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  • Articles  (236)
  • Adult  (236)
  • American Association for the Advancement of Science (AAAS)  (236)
  • American Association of Petroleum Geologists (AAPG)
  • American Institute of Physics (AIP)
  • Wiley
  • 1985-1989  (87)
  • 1980-1984  (149)
  • 1955-1959
Collection
  • Articles  (236)
Publisher
  • American Association for the Advancement of Science (AAAS)  (236)
  • American Association of Petroleum Geologists (AAPG)
  • American Institute of Physics (AIP)
  • Wiley
  • Springer  (4)
Years
Year
  • 1
    Publication Date: 1989-06-16
    Description: Secretory chloride channels can be activated by adenosine 3',5'-monophosphate (cAMP)-dependent protein kinase in normal airway epithelial cells but not in cells from individuals with cystic fibrosis (CF). In excised, inside-out patches of apical membrane of normal human airway cells and airway cells from three patients with CF, the chloride channels exhibited a characteristic outwardly rectifying current-voltage relation and depolarization-induced activation. Channels from normal tissues were activated by both cAMP-dependent protein kinase and protein kinase C. However, chloride channels from CF patients could not be activated by either kinase. Thus, gating of normal epithelial chloride channels is regulated by both cAMP-dependent protein kinase and protein kinase C, and regulation by both kinases is defective in CF.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hwang, T C -- Lu, L -- Zeitlin, P L -- Gruenert, D C -- Huganir, R -- Guggino, W B -- 1-K08-HL02188/HL/NHLBI NIH HHS/ -- R01-DK 39619/DK/NIDDK NIH HHS/ -- R01-HL 40178/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1989 Jun 16;244(4910):1351-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Physiology, Johns Hopkins University, Baltimore, MD 21205.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2472005" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Chloride Channels ; Chlorides/*physiology ; Cystic Fibrosis/*physiopathology ; Electrophysiology ; Fetus ; Humans ; In Vitro Techniques ; Ion Channels/*physiology ; Membrane Proteins/*physiology ; Protein Kinase C/*physiology ; Protein Kinases/*physiology ; Respiratory System/cytology/physiopathology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1989-09-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1989 Sep 15;245(4923):1185.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2781278" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Bone and Bones/*analysis/anatomy & histology ; Female ; *Forensic Medicine ; *Fossils ; Humans ; Infant ; Male ; *Paleontology
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  • 3
    Publication Date: 1989-01-27
    Description: Techniques of gene amplification, molecular cloning, and sequence analysis were used to test for the presence of sequences related to human T-lymphotropic virus type I (HTLV-I) in peripheral blood mononuclear cells of six patients with multiple sclerosis (MS) and 20 normal individuals. HTLV-I sequences were detected in all six MS patients and in one individual from the control group by DNA blot analysis and molecular cloning of amplified DNAs. The viral sequence in MS patients were associated with adherent cell populations consisting predominantly of monocytes and macrophages. Molecular cloning and nucleotide sequence analysis indicated that these amplified viral sequences were related to the HTLV-I proviral genome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Reddy, E P -- Sandberg-Wollheim, M -- Mettus, R V -- Ray, P E -- DeFreitas, E -- Koprowski, H -- CA-10815/CA/NCI NIH HHS/ -- NS-11036/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1989 Jan 27;243(4890):529-33.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wistar Institute of Anatomy and Biology, Philadelphia, PA 19104.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2536193" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Base Sequence ; Child ; *Cloning, Molecular ; DNA Restriction Enzymes ; DNA, Viral/*genetics ; Female ; *Gene Amplification ; Human T-lymphotropic virus 1/*genetics ; Humans ; Leukocytes, Mononuclear/analysis/microbiology ; Macrophages/analysis/microbiology ; Male ; Molecular Sequence Data ; Multiple Sclerosis/*microbiology ; Nucleic Acid Hybridization ; Oligonucleotide Probes
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1989-10-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Frisch, R E -- New York, N.Y. -- Science. 1989 Oct 27;246(4929):432.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2814472" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Body Weight/*physiology ; Cricetinae ; Female ; Fertility/*physiology ; Humans ; Mesocricetus
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  • 5
    Publication Date: 1989-08-25
    Description: Blue cone monochromacy is a rare X-linked disorder of color vision characterized by the absence of both red and green cone sensitivities. In 12 of 12 families carrying this trait, alterations are observed in the red and green visual pigment gene cluster. The alterations fall into two classes. One class arose from the wild type by a two-step pathway consisting of unequal homologous recombination and point mutation. The second class arose by nonhomologous deletion of genomic DNA adjacent to the red and green pigment gene cluster. These deletions define a 579-base pair region that is located 4 kilobases upstream of the red pigment gene and 43 kilobases upstream of the nearest green pigment gene; this 579-base pair region is essential for the activity of both pigment genes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nathans, J -- Davenport, C M -- Maumenee, I H -- Lewis, R A -- Hejtmancik, J F -- Litt, M -- Lovrien, E -- Weleber, R -- Bachynski, B -- Zwas, F -- New York, N.Y. -- Science. 1989 Aug 25;245(4920):831-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology and Genetics, Wilmer Ophthalmologic Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2788922" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Base Sequence ; Child ; Child, Preschool ; Chromosome Deletion ; Color Vision Defects/*genetics ; DNA/analysis ; Female ; Humans ; Male ; Molecular Sequence Data ; Mutation ; Nucleic Acid Hybridization ; Retinal Pigments/genetics ; Thalassemia/genetics ; X Chromosome
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  • 6
    Publication Date: 1989-07-28
    Description: The purine analog 2',3'-dideoxyinosine (ddI), which has anti-retroviral activity in vitro was administered for up to 42 weeks to 26 patients with acquired immunodeficiency syndrome (AIDS) or severe AIDS-related complex (ARC). Ten of these individuals were AZT-intolerant. Eight dose regimens were studied. The drug was orally bioavailable and penetrated into the cerebrospinal fluid (CSF). Comparatively little evidence of an effect against human immunodeficiency virus (HIV) was seen at the lowest four doses. However, patients in the four highest dose groups (ddI at 1.6 milligrams per kilogram intravenously and then greater than or equal to 3.2 milligrams per kilogram orally at least every 12 hours or higher) had increases in their circulating CD4+ T cells (P less than 0.0005), increased CD4/CD8 T cell ratios (P less than 0.01), and, where evaluable, more than an 80% decrease in serum HIV p24 antigen (P less than 0.05). The patients also had evidence of improved immunologic function, had reduced viremic symptomatology, and gained a mean of 1.6 kilogram with these comparatively infrequent dosing schedules (every 8 or 12 hours). The most notable adverse effects directly attributable to ddI administration at the doses used in this study included increases in serum uric acid (due to hypoxanthine release) and mild headaches and insomnia. These results suggest that serious short-term toxicity at therapeutic doses is not an inherent feature in the profile of agents with clinical anti-HIV activity. Further controlled studies to define the safety and efficacy of this agent may be worth considering.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yarchoan, R -- Mitsuya, H -- Thomas, R V -- Pluda, J M -- Hartman, N R -- Perno, C F -- Marczyk, K S -- Allain, J P -- Johns, D G -- Broder, S -- New York, N.Y. -- Science. 1989 Jul 28;245(4916):412-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Clinical Oncology Program, National Cancer Institute, Bethesda, MD 20892.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2502840" target="_blank"〉PubMed〈/a〉
    Keywords: AIDS-Related Complex/*drug therapy/immunology ; Acquired Immunodeficiency Syndrome/*drug therapy/immunology ; Adult ; Antiviral Agents/adverse effects/cerebrospinal fluid/pharmacology/*therapeutic ; use ; Biological Availability ; Clinical Trials as Topic ; Didanosine ; Dideoxynucleosides/adverse effects/cerebrospinal fluid/pharmacology/*therapeutic ; use ; Dose-Response Relationship, Drug ; Female ; HIV/*drug effects ; HIV Antigens/analysis ; HIV Core Protein p24 ; Humans ; Hypersensitivity, Delayed ; Immunity, Cellular ; Leukocyte Count ; Male ; Middle Aged ; Molecular Structure ; Retroviridae Proteins/analysis ; T-Lymphocytes/immunology
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  • 7
    Publication Date: 1989-04-07
    Description: Low-density lipoprotein (LDL) concentrations correlate with risk of coronary heart disease, and genetic variation affecting LDL levels influences atherosclerosis susceptibility. The principal LDL protein is apolipoprotein B (apoB); apoB is not exchangeable between lipoprotein particles and there is only one apoB per LDL particle. Plasma LDL therefore consists of two populations, one containing apoB derived from the maternal and one from the paternal apoB alleles. Products of the apob gene with high or low affinity for the MB-19 monoclonal antibody can be distinguished, and this antibody was used to identify heterozygotes with allele-specific differences in the amount of apoB in their plasma. A family study confirmed that the unequal expression phenotype was inherited in an autosomal dominant manner and was linked to the apob gene locus. Significant apoB genetic variation affecting plasma LDL levels may be more common than previously appreciated.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gavish, D -- Brinton, E A -- Breslow, J L -- HL32435/HL/NHLBI NIH HHS/ -- HL33714/HL/NHLBI NIH HHS/ -- HL36461/HL/NHLBI NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1989 Apr 7;244(4900):72-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Rockefeller University, New York 10021.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2565046" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; *Alleles ; Apolipoproteins B/blood/*genetics ; Binding Sites, Antibody ; Child ; Child, Preschool ; Genetic Linkage ; Genotype ; Humans ; Lipoproteins, LDL/blood/*genetics ; Pedigree ; Phenotype ; Polymorphism, Restriction Fragment Length
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  • 8
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1989-11-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 1989 Nov 10;246(4931):821-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2683085" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Base Sequence ; DNA, Viral/*analysis/genetics ; Gene Products, env/genetics ; Gene Products, gag/genetics ; Gene Products, pol/genetics ; HTLV-I Infections/*complications ; Human T-lymphotropic virus 1/genetics/*isolation & purification ; Humans ; Middle Aged ; Molecular Sequence Data ; Multiple Sclerosis/complications/*microbiology ; Polymerase Chain Reaction
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  • 9
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1989-01-20
    Description: The prevalence and patterns of same-gender sexual contact among men are key components of models of the spread of HIV infection and AIDS in the U.S. population. Previous estimates by Kinsey et al. from data collected between 1938 and 1948 have been widely criticized for inadequacies of sample design. New lower-bound estimates of prevalence developed from data from a national sample survey conducted in 1970 indicate that minimums of 20.3 percent of adult men in the United States in 1970 had sexual contact to orgasm with another man at some time in life; 6.7 percent had such contact after age 19; and between 1.6 and 2.0 percent had such contact within the previous year. Although these estimates incorporate adjustments for missing data, the likelihood of underreporting suggests that these estimates might be lower bounds on the prevalence of same-gender sex among men. Two sets of alternative estimates are derived to assess the sensitivity of these estimates to the assumptions made in imputing values to missing data. Detailed estimates are presented by frequency of contact, age, education, and marital status; and supporting estimates are derived from a 1988 national survey. Data from both the 1970 and 1988 surveys indicate that never-married men are more likely than other men to have had same-gender sexual contacts within the last year. The 1970 survey also indicates, however, that approximately half the men estimated to have such contacts are found among the more numerous population of currently or previously married men.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fay, R E -- Turner, C F -- Klassen, A D -- Gagnon, J H -- New York, N.Y. -- Science. 1989 Jan 20;243(4889):338-48.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Committee on AIDS Research, National Academy of Sciences, Washington, DC 20418.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2911744" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Educational Status ; Homosexuality/*statistics & numerical data ; Humans ; Male ; Marriage ; Middle Aged ; Surveys and Questionnaires ; United States
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  • 10
    Publication Date: 1989-06-16
    Description: The response of the human circadian pacemaker to light was measured in 45 resetting trials. Each trial consisted of an initial endogenous circadian phase assessment, a three-cycle stimulus which included 5 hours of bright light per cycle, and a final phase assessment. The stimulus induced strong (type 0) resetting, with responses highly dependent on the initial circadian phase of light exposure. The magnitude and direction of the phase shifts were modulated by the timing of exposure to ordinary room light, previously thought to be undetectable by the human pacemaker. The data indicate that the sensitivity of the human circadian pacemaker to light is far greater than previously recognized and have important implications for the therapeutic use of light in the management of disorders of circadian regulation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Czeisler, C A -- Kronauer, R E -- Allan, J S -- Duffy, J F -- Jewett, M E -- Brown, E N -- Ronda, J M -- 1-RO1-AG06072/AG/NIA NIH HHS/ -- 2-S07-RR-05950/RR/NCRR NIH HHS/ -- 5-M01-RR00888/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1989 Jun 16;244(4910):1328-33.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Boston, MA 02115.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2734611" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Circadian Rhythm ; Humans ; Male ; Models, Biological ; *Phototherapy ; Time Factors
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  • 11
    Publication Date: 1988-04-29
