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  • Journals
  • Articles  (122)
  • Female  (122)
  • 1975-1979  (122)
  • 1960-1964
  • 1955-1959
  • 1978  (122)
  • Science. 199(4324): 22-30.  (1)
  • Science. 199(4324): 83-4.  (1)
  • Science. 199(4325): 181-3.  (1)
  • Science. 199(4325): 200-1.  (1)
  • Science. 199(4326): 303-5.  (1)
  • Science. 199(4327): 429-31.  (1)
  • Science. 199(4327): 431-2.  (1)
  • Science. 199(4327): 437-9.  (1)
  • Science. 199(4328): 539-41.  (1)
  • Science. 199(4328): 544-5.  (1)
  • Science. 199(4328): 545-7.  (1)
  • Science. 199(4329): 686-8.  (1)
  • Science. 199(4330): 748-9.  (1)
  • Science. 199(4330): 778-81.  (1)
  • Science. 199(4330): 783-6.  (1)
  • Science. 199(4330): 786-7.  (1)
  • Science. 199(4330): 804-6.  (1)
  • Science. 199(4331): 904-6.  (1)
  • Science. 199(4331): 909-11.  (1)
  • Science. 199(4331): 911-2.  (1)
  • 25
Collection
  • Journals
  • Articles  (122)
Source
Keywords
Publisher
Years
  • 1975-1979  (122)
  • 1960-1964
  • 1955-1959
Year
Journal
Topic
  • 1
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    Estrogens: hormones' link to cancer disputed (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-12-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J L -- New York, N.Y. -- Science. 1978 Dec 22;202(4374):1270-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/725601" target="_blank"〉PubMed〈/a〉
    Keywords: Dose-Response Relationship, Drug ; Estrogens/*adverse effects ; Female ; Hemorrhage/etiology ; Humans ; Risk ; Uterine Diseases/etiology ; Uterine Neoplasms/diagnosis/*etiology
    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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    Intraventricular alloxan eliminates feeding elicited by 2-deoxyglucose (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-12-15
    Description: Evidence suggests that alloxan reacts with membrane-bound glucoreceptors and that it competes with glucose molecules for these sites. We therefore administered small quantities of alloxan into the cerebrospinal fluid of rats to determine what effect this might have on their ability to react to changes of glucose concentration. Rats treated in this manner did not eat as much as controls in response to the intraperitoneal administration of 2-deoxyglucose or to a 24-hour fast, and they became hypoglycemic significantly sooner than controls when fasted. The data suggest that the function of brain glucoreceptors is to protect the body from sudden decreases of glucose and that these glucoreceptors play little if any role in the normal regulation or maintenance of feeding, body weight, or blood glucose concentrations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Woods, S C -- McKay, L D -- New York, N.Y. -- Science. 1978 Dec 15;202(4373):1209-11.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/725595" target="_blank"〉PubMed〈/a〉
    Keywords: Alloxan/administration & dosage/*pharmacology ; Animals ; Deoxyglucose/antagonists & inhibitors/pharmacology ; Eating/*drug effects ; Female ; Glucose ; Injections, Intraventricular ; Rats ; Receptors, Drug/*drug effects
    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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  • 3
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    Restriction enzymes: prenatal diagnosis of genetic disease (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-12-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J L -- New York, N.Y. -- Science. 1978 Dec 8;202(4372):1068-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/715458" target="_blank"〉PubMed〈/a〉
    Keywords: Anemia, Sickle Cell/*diagnosis/genetics ; DNA Restriction Enzymes/*metabolism ; Female ; Globins/genetics ; Humans ; Pregnancy ; Prenatal Diagnosis/*methods ; Thalassemia/*diagnosis
    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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  • 4
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    Child spacing and birth order: effect on intellectual ability in two-child families (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-12-01
    Description: The effect on intellectual ability of the spacing of the birth of siblings was studied in two series of young men from two-child families: (i) 535 pairs of brothers and (ii) 1511 unrelated firstborn and secondborn. Birth-order effect and level of ability were not influenced by length of interval between firstborn and secondborn.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Belmont, L -- Stein, Z -- Zybert, P -- New York, N.Y. -- Science. 1978 Dec 1;202(4371):995-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/568823" target="_blank"〉PubMed〈/a〉
    Keywords: *Birth Order ; Family ; Female ; Humans ; *Intelligence ; Male ; Maternal Age ; Socioeconomic Factors ; Time Factors
    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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  • 5
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    beta-Endorphin is associated with overeating in genetically obese mice (ob/ob) and rats (fa/fa) (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-12-01
    Description: Small doses of the opiate antagonist naloxone selectively abolished overeating in genetically obese mice (ob/ob) and rats (fa/fa). Elevated concentrations of the naturally occurring opiate beta-endorphin were found in the pituitaries of both obese species and in the blood plasma of the obese rats. Brain levels of beta-endorphin and Leu-enkephalin were unchanged. These data suggest that excess pituitary beta-endorphin may play a role in the development of the overeating and obesity syndrome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Margules, D L -- Moisset, B -- Lewis, M J -- Shibuya, H -- Pert, C B -- New York, N.Y. -- Science. 1978 Dec 1;202(4371):988-91.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/715455" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Disease Models, Animal ; Eating/drug effects ; Endorphins/antagonists & inhibitors/blood/*physiology ; Feeding Behavior/*physiology ; Female ; Male ; Mice ; Mice, Obese/*physiology ; Naloxone/pharmacology ; Obesity/genetics/*physiopathology ; Pituitary Gland/physiology ; Rats
