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  • Humans  (33)
  • 2010-2014
  • 1985-1989
  • 1975-1979  (33)
  • 1945-1949
  • 1978  (33)
  • 1
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    beta-Endorphin is not detectable in plasma from normal human subjects (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-10-13
    Description: beta-Endorphin is not detectable in plasma from normal human subjects when measured under baseline conditions or after the subjects have received vasopressin, an agent that elevates beta-lipotropin and adrenocorticotropic hormone (ACTH). Significant amounts of beta-endorphin are present in plasma of patients with endocrine disorders associated with increased ACTH and beta-lipotropin production. Highly purified, natural beta-lipotropin is not peripherally converted to beta-endorphin in vivo in normal subjects.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Suda, T -- Liotta, A S -- Krieger, D T -- New York, N.Y. -- Science. 1978 Oct 13;202(4364):221-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/211585" target="_blank"〉PubMed〈/a〉
    Keywords: Addison Disease/blood ; Adrenocorticotropic Hormone/*blood ; Cushing Syndrome/blood ; Endorphins/*blood ; Humans ; Nelson Syndrome/blood ; Pituitary Gland/metabolism ; beta-Lipotropin/*blood
    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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    Deficiencies of glucosamine-6-sulfate or galactosamine-6-sulfate sulfatases are responsible for different mucopolysaccharidoses (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-01-06
    Description: [1-3H]Galactitol-6-sulfate, N- [1-3H]acetylgalactosaminitol-6-sulfate, N-[1-3H]acetylglucosaminitol-6-sulfate, N-acetylglucosamine-6-sulfate, and 6-sulfated tetrasaccharides from chondroitin-6-sulfate have been used for the measurement of 6-sulfatase activity of extracts of normal skin fibroblasts and of fibroblasts cultured from patients with genetic mucopolysaccharidoses. With these substrates, extracts of fibroblasts derived from Morquio patients lack or have greatly reduced activities for galactitol-6-sulfate, N-acetylgalactosaminitol-6-sulfate, and 6-sulfated tetrasaccharides but have normal activity for N-acetylglucosamine-6-sulfate and its alditol; those derived from a patient with a newly discovered mucopolysaccharidosis have greatly reduced activity for N-acetylglucosamine-6-sulfate and its alditol but normal activity for galactitol-6-sulfate, N-acetylgalactosaminitol-6-sulfate, and the 6-sulfated tetrasaccharides. These findings demonstrate the existence of two different hexosamine-6-sulfate sulfatases, specific for the glucose or galactose configuration of their substrates. Their respective deficiencies, causing inability to degrade keratan sulfate and heparan sulfate in one case and keratan sulfate and chondroitin-6-sulfate in the other, are responsible for different clinical phenotypes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Di Ferrante, N -- Ginsberg, L C -- Donnelly, P V -- Di Ferrante, D T -- Caskey, C T -- New York, N.Y. -- Science. 1978 Jan 6;199(4324):79-81.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratories of Connective Tissue Research, Department of Biochemistry, Baylor College of Medicine, Houston, Texas 77030, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17569489" target="_blank"〉PubMed〈/a〉
    Keywords: Acetylgalactosamine/analogs & derivatives/metabolism ; Acetylglucosamine/analogs & derivatives/metabolism ; Cells, Cultured ; Child, Preschool ; Chondroitin Sulfates/metabolism ; Chondroitinsulfatases/*deficiency/metabolism ; Fibroblasts/enzymology ; Galactitol/metabolism ; Heparitin Sulfate/metabolism ; Humans ; Hydrogen-Ion Concentration ; Keratan Sulfate/metabolism ; Male ; Mucopolysaccharidoses/*enzymology ; Mucopolysaccharidosis III/enzymology ; Mucopolysaccharidosis IV/*enzymology ; Skin/cytology/enzymology ; Substrate Specificity ; Sulfatases/*deficiency/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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  • 3
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    Hepatitis B virus and sex ratio of offspring (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-08-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Drew, J S -- London, W T -- Lustbader, E D -- Hesser, J E -- Blumberg, B S -- New York, N.Y. -- Science. 1978 Aug 25;201(4357):687-92.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/566954" target="_blank"〉PubMed〈/a〉
    Keywords: Age Factors ; Birth Order ; Cross Reactions ; Female ; Fetal Death ; Graft Survival ; Hepatitis B/immunology/*physiopathology/transmission ; Hepatitis B Surface Antigens/analysis ; Humans ; Male ; Parity ; Pregnancy ; Sex Factors ; *Sex Ratio
    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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    Lymphocyte ecto-5'-nucleotidase deficiency in agammaglobulinemia (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-08-18