    Description: Screening for human T-lymphotropic virus type I (HTLV-I) antibodies was performed on sera from 39,898 blood donors at eight blood centers in geographically distinct areas of the United States. Ten donors (0.025 percent) showed evidence of HTLV-I seropositivity by enzyme immunoassays; this was confirmed by protein immunoblot and radioimmunoprecipitation. Seroprevalence rates ranged from 0 to 0.10 percent at the locations sampled, with HTLV-I antibodies found predominantly in donors from the southeastern and southwestern United States. Matched case-control interviews and laboratory studies were performed on five seropositive women and two seropositive men who participated in an identity-linked collection of sera from a subset of 33,893 donors at six of the eight blood centers. Four of the women and both men are black; one woman is Caucasian. Four of the seven seropositive individuals admitted to prior intravenous drug abuse or sexual contact with an intravenous drug user. Sexual contact with native inhabitants of an HTLV-I endemic area was the only identified risk factor for one male. The distribution of HTLV-I antibodies in this U.S. blood donor sample corroborates the previously reported epidemiology of this agent and suggests that additional donor screening measures, including the testing of donated blood for HTLV-I markers, may be necessary to prevent the spread of HTLV-I to transfusion recipients.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Williams, A E -- Fang, C T -- Slamon, D J -- Poiesz, B J -- Sandler, S G -- Darr, W F 2nd -- Shulman, G -- McGowan, E I -- Douglas, D K -- Bowman, R J -- New York, N.Y. -- Science. 1988 Apr 29;240(4852):643-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉American Red Cross Jerome H. Holland Laboratory, Rockville, MD 20855.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2896386" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Antibodies, Viral/*analysis ; *Blood Donors ; Deltaretrovirus/*immunology/isolation & purification ; Deltaretrovirus Infections/diagnosis/*epidemiology/transmission ; Female ; Humans ; Immunoenzyme Techniques ; Immunosorbent Techniques ; Japan ; Male ; Middle Aged ; Risk Factors ; Sexual Partners ; Substance-Related Disorders ; United States
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  • 12
    Publication Date: 1988-05-06
    Description: A point mutation in the human insulin receptor gene in a patient with type A insulin resistance alters the amino acid sequence within the tetrabasic processing site of the proreceptor molecule from Arg-Lys-Arg-Arg to Arg-Lys-Arg-Ser. Epstein-Barr virus-transformed lymphocytes from this patient synthesize an insulin receptor precursor that is normally glycosylated and inserted into the plasma membrane but is not cleaved to mature alpha and beta subunits. Insulin binding to these cells is severely reduced but can be increased about fivefold by gentle treatment with trypsin, accompanied by the appearance of normal alpha subunits. These results indicate that proteolysis of the proreceptor is necessary for its normal full insulin-binding sensitivity and signal-transducing activity and that a cellular protease that is more stringent in its specificity than trypsin is required to process the receptor precursor.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yoshimasa, Y -- Seino, S -- Whittaker, J -- Kakehi, T -- Kosaki, A -- Kuzuya, H -- Imura, H -- Bell, G I -- Steiner, D F -- AM 13914/AM/NIADDK NIH HHS/ -- AM 20595/AM/NIADDK NIH HHS/ -- New York, N.Y. -- Science. 1988 May 6;240(4853):784-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Molecular Biology, University of Chicago, IL 60637.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3283938" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Amino Acid Sequence ; Cell Membrane/metabolism ; Cells, Cultured ; DNA/genetics ; Diabetes Mellitus/*genetics/metabolism ; Female ; Glycosylation ; Humans ; Insulin/metabolism ; Insulin Resistance/*genetics ; Lymphocytes/metabolism ; Molecular Sequence Data ; Mutation ; Nucleic Acid Hybridization ; Protein Precursors/*genetics/metabolism ; RNA, Messenger/metabolism ; Receptor, Insulin/*genetics/metabolism ; Trypsin/metabolism
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  • 13
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1988-04-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roberts, L -- New York, N.Y. -- Science. 1988 Apr 1;240(4848):27.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3353707" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; China ; *Diet ; Diet Surveys ; Female ; *Health ; Humans ; Male ; Middle Aged ; Neoplasms/epidemiology
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  • 14
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1988-01-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roberts, L -- New York, N.Y. -- Science. 1988 Jan 29;239(4839):457.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3340829" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Aging/*physiology ; Humans ; Middle Aged ; Skin Diseases/*drug therapy/etiology ; Sunlight/*adverse effects ; Tretinoin/adverse effects/*therapeutic use
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  • 15
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1988-02-05
    Description: The epidemic of infection with the human immunodeficiency virus (HIV) and the acquired immunodeficiency syndrome (AIDS) poses a major ethical question: How can we control the epidemic and the harm that it causes without unjustly discriminating against particular social groups and without unnecessarily infringing on the freedom of individuals? This question pertains to three spheres of public policy in the United States: public health, the delivery of health care, and research. In the public health sphere, vigorous educational efforts will be required, as will modified approaches to intravenous drug use, prostitution, and homosexual and bisexual sexual activity. Carefully targeted, voluntary testing and screening programs should be coupled with counseling and with guarantees of confidentiality and nondiscrimination where these are appropriate. Both health care workers and the health care system have a moral obligation to provide care to people with HIV infection, but heroic self-sacrifice should not be required provided that infection control precautions are observed. Patients with neurological involvement and terminally ill patients will benefit from statutes allowing recognition of advance directives about preferred modes of care or nontreatment. There is a moral imperative to perform intensive research directed toward the understanding, treatment, and prevention of HIV infection and AIDS. The research process will raise challenging ethical questions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Walters, L -- New York, N.Y. -- Science. 1988 Feb 5;239(4840):597-603.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Bioethics, Kennedy Institute of Ethics, Washington, DC 20057.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3340846" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/*prevention & control/therapy ; Adult ; Beneficence ; Biomedical Research ; Bisexuality ; Brain Diseases ; Delivery of Health Care ; *Ethics, Medical ; Female ; Government Regulation ; Health Education ; Health Policy ; Homosexuality ; Humans ; Male ; Mandatory Programs ; *Moral Obligations ; Personal Autonomy ; Resource Allocation ; Risk Assessment ; Social Justice ; Substance-Related Disorders ; United States ; *Voluntary Programs
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  • 16
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1988-03-11
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bloom, M -- New York, N.Y. -- Science. 1988 Mar 11;239(4845):1235-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3344431" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; American Medical Association ; *Editorial Policies ; Ethicists ; *Ethics, Medical ; *Euthanasia ; *Euthanasia, Active ; Euthanasia, Active, Voluntary ; Female ; Humans ; Morphine ; Ovarian Neoplasms/physiopathology ; Pain, Intractable/physiopathology ; *Periodicals as Topic ; United States
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  • 17
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1988-12-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barnes, D M -- New York, N.Y. -- Science. 1988 Dec 16;242(4885):1509.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3201238" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Estrogens/*physiology ; Female ; Humans ; Menstrual Cycle ; Progesterone/*physiology ; *Task Performance and Analysis
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  • 18
    Publication Date: 1988-02-05
    Description: By the end of 1987, nearly 50,000 cases of acquired immunodeficiency syndrome (AIDS) had been reported since 1981, 20,745 in the past year alone. Black and Hispanic adults and children have reported rates 3 to 12 times as high as whites. This can be largely attributed to higher reported rates in black and Hispanic intravenous (IV) drug abusers, their sex partners, and infants. In 1986, reported AIDS deaths increased adult male and female mortality in the United States by an estimated 0.7 and 0.07%, respectively, with much greater increases in selected age groups or areas of the country. The greatest variation in infection with the human immunodeficiency virus (HIV) (0 to 70%) has been found in surveys of IV drug abusers, while surveys of homosexual men reveal infection rates of 20 to 50%. Infection with HIV ranged from 0 to 2.6% in limited sexually transmitted disease clinic surveys of heterosexual men and women without a history of IV drug abuse or known sexual contact with persons at increased risk. The modes of HIV transmission are now well understood, but a large amount of biologic variability in efficiency of transmission remains to be explained. The period between initial infection with HIV and the development of AIDS is variable, but the risk for disease progression increases with duration of infection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Curran, J W -- Jaffe, H W -- Hardy, A M -- Morgan, W M -- Selik, R M -- Dondero, T J -- New York, N.Y. -- Science. 1988 Feb 5;239(4840):610-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉AIDS Program, Centers for Disease Control, Atlanta, Georgia 30333.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3340847" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/*epidemiology/mortality ; Adult ; Child ; Continental Population Groups ; Ethnic Groups ; Female ; HIV Seropositivity ; Humans ; Male ; Risk Factors ; United States
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  • 19
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1988-01-29
    Description: A central question in the debate about the effects of welfare programs is whether their intended positive results--providing needed resources to recipients and their children--outweigh any unintended negative results--for example, the breaking up of families, reduction in work effort, or the fostering of a welfare "culture" that is passed on from parent to child. Recent research shows that although work effort is affected adversely by the generosity of welfare programs, effects on family structure appear quite weak, most welfare experiences are relatively short, and the majority of women who grew up in homes heavily dependent on welfare do not rely on those programs when they are young adults.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Duncan, G J -- Hill, M S -- Hoffman, S D -- New York, N.Y. -- Science. 1988 Jan 29;239(4839):467-71.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Social Research, University of Michigan, Ann Arbor 48106.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3277267" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Attitude ; Behavior ; Child ; *Dependency (Psychology) ; Family ; Female ; Humans ; *Personality ; Poverty ; *Public Assistance ; United States
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  • 20
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-10-09
    Description: In sharp contrast with the experiences of all other industrialized nations, the size of the labor force of the United States is growing rapidly while, simultaneously, its age, gender, and ethnic composition are changing markedly. Consequently, human resource issues present an unprecedented challenge in the nation's quest to achieve a fully employed and equitable society. New public policies that focus on labor market adjustment policies will be required if these developments are to be a boon rather than a bane to the emerging postindustrial economy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Briggs, V M Jr -- New York, N.Y. -- Science. 1987 Oct 9;238(4824):176-80.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉New York State School of Industrial and Labor Relations, Cornell University, Ithaca 14851.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3659908" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Age Factors ; Australia ; Canada ; Emigration and Immigration ; *Employment ; Europe ; Female ; Humans ; Japan ; Male ; *Population ; Unemployment ; United States
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  • 21
    Publication Date: 1987-03-27
    Description: Myotonic muscular dystrophy (DM) is the most common muscular dystrophy, affecting adults as well as children. It is inherited as an autosomal dominant trait and is characterized by variable expressivity and late age-of-onset. Linkage studies have established the locus on chromosome 19. In order to identify tightly linked probes for diagnosis as well as to define in detail the DM gene region, chromosome 19 libraries were constructed and screened for restriction fragment length polymorphisms tightly linked to DM. A genomic clone, LDR152 (D19S19), was isolated that is tightly linked to DM; recombination fraction = 0.0 (95% confidence limits 0.0-0.03); lod score, 15.4.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bartlett, R J -- Pericak-Vance, M A -- Yamaoka, L -- Gilbert, J -- Herbstreith, M -- Hung, W Y -- Lee, J E -- Mohandas, T -- Bruns, G -- Laberge, C -- NS19999/NS/NINDS NIH HHS/ -- RR-30/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1987 Mar 27;235(4796):1648-50.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3029876" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Autoradiography ; Child ; Chromosome Mapping ; Chromosomes, Human, Pair 19 ; DNA Restriction Enzymes/metabolism ; Genetic Linkage ; Humans ; Muscular Dystrophies/*diagnosis/genetics ; Pedigree ; Polymorphism, Genetic
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  • 22
    Publication Date: 1987-05-15
    Description: A new human T-lymphotropic virus (HTLV-4) was recently described in healthy people from Senegal. This virus has many properties in common with members of the human T-lymphotropic viruses, particularly the human immunodeficiency virus or HIV, the etiologic agent of acquired immune deficiency syndrome (AIDS), but does not appear to be associated with immunodeficiency-related disorders. In the present study, serum samples were obtained from 4248 individuals from six West African countries, including Senegal, Guinea, Guinea Bissau, Mauritania, Burkina Faso, and Ivory Coast. These samples, collected during 1985-1987, were from people categorized as healthy control, sexually active risk, and disease populations. All samples were analyzed for reactivity to HTLV-4 and HIV by radioimmunoprecipitation-sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotting. Evidence for HTLV-4 infection was found in five of the six countries. The seroprevalence varied markedly from country to country. Healthy sexually active individuals in the risk category had the highest levels of HTLV-4 infection compared to individuals in the healthy control category and the disease category, the latter including AIDS patients. The seroprevalence of HIV infection in most of these countries was quite low, although tightly associated with the rare cases of AIDS. The biology of HTLV-4 infection thus differs from that of HIV in Central Africa or the United States and Europe. The presence of these viruses and their different pathogenicities in several countries of West Africa indicate the necessity for serologic assays that will distinguish between them. Further studies of their origin and distribution as well as of their biology will be important in advancing our understanding of AIDS.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kanki, P J -- M'Boup, S -- Ricard, D -- Barin, F -- Denis, F -- Boye, C -- Sangare, L -- Travers, K -- Albaum, M -- Marlink, R -- CA 18216/CA/NCI NIH HHS/ -- CA 37466/CA/NCI NIH HHS/ -- FOD 630/OD/NIH HHS/ -- New York, N.Y. -- Science. 1987 May 15;236(4803):827-31.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3033826" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/epidemiology ; Adult ; Africa, Western ; Deltaretrovirus/*isolation & purification ; Demography ; Female ; HIV/*isolation & purification ; Humans ; Inpatients ; Male ; Pregnancy ; Prisoners ; Prostitution ; Reference Values ; Risk
