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  • Pregnancy  (26)
  • American Association for the Advancement of Science (AAAS)  (26)
  • Annual Reviews
  • 1980-1984
  • 1975-1979  (26)
  • 1945-1949
  • 1930-1934
  • 1979  (26)
Collection
Publisher
  • American Association for the Advancement of Science (AAAS)  (26)
  • Annual Reviews
Years
  • 1980-1984
  • 1975-1979  (26)
  • 1945-1949
  • 1930-1934
Year
  • 1
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-03-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Frisch, R E -- McArthur, J W -- New York, N.Y. -- Science. 1979 Mar 2;203(4383):921-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/419411" target="_blank"〉PubMed〈/a〉
    Keywords: Amenorrhea/*etiology/physiopathology ; Body Weight ; Female ; Humans ; Lactation ; Nutrition Disorders/complications ; Pregnancy ; 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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  • 2
    Publication Date: 1979-02-09
    Description: A sensitive and specific radioimmunoassay for the insulin receptor has been developed employing receptor autoantibodies from the serum of a patient with insulin-resistant diabetes. The assay detects insulin binding sites at concentrations as low as 0.1 nanomolar; distinguishes between receptors originating from human placental membranes, human lymphoblastoid cells, and mouse liver membranes; and measures the receptor independently of its binding function. Down-regulation, or loss of binding after exposure to insulin, is associated with loss of immunoreactive receptor.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Harrison, L C -- Flier, J -- Itin, A -- Kahn, C R -- Roth, J -- New York, N.Y. -- Science. 1979 Feb 9;203(4380):544-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/83675" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigen-Antibody Reactions ; Binding Sites ; Binding Sites, Antibody ; Epitopes ; Female ; Humans ; Liver/analysis ; Lymphocytes/analysis ; Mice ; Placenta/analysis ; Pregnancy ; Radioimmunoassay/methods ; Receptor, Insulin/analysis/*immunology ; Solubility
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    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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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-04-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G B -- New York, N.Y. -- Science. 1979 Apr 27;204(4391):391-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/87012" target="_blank"〉PubMed〈/a〉
    Keywords: Anesthesia, Obstetrical/*adverse effects ; Child ; Child Development/*drug effects ; Child, Preschool ; Delivery, Obstetric/methods ; Developmental Disabilities/chemically induced ; Female ; Humans ; Infant ; Infant, Newborn ; Labor, Obstetric ; Methods ; Pregnancy
    Print ISSN: 0036-8075
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  • 4
    Publication Date: 1979-05-11
    Description: In rats, a single injection of clomiphene citrate (Clomid) during pregnancy causes multiple abnormalities of the reproductive tract in the offspring and mothers. These abnormalities probably result from the ability of Clomid to cause long-term estrogenic stimulation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McCormack, S -- Clark, J H -- New York, N.Y. -- Science. 1979 May 11;204(4393):629-31.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/432668" target="_blank"〉PubMed〈/a〉
    Keywords: Abnormalities, Drug-Induced/*pathology ; Animals ; Clomiphene/*toxicity ; Fallopian Tubes/pathology ; Female ; Metaplasia ; Pregnancy ; Pregnancy, Animal/*drug effects ; Rats ; Uterine Diseases/chemically induced/pathology ; Vaginal Diseases/chemically induced
    Print ISSN: 0036-8075
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  • 5
    Publication Date: 1979-06-29
    Description: The concentrations of 1,25-dihydroxyvitamin D [1,25-(OH)2D], calcium, and phosphorus were measured in the serum of rats during pregnancy and at various stages of lactation. The concentration of 1,25-(OH)2D hormone increased almost two-fold during pregnancy and the latter part of lactation, but decreased to control levels or very low values immediately after birth and weaning, respectively. Furthermore, the concentration of 1,25-(OH)2D was inversely correlated with the concentration of calcium, suggesting that circulating 1,25-(OH)2D fluctuates in concert with calcium demands during the reproductive cycle. Parathyroidectomy in lactating rats caused a 70 percent inhibition of the normally observed 1,25-(OH)2D increase, indicating that parathyroid hormone, in response to changes in serum calcium, is a primary modulator of 1,25-(OH)2D during lactation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pike, J W -- Parker, J B -- Haussler, M R -- Boass, A -- Toverud, S V -- New York, N.Y. -- Science. 1979 Jun 29;204(4400):1427-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/451573" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Calcium/blood ; Dihydroxycholecalciferols/*blood ; Female ; Hydroxycholecalciferols/*blood ; *Lactation ; Parathyroid Glands/physiology ; Parathyroid Hormone/physiology ; Phosphorus/blood ; Pregnancy ; *Pregnancy, Animal ; Rats
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  • 6