    Description: Fresh peripheral blood lymphocytes from eight patients with congenital agammaglobulinemia demonstrate reduced ecto-5'-nucleotidase activity when compared to the mean activity of normal subjects and patients with other forms of immunoglobulin deficiency. A specific defect of ecto-5'-nucleotidase is further suggested by normal values for lymphocyte ecto-adenosinetriphosphatase and ecto-nonspecific phosphatase. The data provide evidence for an enzyme deficiency in this X-linked, B lymphocyte deficiency syndrome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Edwards, N L -- Magilavy, D B -- Cassidy, J T -- Fox, I H -- New York, N.Y. -- Science. 1978 Aug 18;201(4356):628-30.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/27864" target="_blank"〉PubMed〈/a〉
    Keywords: Agammaglobulinemia/*enzymology/genetics ; Cell Membrane/enzymology ; Female ; Genetic Linkage ; Humans ; Hydrogen-Ion Concentration ; IgA Deficiency ; Lymphocytes/*enzymology ; Male ; Nucleotidases/blood/*deficiency ; Rosette Formation ; T-Lymphocytes/immunology ; X Chromosome
    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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    Right-left asymmetrics in the brain (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-02-24
    Description: Structural asymmetries between the hemispheres are found in the human brain. Asymmetries in the auditory regions and in the Sylvian fissures are present even in the fetus. The Sylvian asymmetries may have existed in Neanderthal man and are found consistently in some apes. They may relate to right-left differences infunction. Thus, the striking auditory asymmetries could underlie language lateralization. The asymmetries in the frontal and occipital lobes and the lateral ventricles are correlated with hand preference. Anatomical asymmetries may help to explain the range of human talents, recovery from acquired disorders of language function, certain childhood learning disabilities, some dementing illnesses of middle life, and the evidence for behavioral lateralization in nonhuman primates.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Galaburda, A M -- LeMay, M -- Kemper, T L -- Geschwind, N -- New York, N.Y. -- Science. 1978 Feb 24;199(4331):852-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/341314" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/*anatomy & histology/physiology/radiography ; Cerebral Cortex/anatomy & histology ; Dementia/etiology ; Dyslexia/etiology ; Fossils ; *Functional Laterality ; Humans ; Primates/anatomy & histology ; Pyramidal Tracts/anatomy & histology ; Temporal Lobe/anatomy & histology ; Tomography, X-Ray Computed
    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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    Thrombin-induced platelet aggregation is mediated by a platelet plasma membrane-bound lectin (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-06-16
    Description: Throbin-activated human platelets cause agglutination of trypsinized, formalinized bovine erythrocytes. This lectin activity of stimulated platelets was blocked by galactosamine, glucosamine, mannosamine, lysine, and arginine, but not by N-acetylated sugars, other neutral sugars, or other amino acids. Inhibitors of the thrombin-induced lectin activity also blocked thrombin-induced platelet aggregation. It appears that a membrane surface component that has lectin activity mediates platelet aggregation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gartner, T K -- Williams, D C -- Minion, F C -- Phillips, D R -- New York, N.Y. -- Science. 1978 Jun 16;200(4347):1281-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/663608" target="_blank"〉PubMed〈/a〉
    Keywords: *Agglutinins ; Amino Acids/pharmacology ; Amino Sugars/pharmacology ; Animals ; Binding Sites ; Cytochalasin B/pharmacology ; *Hemagglutinins ; Humans ; Membrane Proteins/blood ; Platelet Aggregation/*drug effects ; Prostaglandins E/pharmacology ; Species Specificity ; Thrombin/*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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  • 7
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    B lymphocyte antigens in sicca syndrome (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-03-31
    Description: All individuals tested in this study with sicca syndrome, a human autoimmune disease, bear two immunologically distinct and genetically unrelated B lymphocyte antigens that appear similar to the immune response associated (Ia) antigens of the mouse. The genes coding for these two antigens are present in only 37 and 24 percent of normal controls. In animal models Ia antigen genes are closely linked to immune response genes. Our findings suggest that two such genes may be required for the development of sicca syndrome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moutsopoulos, H M -- Chused, T M -- Johnson, A H -- Khudsen, B -- Mann, D L -- New York, N.Y. -- Science. 1978 Mar 31;199(4336):1441-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/415366" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Autoimmune Diseases/*immunology ; B-Lymphocytes/*immunology ; Female ; *Genes, MHC Class II ; Genetic Linkage ; HLA Antigens/analysis/genetics ; Humans ; Isoantigens/*analysis/genetics ; Male ; Middle Aged ; Sjogren's Syndrome/genetics/*immunology
