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  • Male  (122)
  • American Association for the Advancement of Science (AAAS)  (122)
  • 1985-1989
  • 1980-1984  (122)
  • 1983  (122)
  • 1929
Collection
Publisher
  • American Association for the Advancement of Science (AAAS)  (122)
Years
  • 1985-1989
  • 1980-1984  (122)
Year
  • 101
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-09-02
    Description: Rats trained on an eight-arm radial maze were challenged by placing the maze in new spatial environments. Administration of opiate antagonists, either naloxone or diprenorphine, after exposure to the new environments significantly improved subsequent performance. The effect of naloxone on spatial memory was attenuated when drug administration occurred 2 hours after maze exposure.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gallagher, M -- King, R A -- Young, N B -- K02 MH00406/MH/NIMH NIH HHS/ -- MH35554/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1983 Sep 2;221(4614):975-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6879198" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal ; Male ; Memory/*drug effects ; Naloxone/*pharmacology ; Rats ; Spatial Behavior
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  • 102
    Publication Date: 1983-05-20
    Description: Several isolates of a human type-C retrovirus belonging to one group, known as human T-cell leukemia virus (HTLV), have previously been obtained from patients with adult T-cell leukemia or lymphoma. The T-cell tropism of HTLV and its prevalence in the Caribbean basin prompted a search for it in patients with the epidemic T-cell immune deficiency disorder known as AIDS. Peripheral blood lymphocytes from one patient in the United States and two in France were cultured with T-cell growth factor (TCGF) an shown to express HTLV antigens. Virus from the U.S. patient was isolated and characterized and shown to be related to HTLV subgroup I. The virus was also transmitted into normal human T cells from umbilical cord blood of a newborn. Whether or not HTLV-I or other retroviruses of this family with T-cell tropism cause AIDS, it is possible that patients from whom the virus can be isolated can also transmit it to others. If the target cell of AIDS is the mature T cell as suspected, the methods used in these studies may prove useful for the long-term growth of these cells and for the identification of antigens specific for the etiological agent of AIDS.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gallo, R C -- Sarin, P S -- Gelmann, E P -- Robert-Guroff, M -- Richardson, E -- Kalyanaraman, V S -- Mann, D -- Sidhu, G D -- Stahl, R E -- Zolla-Pazner, S -- Leibowitch, J -- Popovic, M -- New York, N.Y. -- Science. 1983 May 20;220(4599):865-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6601823" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/etiology/immunology/*microbiology ; Animals ; Antibodies, Monoclonal/immunology ; Antibodies, Viral/immunology ; Female ; Humans ; Immunity, Cellular ; Male ; Retroviridae/*isolation & purification ; T-Lymphocytes/microbiology ; Tumor Virus Infections/complications/*microbiology/transmission
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  • 103
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-10-21
    Description: Male and female rats exhibit sex differences in binding by serotonin 1 receptors in discrete areas of the brain, some of which have been implicated in the control of ovulation and of gonadotropin release. The sex-specific changes in binding, which occur in response to the same hormonal (estrogenic) stimulus, are due to changes in the number of binding sites. Castration alone also affects the number of binding sites in certain areas. The results lead to the conclusion that peripheral hormones modulate binding by serotonin 1 receptors. The status of the serotonin receptor system may affect the reproductive capacity of an organism and may be related to sex-linked emotional disturbances in humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fischette, C T -- Biegon, A -- McEwen, B S -- AM06122/AM/NIADDK NIH HHS/ -- NS06080/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1983 Oct 21;222(4621):333-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6623080" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/*metabolism ; Brain Mapping ; Castration ; Cell-Free System ; Estradiol/*pharmacology ; Female ; Glucosephosphate Dehydrogenase/metabolism ; Kinetics ; Male ; Pituitary Gland/enzymology ; Rats ; Receptors, Serotonin/drug effects/*metabolism ; *Sex Factors
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  • 104
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-07-01
    Description: A temperature-sensitive lethal mutant of Drosophila melanogaster was used to identify an essential cell cycle function that is necessary for the mitotic condensation of heterochromatic but not of euchromatic portions of the genome. This mutant is an allele at a locus (mus-101) identified earlier by the use of mutagen-sensitive mutants. The data suggest that the mutagen-sensitive and repair-defective phenotypes of viable mus-101 mutants result from a disruption in chromosome organization.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gatti, M -- Smith, D A -- Baker, B S -- GM23345/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1983 Jul 1;221(4605):83-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6407113" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Cycle ; Chromosomes/ultrastructure ; Drosophila melanogaster ; Female ; *Genes ; Heterochromatin/*genetics/physiology ; Male ; Mutation