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-03-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Warner, J S -- New York, N.Y. -- Science. 1979 Mar 23;203(4386):1194-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/424746" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Dose-Response Relationship, Drug ; Female ; Humans ; Ketones/*toxicity ; Nickel/*toxicity ; Occupational Medicine ; Pregnancy ; Rats ; *Teratogens
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
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  • 7
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-02-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1979 Feb 23;203(4382):705.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/419403" target="_blank"〉PubMed〈/a〉
    Keywords: *Abnormalities, Drug-Induced ; Abortion, Spontaneous/*chemically induced ; Anesthetics/*adverse effects ; Female ; Humans ; Male ; Pregnancy
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    Electronic ISSN: 1095-9203
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  • 8
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-06-22
    Description: The kidneys are thought to be the only organs capable of 1 alpha-hydroxylation of vitamin D and its metabolites. We have examined the in vivo conversion of 3H-(25,26)-25-hydroxyvitamin D3(25OHD3) to 3H-(25,26)-1 alpha,25-dihydroxyvitamin D3 [1 alpha,25(OH)2D3] in vitamin D-deficient, pregnant and nonpregnant rats. As expected, nephrectomy of nonpregnant, vitamin D-deficient rats prevented the conversion of 25OHD3 to 1 alpha,25(OH)2D3. In contrast, nephrectomy of pregnant, vitamin D-deficient rats reduced but did not abolish the formation of 1 alpha,25(OH)2D3 from its precursor. The identity of the radioactive metabolite formed from 3H-25OHD3 which circulated in nephrectomized, pregnant rats was established as 1 alpha,25(OH)2D3 by comigration with synthetic 1 alpha,25(OH)2D3 on high-pressure liquid chromatography. The simultaneous absence of 1 alpha,25(OH)2D3 in the fetal kidneys indicated that the site of 1 alpha-hydroxylation after nephrectomy of the pregnant rat was probably extra-renal in origin. Two sites of 1 alpha-hydroxylation of 25OHD3, one renal and the other extra-renal, either fetoplacental or maternal, may exist in the pregnant, vitamin D-deficient rat.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gray, T K -- Lester, G E -- Lorenc, R S -- New York, N.Y. -- Science. 1979 Jun 22;204(4399):1311-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/451538" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Dihydroxycholecalciferols/biosynthesis ; Female ; Fetal Blood/metabolism ; Hydroxycholecalciferols/*metabolism ; Hydroxylation ; Kidney/embryology/metabolism ; *Nephrectomy ; Placenta/metabolism ; Pregnancy ; *Pregnancy, Animal
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  • 9
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-10-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brackbill, Y -- New York, N.Y. -- Science. 1979 Oct 26;206(4417):404-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/504983" target="_blank"〉PubMed〈/a〉
    Keywords: Abortion, Induced ; Disclosure ; *Ethics, Medical ; Female ; Fetus/*physiology ; Humans ; Informed Consent ; Pregnancy ; *Risk Assessment
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  • 10
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-11-02
    Description: Exposure to ethanol retards growth and differentiation in cultured rat embryos during organogenesis. The development of untreated embryos is indistinguishable from growth in utero. These data suggest that the hypoplastic features of children born to chronically alcoholic mothers are due, at least in part, to a direct action of ethanol, which causes reduced embryonic cellular proliferation early in gestation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brown, N A -- Goulding, E H -- Fabro, S -- New York, N.Y. -- Science. 1979 Nov 2;206(4418):573-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/573922" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Dose-Response Relationship, Drug ; Ectogenesis/*drug effects ; Embryo, Mammalian/*drug effects ; Ethanol/*toxicity ; Female ; Fetal Growth Retardation/chemically induced ; Pregnancy ; Rats ; *Teratogens
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  • 11
    Publication Date: 1979-11-30
    Description: Male mice release luteinizing hormone when exposed for a short time to a female. In this experiment, multiple blood samples were withdrawn by atrial cannulas from tethered males during either continuous or intermittent exposure to nonreceptive females. After an immediate, transient release of luteinizing hormone, continuous exposure to the same female was accompanied by only random, spontaneous elevations in plasma levels of this hormone. Successive presentations of the same female at 2-hour intervals elicited gradually diminishing luteinizing hormone responses. Exposing such unresponsive males to novel, diestrous females, however, dramatically stimulated their release of the hormone. These results demonstrate habituation of a socially induced, neuroendocrine response involving reproductive hormones.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Coquelin, A -- Bronson, F H -- New York, N.Y. -- Science. 1979 Nov 30;206(4422):1099-101.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/573924" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arousal/physiology ; Diestrus ; Female ; Habituation, Psychophysiologic/*physiology ; Luteinizing Hormone/*metabolism ; Male ; Mice ; Pregnancy ; Sexual Behavior, Animal/physiology