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  • 23
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-08-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lewin, R -- New York, N.Y. -- Science. 1987 Aug 28;237(4818):978.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3616630" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Age Factors ; Aged ; Humans ; Middle Aged ; Parkinson Disease/*etiology
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  • 24
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-12-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Olson, R E -- New York, N.Y. -- Science. 1987 Dec 18;238(4834):1635.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3685999" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Cholesterol, Dietary ; Dietary Fats ; Humans ; National Institutes of Health (U.S.) ; United States
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  • 25
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-10-30
    Description: The progressive deposition in the human brain of amyloid filaments composed of the amyloid beta protein is a principal feature of Alzheimer's disease (AD). Densitometric analysis of Southern blots probed with a complementary DNA for the amyloid protein has been carried out to determine the relative dosage of this gene in genomic DNA of 14 patients with AD, 12 aged normal subjects, and 10 patients with trisomy 21 (Down syndrome). Whereas patients in the last group showed the expected 1.5-fold increase in dosage of this gene, none of the patients with AD had a gene dosage higher than that of the normal controls. These results do not support the hypothesis that the genetic defect in AD involves duplication of a segment of chromosome 21 containing the amyloid gene. Alternative mechanisms for the brain-specific increase in amyloid protein deposition in AD should be considered.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Podlisny, M B -- Lee, G -- Selkoe, D J -- AGO2741/AG/NIA NIH HHS/ -- AGO6173/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 1987 Oct 30;238(4827):669-71.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurology, Harvard Medical School, Boston, MA 02115.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2960019" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Aged, 80 and over ; Alzheimer Disease/*genetics ; Amyloid/*genetics ; Amyloid beta-Peptides ; Chromosomes, Human, Pair 21 ; DNA/genetics ; Down Syndrome/genetics ; Genes ; Humans ; Leukocytes/physiology
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  • 26
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-07-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roberts, L -- New York, N.Y. -- Science. 1987 Jul 3;237(4810):28-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3603009" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Arteriosclerosis/*therapy ; Cholesterol/*adverse effects ; Colestipol/therapeutic use ; Dietary Fats/adverse effects ; Humans ; Male ; Middle Aged ; Niacin/therapeutic use
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  • 27
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-05-29
    Description: The development of the cerebral hemispheres was assessed by using measures of electroencephalographic coherence and phase in 577 children ranging in age from 2 months to early adulthood. Two categories of age-dependent change in electroencephalographic coherence and phase were noted: continuous growth processes that were described best by an exponential growth function, and discrete growth spurts that appeared in specific anatomical locations at specific postnatal periods. The left and right hemispheres developed at different rates and with different postnatal onset times with the timing of growth spurts overlapping the timing of the major developmental stages described by Piaget.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Thatcher, R W -- Walker, R A -- Giudice, S -- RR08079-0951/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1987 May 29;236(4805):1110-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3576224" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Age Factors ; Brain/*growth & development ; Child ; Child, Preschool ; Electroencephalography ; Functional Laterality ; Humans ; Infant ; Intelligence
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  • 28
    Publication Date: 1987-01-23
    Description: The regional distributions of monoamine oxidase (MAO) types A and B have been identified in human brain in vivo with intravenously injected 11C-labeled suicide enzyme inactivators, clorgyline and L-deprenyl, and positron emission tomography. The rapid brain uptake and retention of radioactivity for both 11C tracers indicated irreversible trapping. The anatomical distribution of 11C paralleled the distribution of MAO A and MAO B in human brain in autopsy material. The corpus striatum, thalamus, and brainstem contained high MAO activity. The magnitudes of uptake of both [11C]clorgyline and L-[11C]deprenyl were markedly reduced in one subject treated with the antidepressant MAO inhibitor phenelzine. A comparison of the brain uptake and retention of the 11C-labeled inactive (D-) and active (L-) enantiomers of deprenyl showed rapid clearance of the inactive enantiomer and retention of the active enantiomer within MAO B-rich brain structures, in agreement with the known stereoselectivity of MAO B for L-deprenyl. Prior treatment with unlabeled L-deprenyl prevented retention of L-[11C]deprenyl. Thus, suicide enzyme inactivators labeled with positron emitters can be used to quantitate the distribution and kinetic characteristics of MAO in human brain structures.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fowler, J S -- MacGregor, R R -- Wolf, A P -- Arnett, C D -- Dewey, S L -- Schlyer, D -- Christman, D -- Logan, J -- Smith, M -- Sachs, H -- NS-15638/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1987 Jan 23;235(4787):481-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3099392" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Aged, 80 and over ; Brain/*enzymology ; Brain Stem/enzymology ; Cerebral Cortex/enzymology ; Clorgyline ; Corpus Striatum/enzymology ; Humans ; Monoamine Oxidase/*metabolism ; Selegiline ; Thalamus/enzymology ; Tomography, Emission-Computed
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  • 29
    Publication Date: 1987-01-30
    Description: In seven right-handed adults, the brain electrical patterns before accurate performance differed from the patterns before inaccurate performance. Activity overlying the left frontal cortex and the motor and parietal cortices contralateral to the performing hand preceded accurate left- or right-hand performance. Additional strong activity overlying midline motor and premotor cortices preceded left-hand performance. These measurements suggest that brief, spatially distributed neural activity patterns, or "preparatory sets," in distinct cognitive, somesthetic-motor, and integrative motor areas of the human brain may be essential precursors of accurate visuomotor performance.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gevins, A S -- Morgan, N H -- Bressler, S L -- Cutillo, B A -- White, R M -- Illes, J -- Greer, D S -- Doyle, J C -- Zeitlin, G M -- New York, N.Y. -- Science. 1987 Jan 30;235(4788):580-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3810158" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Cerebral Cortex/*physiology ; Cognition/physiology ; Electroencephalography ; Electrophysiology ; Functional Laterality ; Humans ; Male ; Motor Activity/physiology ; Time Factors ; Visual Perception/physiology
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  • 30
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-11-06
    Description: Diversification of the antibody repertoire in mammals results from a series of apparently random somatically propagated gene rearrangement and mutational events. Nevertheless, it is well known that the adult repertoire of antibody specificities is acquired in a developmentally programmed fashion. As previously shown, rearrangement of the gene segments encoding the heavy-chain variable regions (VH) of mouse antibodies is also developmentally ordered: the number of VH gene segments rearranged in B lymphocytes of fetal mice is small but increased progressively after birth. In this report, human fetal B-lineage cells were also shown to rearrange a highly restricted set of VH gene segments. In a sample of heavy-chain transcripts from a 130-day human fetus the most frequently expressed human VH element proved to be closely related to the VH element most frequently expressed in murine fetal B-lineage cells. These observations are important in understanding the development of immunocompetence.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schroeder, H W Jr -- Hillson, J L -- Perlmutter, R M -- AI07470/AI/NIAID NIH HHS/ -- GM07454/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1987 Nov 6;238(4828):791-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, University of Washington, Seattle 98195.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3118465" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Amino Acid Sequence ; Animals ; B-Lymphocytes/immunology ; Base Sequence ; Fetus ; *Genes, Immunoglobulin ; Humans ; Immunoglobulin Heavy Chains/genetics ; Immunoglobulin Variable Region/genetics ; Mice ; Molecular Sequence Data ; Mutation ; Sequence Homology, Nucleic Acid
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  • 31
    Publication Date: 1987-03-13
    Description: With the recently cloned complementary DNA probe, lambda Am4 for the chromosome 21 gene encoding brain amyloid polypeptide (beta amyloid protein) of Alzheimer's disease, leukocyte DNA from three patients with sporadic Alzheimer's disease and two patients with karyotypically normal Down syndrome was found to contain three copies of this gene. Because a small region of chromosome 21 containing the ets-2 gene is duplicated in patients with Alzheimer's disease, as well as in karyotypically normal Down syndrome, duplication of a subsection of the critical segment of chromosome 21 that is duplicated in Down syndrome may be the genetic defect in Alzheimer's disease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Delabar, J M -- Goldgaber, D -- Lamour, Y -- Nicole, A -- Huret, J L -- de Grouchy, J -- Brown, P -- Gajdusek, D C -- Sinet, P M -- New York, N.Y. -- Science. 1987 Mar 13;235(4794):1390-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2950593" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Alzheimer Disease/*genetics ; Amyloid/*genetics ; *Chromosomes, Human, Pair 21 ; DNA/genetics ; Down Syndrome/*genetics ; Humans ; Leukocytes/analysis ; *Multigene Family
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  • 32
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-05-22
    Description: The American family income distribution now lies at the center of several controversies. Some observers argue that the American middle class is vanishing, but U.S. census income statistics show income inequality has not changed appreciably since 1947. A second controversy involves whether average living standards have risen or fallen since the major oil price increase of 1973-74. These controversies can be partially resolved by understanding the sharp slowdown in the growth of workers' wages which occurred after 1973 and the demographic trends which kept per capita living standards rising despite stagnant wages, including more working women and low birthrates.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Levy, F -- New York, N.Y. -- Science. 1987 May 22;236(4804):923-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3576210" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Demography ; Female ; Humans ; *Income ; Male ; Middle Aged ; Social Class ; *Socioeconomic Factors ; United States
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  • 33
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-07-10
    Description: Some components of a speech signal, when made more intense, are heard simultaneously as speech and nonspeech--a form of duplex perception. At lower intensities, the speech alone is heard. Such intensity-dependent duplexity implies the existence of a phonetic mode of perception that takes precedence over auditory modes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Whalen, D H -- Liberman, A M -- HD-01994/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1987 Jul 10;237(4811):169-71.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3603014" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Attention ; Auditory Threshold ; Female ; Hearing ; Humans ; Male ; Perception ; *Phonetics ; Speech ; Speech Discrimination Tests ; *Speech Perception
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  • 34
    Publication Date: 1987-08-07
    Description: The first human vaccines against the malaria parasite have been designed to elicit antibodies to the circumsporozoite protein of Plasmodium falciparum. However, it is not known whether any level of naturally acquired antibodies to the circumsporozoite protein can predict resistance to Plasmodium falciparum malaria. In this study, 83 adults in a malaria-endemic region of Kenya were tested for circumsporozoite antibodies and then treated for malaria. They were monitored for the development of new malaria infections for 98 days. Antibody levels, as determined by four assays in vitro, were indistinguishable between the 60 individuals who did and the 23 who did not develop parasitemia during follow-up, and there was no apparent relation between day of onset of parasitemia and level of antibodies to circumsporozoite protein. Unless immunization with sporozoite vaccines induces antibodies that are quantitatively or qualitatively superior to the circumsporozoite antibodies in these adults, it is unlikely that such antibodies will prevent infection in areas with as intense malaria transmission as western Kenya.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hoffman, S L -- Oster, C N -- Plowe, C V -- Woollett, G R -- Beier, J C -- Chulay, J D -- Wirtz, R A -- Hollingdale, M R -- Mugambi, M -- New York, N.Y. -- Science. 1987 Aug 7;237(4815):639-42.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3299709" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Antibodies/*analysis ; Antigens, Protozoan ; Antigens, Surface/*immunology ; Humans ; Kenya ; Malaria/*prevention & control ; Male ; Middle Aged ; Plasmodium falciparum/*immunology ; Prospective Studies ; *Protozoan Proteins ; Spores/immunology ; Time Factors ; *Vaccines
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  • 35
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-01-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Soloway, A H -- New York, N.Y. -- Science. 1986 Jan 31;231(4737):442.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3941905" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Child ; Drug Therapy/*standards ; *Government Agencies ; Humans ; *Patient Participation ; Social Responsibility ; United States
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  • 36
    Publication Date: 1986-12-12