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  • 105
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-11-04
    Description: A pseudomemory of having been awakened by some loud noises during a night of the previous week was suggested to 27 highly hypnotizable subjects during hypnosis. Posthypnotically, 13 of them stated that the suggested event had actually occurred. This finding has implications for the investigative use of hypnosis in a legal context.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Laurence, J R -- Perry, C -- New York, N.Y. -- Science. 1983 Nov 4;222(4623):523-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6623094" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Female ; Humans ; *Hypnosis ; Male ; *Memory ; Middle Aged ; Personality
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  • 106
    Publication Date: 1983-05-13
    Description: A cell-free preparation of the cytoplasm from activated eggs of Rana pipiens induces, in demembranated sperm nuclei of Xenopus laevis, formation of a nuclear envelope, chromatin decondensation, initiation of DNA synthesis, and chromosome condensation. Both soluble and particulate cytoplasmic constituents are required to initiate these processes in vitro. The observed changes resemble processes occurring during fertilization and the mitotic cycle in early amphibian embryos. Therefore, this cell-free system may be useful in biochemical analysis of the interactions of nucleus and cytoplasm that control nuclear behavior.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lohka, M J -- Masui, Y -- New York, N.Y. -- Science. 1983 May 13;220(4598):719-21.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6601299" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Nucleus/*physiology/ultrastructure ; Chromatin/physiology ; Chromosomes/ultrastructure ; Female ; Fertilization ; Male ; Metaphase ; Nuclear Envelope/ultrastructure ; Ovum/*physiology ; Prophase ; Rana pipiens ; Spermatozoa/*physiology/ultrastructure ; Xenopus laevis
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  • 107
    Publication Date: 1983-05-13
    Description: Socially stressed adult male cynomolgus monkeys (Macaca fascicularis) fed a low fat, low cholesterol diet developed more extensive coronary artery atherosclerosis than unstressed controls. Groups did not differ in serum lipids, blood pressure, serum glucose, or ponderosity. These results suggest that psychosocial factors may influence atherogenesis in the absence of elevated serum lipids. Psychosocial factors thus may help explain the presence of coronary artery disease (occasionally severe) in people with low or normal serum lipids and normal values for the other "traditional" risk factors.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaplan, J R -- Manuck, S B -- Clarkson, T B -- Lusso, F M -- Taub, D M -- Miller, E W -- HL 14164/HL/NHLBI NIH HHS/ -- R01 HL 26561/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1983 May 13;220(4598):733-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6836311" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arteriosclerosis/*etiology/pathology ; Blood Pressure ; Cholesterol/blood ; Coronary Vessels/pathology ; Group Structure ; Humans ; Macaca fascicularis ; Male ; Social Environment ; Stress, Psychological/*complications
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  • 108
    Publication Date: 1983-12-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J L -- New York, N.Y. -- Science. 1983 Dec 2;222(4627):1001-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6417788" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cloning, Molecular ; Female ; *Gene Expression Regulation ; *Genetic Engineering ; Immunoglobulin Light Chains/*genetics ; Immunoglobulin kappa-Chains/biosynthesis/*genetics ; Liver/metabolism ; Male ; Mice ; Organ Specificity ; Spleen/metabolism ; Transferrin/biosynthesis/*genetics
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  • 109
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-04-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J L -- New York, N.Y. -- Science. 1983 Apr 29;220(4596):488-90.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6132445" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal/physiology ; Birds/physiology ; Dominance, Cerebral/*physiology ; Dyslexia/physiopathology ; Female ; Functional Laterality/physiology ; Humans ; Male ; Mice ; Neurotransmitter Agents/physiology ; Rats
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  • 110
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-06-10