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  • 12
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-11-30
    Description: Female rats subjected to prenatal stress later experienced fewer conceptions, more spontaneous abortions and vaginal hemorrhaging, longer pregnancies, and fewer viable young than nonstressed rats. The offspring of the prenatally stressed rats were lighter in weight and less likely to survive the neonatal period. Prenatal stress may influence the balance of adrenal and gonadal hormones during a critical stage of fetal hypothalamic differentiation, thereby producing a variety of reproductive dysfunctions in adulthood.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Herrenkohl, L R -- New York, N.Y. -- Science. 1979 Nov 30;206(4422):1097-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/573923" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Disorders of Sex Development/etiology ; Female ; Gestational Age ; Humans ; Infertility, Female/*etiology ; Lighting ; Litter Size ; Maternal Behavior ; Pregnancy ; Rats ; Reproduction ; Stress, Psychological/*complications
    Print ISSN: 0036-8075
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  • 13
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-12-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lowry, J T -- New York, N.Y. -- Science. 1979 Dec 21;206(4425):1428.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/505019" target="_blank"〉PubMed〈/a〉
    Keywords: Female ; Fetal Death/*epidemiology ; Humans ; Male ; Pregnancy ; *Sex Ratio
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  • 14
    Publication Date: 1979-09-28
    Description: A reactive metabolite of acetaminophen is hepatotoxic in humans when the drug is ingested in large overdoses. The ability of the human fetal and adult liver to oxidize acetaminophen by trapping the potentially toxic metabolite as a glutathione conjugate has been measured. Oxidation by fetal liver was approximately ten times slower than by adult liver. However, there was a definite increase in acetaminophen oxidation with fetal age. Isolated human fetal liver cells conjugated acetaminophen with sulfate but not with glucuronic acid. The results indicate that the human fetal liver is able to detoxify acetaminophen by conjugation. However, it also catalyzes the formation of an active metabolite of acetaminophen through oxidation. Hence the fetus remains at risk should a large dose of the drug cross into the fetal circulation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rollins, D E -- von Bahr, C -- Glaumann, H -- Moldeus, P -- Rane, A -- New York, N.Y. -- Science. 1979 Sep 28;205(4413):1414-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/38505" target="_blank"〉PubMed〈/a〉
    Keywords: Acetaminophen/*metabolism/toxicity ; Biotransformation ; Cytochrome P-450 Enzyme System/metabolism ; Female ; Glutathione/metabolism ; Humans ; Liver/embryology ; Maternal-Fetal Exchange ; Microsomes, Liver/*metabolism ; NADP/metabolism ; Pregnancy
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  • 15
    Publication Date: 1979-09-14
    Description: The multiple relationships within kinships of adult monozygotic twins permit incisive analyses to be made of genetic and environmental effects on behavioral traits. Data from families of 65 monozygotic twin pairs yield evidence of genetic variance on the Block Design Test, a nonverbal measure of general intelligence.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rose, R J -- Harris, E L -- Christian, J C -- Nance, W E -- New York, N.Y. -- Science. 1979 Sep 14;205(4411):1153-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/572991" target="_blank"〉PubMed〈/a〉
    Keywords: Female ; Humans ; *Intelligence ; Pedigree ; Pregnancy ; *Twins ; *Twins, Monozygotic ; Wechsler Scales
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 16
    Publication Date: 1979-03-16
    Description: A decrease in specific [3H]spiroperidol binding to rat caudate tissue and a parallel decrease in sensitivity to apomorphine in eliciting stereotyped behavior was observed in the offspring of rat mothers treated with either haloperidol or alpha-methyl-p-tyrosine-methyl ester during pregnancy. In contrast, evidence of increased dopamine-receptor sensitivity was observed in the pups if haloperidol was administered to their mothers postpartum during nursing rather than during pregnancy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rosengarten, H -- Friedhoff, A J -- New York, N.Y. -- Science. 1979 Mar 16;203(4385):1133-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/570724" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal/drug effects ; Corpus Striatum/*drug effects/embryology/growth & development ; Female ; Fetus/*drug effects ; Haloperidol/*pharmacology ; Humans ; *Lactation ; Maternal-Fetal Exchange ; Methyltyrosines/*pharmacology ; Pregnancy ; Rats ; Receptors, Dopamine/*drug effects ; Stereotyped Behavior/drug effects