    Description: When isolated adult oligodendrocytes adhere to a substratum myelinogenesis occurs. Investigation of the mechanism by which this happens indicated that the oligodendrocyte-substratum interaction activated protein kinase C-dependent phosphorylation of myelin basic protein and promoted the synthesis of myelin basic protein. In addition, when agents that activate protein kinase C (second messenger diacylglycerol or a tumor-promoting phorbol ester) were added to nonattached oligodendrocytes, they mimicked the influence of the substratum by inducing phosphorylation of myelin basic protein; and reagents that increase cellular adenosine 3', 5'-monophosphate (cyclic AMP) inhibited phosphorylation of myelin basic protein. Thus, at least in vitro, the interaction between oligodendrocytes and the substratum may mediate myelinogenic events, and phosphorylation of myelin basic protein may be an early requirement in the sequence of steps that ultimately results in myelin formation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vartanian, T -- Szuchet, S -- Dawson, G -- Campagnoni, A T -- GM-07183/GM/NIGMS NIH HHS/ -- HD-04583/HD/NICHD NIH HHS/ -- HD-06426/HD/NICHD NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1986 Dec 12;234(4782):1395-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2431483" target="_blank"〉PubMed〈/a〉
    Keywords: 1-Methyl-3-isobutylxanthine/pharmacology ; Adult ; Calcimycin/pharmacology ; Cell Adhesion ; Colforsin/pharmacology ; Cyclic AMP/metabolism ; Enzyme Activation ; Humans ; Myelin Basic Protein/*metabolism ; Neuroglia/*cytology ; Oligodendroglia/*cytology ; Phosphorylation ; Protein Kinase C/*metabolism ; Tetradecanoylphorbol Acetate/pharmacology
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  • 37
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-10-31
    Description: From the postwar high of 3.8 births per woman at the peak of the baby boom, the total fertility rate in the United States has fallen to 1.8, where it has remained unchanged for nearly a decade. This below-replacement level of fertility has, in recent decades, characterized most Western countries, some of which have shown declines to well below 1.5 births per woman. Were it not for the continued infusion of immigrants, the U.S. population, which already shows the aging characteristic of low fertility, would stop growing and begin to decline before the middle of the next century. The low fertility in the United States has been accomplished by a postponement of marriage and by the widespread use of contraception, with heavy reliance on surgical sterilization as a contraceptive method. Judging from the experience of other Western countries and from our own historical experience of two centuries of fertility decline interrupted only by the baby boom, as well as from the absence of social trends that would counteract those contributing to that decline, the prognosis is for a continued low level of fertility in the United States.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Westoff, C F -- New York, N.Y. -- Science. 1986 Oct 31;234(4776):554-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3532324" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; *Birth Rate ; Contraception/history ; Ethnic Groups ; Female ; Fertility ; Forecasting ; History, 20th Century ; Humans ; Population Dynamics ; Population Growth ; Pregnancy ; Pregnancy in Adolescence ; United States
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  • 38
    Publication Date: 1986-03-07
    Description: A sensitive radioimmunoassay for atrial natriuretic peptide was used to examine the relation between circulating atrial natriuretic peptide and cardiac filling pressure in normal human subjects, in patients with cardiovascular disease and normal cardiac filling pressure, and in patients with cardiovascular disease and elevated cardiac filling pressure with and without congestive heart failure. The present studies establish a normal range for atrial natriuretic peptide in normal human subjects. These studies also establish that elevated cardiac filling pressure is associated with increased circulating concentrations of atrial natriuretic peptide and that congestive heart failure is not characterized by a deficiency in atrial natriuretic peptide, but with its elevation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Burnett, J C Jr -- Kao, P C -- Hu, D C -- Heser, D W -- Heublein, D -- Granger, J P -- Opgenorth, T J -- Reeder, G S -- New York, N.Y. -- Science. 1986 Mar 7;231(4742):1145-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2935937" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Atrial Natriuretic Factor/*blood ; Cardiovascular Diseases/blood ; Female ; Heart Failure/*blood ; Hemodynamics ; Humans ; Male ; Middle Aged ; Radioimmunoassay
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  • 39
    Publication Date: 1986-04-25
    Description: Immunoreactive oxytocin and neurophysin were identified and measured by radioimmunoassay in human thymus extracts. Serial dilutions of extracts paralleled the appropriate standard curves. Thymus-extracted oxytocin and neurophysin eluted in the same positions as reference preparations on Sephadex G-75. Authenticity of oxytocin was confirmed by biological assay and high-performance liquid chromatography analysis. In most instances, thymus contents of oxytocin and neurophysin were far greater than those expected from known circulating concentrations and declined with increasing age. The molar ratio of oxytocin to neurophysin in thymus was similar to that found in the hypothalamo-neurohypophyseal system, which strongly suggested with the other data a local synthesis of oxytocin. These findings indicate the presence of neurohypophyseal peptides in the human thymus and further support the concept of a neuroendocrine function integrated in an immune structure.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Geenen, V -- Legros, J J -- Franchimont, P -- Baudrihaye, M -- Defresne, M P -- Boniver, J -- New York, N.Y. -- Science. 1986 Apr 25;232(4749):508-11.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3961493" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Age Factors ; Child ; Chromatography, Gel ; Chromatography, High Pressure Liquid ; Female ; Humans ; Infant, Newborn ; Male ; Middle Aged ; Myasthenia Gravis/physiopathology ; Neurophysins/*analysis/isolation & purification/physiology ; Oxytocin/*analysis/isolation & purification/physiology ; Radioimmunoassay ; Thymus Gland/*analysis/physiology/physiopathology
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  • 40
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-09-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 1986 Sep 26;233(4771):1377-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3749882" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; *Adolescent Behavior ; Adult ; *Crime ; Government Agencies ; Humans ; Middle Aged ; United States
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  • 41
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-09-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 1986 Sep 19;233(4770):1249-51.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3749875" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Female ; Humans ; *Mmpi ; Male ; United States
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  • 42
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-09-26
    Description: Direct evidence on age patterns of infecundity and sterility cannot be obtained from contemporary populations because such large fractions of couples use contraception or have been sterilized. Instead, historical data are exploited to yield upper bounds applicable to contemporary populations on the proportions sterile at each age. Examination of recent changes in sexual behavior that may increase infecundity indicates that sexually transmitted infections, the prime candidate for hypothesized rises in infertility, are unlikely to have added to infecundity to any great extent. These results imply that a woman in a monogamous union faces only moderate increases in the probability of becoming sterile (or infecund) until her late thirties. Nevertheless, it appears that recent changes in reproductive behavior were guaranteed to result in the perception that infecundity is on the rise.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Menken, J -- Trussell, J -- Larsen, U -- HD11720/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1986 Sep 26;233(4771):1389-94.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3755843" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Age Factors ; *Aging ; Female ; *Fertility ; Humans ; Infertility, Female/*epidemiology ; Infertility, Male/*epidemiology ; Male ; Marriage ; Middle Aged ; United States
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  • 43
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-11-21
    Description: Issues regarding the use of epidemiology in drug abuse research are discussed and systems for monitoring national trends and identifying risk factors are described. Data indicate a general decline in marijuana use among youth, a cohort aging effect among heroin and marijuana users, and increased prevalence and health consequences associated with cocaine use.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kozel, N J -- Adams, E H -- New York, N.Y. -- Science. 1986 Nov 21;234(4779):970-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3490691" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/complications ; Adolescent ; Adult ; Child ; Cocaine ; Epidemiologic Methods ; Female ; Heroin ; Humans ; Male ; Marijuana Abuse/epidemiology ; Population Surveillance ; Risk ; Substance-Related Disorders/*epidemiology
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  • 44
    Publication Date: 1986-01-10
    Description: Red blood cells that are infected with the malaria parasite Plasmodium falciparum express new antigens on their surface. In a study of these antigens in the erythrocytes of naturally infected children in the Gambia, an antibody-mediated agglutination assay revealed an extreme degree of antigenic diversity. Serum samples from each of ten children in the convalescent stage of malaria infection reacted with infected cells from the same child but generally not with infected cells from the other children. The Gambian children's erythrocytes also expressed shared determinants: sera from Gambian adults often reacted with the surface of infected cells from all of the children and were shown by adsorption and elution experiments to contain antibodies that recognized several isolates. Conserved determinants exposed on infected erythrocytes may be important for development of antimalarial immunity either naturally or through vaccination.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marsh, K -- Howard, R J -- New York, N.Y. -- Science. 1986 Jan 10;231(4734):150-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2417315" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Agglutination Tests ; Antigens, Protozoan/*immunology ; Child ; *Epitopes ; Erythrocytes/immunology/*parasitology ; Gambia ; Humans ; Malaria/*immunology ; Plasmodium falciparum
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  • 45
    Publication Date: 1986-05-30
    Description: An antiserum prepared against thymosin alpha 1, a hormone secreted by the thymus gland, effectively neutralized the AIDS-associated virus [HTLV-III/LAV (clone BH-10)] and blocked its replication in H9 cells. Reverse transcriptase activity and expression of the HTLV-III/LAV antigens p15 and p24 were inhibited by purified immunoglobulin G preparations of antisera to thymosin alpha 1. The antiviral activity of the antiserum was found to be due to a region of homology between thymosin alpha 1 and p17, a product of the gag gene of HTLV-III/LAV. Comparison of the primary sequences of thymosin alpha 1 and the gag protein revealed a 44% to 50% homology in an 18-amino acid region, between positions 11 and 28 on thymosin alpha 1 and 92 and 109 on the gag protein. The effectiveness of the thymosin alpha 1 antiserum and of immunoglobulin G-enriched preparations in blocking replication of HTLV-III(BH-10) in H9 cells suggests a novel approach to the development of an AIDS vaccine. A vaccine directed against the gag protein might overcome the problem of genetic drift in the envelope region of the virus and be useful against all genetic variants of HTLV-III/LAV.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sarin, P S -- Sun, D K -- Thornton, A H -- Naylor, P H -- Goldstein, A L -- CA 24974/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1986 May 30;232(4754):1135-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3010464" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/microbiology ; Adult ; Animals ; Child ; Deltaretrovirus/*drug effects/physiology ; Gene Products, gag ; Humans ; Immune Sera/immunology/*pharmacology ; Immunoglobulin G/immunology ; Rabbits/immunology ; Retroviridae Proteins/immunology ; Thymosin/*analogs & derivatives/immunology ; Virus Replication/*drug effects
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  • 46
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-08-15
    Description: The kappa opioid agonists are analgesics that seem to be free of undesired morphine-like effects. Their dysphoric actions observed with the kappa agonist cyclazocine are thought to be mediated by an action at sigma-phencyclidine receptors. The benzomorphan kappa agonist MR 2033 is inactive at sigma-phencyclidine receptors. In male subjects, the opiate-active (-)-isomer, but not the (+)-isomer, elicited dose-dependent dysphoric and psychotomimetic effects that were antagonized by naloxone. Thus, kappa opiate receptors seem to mediate psychotomimetic effects. In view of the euphorigenic properties of mu agonists, our results imply the existence of opposed opioid systems affecting emotional and perceptual experiences.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pfeiffer, A -- Brantl, V -- Herz, A -- Emrich, H M -- New York, N.Y. -- Science. 1986 Aug 15;233(4765):774-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3016896" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Anxiety ; Benzomorphans/adverse effects/*pharmacology ; Humans ; Male ; Middle Aged ; Morphinans/*pharmacology ; Naloxone/pharmacology ; Personality Tests ; Phencyclidine/pharmacology ; Receptors, Opioid/drug effects/*physiology ; Receptors, Opioid, kappa
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  • 47
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-01-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Motulsky, A G -- New York, N.Y. -- Science. 1986 Jan 10;231(4734):126-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3510453" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Arteriosclerosis/therapy ; Cholesterol/blood/metabolism ; Endocytosis ; History, 20th Century ; Humans ; Hyperlipoproteinemia Type II/genetics/therapy ; Lipoproteins/metabolism ; Male ; Middle Aged ; Mutation ; *Nobel Prize ; Receptors, LDL/genetics ; United States
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  • 48
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-11-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1986 Nov 28;234(4780):1066-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3775375" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Child ; Humans ; Tobacco Smoke Pollution/*adverse effects
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  • 49
    Publication Date: 1986-12-19