    Description: Exposure of C57BL/6J mice to ionizing radiation caused stereotypical locomotor hyperactivity similar to that produced by morphine. Naloxone administration prevented this radiation-induced behavioral activation. These results support the hypothesis that endorphins are involved in some aspects of radiogenic behavioral change.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mickley, G A -- Stevens, K E -- White, G A -- Gibbs, G L -- New York, N.Y. -- Science. 1983 Jun 10;220(4602):1185-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6857244" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal/drug effects/physiology/*radiation effects ; Dose-Response Relationship, Radiation ; Endorphins/*physiology ; Male ; Mice ; Mice, Inbred C57BL ; Motor Activity/radiation effects ; Naloxone/pharmacology
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  • 111
    Publication Date: 1983-02-25
    Description: There is evidence that the mammalian female genital tract is capable of responding immunologically when challenged with alloantigens. The antigenic properties of male gametes have been well delineated. However, it is only rarely that a female mammal ever responds immunologically to the male gametic antigens as a result of coitus. When a proposed mechanism of suppression of antigenicity of epididymal spermatozoa was tested experimentally, the results indicated that two proteins (uteroglobin and transglutaminase) present in the prostate may be responsible for suppressing sperm antigenicity in the rabbit.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mukherjee, D C -- Agrawal, A K -- Manjunath, R -- Mukherjee, A B -- New York, N.Y. -- Science. 1983 Feb 25;219(4587):989-91.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6130601" target="_blank"〉PubMed〈/a〉
    Keywords: Acyltransferases/*immunology/metabolism ; Animals ; Epididymis/immunology ; Female ; Glycoproteins/*immunology ; *Immune Tolerance ; Lymphocyte Activation ; Male ; Rabbits ; Semen/enzymology/*immunology ; Spermatozoa/*immunology ; Transglutaminases ; Uteroglobin/*immunology
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  • 112
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-12-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G -- New York, N.Y. -- Science. 1983 Dec 23;222(4630):1312.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6658454" target="_blank"〉PubMed〈/a〉
    Keywords: Child ; *Child, Gifted ; Female ; Humans ; Infant ; Male ; *Mathematics ; Sex Factors ; Testosterone/*physiology
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  • 113
    Publication Date: 1983-04-29
    Description: Urine of the human fetus stimulated prostaglandin biosynthesis in vitro by increasing the conversion of arachidonic acid into prostaglandins. The stimulatory activity in urine from fetuses delivered at term after labor of spontaneous onset was greater than that in urine from fetuses delivered by cesarean section at term before the onset of labor. Such stimulation of prostaglandin biosynthesis by the fetal membranes, by way of a substance released into the urine and thence into amniotic fluid, could serve as a signal for the initiation of parturition.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Strickland, D M -- Saeed, S A -- Casey, M L -- Mitchell, M D -- 5-P50-HD11149/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1983 Apr 29;220(4596):521-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6573023" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Dinoprostone ; Extraembryonic Membranes/physiology ; Female ; Fetus/*physiology ; Humans ; *Labor Onset ; *Labor, Obstetric ; Male ; Pregnancy ; Prostaglandins/*biosynthesis ; Prostaglandins E/biosynthesis ; *Urine
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  • 114
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-08-12
    Description: Naltrexone, an opiate antagonist, had both stimulatory and inhibitory effects, depending on the dosage, on the growth of S20Y neuroblastoma in A/Jax mice. Daily injections of 0.1 milligram of naltrexone per kilogram of body weight, which blocked morphine-induced analgesia for 4 to 6 hours per day, resulted in a 33 percent tumor incidence, a 98 percent delay in the time before tumor appearance, and a 36 percent increase in survival time. Neuroblastoma-inoculated mice receiving 10 milligrams of naltrexone per kilogram, which blocked morphine-induced analgesia for 24 hours per day, had a 100 percent tumor incidence, a 27 percent reduction in the time before tumor appearance, and a 19 percent decrease in survival time. Inoculation of neuroblastoma cells in control subjects resulted in 100 percent tumor incidence within 29 days. These results show that naltrexone can modulate tumor response and suggest a role for the endorphin-opiate receptor system in neuro-oncogenic events.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zagon, I S -- McLaughlin, P J -- New York, N.Y. -- Science. 1983 Aug 12;221(4611):671-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6867737" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Dose-Response Relationship, Drug ; Endorphins/physiology ; Male ; Mice ; Mice, Inbred Strains ; Naloxone/*analogs & derivatives ; Naltrexone/*therapeutic use ; Neoplasm Transplantation ; Neoplasms, Experimental/drug therapy ; Neuroblastoma/*drug therapy