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  • 17
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-03-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, J -- New York, N.Y. -- Science. 1979 Mar 16;203(4385):1090-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/424734" target="_blank"〉PubMed〈/a〉
    Keywords: 2,4,5-Trichlorophenoxyacetic Acid/adverse effects/*standards ; Abortion, Spontaneous/*chemically induced ; Female ; Government Agencies ; Humans ; Legislation, Drug ; Pregnancy ; Tetrachlorodibenzodioxin/toxicity ; United States
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  • 18
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-10-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, K D -- Steinberger, E -- Rodriguez-Rigau, L J -- New York, N.Y. -- Science. 1979 Oct 5;206(4414):96-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/482933" target="_blank"〉PubMed〈/a〉
    Keywords: Birth Weight/*drug effects ; Female ; Humans ; Prednisone/*adverse effects ; Pregnancy
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  • 19
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-06-22
    Description: Specific binding of tritiated oxytocin to uterine receptors of pregnant rats increases dramatically at term and is maximal during labor. In mammary glands the increase in binding is gradual, reaching a maximum during the lactation period. Concomitant changes in the sensitivity of the uterus and mammary gland to oxytocin indicate that the receptor concentration is of functional significance. Oxytocin receptors, therefore, may regulate the response of the target organs to circulating oxytocin and thereby control the onset of labor and lactation. Ovarian steroids participate in the regulation of oxytocin receptors in a manner as yet unclarified.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Soloff, M S -- Alexandrova, M -- Fernstrom, M J -- New York, N.Y. -- Science. 1979 Jun 22;204(4399):1313-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/221972" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Estradiol/blood ; Female ; Kinetics ; *Labor, Obstetric ; *Lactation ; Mammary Glands, Animal/metabolism ; Myometrium/*metabolism ; Oxytocin/blood/*metabolism ; Pregnancy ; Progesterone/blood ; Receptors, Cell Surface/*metabolism ; Uterus/*metabolism
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  • 20
    Publication Date: 1979-02-09
    Description: Exposure of pregnant rats to inhalation of nickel carbonyl on days 7 or 8 of gestation frequently causes the progeny to develop ocular anomalies, including anophthalmia and microphthalmia. The incidence of extraocular anomalies is very low. The specificity of nickel carbonyl for induction of ocular anomalies in rats appears to be unique among known teratogenic agents.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sunderman, F W Jr -- Allpass, P R -- Mitchell, J M -- Baselt, R C -- Albert, D M -- New York, N.Y. -- Science. 1979 Feb 9;203(4380):550-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/104388" target="_blank"〉PubMed〈/a〉
    Keywords: Abnormalities, Drug-Induced/*embryology/pathology ; Animals ; Anophthalmos/chemically induced ; Carcinogens ; *Eye Abnormalities ; Female ; Gestational Age ; Ketones/*toxicity ; Microphthalmos/chemically induced ; Nickel/*toxicity ; Pregnancy ; Rats ; Teratogens
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  • 21
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-08-03
    Description: The administration of iodide to pregnant and nursing rats induces hypothyroidism in the term fetus and neonatal rat through age 10 days as indicated by an increase in the serum concentration of thyroid-stimulating hormone and a decrease in the serum of thyroxine and triiodothyronine. Thyroid function returned to normal from age 18 through 60 days in spite of continued iodide administration, strongly suggesting that resistance to the inhibitory effect of iodide on thyroid hormone synthesis is developed at approximately 18 days of age. This perinatal rat model can be used to study the mechanisms responsible for iodide-induced hypothyroidism and goiter in human newborns whose mothers received iodide-containing medications during pregnancy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Theodoropoulos, T -- Braverman, L E -- Vagenakis, A G -- New York, N.Y. -- Science. 1979 Aug 3;205(4405):502-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/451615" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Female ; Fetus ; Hypothyroidism/chemically induced/*physiopathology ; *Iodides ; Lactation ; Pregnancy ; Rats ; Thyrotropin/blood ; Thyroxine/blood ; Triiodothyronine/blood
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  • 22
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-09-21