    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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  • 6
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    Synchronies in mental development: an epigenetic perspective (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-12-01
    Description: Early mental development is analyzed from an evolutionary viewpoint and related to the dynamic interplay of genetic programming, maturational status, and environmental influence. Data are reported from a large sample of twins and siblings who have been tested longitudinally from 3 months to 6 years of age. Monozygotic twins became increasingly concordant with age and also paralleled each other for the spurts and lags in development. Dizygotic twins became less concordant with age and eventually matched their singleton siblings as closely as one another. The overall results suggested that the course of mental development is guided by the intrinsic scheduling of the genetic program acting in concert with maturational status and environmental influence.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wilson, R S -- New York, N.Y. -- Science. 1978 Dec 1;202(4371):939-48.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/568822" target="_blank"〉PubMed〈/a〉
    Keywords: Behavior/physiology ; *Biological Evolution ; Child ; Child, Preschool ; Environment ; Female ; Genes ; *Growth ; Humans ; Infant ; Infant, Newborn ; Infant, Premature ; Intelligence ; Mental Processes/*physiology ; Pregnancy ; *Twins
    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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    NAS saccharin report sweetens FDA position, but not by much (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-11-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, R J -- New York, N.Y. -- Science. 1978 Nov 24;202(4370):852-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/715446" target="_blank"〉PubMed〈/a〉
    Keywords: Age Factors ; *Carcinogens ; Cocarcinogenesis ; Female ; Humans ; Male ; Risk ; Saccharin/*adverse effects ; United States ; United States Food and Drug Administration
    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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    S-adenosylhomocysteine hydrolase is an adenosine-binding protein: a target for adenosine toxicity (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-11-17
    Description: When adenosine deaminase activity is inhibited, low concentrations of adenosine are toxic to human lymphoblast mutants that are unable to convert adenosine to intracellular nucleotides. In order to identify the mediator of this cytotoxicity, we searched for a cytoplasmic protein capable of binding adenosine with high affinity. Such a protein was identified in extracts of human lymphoblasts and placenta as the enzyme S-adenosylhomocysteine hydrolase.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hershfield, M S -- Krodich, N M -- New York, N.Y. -- Science. 1978 Nov 17;202(4369):757-60.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/715439" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine/*metabolism ; Adenosine Deaminase/*deficiency ; Carrier Proteins/*metabolism ; Female ; Humans ; Hydrolases/*metabolism ; Kinetics ; Lymphocytes/metabolism ; Nucleoside Deaminases/*deficiency ; Placenta/metabolism ; Pregnancy ; S-Adenosylhomocysteine/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
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    Behavioral teratology: birth defects of the mind (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-11-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G B -- New York, N.Y. -- Science. 1978 Nov 17;202(4369):732-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/568821" target="_blank"〉PubMed〈/a〉
    Keywords: Anesthesia, Obstetrical/adverse effects ; Behavior/*drug effects ; Female ; Gonadal Steroid Hormones/adverse effects ; Humans ; Infant ; Infant, Newborn ; Infant, Newborn, Diseases/chemically induced ; Male ; Mental Disorders/*chemically induced ; Narcotics ; Pregnancy ; Semen/metabolism ; Spermatozoa/drug effects ; Substance Withdrawal Syndrome/etiology ; *Teratogens/metabolism
    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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  • 10
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    Gene dosage compensation and the evolution of sex chromosomes (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-11-17
    Description: Dosage compensation is a mechanism by means of which the activity of X-linked or Z-linked genes is made equal in the two sexes of organisms with an XX compared to XY or ZZ compared to ZW basis of sex determination. In mammals, compensation is achieved by the inactivation of one X chromosome in somatic cells of females. In Drosophila, compensation does not involve inactivation. The two X chromosomes in females as well as the single X in males are regulated, and individual genes are thought to respond independently to the regulatory mechanism. It is proposed that in both groups of organisms the evolution of heteromorphic sex chromosomes was gradual and occurred as the direct result of the evolution of dosage compensation rather than the reverse.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lucchesi, J C -- New York, N.Y. -- Science. 1978 Nov 17;202(4369):711-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/715437" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; *Biological Evolution ; Drosophila/*genetics ; Female ; Genes, Regulator ; Genetic Linkage ; Haploidy ; Male ; Mammals/physiology ; Sex Chromosomes/*physiology
    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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