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  • 115
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-06-03
    Description: Vasoactive intestinal polypeptide stimulated serotonin N-acetyltransferase activity in rat pineal glands in organ culture by a postsynaptic action that was independent of the beta-receptor. The magnitude of stimulation could be altered by environmental lighting conditions and by prior exposure to the agonist. Such up- and down-regulation, well known for catecholaminergic stimulation of this system, is compatible with a possible control of the pineal by vasoactive intestinal polypeptide as well as by catecholamines.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yuwiler, A -- RR 05756/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1983 Jun 3;220(4601):1082-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6844931" target="_blank"〉PubMed〈/a〉
    Keywords: Acetyltransferases/*metabolism ; Animals ; Arylamine N-Acetyltransferase/antagonists & inhibitors/*metabolism ; Gastrointestinal Hormones/*pharmacology ; Isoproterenol/pharmacology ; *Lighting ; Male ; Pineal Gland/drug effects/*enzymology/radiation effects ; Propranolol/pharmacology ; Rats ; Vasoactive Intestinal Peptide/*pharmacology
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  • 116
    Publication Date: 1983-09-09
    Description: The resources allocated to a primary and secondary task are reciprocal. Subjects performed a tracking task in which the discrete displacements of the tracking cursor could be used to elicit event-related brain potentials. As the resource demands of the tracking task were increased, potentials elicited by the task-defined events increased in amplitude, whereas those elicited by secondary task auditory stimuli decreased.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wickens, C -- Kramer, A -- Vanasse, L -- Donchin, E -- New York, N.Y. -- Science. 1983 Sep 9;221(4615):1080-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6879207" target="_blank"〉PubMed〈/a〉
    Keywords: Evoked Potentials ; Female ; Humans ; Male ; *Psychomotor Performance ; *Thinking
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  • 117
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-06-03
    Description: Veratridine-stimulated uptake of sodium-22 in brain synaptosomes was significantly reduced by ionizing radiation over a dose range of 10 to 1000 rads. The response was dose-dependent and involved a decrease in the maximum effect of veratridine on uptake. The central nervous system may be more sensitive to ionizing radiation than generally thought, perhaps through a loss of the ability of the sodium channel to respond properly to stimulation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wixon, H N -- Hunt, W A -- New York, N.Y. -- Science. 1983 Jun 3;220(4601):1073-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6302846" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/drug effects/*radiation effects ; Dose-Response Relationship, Drug ; Dose-Response Relationship, Radiation ; Ion Channels/drug effects/radiation effects ; Male ; Rats ; Rats, Inbred Strains ; Sodium/*metabolism ; Synaptosomes/drug effects/*radiation effects ; Veratridine/*pharmacology ; Veratrine/*analogs & derivatives
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  • 118
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-12-02
    Description: Mouse eggs with different genetic constitutions were prepared by micromanipulation of fertilized diploids and triploids. The diploid gynogenones, activated by the male gamete which was then removed, developed at best to about the 25-somite stage as did the genetically similar diploid parthenogenones stimulated to develop in the complete absence of the male gamete. The failure of development to term in both cases may be due to homozygosity and does not appear to be due to a lack of extragenetic contribution from spermatozoa.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Surani, M A -- Barton, S C -- New York, N.Y. -- Science. 1983 Dec 2;222(4627):1034-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6648518" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Division ; Cytoplasm/physiology ; Embryo Implantation ; Embryo Transfer ; Embryo, Mammalian/*physiology ; Female ; Genes, Lethal ; Homozygote ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; *Parthenogenesis ; Spermatozoa/physiology
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  • 119
    Publication Date: 1983-06-17
    Description: In the house mouse (Mus musculus), fetuses may develop in utero next to siblings of the same or opposite sex. The amniotic fluid of the female fetuses contains higher concentrations of estradiol than that of male fetuses. Male fetuses that developed in utero between female fetuses had higher concentrations of estradiol in their amniotic fluid than males that were located between other male fetuses during intrauterine development. They were also more sexually active as adults, less aggressive, and had smaller seminal vesicles than males that had developed between other male fetuses in utero. These findings raise the possibility that during fetal life circulating estrogens may interact with circulating androgens both in regulating the development of sex differences between males and females and in producing variation in phenotype among males and among females.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉vom Saal, F S -- Grant, W M -- McMullen, C W -- Laves, K S -- MH35079/MH/NIMH NIH HHS/ -- RR07053/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1983 Jun 17;220(4603):1306-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6857252" target="_blank"〉PubMed〈/a〉