    Description: Three psychotropic drugs were administered to pregnant rats and were then evaluated for their behavioral and reproductive effects in the offspring. Control rats received either saline or vitamin A. Prochlorperazine had the most disruptive effects on reproduction and growth, but had the least effect on behavior. Propoxyphene had no apparent effects on reproduction or growth, but produced a variety of behavioral changes. Fenfluramine was intermediate in its effects on reproduction and growth and had behavioral effects that were revealed in tests of preweaning development. The data suggest that systematic tests of behavior add important information to evaluations of reproductive toxicity that cannot, at present, be obtained by other means.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vorhees, C V -- Brunner, R L -- Butcher, R E -- New York, N.Y. -- Science. 1979 Sep 21;205(4412):1220-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/472738" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal/*drug effects ; Brain Chemistry/drug effects ; Dextropropoxyphene/*pharmacology ; *Disease Models, Animal ; Female ; Fenfluramine/*pharmacology ; Humans ; Litter Size/drug effects ; Male ; Movement Disorders/chemically induced ; Pregnancy ; Pregnancy, Animal/*drug effects ; Prochlorperazine/*pharmacology ; Rats ; Reproduction/drug effects ; Sex Ratio/drug effects ; Swimming
    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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  • 23
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-04-20
    Description: The normal ovarian cycle of female rats is typically replaced by persistent estrus when these animals are housed under constant light. Evidence presented here shows that the maintenance of periodicity in the environment can at least delay (if not prevent) the photic induction of persistent vaginal estrus. Female rats in constant light were exposed to vaginal smearing at random times or at the same time every day. In another experiment, female rats were exposed to either constant bright light, constant dim light, or a 24-hour photic cycle of bright and dim light. The onset of persistent vaginal estrus was delayed in rats exposed to 24-hour time cues even though the light intensities were the same as or greater than those for the aperiodic control groups. The results suggest that the absence of 24-hour time cues in constant light contributes to the induction of persistent estrus.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Weber, A L -- Adler, N T -- New York, N.Y. -- Science. 1979 Apr 20;204(4390):323-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/571146" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Clocks ; Dose-Response Relationship, Radiation ; Estrus/*radiation effects ; Female ; *Light ; Periodicity/radiation effects ; Pregnancy ; Rats ; 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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  • 24
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-02-09
    Description: Methyl p-hydroxybenzoate has been identified in the vaginal secretions of female dogs in estrus. When small amounts of this compound were applied to the vulvas of anestrous or spayed females, males placed with these females became sexually aroused and attempted to mount them.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Goodwin, M -- Gooding, K M -- Regnier, F -- New York, N.Y. -- Science. 1979 Feb 9;203(4380):559-61.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/569903" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Dogs/*physiology ; *Estrus ; Female ; Hydroxybenzoates ; Male ; Pheromones/*physiology ; Posture ; Pregnancy ; Proestrus ; Sex Attractants/*physiology ; Sexual Behavior, Animal/physiology ; Smell ; Vagina/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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  • 25
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-10-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jefferies, W M -- New York, N.Y. -- Science. 1979 Oct 5;206(4414):96-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/482932" target="_blank"〉PubMed〈/a〉
    Keywords: Adrenal Cortex Hormones/*adverse effects ; Birth Weight/drug effects ; Cortisone/adverse effects ; Dose-Response Relationship, Drug ; Female ; Humans ; Hydrocortisone/adverse effects ; Prednisone/*adverse effects ; Pregnancy
    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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  • 26
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-04-06
    Description: Vital statistics data for the United States from 1922 to 1936 and from 1950 to 1972 were used to analyze fetal and early neonatal mortality. This analysis corroborates the previously established pattern of the sex ratio of fetal deaths--highest from months 3 to 5, lower from months 6 to 7 or 8, and increasing at term. It also indicates a postponement of late fetal deaths into the early infant period. Whereas earlier research reports have described the pattern of the sex ratio of fetal deaths, this report repeats this analysis for a recent national data base. This line of analysis is extended by using the patterns observed in the data to produce an empirical estimate of the primary sex ratio. For 1950 to 1972, this ratio (male to female) is conservatively estimated to be 120:100.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McMillen, M M -- New York, N.Y. -- Science. 1979 Apr 6;204(4388):89-91.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/571144" target="_blank"〉PubMed〈/a〉
    Keywords: Female ; Fetal Death/*epidemiology ; Humans ; *Infant Mortality ; Male ; Pregnancy ; *Sex Ratio ; United States
    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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