    Description: In postmortem studies of patients with schizophrenia, D2 dopamine receptors in the basal ganglia have been observed to be more numerous than in patients with no history of neurological or psychiatric disease. Because most patients with schizophrenia are treated with neuroleptic drugs that block D2 dopamine receptors in the caudate nucleus, it has been suggested that this increase in the number of receptors is a result of adaptation to these drugs rather than a biochemical abnormality intrinsic to schizophrenia. With positron emission tomography (PET), the D2 dopamine receptor density in the caudate nucleus of living human beings was measured in normal volunteers and in two groups of patients with schizophrenia--one group that had never been treated with neuroleptics and another group that had been treated with these drugs. D2 dopamine receptor densities in the caudate nucleus were higher in both groups of patients than in the normal volunteers. Thus, schizophrenia itself is associated with an increase in brain D2 dopamine receptor density.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wong, D F -- Wagner, H N Jr -- Tune, L E -- Dannals, R F -- Pearlson, G D -- Links, J M -- Tamminga, C A -- Broussolle, E P -- Ravert, H T -- Wilson, A A -- Toung, J K -- Malat, J -- Williams, J A -- O'Tuama, L A -- Snyder, S H -- Kuhar, M J -- Gjedde, A -- 1RO1 53146/PHS HHS/ -- NS15080/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1986 Dec 19;234(4783):1558-63.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2878495" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Antipsychotic Agents/*therapeutic use ; Caudate Nucleus/*metabolism ; Haloperidol/therapeutic use ; Humans ; Kinetics ; Receptors, Dopamine/*metabolism ; Receptors, Dopamine D2 ; Schizophrenia/drug therapy/*metabolism ; Spiperone/analogs & derivatives/metabolism ; Tomography, Emission-Computed
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  • 50
    Publication Date: 1986-02-21
    Description: 2-Deoxy-2[18F]fluoro-D-glucose positron emission tomography performed in human infants during development revealed progressive changes in local cerebral glucose utilization. In infants 5 weeks of age and younger, glucose utilization was highest in the sensorimotor cortex, thalamus, midbrain-brainstem, and cerebellar vermis. By 3 months, glucose metabolic activity had increased in the parietal, temporal, and occipital cortices and the basal ganglia, with subsequent increases in frontal and various association regions occurring by 8 months. These functional changes measured with positron emission tomography are in agreement with behavioral, neurophysiological, and anatomical alterations known to occur during infant development.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chugani, H T -- Phelps, M E -- 2P50-NS-02808/NS/NINDS NIH HHS/ -- 7ROI-GM-24839/GM/NIGMS NIH HHS/ -- IPOI-NS-15654/NS/NINDS NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1986 Feb 21;231(4740):840-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3945811" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Brain/growth & development/*physiology/radionuclide imaging ; Brain Stem/metabolism ; Caudate Nucleus/metabolism ; Cerebellum/metabolism ; Cerebral Cortex/metabolism ; Child, Preschool ; Deoxyglucose/analogs & derivatives/metabolism ; Fluorodeoxyglucose F18 ; Humans ; Infant ; Infant, Newborn ; Intellectual Disability/metabolism/radionuclide imaging ; Thalamus/metabolism
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  • 51
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-10-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1986 Oct 10;234(4773):127.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3749895" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Child Abuse ; Depression ; Humans ; Sex Offenses ; *Suicide
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  • 52
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-12-05
    Description: New methods were used to identify the abnormality in a patient who showed evidence of neuromuscular dysfunction on extensive clinical examination. The methods revealed that the lactate content of the patient's skeletal muscle does not decline normally after exercise and that his red cells are defective in lactate transport. These results suggest that skeletal muscle and erythrocyte membranes share the same genetic lactate transporter (or a common subunit), which is deficient in this patient. This defect may be a common cause of elevated serum creatine kinase levels, as seen in the patient described here and of unexplained episodes of rhabdomyolysis and myoglobinuria.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fishbein, W N -- New York, N.Y. -- Science. 1986 Dec 5;234(4781):1254-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3775384" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Carrier Proteins/*metabolism ; Creatine Kinase/blood ; Erythrocyte Membrane/metabolism ; Erythrocytes/analysis ; Humans ; Lactates/blood/*metabolism ; Male ; Monocarboxylic Acid Transporters ; Muscular Diseases/*metabolism ; Physical Exertion
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  • 53
    Publication Date: 1986-01-17
    Description: D2 dopamine receptors in the putamen of living human subjects were characterized by using the selective, high-affinity D2 dopamine receptor antagonist carbon-11-labeled raclopride and positron emission tomography. Experiments in four healthy men demonstrated saturability of [11C]raclopride binding to an apparently homogeneous population of sites with Hill coefficients close to unity. In the normal putamen, maximum binding ranged from 12 to 17 picomoles per cubic centimeter and dissociation constants from 3.4 to 4.7 nanomolar. Maximum binding for human putamen at autopsy was 15 picomoles per cubic centimeter. Studies of [11C]raclopride binding indicate that clinically effective doses of chemically distinct neuroleptic drugs result in 85 to 90 percent occupancy of D2 dopamine receptors in the putamen of schizophrenic patients.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Farde, L -- Hall, H -- Ehrin, E -- Sedvall, G -- New York, N.Y. -- Science. 1986 Jan 17;231(4735):258-61.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2867601" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Antipsychotic Agents/metabolism ; Benzamides/metabolism ; Brain/*metabolism ; Cerebellum/metabolism ; Humans ; Male ; Middle Aged ; Putamen/metabolism ; Raclopride ; Receptors, Dopamine/*metabolism ; Receptors, Dopamine D2 ; Rodentia ; Schizophrenia/metabolism ; *Tomography, Emission-Computed
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  • 54
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-08-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 1986 Aug 22;233(4766):839-41.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3738513" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Depressive Disorder/psychology ; Female ; Humans ; Male ; Mental Disorders/psychology ; Research ; Sex Factors ; Suicide/*prevention & control/psychology
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  • 55
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-08-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G -- New York, N.Y. -- Science. 1986 Aug 1;233(4763):519-20.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3726543" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Calcium, Dietary/*therapeutic use ; Female ; Humans ; Middle Aged ; Osteoporosis/*prevention & control
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  • 56
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-04-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G -- New York, N.Y. -- Science. 1986 Apr 4;232(4746):20-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3952499" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; *Child ; Child, Preschool ; Diet, Reducing ; Environment ; Humans ; Infant ; Obesity/etiology/*prevention & control
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  • 57
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-04-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G -- New York, N.Y. -- Science. 1986 Apr 18;232(4748):317-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2938255" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Alzheimer Disease/genetics ; Child ; Employment ; *Ethics, Medical ; Female ; Genetic Diseases, Inborn ; *Genetic Testing ; Humans ; Huntington Disease/genetics ; Insurance, Health ; Risk Assessment ; United States ; develop later in life or under certain environmental conditions raises many ; ethical concerns. Among these are the experimental nature of these tests, the age ; at which they should be offered to individuals, and the repercussions of ; disclosing test results to patients, employers, and insurance companies. At ; present, research is most advanced on the marker for Huntington's disease, and ; Massachusetts General Hospital and Johns Hopkins University Hospital soon will ; become the first institutions to offer screening for this disorder. Although ; Johns Hopkins plans to treat the results as confidential research data, many ; investigators acknowledge that it will be difficult in the future to keep the ; information from third parties. Kolata warns that now is the time to develop ; policies for handling data, before widespread genetic testing becomes a reality.
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  • 58
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1986-07-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barnes, D M -- New York, N.Y. -- Science. 1986 Jul 18;233(4761):282-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3014650" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/epidemiology/*microbiology ; Adolescent ; Adult ; Africa ; Animals ; Deltaretrovirus/pathogenicity ; Female ; Guinea Pigs ; Humans ; Male ; Military Personnel ; Rabbits ; United States
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  • 59
    Publication Date: 1986-07-18
    Description: The etiological agent of AIDS, LAV/HTLV-III, is common in Central Africa but is not endemic in other areas of that continent. A novel human retrovirus, distinct from LAV/HTLV-III, has now been isolated from two AIDS patients from West Africa. Partial characterization of this virus revealed that it has biological and morphological properties very similar to LAV but that it differs in some of its antigenic components. Although the core antigens may share some common epitopes, the West African AIDS retrovirus and LAV differ substantially in their envelope glycoproteins. The envelope antigen of the West African virus can be recognized by serum from a macaque with simian AIDS infected by the simian retrovirus termed STLV-IIImac, suggesting that the West African AIDS virus may be more closely related to this simian virus than to LAV. Hybridization experiments with LAV subgenomic probes further established that this new retrovirus, here referred to as LAV-II, is distantly related to LAV and distinct from STLV-IIImac.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Clavel, F -- Guetard, D -- Brun-Vezinet, F -- Chamaret, S -- Rey, M A -- Santos-Ferreira, M O -- Laurent, A G -- Dauguet, C -- Katlama, C -- Rouzioux, C -- New York, N.Y. -- Science. 1986 Jul 18;233(4761):343-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2425430" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/*microbiology ; Adult ; Africa, Western ; Antigens, Viral/analysis ; Deltaretrovirus/analysis/genetics/immunology ; Electrophoresis, Polyacrylamide Gel ; Enzyme-Linked Immunosorbent Assay ; Epitopes/analysis ; Humans ; Male ; Microscopy, Electron ; RNA, Viral/analysis ; Retroviridae/genetics/immunology/*isolation & purification ; Viral Proteins/analysis
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  • 60
    Publication Date: 1985-07-19
    Description: Somatostatin receptor concentrations were measured in patients with Alzheimer's disease and controls. In the frontal cortex (Brodmann areas 6, 9, and 10) and temporal cortex (Brodmann area 21), the concentrations of somatostatin in receptors in the patients were reduced to approximately 50 percent of control values. A 40 percent reduction was seen in the hippocampus, while no significant changes were found in the cingulate cortex, postcentral gyrus, temporal pole, and superior temporal gyrus. Scatchard analysis showed a reduction in receptor number rather than a change in affinity. Somatostatin-like immunoreactivity was significantly reduced in both the frontal and temporal cortex. Somatostatin-like immunoreactivity was linearly related to somatostatin-receptor binding in the cortices of Alzheimer's patients. These findings may reflect degeneration of postsynaptic neurons or cortical afferents in the patients' cerebral cortices. Alternatively, decreased somatostatin-like immunoreactivity in Alzheimer's disease might indicate increased release of somatostatin and down regulation of postsynaptic receptors.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Beal, M F -- Mazurek, M F -- Tran, V T -- Chattha, G -- Bird, E D -- Martin, J B -- 1P50AG05134/AG/NIA NIH HHS/ -- IR23NS19867-1/NS/NINDS NIH HHS/ -- MN/NS31862/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1985 Jul 19;229(4710):289-91.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2861661" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Alzheimer Disease/*metabolism ; Cerebral Cortex/*analysis ; Chromatography, High Pressure Liquid ; Female ; Frontal Lobe/analysis ; Humans ; Male ; Middle Aged ; Neurons/metabolism/physiology ; Radioimmunoassay ; Receptors, Cell Surface/*analysis ; Receptors, Somatostatin ; Somatostatin/metabolism/physiology ; Temporal Lobe/analysis
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  • 61
    Publication Date: 1985-09-27
    Description: The reported incidence of acquired immune deficiency syndrome (AIDS) continues to increase in countries throughout the world. On the basis of a polynomial model for extrapolation, the cumulative number of cases diagnosed and reported since 1981 in the United States is expected to double during the next year with over 12,000 additional cases projected to be diagnosed by July 1986. The annual incidence rates for single (never-married) men in Manhattan and San Francisco, intravenous drug users in New York City and New Jersey, and persons with hemophilia A ranged from 261 to 350 per 100,000 population during 1984. For single men aged 25 to 44 years in Manhattan and San Francisco, AIDS was the leading cause of premature mortality in 1984 as measured by years of potential life lost. Infection with HTLV-III/LAV is considerably more common than reported AIDS in high-risk populations and can persist at least for several years, so the presence of specific antibody should be considered presumptive evidence of current infection. The screening of donated blood and plasma for antibody to HTLV-III/LAV and use of safer clotting factor concentrates should greatly reduce HTLV-III/LAV transmission through blood and blood products. Most HTLV-III/LAV infections occur through sexual transmission, use of contaminated needles, and as a result of infected mothers passing the virus to newborns. Continued research commitment is needed to develop an HTLV-III/LAV vaccine and therapy for this infection. In the interim, widespread community efforts are needed to minimize transmission.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Curran, J W -- Morgan, W M -- Hardy, A M -- Jaffe, H W -- Darrow, W W -- Dowdle, W R -- New York, N.Y. -- Science. 1985 Sep 27;229(4720):1352-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2994217" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency ; Syndrome/complications/*epidemiology/microbiology/mortality/prevention & ; control/transmission ; Adult ; Antibodies, Viral/immunology ; Blood Donors ; California ; Child ; Deltaretrovirus/immunology ; Female ; Hemophilia A/complications ; Homosexuality ; Humans ; Infant ; Infant, Newborn ; Male ; New York City ; Pregnancy ; Retroviridae Infections/epidemiology ; Risk ; Sarcoma, Kaposi/complications ; Substance-Related Disorders/complications ; United States
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  • 62
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-03-15
