformation by SSV. It is now reported that SSV-transformed cells but not control cells contain a growth factor activity that is identical to PDGF in immunoassay, in mitogenic dose response, and in specific mitogenic activity. The protein immunoprecipitated by antiserum to human PDGF has an apparent molecular weight of 20,000, identical to that of p20sis, the putative intracellular degradation product of p28sis. The results support the concept that expression of a PDGF-like molecule, which appears to be the product of the viral-sis gene, is responsible for the abnormal regulation of growth is SSV-transformed cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Deuel, T F -- Huang, J S -- Huang, S S -- Stroobant, P -- Waterfield, M D -- New York, N.Y. -- Science. 1983 Sep 30;221(4618):1348-50.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6310754" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; *Cell Transformation, Viral ; Cross Reactions ; DNA Replication/drug effects ; *Genes, Viral ; Growth Substances/*genetics/immunology ; Mice ; Molecular Weight ; Peptides/*genetics/immunology ; Platelet-Derived Growth Factor ; Retroviridae/*genetics ; Sarcoma Virus, Woolly Monkey/*genetics ; Sarcoma, Experimental/*physiopathology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 10
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    Laser microsurgery in cell and developmental biology (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-07-31
    Description: New applications of laser microbeam irradiation to cell and developmental biology include a new instrument with a tunable wavelength (217- to 800-nanometer) laser microbeam and a wide range of energies and exposure durations (down to 25 X 10(-12) second). Laser microbeams can be used for microirradiation of selected nucleolar genetic regions and for laser microdissection of mitotic and cytoplasmic organelles. They are also used to disrupt the developing neurosensory appendages of the cricket and the imaginal discs of Drosophila.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Berns, M W -- Aist, J -- Edwards, J -- Strahs, K -- Girton, J -- McNeill, P -- Rattner, J B -- Kitzes, M -- Hammer-Wilson, M -- Liaw, L H -- Siemens, A -- Koonce, M -- Peterson, S -- Brenner, S -- Burt, J -- Walter, R -- Bryant, P J -- van Dyk, D -- Coulombe, J -- Cahill, T -- Berns, G S -- New York, N.Y. -- Science. 1981 Jul 31;213(4507):505-13.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7017933" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Cell Physiological Phenomena ; Chloroplasts/physiology ; Drosophila ; *Lasers ; Microscopy, Phase-Contrast ; Microsurgery/*methods ; Mitochondria/physiology ; Mitosis ; Neurons/physiology ; Plant Physiological Phenomena
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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