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  • Articles  (7)
  • Middle Aged  (7)
  • American Association for the Advancement of Science (AAAS)  (7)
  • American Chemical Society
  • American Geophysical Union
  • International Union of Crystallography (IUCr)
  • 1980-1984  (7)
  • 1975-1979
  • 1955-1959
  • 1984  (7)
  • 1977
  • 1955
Collection
  • Articles  (7)
Source
Keywords
Publisher
  • American Association for the Advancement of Science (AAAS)  (7)
  • American Chemical Society
  • American Geophysical Union
  • International Union of Crystallography (IUCr)
Years
  • 1980-1984  (7)
  • 1975-1979
  • 1955-1959
Year
Journal
Topic
  • 1
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    Transfusion-associated AIDS: serologic evidence of human T-cell leukemia virus infection of donors (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-03-23
    Description: An assay for antibodies to membrane antigens of cells infected by human T-cell leukemia virus was used to examine serum from persons who donated blood to 12 patients with acquired immunodeficiency syndrome (AIDS) associated with blood transfusions. The occurrence of positive results in the assay was significantly greater among donors to the AIDS patients (9 of 117; 7.7 percent) than among random donors (1 of 298; 0.3 percent). Of 12 sets of donors examined, 9 sets included a donor whose serum gave positive results for the presence of the antibodies. In six of these nine sets, the seropositive donor was an individual who was also identified as a possible source of AIDS transmission when epidemiologic and immunologic criteria were used.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jaffe, H W -- Francis, D P -- McLane, M F -- Cabradilla, C -- Curran, J W -- Kilbourne, B W -- Lawrence, D N -- Haverkos, H W -- Spira, T J -- Dodd, R Y -- New York, N.Y. -- Science. 1984 Mar 23;223(4642):1309-12.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6322301" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/*etiology/immunology/transmission ; Adult ; Aged ; Antibodies, Viral/*analysis ; Antigens, Surface/immunology ; Antigens, Viral/immunology ; *Blood Donors ; Blood Transfusion/*adverse effects ; Deltaretrovirus/immunology/*pathogenicity ; Female ; Homosexuality ; Humans ; Male ; Middle Aged ; Retroviridae/*immunology ; Retroviridae Infections/*epidemiology ; Risk
    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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    Blood pressure and nutrient intake in the United States (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-06-29
    Description: A data base of the National Center for Health Statistics, Health and Nutrition Examination Survey I (HANES I), was used to perform a computer-assisted, comprehensive analysis of the relation of 17 nutrients to the blood pressure profile of adult Americans. Subjects were 10,372 individuals, 18 to 74 years of age, who denied a history of hypertension and intentional modification of their diet. Significant decreases in the consumption of calcium, potassium, vitamin A, and vitamin C were identified as the nutritional factors that distinguished hypertensive from normotensive subjects. Lower calcium intake was the most consistent factor in hypertensive individuals. Across the population, higher intakes of calcium, potassium, and sodium were associated with lower mean systolic blood pressure and lower absolute risk of hypertension. Increments of dietary calcium were also negatively correlated with body mass. Even though these correlations cannot be accepted as proof of causation, they have implications for future studies of the association of nutritional factors and dietary patterns with hypertension in America.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McCarron, D A -- Morris, C D -- Henry, H J -- Stanton, J L -- New York, N.Y. -- Science. 1984 Jun 29;224(4656):1392-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6729459" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Age Factors ; Aged ; Ascorbic Acid/metabolism ; *Blood Pressure/drug effects ; Calcium/metabolism ; Continental Population Groups ; Energy Intake ; Female ; Humans ; Hypertension/metabolism ; Male ; Middle Aged ; National Center for Health Statistics (U.S.) ; Nutrition Surveys ; *Nutritional Physiological Phenomena ; Obesity/metabolism ; Potassium/metabolism ; Sex Factors ; Sodium/metabolism ; United States ; Vitamin A/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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    Elevated concentrations of CSF corticotropin-releasing factor-like immunoreactivity in depressed patients (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-12-14
    Description: The possibility that hypersecretion of corticotropin-releasing factor (CRF) contributes to the hyperactivity of the hypothalamo-pituitary-adrenal axis observed in patients with major depression was investigated by measuring the concentration of this peptide in cerebrospinal fluid of normal healthy volunteers and in drug-free patients with DSM-III diagnoses of major depression, schizophrenia, or dementia. When compared to the controls and the other diagnostic groups, the patients with major depression showed significantly increased cerebrospinal fluid concentrations of CRF-like immunoreactivity; in 11 of the 23 depressed patients this immunoreactivity was greater than the highest value in the normal controls. These findings are concordant with the hypothesis that CRF hypersecretion is, at least in part, responsible for the hyperactivity of the hypothalamo-pituitary-adrenal axis characteristic of major depression.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nemeroff, C B -- Widerlov, E -- Bissette, G -- Walleus, H -- Karlsson, I -- Eklund, K -- Kilts, C D -- Loosen, P T -- Vale, W -- MH-36157/MH/NIMH NIH HHS/ -- MH-39415/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1984 Dec 14;226(4680):1342-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6334362" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Corticotropin-Releasing Hormone/*cerebrospinal fluid ; Dementia/cerebrospinal fluid ; Depressive Disorder/*cerebrospinal fluid ; Female ; Humans ; Male ; Middle Aged ; Radioimmunoassay ; Schizophrenia/cerebrospinal fluid
    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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    Estrogen-dependent Leydig cell protein recognized by monoclonal antibody to MCF-7 cell line (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-10-26