    Description: Antiviral compounds have been developed for use in chemoprophylaxis and chemotherapy of a variety of infections in humans, including those caused by influenza viruses, respiratory syncytial virus, and herpesviruses. The efficacy of several of these compounds has been demonstrated in rigorously controlled trials. Advances in molecular virology have led to the identification of biochemically defined, virus-specific functions that serve as appropriate targets for the future development of antiviral compounds. Clinical investigators and practicing physicians are now confronting questions previously raised with the use of antibacterial antibiotics. These questions concern appropriate routes of administration for antiviral compounds, optimal dosage regimens, risks of long-term prophylaxis, and the emergence of resistant organisms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dolin, R -- N0I AI 02653/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 1985 Mar 15;227(4692):1296-303.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2983421" target="_blank"〉PubMed〈/a〉
    Keywords: Acyclovir/therapeutic use ; Adult ; Aged ; Amantadine/therapeutic use ; Antiviral Agents/pharmacology/*therapeutic use ; Chickenpox/drug therapy ; Clinical Trials as Topic ; Cytomegalovirus/drug effects ; Encephalitis/drug therapy ; Foscarnet ; Guanosine Triphosphate/analogs & derivatives/therapeutic use ; Herpes Simplex/drug therapy ; Herpes Zoster/drug therapy ; Herpesviridae Infections/drug therapy ; Humans ; Infant, Newborn ; Infant, Newborn, Diseases/drug therapy ; Influenza A virus/drug effects ; Influenza, Human/drug therapy/prevention & control ; Phosphonoacetic Acid/analogs & derivatives/therapeutic use ; Respiratory Tract Infections/drug therapy ; Ribavirin/therapeutic use ; Rimantadine/therapeutic use ; Vidarabine/therapeutic use ; Virus Diseases/*drug therapy/prevention & control
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  • 63
    Publication Date: 1985-02-08
    Description: Phenylmercury absorbed through the skin from contaminated diapers affected urinary excretion in infants in Buenos Aires. The effects were reversible and quantitatively related to the concentration of urinary mercury. Excretion of gamma-glutamyl transpeptidase, an enzyme in the brush borders of renal tubular cells, increased in a dose-dependent manner when mercury excretion exceeded a "threshold" value. Urine volume also increased but at a higher threshold with respect to mercury. The results support the threshold concept of the systemic toxicity of metals. gamma-Glutamyl transpeptidase is a useful and sensitive marker for preclinical effects of toxic metals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gotelli, C A -- Astolfi, E -- Cox, C -- Cernichiari, E -- Clarkson, T W -- ES01247/ES/NIEHS NIH HHS/ -- ES01248/ES/NIEHS NIH HHS/ -- New York, N.Y. -- Science. 1985 Feb 8;227(4687):638-40.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2857500" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Argentina ; Creatinine/urine ; Dose-Response Relationship, Drug ; Fungicides, Industrial/*pharmacology ; Humans ; Infant ; Mercury/urine ; Mercury Poisoning/etiology ; Phenylmercury Compounds/*pharmacology ; Proteinuria/metabolism ; Urodynamics/drug effects ; gamma-Glutamyltransferase/urine
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  • 64
    Publication Date: 1985-09-27
    Description: The innervation of acini and ducts of eccrine sweat glands by immunoreactive, vasoactive intestinal peptide-containing nerve fibers was sharply reduced in seven patients with cystic fibrosis compared to eight normal subjects. The decrease in innervation by this neuropeptide, which has been shown to promote blood flow and the movement of water and chloride across epithelial surfaces in other systems, may be a basic mechanism for the decreased water content and relative impermeability of the epithelium to chloride and other ions that characterize cystic fibrosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Heinz-Erian, P -- Dey, R D -- Flux, M -- Said, S I -- HL30450/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1985 Sep 27;229(4720):1407-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/4035357" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Chlorides/metabolism ; Cystic Fibrosis/*physiopathology ; Female ; Humans ; Male ; Middle Aged ; Sweat Glands/*innervation/physiopathology ; Vasoactive Intestinal Peptide/*physiology
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  • 65
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-03-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Olson, R E -- New York, N.Y. -- Science. 1985 Mar 8;227(4691):1154.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3975606" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Child ; Child, Preschool ; Coronary Disease/etiology/prevention & control ; Dietary Fats/*adverse effects ; Female ; Humans ; Male ; Middle Aged
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  • 66
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-05-31
    Description: A sexually dimorphic cell group is described in the preoptic area of the human hypothalamus. Morphometric analysis revealed that the volume of this nucleus is 2.5 +/- 0.6 times (mean +/- standard error of the mean) as large in men as in women, and contains 2.2 +/- 0.5 times as many cells. Between the ages of 10 and 93 years, the nucleus decreases greatly in volume and in cell number. Although no function has yet been established for this nucleus, it is located within an area that is essential for gonadotropin release and sexual behavior in other mammals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Swaab, D F -- Fliers, E -- New York, N.Y. -- Science. 1985 May 31;228(4703):1112-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3992248" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Child ; Female ; Humans ; Male ; Middle Aged ; Preoptic Area/*anatomy & histology/cytology ; *Sex Characteristics
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  • 67
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-06-21
    Description: Prosopagnosia, the inability to recognize visually the faces of familiar persons who continue to be normally recognized through other sensory channels, is caused by bilateral cerebral lesions involving the visual system. Two patients with prosopagnosia generated frequent and large electrodermal skin conductance responses to faces of persons they had previously known but were now unable to recognize. They did not generate such responses to unfamiliar faces. The results suggest that an early step of the physiological process of recognition is still taking place in these patients, without their awareness but with an autonomic index.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tranel, D -- Damasio, A R -- NS 19632-02/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1985 Jun 21;228(4706):1453-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/4012303" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Agnosia/*physiopathology ; *Awareness ; *Cognition ; *Face ; Female ; Galvanic Skin Response ; Humans ; Middle Aged ; *Visual Perception
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  • 68
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-08-16
    Description: The size of the midsagittal area of the human corpus callosum obtained from postmortem measurement varied with tested hand preference. The corpus callosum, the main fiber tract connecting the two cerebral hemispheres, was larger by about 0.75 square centimeter, or 11 percent, in left-handed and ambidextrous people than in those with consistent right-hand preference. The difference was present in both the anterior and posterior halves, but not in the region of the splenium itself. This callosal morphology, which varied with hand preference, may also be related to individual differences in the pattern of hemispheric functional specialization. The greater bihemispheric representation of cognitive functions in left- and mixed-handers may be associated with greater anatomical connection between the hemispheres. The naturally occurring regressive events in neurogenesis, such as neuronal cell death and axonal elimination, may be factors in the individual differences in brain morphology and in functional lateralization. Specifically, right-handers may be those with more extensive early elimination of neural components.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Witelson, S F -- N01-NS-6-2344/NS/NINDS NIH HHS/ -- R01-NS 18954/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1985 Aug 16;229(4714):665-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/4023705" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Brain/anatomy & histology ; Corpus Callosum/*anatomy & histology ; Female ; *Functional Laterality ; Humans ; Male ; Middle Aged ; Organ Size ; Sex Factors
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  • 69
    Publication Date: 1985-07-19
    Description: List memory of pigeons, monkeys, and humans was tested with lists of four visual items (travel slides for animals and kaleidoscope patterns for humans). Retention interval increases for list-item memory revealed a consistent modification of the serial-position function shape: a monotonically increasing function at the shortest interval, a U-shaped function at intermediate intervals, and a monotonically decreasing function at the longest interval. The time course of these changes was fastest for pigeons, intermediate for monkeys, and slowest for humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wright, A A -- Santiago, H C -- Sands, S F -- Kendrick, D F -- Cook, R G -- New York, N.Y. -- Science. 1985 Jul 19;229(4710):287-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Sensory Sciences Center, Graduate School of Biomedical Sciences, University of Texas Health Science Center, Houston 77030, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9304205" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Columbidae ; Female ; Humans ; Macaca mulatta ; Male ; Random Allocation ; *Retention (Psychology) ; Serial Learning
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  • 70
    Publication Date: 1985-06-21
    Description: Protective immunity against malaria can be obtained by vaccination with irradiated sporozoites. The protective antigens known as circumsporozoite (CS) proteins, are polypeptides that cover the surface membrane of the parasite. The CS proteins contain species-specific immunodominant epitopes formed by tandem repeated sequences of amino acids. Here it is shown that the dominant epitope of Plasmodium falciparum is contained in the synthetic dodecapeptide Asn-Ala-Asn-Pro-Asn-Ala-Asn-Pro-Asn-Ala-Pro or (NANP)3. Monoclonal antibodies and most or all polyclonal human antibodies to the sporozoites react with (NANP)3, and polyclonal antibodies raised against the synthetic peptide (NANP)3 react with the surface of the parasite and neutralize its infectivity. Since (NANP)3 repeats are present in CS proteins of P. falciparum from many parts of the world, this epitope is a logical target for vaccine development.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zavala, F -- Tam, J P -- Hollingdale, M R -- Cochrane, A H -- Quakyi, I -- Nussenzweig, R S -- Nussenzweig, V -- New York, N.Y. -- Science. 1985 Jun 21;228(4706):1436-40.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2409595" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Antibodies, Monoclonal ; Child ; Epitopes/*immunology ; Humans ; Malaria/*prevention & control ; Peptides/immunology ; Plasmodium falciparum/*immunology ; *Vaccines
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  • 71
    Publication Date: 1985-03-29
    Description: Concentrations of plasma homovanillic acid before treatment were highly correlated with global severity of illness in schizophrenic patients, both before and after treatment. In contrast, a fixed dose of haloperidol did not affect those concentrations. Thus, in patients with a diagnosis of schizophrenia, plasma homovanillic acid may reflect the severity of illness, but not be influenced by short-term pharmacological perturbations by neuroleptics.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Davis, K L -- Davidson, M -- Mohs, R C -- Kendler, K S -- Davis, B M -- Johns, C A -- DeNigris, Y -- Horvath, T B -- MH37922/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1985 Mar 29;227(4694):1601-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3975630" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Haloperidol/pharmacology ; Homovanillic Acid/*blood ; Humans ; Male ; Phenylacetates/*blood ; Schizophrenia/*blood
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  • 72
    Publication Date: 1985-11-01
    Description: A distinct subpopulation of striatal aspiny neurons, containing the enzyme nicotinamide adenine dinucleotide phosphate diaphorase, is preserved in the caudate nucleus in Huntington's disease. Biochemical assays confirmed a significant increase in the activity of this enzyme in both the caudate nucleus and putamen in postmortem brain tissue from patients with this disease. The resistance of these neurons suggests that the gene defect in Huntington's disease may be modifiable by the local biochemical environment. This finding may provide insight into the nature of the genetically programmed cell death that is a characteristic of the disease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ferrante, R J -- Kowall, N W -- Beal, M F -- Richardson, E P Jr -- Bird, E D -- Martin, J B -- IR 23NS 19867-1/NS/NINDS NIH HHS/ -- MN1NS-3187/NS/NINDS NIH HHS/ -- NS 16367/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1985 Nov 1;230(4725):561-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2931802" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Caudate Nucleus/enzymology/pathology ; Corpus Striatum/enzymology/*pathology ; Humans ; Huntington Disease/enzymology/*pathology ; Middle Aged ; NADPH Dehydrogenase/analysis ; Nerve Tissue Proteins/analysis ; Neurons/enzymology/*pathology ; Neuropeptide Y
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  • 73
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-11-01
    Description: Figure 10 on page 351 of the Research Article "Constitutive and conditional suppression of exogenous and endogenous genes by anti-sense RNA" by J. G. Izant and H. Weintraub (26 July, p. 345) was reproduced erroneously, so that the green stain (NBD-phallacidin) of the actin filaments was not chromatically resolved. The micrographs are intended to document the specific disruption of the actin microfilament distribution, while the RNA and DNA staining pattern (orange-red) was unaffected. The correct figure and legend appear below.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Franco, V W -- New York, N.Y. -- Science. 1985 Nov 1;230(4725):496.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/4048943" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Clinical Enzyme Tests ; Colon/enzymology ; Colonic Neoplasms/*diagnosis/genetics ; Humans ; Ornithine Decarboxylase/analysis ; Risk
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  • 74
    Publication Date: 1985-01-04
    Description: Accumulation of very long chain fatty acids in X-linked and neonatal forms of adrenoleukodystrophy (ALD) appears to be a consequence of deficient peroxisomal oxidation of very long chain fatty acids. Peroxisomes were readily identified in liver biopsies taken from a patient having the X-linked disorder. However, in liver biopsies from a patient having neonatal-onset ALD, hepatocellular peroxisomes were greatly reduced in size and number, and sedimentable catalase was markedly diminished. The presence of increased concentrations of serum pipecolic acid and the bile acid intermediate, trihydroxycoprostanic acid, in the neonatal ALD patient are associated with a generalized diminution of peroxisomal activities that was not observed in the patient with X-linked ALD.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Goldfischer, S -- Collins, J -- Rapin, I -- Coltoff-Schiller, B -- Chang, C H -- Nigro, M -- Black, V H -- Javitt, N B -- Moser, H W -- Lazarow, P B -- AG-01468/AG/NIA NIH HHS/ -- AM-17702/AM/NIADDK NIH HHS/ -- N5-03356/PHS HHS/ -- etc. -- New York, N.Y. -- Science. 1985 Jan 4;227(4682):67-70.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3964959" target="_blank"〉PubMed〈/a〉