    Keywords: Aggression/*drug effects ; Amniotic Fluid/analysis ; Animals ; Estradiol/analysis/*pharmacology/physiology ; Female ; Fetus/*drug effects/physiology ; Humans ; Male ; Mice ; Progesterone/pharmacology ; Rats ; Rats, Inbred Strains ; Sex Differentiation/drug effects ; Sexual Behavior, Animal/*drug effects/physiology ; Testosterone/analysis/pharmacology
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  • 120
    Publication Date: 1983-04-29
    Description: A syndrome of spontaneous orofacial dyskinesia was identified in groups of rats treated for 6 months with a wide range of neuroleptic drugs. Phenothiazines, thioxanthenes, and substituted benzamides were particularly likely to induce the syndrome. It was observed in the presence of a functional blockade of dopamine receptors and endured for at least 2.5 months after drug withdrawal. There was no relation between the syndrome and changes in striatal dopamine receptors, as indexed by the binding of tritiated spiperone and tritiated cis(Z)-flupenthixol. The syndrome parallels several of the features of clinical tardive dyskinesia, whose pathophysiology thus may not involve changes in the characteristics of striatal dopamine receptors.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Waddington, J L -- Cross, A J -- Gamble, S J -- Bourne, R C -- New York, N.Y. -- Science. 1983 Apr 29;220(4596):530-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6132447" target="_blank"〉PubMed〈/a〉
    Keywords: Administration, Oral ; Animals ; Antipsychotic Agents/*adverse effects ; Dyskinesia, Drug-Induced/*etiology ; Fluphenazine/administration & dosage/adverse effects/analogs & derivatives ; Haloperidol/adverse effects/pharmacology ; Humans ; Injections, Intramuscular ; Male ; Rats ; Rats, Inbred Strains ; Receptors, Dopamine/*drug effects/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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  • 121
    Publication Date: 1983-09-09
    Description: Prolonged treatment with classical antipsychotic drugs decreased the number of spontaneously active dopamine neurons in both the substantia nigra (A9) and the ventral tegmental area (A10) of the rat brain. In contrast, treatment with atypical antipsychotic drugs selectively decreased the number of A10 dopamine neurons. Related drugs lacking antipsychotic efficacy failed to decrease dopamine activity. These findings suggest that the inability of atypical antipsychotic drugs to decrease A9 dopamine neuronal activity may be related to their lower potential for causing tardive dyskinesia and that the inactivation of A10 neurons may be involved in the delayed onset of therapeutic effects during treatment.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉White, F J -- Wang, R Y -- MH 00378/MH/NIMH NIH HHS/ -- MH-34424/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1983 Sep 9;221(4615):1054-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6136093" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antipsychotic Agents/*pharmacology ; Dopamine/*metabolism ; Male ; Metoclopramide/pharmacology ; Mice ; Neurons/metabolism ; Pons/*metabolism ; Rats ; Rats, Inbred Strains ; Substantia Nigra/*metabolism ; 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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  • 122
    Publication Date: 1983-07-08
    Description: Inbred BALB/c females were mated and subsequently exposed in a divided cage to "stimulus" males or females whose H-2 type was similar or dissimilar to the stud male's. The incidence of pregnancy blocking was considerably higher when stud and stimulus males differed in H-2 type than when they did not. Similar results were obtained with urine samples of H-2 identical and nonidentical males. Females exposed after mating to other females whose H-2 type differed from the stud male, under the same experimental conditions, also showed an appreciable incidence of pregnancy block. It is therefore concluded that chemosensory recognition of H-2 types affects the reproductive hormonal status of the pregnant female.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yamazaki, K -- Beauchamp, G K -- Wysocki, C J -- Bard, J -- Thomas, L -- Boyse, E A -- CA-29979/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1983 Jul 8;221(4606):186-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6857281" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Embryonic Development ; Estrus ; Female ; H-2 Antigens/*immunology ; Homozygote ; Male ; Mice ; Mice, Inbred BALB C ; Pregnancy ; *Pregnancy, Animal
    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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