    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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    Pharmacologic effects in man of a specific serotonin-reuptake inhibitor (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-01-27
    Description: Fluoxetine (Li-ly 110140) caused a 63 percent inhibition of [3H]serotonin uptake into platelets obtained from normal volunteers to whom the drug was administered daily for 7 days. This dose had no effect on the usual pressor response produced by injections of norepinephrine or tyramine.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lemberger, L -- Rowe, H -- Carmichael, R -- Oldham, S -- Horng, J S -- Bymaster, F P -- Wong, D T -- New York, N.Y. -- Science. 1978 Jan 27;199(4327):436-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/619465" target="_blank"〉PubMed〈/a〉
    Keywords: Behavior/drug effects ; Blood Platelets/*drug effects/metabolism ; Blood Pressure/drug effects ; Humans ; Norepinephrine/pharmacology ; Phenyl Ethers/pharmacology ; Propylamines/*pharmacology ; Serotonin/*blood ; Serotonin Antagonists/pharmacology ; Tyramine/pharmacology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
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  • 9
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    Giemsa-11 staining of chromosome 1: a newly described heteromorphism (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-10-06
    Description: Sequential Giemsa-11 and C-band staining of the heterochromatic region of chromosome 1 from 30 unrelated individuals revealed a high degree of variability within this region, more than was identifiable with either stain alone. The Giemsa-11 stained material usually appeared as a single band of only slightly varying size within the heterochromatic region. The position of this band ranged from a location immediately adjacent to the centromere, to one farther along the long arm or at the junction of the C-band heterochromatin and euchromatin. Two individuals had a chromosome 1 with no detectable Giemsa-11 band but an average-size C-band. Two others with a large heterochromatic segment by C-banding had two Giemsa-11 positive bands. Additional studies of five members of one family were consistent with transmission of these hetermorphisms in codominant Mendelian fashion.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Maegenis, R E -- Donlon, T A -- Wyandt, H E -- New York, N.Y. -- Science. 1978 Oct 6;202(4363):64-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/694520" target="_blank"〉PubMed〈/a〉
    Keywords: Azure Stains ; Centromere/ultrastructure ; Chromosomes, Human, 1-3/*ultrastructure ; Genes, Dominant ; Heterochromatin/ultrastructure ; Humans
    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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    Kainic acid lesions of the striatum dissociate amphetamine and apomorphine stereotypy: similarities to Huntingdon's chorea (1978)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1978-07-28
    Description: Kainic acid lesion of cell bodies in the dorsal striatum enhanced the stereotypy-producing effects of d-amphetamine without affecting the sterotypy produced by the direct receptor agonist apomorphine. This pattern of results parallels that found in patients suffering from Hungtington's chorea, thus strengthening the parallels between the kainic acid animal model and the human disease state initially suggested on biochemical gounds. The present results further suggest a dissociation of the mechanisms involved in the production of stereotypy by these two drugs, perhaps in terms of differential involvement of the striato-nigral negative feedback loop.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mason, S T -- Sanberg, P R -- Fibiger, H C -- New York, N.Y. -- Science. 1978 Jul 28;201(4353):352-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26976" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apomorphine/*pharmacology ; Behavior/*drug effects ; Choline O-Acetyltransferase/metabolism ; Corpus Striatum/*drug effects/enzymology/pathology ; Dextroamphetamine/*pharmacology ; Disease Models, Animal ; Glutamate Decarboxylase/metabolism ; Humans ; Huntington Disease/*physiopathology ; *Kainic Acid/pharmacology ; Male ; Nucleus Accumbens/enzymology ; *Pyrrolidines/pharmacology ; Rats ; Stereotyped Behavior/*drug effects ; Tyrosine 3-Monooxygenase/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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