    Keywords: Adrenoleukodystrophy/genetics/metabolism/*pathology ; Adult ; Animals ; Bile Acids and Salts/metabolism ; Catalase/metabolism ; Child ; Child, Preschool ; Diffuse Cerebral Sclerosis of Schilder/*pathology ; Female ; Humans ; Liver/pathology ; Male ; Microbodies/*pathology ; Oxidation-Reduction ; Pipecolic Acids/blood ; Rats ; *X Chromosome
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  • 75
    Publication Date: 1985-05-03
    Description: The T-cell receptor is formed by two chains, alpha and beta, for which specific clones were recently obtained. In this report the gene for the beta chain of the human T-cell receptor was located on the long arm of chromosome 7, band q35, by means of in situ hybridization. This chromosome region in T cells is unusually prone to develop breaks in vivo, perhaps reflecting instability generated by somatic rearrangement of T-cell receptor genes during normal differentiation in this cell lineage.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Isobe, M -- Erikson, J -- Emanuel, B S -- Nowell, P C -- Croce, C M -- CA15822/CA/NCI NIH HHS/ -- CA16685/CA/NCI NIH HHS/ -- GM20700/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1985 May 3;228(4699):580-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3983641" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Ataxia Telangiectasia/genetics ; Chromosome Aberrations/genetics ; Chromosome Disorders ; *Chromosome Mapping ; Chromosomes, Human, 13-15 ; Chromosomes, Human, 6-12 and X ; Female ; Humans ; Male ; Mice ; Receptors, Antigen, T-Cell/*genetics
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  • 76
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-12-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G -- New York, N.Y. -- Science. 1985 Dec 6;230(4730):1152-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2933807" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Alzheimer Disease/*pathology ; Brain/pathology ; Down Syndrome/*pathology ; Female ; Humans ; Middle Aged
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 77
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-09-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G -- New York, N.Y. -- Science. 1985 Sep 27;229(4720):1378.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3898364" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Breast Neoplasms/*drug therapy/pathology/therapy ; Clinical Trials as Topic ; Female ; Humans ; Lymphatic Metastasis ; Menopause ; Middle Aged ; National Institutes of Health (U.S.) ; Receptors, Estrogen/drug effects ; Tamoxifen/therapeutic use ; United States
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  • 78
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-03-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G -- New York, N.Y. -- Science. 1985 Mar 1;227(4690):1019-20.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3975599" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Body Weight ; Child ; Female ; Humans ; Male ; Middle Aged ; *Obesity/complications
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  • 79
    Publication Date: 1985-01-11
    Description: Unexplained debilitating dementia or encephalopathy occurs frequently in adults and children with the acquired immune deficiency syndrome (AIDS). Brains from 15 individuals with AIDS and encephalopathy were examined by Southern analysis and in situ hybridization for the presence of human T-cell leukemia (lymphotropic) virus type III (HTLV-III), the virus believed to be the causative agent of AIDS. HTLV-III DNA was detected in the brains of five patients, and viral-specific RNA was detected in four of these. In view of these findings and the recent demonstration of morphologic and genetic relatedness between HTLV-III and visna virus, a lentivirus that causes a chronic degenerative neurologic disease in sheep, HTLV-III should be evaluated further as a possible cause of AIDS encephalopathy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shaw, G M -- Harper, M E -- Hahn, B H -- Epstein, L G -- Gajdusek, D C -- Price, R W -- Navia, B A -- Petito, C K -- O'Hara, C J -- Groopman, J E -- New York, N.Y. -- Science. 1985 Jan 11;227(4683):177-82.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2981429" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/microbiology ; Adult ; Antibodies, Viral/analysis ; Brain Diseases/*microbiology ; Cerebral Cortex/analysis/*microbiology ; Child ; Deltaretrovirus/*isolation & purification ; Dementia/microbiology ; Female ; Humans ; Infant ; Male ; Middle Aged ; Nucleic Acid Hybridization ; RNA, Viral/analysis
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  • 80
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-05-24
    Description: Human tissues have carbon-isotope ratios (13C/12C) that reflect dietary ratios. This observation has been used to determine the extent of metabolic turnover of DNA in cells of the adult human cerebellum (90 percent of which are neuronal). If adult human neuronal DNA were metabolically stable, its 13C/12C would reflect that in the maternal diet during fetal development as nearly all neurons are formed during maturation of the fetal brain and do not undergo cell division thereafter. The 13C/12C ratios in the food chains and body tissues of Europeans differ from corresponding American ratios by about 50 parts per million on the average. Therefore, turnover was studied by comparing 13C/12C ratios in cerebellar DNA of American-born Americans, European-born Americans, and European-born Europeans. The 13C/12C ratios in cerebellar DNA from European-born Americans were closer to 13C/12C ratios in cerebellar DNA from European-born Europeans than from American-born Americans, indicating that there was little or no turnover of neuronal DNA.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Slatkin, D N -- Friedman, L -- Irsa, A P -- Micca, P L -- NS 17822-01 RNM/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1985 May 24;228(4702):1002-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/4001927" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Aging ; Carbon ; Carbon Isotopes ; Cerebellum/cytology/*metabolism ; DNA/*metabolism ; Europe/ethnology ; Female ; Humans ; Male ; Middle Aged ; Neurons/*metabolism ; United States
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  • 81
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-09-06
    Description: Gonadotropin-releasing hormone analogs can cause regression of hormone-dependent breast carcinomas. These effects are thought to be mediated through the inhibition of gonadotropic and steroid hormones. These analogs may also act directly on the tumor because they are effective in treating breast cancer in some postmenopausal women. The presence of specific binding sites for gonadotropin-releasing hormone was demonstrated in human breast carcinomas by means of a novel approach of ligand immunoblotting. The results indicate a possible mechanism by which the peptide has direct effects on this tissue. These binding proteins were not detectable in non-neoplastic breast tissue.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Eidne, K A -- Flanagan, C A -- Millar, R P -- New York, N.Y. -- Science. 1985 Sep 6;229(4717):989-91.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2992093" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Breast Neoplasms/*metabolism ; Female ; Gonadotropin-Releasing Hormone/*metabolism ; Humans ; Membrane Proteins/metabolism ; Menopause ; Middle Aged ; Molecular Weight ; Receptors, Cell Surface/*metabolism ; Receptors, LHRH
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  • 82
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-05-24
    Description: Direct scanning electron microscopy of material obtained during surgical debridement of osteomyelitic bone showed that the infecting bacteria grew in coherent microcolonies in an adherent biofilm so extensive it often obscured the infected bone surfaces. Transmission electron microscopy showed this biofilm to have a fibrous matrix, to contain some host cells, and to contain many bacteria around which matrix fibers were often concentrated. Many bacterial morphotypes were present in these biofilms, and each bacterium was surrounded by exopolysaccharide polymers, which are known to mediate formation of microcolonies and adhesion of bacteria to surfaces in natural ecosystems and in infections related biomaterials. The adherent mode of growth may reduce the susceptibility of these organisms to host clearance mechanisms and antibiotic therapy and thus may be a fundamental factor in acute and chronic osteomyelitis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gristina, A G -- Oga, M -- Webb, L X -- Hobgood, C D -- AM26957-03/AM/NIADDK NIH HHS/ -- New York, N.Y. -- Science. 1985 May 24;228(4702):990-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/4001933" target="_blank"〉PubMed〈/a〉
    Keywords: Acute Disease ; Adhesiveness ; Adult ; Aged ; Bacteria/ultrastructure ; Bacterial Infections/microbiology ; *Bacterial Physiological Phenomena ; Bone and Bones/*microbiology ; Chronic Disease ; Humans ; Male ; Microscopy, Electron ; Microscopy, Electron, Scanning ; Middle Aged ; Models, Biological ; Osteomyelitis/etiology/*microbiology ; Polysaccharides, Bacterial/physiology
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  • 83
    Publication Date: 1985-08-09
    Description: The human T-cell lines MT-2 and MT-4 carry the human T-cell leukemia virus type I (HTLV-I). When MT-2 and MT-4 were infected with HTLV-III, the probable etiologic agent of the acquired immune deficiency syndrome (AIDS), rapid cytopathogenic effects and cytotoxicity were observed that made it possible to titrate the biologically active virus in a plaque-forming assay. The cytopathogenic effects were preceded by the rapid induction and increase of HTLV-III antigens as revealed by immunofluorescence and immunoprecipitation. Activities of HTLV-III were neutralized by the human antibodies against the virus when immunofluorescence and plaque assays were used. Essentially the same results were obtained with the lymphadenopathy-associated virus (LAV1).〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Harada, S -- Koyanagi, Y -- Yamamoto, N -- New York, N.Y. -- Science. 1985 Aug 9;229(4713):563-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2992081" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Antigens, Viral/analysis ; Chemical Precipitation ; Cytopathogenic Effect, Viral ; Deltaretrovirus/*growth & development/immunology ; Fetal Blood/cytology ; Fluorescent Antibody Technique ; Humans ; Immunochemistry ; Leukemia ; T-Lymphocytes ; Viral Plaque Assay ; Virus Cultivation/methods ; Virus Replication
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  • 84
    Publication Date: 1985-11-08
    Description: A skin equivalent model has been used to fabricate tissues with psoriatic and normal cells. Psoriatic fibroblasts can induce hyperproliferative activity in normal keratinocytes. The psoriatic epidermis from lesions continues to proliferate at high rates for at least 15 days in this model, and normal fibroblasts are unable to suppress this hyperproliferation. The primary defect in psoriatic skin may reside in the dermal fibroblast.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Saiag, P -- Coulomb, B -- Lebreton, C -- Bell, E -- Dubertret, L -- New York, N.Y. -- Science. 1985 Nov 8;230(4726):669-72.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2413549" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Collagen/physiology ; Epidermis/*cytology ; Female ; Fibroblasts/*physiology ; Humans ; In Vitro Techniques ; Keratins/*physiology ; Male ; Mice ; Mice, Nude ; Psoriasis/*physiopathology ; Skin/*cytology/growth & development
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  • 85
    Publication Date: 1985-06-07
    Description: A set of naturally occurring immunoglobulin M (IgM) antibodies that are reactive with a defined subset of proteins in the acrosomal cap region of human sperm has been identified. These antibodies are present in a broad spectrum of human sera from males and females, 1 day to 40 years of age, and are absent or markedly deficient in a large proportion of sera from individuals with the acquired immune deficiency syndrome (AIDS) or at risk for AIDS. The subset of proteins with which the IgM antibodies are reactive includes a factor (or factors) capable of inhibiting lectin-induced T-lymphocyte proliferation. The prevalence of the sperm-reactive IgM antibodies indicates that they are not elicited by sperm. Further, immunoreactivity of the sperm proteins resulting in depletion of specific circulating IgM antibodies, or other interactions between the sperm proteins and elements of the immune system, may be a factor in the suppressed state of the immune system in AIDS.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rodman, T C -- Laurence, J -- Pruslin, F H -- Chiorazzi, N -- Winston, R -- CA 35018-02/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1985 Jun 7;228(4704):1211-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3890184" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/*immunology ; Acrosome/*immunology ; Adolescent ; Adult ; Antibodies/analysis ; Child ; Child, Preschool ; Female ; Fluorescent Antibody Technique ; Humans ; Immunoglobulin M/analysis ; Infant ; Male ; Molecular Weight ; Spermatozoa/*immunology ; T-Lymphocytes/immunology
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  • 86
    Publication Date: 1985-02-15
    Description: Golgi impregnations of neostriatum from deceased Huntington's disease patients and controls were examined. In all cases of Huntington's disease the morphology of dendrites of medium-sized spiny neurons was markedly altered by the appearance of recurved endings and appendages, a decrease or increase in the density of spines, and abnormalities in the size and shape of spines. Pathological changes were rarely observed in medium-sized and large aspiny neostriatal neurons. The findings provide evidence for simultaneous degeneration and growth of spiny neurons in Huntington's disease and support the view that a specific population of neostriatal neurons is selectively involved in its pathogenesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Graveland, G A -- Williams, R S -- DiFiglia, M -- MH-NS31862/MH/NIMH NIH HHS/ -- MH34079/MH/NIMH NIH HHS/ -- NS 16367/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1985 Feb 15;227(4688):770-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3155875" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Corpus Striatum/*pathology ; Dendrites/ultrastructure ; Humans ; Huntington Disease/*pathology ; Middle Aged ; Nerve Degeneration ; Neurons/ultrastructure
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  • 87
    Publication Date: 1985-05-10
    Description: Borna disease virus causes a rare meningoencephalitis in horses and sheep and has been shown to produce behavioral effects in some species. The possibility that the Borna virus is associated with mental disorders in humans was evaluated by examining serum samples from 979 psychiatric patients and 200 normal volunteers for the presence of Borna virus-specific antibodies. Antibodies were detected by the indirect immunofluorescence focus assay. Antibodies to the virus were demonstrated in 16 of the patients but none of the normal volunteers. The patients with the positive serum samples were characterized by having histories of affective disorders, particularly of a cyclic nature. Further studies are needed to define the possible involvement of Borna virus in human psychiatric disturbances.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rott, R -- Herzog, S -- Fleischer, B -- Winokur, A -- Amsterdam, J -- Dyson, W -- Koprowski, H -- MH00044/MH/NIMH NIH HHS/ -- NS-11036/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1985 May 10;228(4700):755-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3922055" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Antibodies, Viral/*immunology ; Bipolar Disorder/microbiology ; Borna disease virus/*immunology ; Depressive Disorder/microbiology ; Female ; Fluorescent Antibody Technique ; Humans ; Male ; Mental Disorders/immunology/*microbiology ; Middle Aged ; Rats ; Tupaiidae ; Viruses, Unclassified/*immunology