    Description: A protein (27,000 molecular weight) was previously found in rat Leydig cells after treatment with estradiol (E2) and human chorionic gonadotropin (hCG) in vitro. The effect of hCG occurred through increased E2 production. This hormone-regulated rat testicular protein was compared to an estrogen-regulated protein of similar physical characteristics isolated from a human mammary cancer cell line (MCF-7) and present in normal human estrogen target organs. The Leydig cells from rat and human tissue showed specific immunofluorescence and immunoperoxidase staining in the cytoplasm upon incubation with a monoclonal antibody (C11) to the estrogen-regulated protein from MCF-7 cells. Leydig cells after exposure to E2 or hCG showed the highest fluorescence intensity; this intensity was reduced by treatment with Tamoxifen. No reaction was associated with other testicular cells. The estrogen-regulated protein from human cell lines is therefore immunologically similar to that from the rat Leydig cell. The monoclonal antibody should be useful for further characterization of the Leydig cell protein.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ciocca, D R -- Dufau, M L -- CA 11378/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1984 Oct 26;226(4673):445-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6387908" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; *Antibodies, Monoclonal ; Breast Neoplasms/metabolism ; Cell Line ; Chorionic Gonadotropin/pharmacology ; Cross Reactions ; Estradiol/pharmacology ; Fluorescent Antibody Technique ; Humans ; Immunoenzyme Techniques ; Leydig Cells/*analysis ; Male ; Middle Aged ; Proteins/*analysis ; 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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  • 5
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    The respiratory sinus arrhythmia: a measure of cardiac age (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-06-01
    Description: A method developed for quantifying respiratory sinus arrhythmia (RSA) during voluntary cardiorespiratory synchronization relies on computer-assisted rhythmometric cosinor analysis of instantaneous heart rate data. The RSA was present in all subjects tested, even those at advanced ages. The amplitude of the RSA falls approximately 10 percent per decade. An individual with a transplanted heart and one with severe diabetic neuropathy each had resting RSA values that were normal for their ages. The shape and amplitude of the RSA during voluntary cardiorespiratory synchronization may reflect the suppleness of the heart and its response to rhythmically changing intrathoracic pressure and the subsequent ebb-and-flow of venous return. Our technology allows objective quantitative assessment of the biologic age of the heart and also the effect of any drug, disease, or behavior that affects the RSA.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hrushesky, W J -- Fader, D -- Schmitt, O -- Gilbertsen, V -- New York, N.Y. -- Science. 1984 Jun 1;224(4652):1001-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6372092" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; *Aging ; Arrhythmia, Sinus/*physiopathology ; Compliance ; Diabetic Neuropathies/physiopathology ; Female ; Heart/*physiology/physiopathology ; Heart Rate ; Heart Transplantation ; Humans ; Male ; Microcomputers ; Middle Aged ; *Respiration
    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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    Elevated beta-endorphin in cerebrospinal fluid after electrical brain stimulation: artifact of contrast infusion? (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-06-01
    Description: Beta-Endorphin-like immunoreactivity in cerebrospinal fluid was assayed in 11 patients receiving electrical stimulation of the brain for chronic pain. Immunoreactivity increased dramatically after contrast ventriculography prior to stimulation. No further elevations were observed after stimulation. The magnitude and time course of elevations were identical after placement of electrodes either in the thalamus or in the periventricular gray matter. These results suggest that previous findings of stimulation-induced elevation of beta-endorphin-like immunoreactivity in cerebrospinal fluid are attributable to an artifact of contrast ventriculography.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fessler, R G -- Brown, F D -- Rachlin, J R -- Mullan, S -- Fang, V S -- New York, N.Y. -- Science. 1984 Jun 1;224(4652):1017-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6326266" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; *Cerebral Ventriculography ; Contrast Media ; *Electronarcosis ; Endorphins/*cerebrospinal fluid ; Female ; Humans ; Male ; Middle Aged ; Pain/physiopathology ; Pain Management ; Radioimmunoassay ; beta-Endorphin
    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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    Common region on chromosome 14 in T-cell leukemia and lymphoma (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-12-21
    Description: Chromosome 14 breakpoints in malignant human lymphocytes cluster on the long (q) arm near bands q11 and q32. An inversion of chromosome 14 due to breaks in q11.2 and q32.3 has now been found in a newly established childhood T-cell lymphoma cell line and confirmed in T-cell chronic lymphocytic leukemia. A translocation was also found between chromosomes 10 and 14 with a breakpoint at 14q11.2 in another T-cell lymphoma cell line. It is proposed that a proximal region on chromosome 14 in or near sub-band q11.2 is related to T-cell function. Rearrangements in this region may affect the growth of T lymphocytes and be involved in the development of T-cell malignancies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hecht, F -- Morgan, R -- Hecht, B K -- Smith, S D -- 25055/PHS HHS/ -- New York, N.Y. -- Science. 1984 Dec 21;226(4681):1445-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6438800" target="_blank"〉PubMed〈/a〉
    Keywords: Cell Line ; *Chromosome Aberrations ; Humans ; Immunoglobulin Heavy Chains/genetics ; Leukemia, Lymphoid/*genetics ; Lymphoma/*genetics ; Male ; Middle Aged ; T-Lymphocytes ; Translocation, Genetic
    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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