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  • 88
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1984-09-28
    Description: Recent neurophysiological findings have demonstrated that abstinent chronic alcoholics manifest deficits in event-related brain potentials. To explore possible biological antecedents of alcoholism the present study examined boys at high risk for alcoholism. Event-related brain potentials were recorded from biological sons of alcoholic fathers and matched control boys. Differences in the P3 component of the potentials were obtained between the high-risk and control subjects.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Begleiter, H -- Porjesz, B -- Bihari, B -- Kissin, B -- AA 05524/AA/NIAAA NIH HHS/ -- New York, N.Y. -- Science. 1984 Sep 28;225(4669):1493-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6474187" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Alcoholism/*genetics/physiopathology ; Analysis of Variance ; Brain/*physiopathology ; Child ; Evoked Potentials ; Fathers ; Humans ; Male ; Memory Disorders/etiology ; Risk
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  • 89
    Publication Date: 1984-12-21
    Description: Smell identification ability was measured in 1955 persons ranging in age from 5 to 99 years. On the average, women outperformed men at all ages, and nonsmokers outperformed smokers. Peak performance occurred in the third through fifth decades and declined markedly after the seventh. More than half of those 65 to 80 years old evidenced major olfactory impairment. After 80 years, more than three-quarters evidenced major impairment. Given these findings, it is not surprising that many elderly persons complain that food lacks flavor and that the elderly account for a disproportionate number of accidental gas poisoning cases each year.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Doty, R L -- Shaman, P -- Applebaum, S L -- Giberson, R -- Siksorski, L -- Rosenberg, L -- NS 16265/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1984 Dec 21;226(4681):1441-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6505700" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; *Aging ; Child ; Child, Preschool ; Female ; Humans ; Male ; Middle Aged ; Sensory Thresholds ; Sex Factors ; Smell/*physiology ; Smoking
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  • 90
    Publication Date: 1984-03-30
    Description: Coronary arteries from hearts of cardiac patients contain significantly higher concentrations of histamine than do those from noncardiac patients. The coronary vessels of cardiac patients are also hyperresponsive to histamine and serotonin. These differences between groups of patients suggest an explanation for coronary artery spasm in heart disease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kalsner, S -- Richards, R -- New York, N.Y. -- Science. 1984 Mar 30;223(4643):1435-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6701530" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Animals ; Arteriosclerosis/physiopathology ; Catecholamines/analysis ; Cattle ; Coronary Vasospasm/*physiopathology ; Coronary Vessels/analysis/drug effects/*physiopathology ; Female ; Histamine/*analysis/pharmacology ; Humans ; Male ; Middle Aged ; Norepinephrine/pharmacology ; Serotonin/analysis/pharmacology
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  • 91
    Publication Date: 1984-05-04
    Description: Peripheral blood lymphocytes from patients with the acquired immunodeficiency syndrome (AIDS) or with signs or symptoms that frequently precede AIDS (pre-AIDS) were grown in vitro with added T-cell growth factor and assayed for the expression and release of human T-lymphotropic retroviruses (HTLV). Retroviruses belonging to the HTLV family and collectively designated HTLV-III were isolated from a total of 48 subjects including 18 of 21 patients wih pre-AIDS, three of four clinically normal mothers of juveniles with AIDS, 26 of 72 adult and juvenile patients with AIDS, and from one of 22 normal male homosexual subjects. No HTLV-III was detected in or isolated from 115 normal heterosexual subjects. The number of HTLV-III isolates reported here underestimates the true prevalence of the virus since many specimens were received in unsatisfactory condition. Other data show that serum samples from a high proportion of AIDS patients contain antibodies to HTLV-III. That these new isolates are members of the HTLV family but differ from the previous isolates known as HTLV-I and HTLV-II is indicated by their morphological, biological, and immunological characteristics. These results and those reported elsewhere in this issue suggest that HTLV-III may be the primary cause of AIDS.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gallo, R C -- Salahuddin, S Z -- Popovic, M -- Shearer, G M -- Kaplan, M -- Haynes, B F -- Palker, T J -- Redfield, R -- Oleske, J -- Safai, B -- New York, N.Y. -- Science. 1984 May 4;224(4648):500-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6200936" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/blood/*microbiology ; Adult ; Antigens, Viral/analysis ; Cells, Cultured ; Cytopathogenic Effect, Viral ; Deltaretrovirus/*isolation & purification/physiology/ultrastructure ; Female ; Homosexuality ; Humans ; Immune Sera/pharmacology ; Interferon Type I/immunology ; Male ; RNA-Directed DNA Polymerase/metabolism ; Risk ; T-Lymphocytes/microbiology
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  • 92
    Publication Date: 1984-11-16
    Description: Clonidine, an alpha-2-adrenergic agonist, significantly reduces opiate withdrawal. Fifteen heavy smokers abstained from cigarettes on three separate occasions and received instead clonidine, placebo, or the benzodiazepine alprazolam. Clonidine and alprazolam diminished withdrawal symptoms. The two drugs suppressed anxiety, tension, irritability, and restlessness equally but clonidine had a greater effect than alprazolam on cigarette craving. These observations suggest that noradrenergic activity is a common feature in the pathophysiology of withdrawal and that a special relationship exists between central noradrenergic activity and craving.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Glassman, A H -- Jackson, W K -- Walsh, B T -- Roose, S P -- Rosenfeld, B -- New York, N.Y. -- Science. 1984 Nov 16;226(4676):864-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6387913" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Alprazolam ; Anxiety/drug therapy ; Benzodiazepines/therapeutic use ; Clinical Trials as Topic ; Clonidine/*therapeutic use ; Double-Blind Method ; Female ; Humans ; Male ; *Smoking ; Substance Withdrawal Syndrome/*drug therapy
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  • 93
    facet.materialart.
    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 1984-01-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G -- New York, N.Y. -- Science. 1984 Jan 27;223(4634):381-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6362006" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Cholesterol/*blood ; Cholesterol, Dietary ; Cholestyramine Resin/*therapeutic use ; Clinical Trials as Topic ; Double-Blind Method ; Heart Diseases/etiology/*prevention & control ; Humans ; Hypercholesterolemia/complications/drug therapy ; Male ; Middle Aged ; Risk
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  • 94
    Publication Date: 1984-06-29
    Description: Human T lymphocytes transformed by human T cell leukemia-lymphoma viruses or activated by lectins were found to produce stimulating factors that promoted both proliferation and maturation of oligodendroglial and astroglial cells in vitro.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Merrill, J E -- Kutsunai, S -- Mohlstrom, C -- Hofman, F -- Groopman, J -- Golde, D W -- CA 30388/CA/NCI NIH HHS/ -- CA 32737/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1984 Jun 29;224(4656):1428-30.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6610212" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Astrocytes/*drug effects ; Cell Division/*drug effects ; Cell Line ; Growth Substances/*pharmacology ; Humans ; Lymphocyte Activation ; Lymphokines/pharmacology ; Neuroglia/*drug effects ; Oligodendroglia/*drug effects ; Rats ; Receptors, Fc/metabolism ; T-Lymphocytes/*physiology
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  • 95
    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
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  • 96
    Publication Date: 1984-09-28
    Description: Antibodies specific for human T-cell leukemia-lymphoma virus type I (HTLV-I) were demonstrated in serum samples from various groups of people in South Africa, Uganda, Ghana, Nigeria, Tunisia, and Egypt. The samples had been collected for other purposes and were presumably selected without bias toward clinical conditions associated with HTLV infections. Regional differences in antibody positivity were observed, indicating widely distributed loci of occurrence of HTLV on the African continent in people of both black and white ancestry. Two patients with high titers of antibody to HTLV-I had some signs of adult T-cell leukemia-lymphoma. In several groups a high frequency of false positive serum reactions was indicated when specific confirmation steps were included in the assay. Further characterization of these sera revealed highly elevated immunoglobulin levels, possibly due to polyclonal activation of immunoglobulin synthesis in these subjects. The possibility that related cross-reactive human retroviruses coexist in the same groups was not eliminated.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Saxinger, W -- Blattner, W A -- Levine, P H -- Clark, J -- Biggar, R -- Hoh, M -- Moghissi, J -- Jacobs, P -- Wilson, L -- Jacobson, R -- New York, N.Y. -- Science. 1984 Sep 28;225(4669):1473-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6089348" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Africa ; African Continental Ancestry Group ; Antibodies, Viral/*analysis ; Burkitt Lymphoma/immunology ; Cross Reactions ; Deltaretrovirus/*immunology ; Enzyme-Linked Immunosorbent Assay ; European Continental Ancestry Group ; False Positive Reactions ; Female ; Humans ; Lymphoma/immunology ; Male ; Middle Aged ; Retroviridae/immunology ; T-Lymphocytes
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  • 97
    Publication Date: 1984-06-15
    Description: Normal sleepers underwent sleep recordings and daytime tests of sleep tendency, performance, and mood while being shifted 180 degrees in their sleep-wake schedule. After two baseline 24-hour periods, subjects postponed sleep until noon. For the next three 24-hour periods, they were in bed from 1200 to 2000 and received triazolam, flurazepam, or placebo at bedtime in parallel groups. Placebo subjects showed significant sleep loss after the shift. Active medication reversed this sleep loss. Despite good sleep, flurazepam subjects appeared most impaired of the three groups on objective assessments of waking function; triazolam subjects were least impaired.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Seidel, W F -- Roth, T -- Roehrs, T -- Zorick, F -- Dement, W C -- NIMH 05804/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1984 Jun 15;224(4654):1262-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6729454" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Arousal/drug effects ; Benzodiazepines/pharmacology/*therapeutic use ; Emotions/drug effects ; Female ; Flurazepam/pharmacology/therapeutic use ; Humans ; Male ; Sleep/drug effects ; Sleep Wake Disorders/*drug therapy ; Triazolam/pharmacology/therapeutic use
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  • 98
    Publication Date: 1984-05-04
    Description: In cats, infection with T-lymphotropic retroviruses can cause T-cell proliferation and leukemia or T-cell depletion and immunosuppression. In humans, some highly T4 tropic retroviruses called HTLV-I can cause T-cell proliferation and leukemia. The subgroup HTLV-II also induces T-cell proliferation in vitro, but its role in disease is unclear. Viruses of a third subgroup of human T-lymphotropic retroviruses, collectively designated HTLV-III, have been isolated from cultured cells of 48 patients with acquired immunodeficiency syndrome (AIDS). The biological properties of HTLV-III and immunological analyses of its proteins show that this virus is a member of the HTLV family, and that it is more closely related to HTLV-II than to HTLV-I. Serum samples from 88 percent of patients with AIDS and from 79 percent of homosexual men with signs and symptoms that frequently precede AIDS, but from less than 1 percent of heterosexual subjects, have antibodies reactive against antigens of HTLV-III. The major immune reactivity appears to be directed against p41, the presumed envelope antigen of the virus.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sarngadharan, M G -- Popovic, M -- Bruch, L -- Schupbach, J -- Gallo, R C -- New York, N.Y. -- Science. 1984 May 4;224(4648):506-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6324345" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/*immunology/microbiology ; Adult ; Antibodies, Viral/*analysis ; Antigens, Viral/immunology ; Child, Preschool ; Deltaretrovirus/*immunology ; Enzyme-Linked Immunosorbent Assay ; Female ; Homosexuality ; Humans ; Infant ; Male ; Middle Aged ; Sarcoma, Kaposi/immunology ; Substance-Related Disorders ; T-Lymphocytes/microbiology ; Viral Envelope Proteins/immunology
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  • 99
    Publication Date: 1984-06-08
    Description: A domain of DNA designated N-myc is amplified 20- to 140-fold in human neuroblastoma cell lines but not in cell lines from other tumor types. N-myc has now been found to be amplified in neuroblastoma tissue from 24 of 63 untreated patients (38 percent). The extent of amplification appears to be bimodal, with amplification of 100- to 300-fold in 12 cases and 3- to 10-fold in 10 others. Amplification was found in 0 of 15 patients with stage 1 or 2 disease, whereas 24 of 48 cases (50 percent) with stage 3 or 4 had evidence of N-myc amplification. These data indicate that N-myc amplification is a common event in untreated human neuroblastomas. Furthermore, N-myc amplification is highly correlated with advanced stages of disease (P less than 0.001) and with the ability to grow in vitro as an established cell line, both of which are associated with a poor prognosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brodeur, G M -- Seeger, R C -- Schwab, M -- Varmus, H E -- Bishop, J M -- CA02971/CA/NCI NIH HHS/ -- CA13539/CA/NCI NIH HHS/ -- CA17829/CA/NCI NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1984 Jun 8;224(4653):1121-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6719137" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Cell Line ; Child ; Child, Preschool ; DNA, Neoplasm/genetics ; Eye Neoplasms/genetics ; *Gene Amplification ; Humans ; Infant ; Lymphatic Metastasis ; Middle Aged ; Neuroblastoma/*genetics/physiopathology ; Nucleic Acid Hybridization ; *Oncogenes ; Prognosis ; Retinoblastoma/genetics
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  • 100
    facet.materialart.
    Unknown
    American Association for the Advancement of Science (AAAS)
    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
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