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  • 1
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1978-08-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Drew, J S -- London, W T -- Lustbader, E D -- Hesser, J E -- Blumberg, B S -- New York, N.Y. -- Science. 1978 Aug 25;201(4357):687-92.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/566954" target="_blank"〉PubMed〈/a〉
    Keywords: Age Factors ; Birth Order ; Cross Reactions ; Female ; Fetal Death ; Graft Survival ; Hepatitis B/immunology/*physiopathology/transmission ; Hepatitis B Surface Antigens/analysis ; Humans ; Male ; Parity ; Pregnancy ; Sex Factors ; *Sex Ratio
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 1979-07-13
    Description: Two different ultrastructural alterations were observed in liver cells of chimpanzees inoculated with plasma derived from two different patients with non-A, non-B hepatitis. During the acute phase of illness in one group of four chimpanzees, peculiar tubular structures, composed of two unit membranes with electron-opaque material in between, were observed in the cytoplasm of hepatocytes. In contrast, these structures were never detected in the liver cells of the second group of five chimpanzees that received the second inoculum, However, nuclear changes, usually associated with aggregates of 20- to 27-nanometer particles, were found in hepatocytes of the latter animals. Although these particles resembled viruses, they were not as uniform as small virus particles often appear. In five other chimpanzees inoculated with non-A, non-B hepatitis material not known to be related to the first two inocula, cytoplasmic structures were found in four, and nuclear structures were found in the remaining one. Thus, all 14 chimpanzees inoculated with transmissible non-A, non-B hepatitis agents could be classified as having either nuclear or cytoplasmic changes. These observations add support to epidemiologic data suggesting that there may be more than one agent of non-A, non-B hepatitis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shimizu, Y K -- Feinstone, S M -- Purcell, R H -- Alter, H J -- London, W T -- New York, N.Y. -- Science. 1979 Jul 13;205(4402):197-200.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/451589" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Nucleus/ultrastructure ; Cytoplasm/ultrastructure ; Hepatitis, Viral, Animal/*microbiology ; Hepatitis, Viral, Human/*microbiology ; Inclusion Bodies, Viral/ultrastructure ; Liver/microbiology/ultrastructure ; Microscopy, Electron ; Pan troglodytes
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 1984-01-06
    Description: Simian acquired immunodeficiency syndrome (SAIDS), a disease clinically and pathologically similar to acquired immunodeficiency syndrome in humans, was transmitted from diseased rhesus monkeys (Macaca mulatta) to normal monkeys by inoculation with heparinized whole blood or plasma that had been passed through filters of 0.45 micrometer pore size. This suggests that the causative agent is small and most probably a virus. No viruses, however, were isolated by standard cell culture techniques from the blood or filtered plasma which caused SAIDS. Both cellular and humoral immunity were markedly depressed in animals with advanced SAIDS.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gravell, M -- London, W T -- Houff, S A -- Madden, D L -- Dalakas, M C -- Sever, J L -- Osborn, K G -- Maul, D H -- Henrickson, R V -- Marx, P A -- RR00169/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1984 Jan 6;223(4631):74-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6318315" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/blood/immunology/*transmission ; Animals ; Blood/microbiology ; Cytomegalovirus/isolation & purification ; Filtration ; Immunoglobulins/analysis ; Lymphatic System/pathology ; Lymphocyte Activation ; Macaca mulatta ; *Plasma/microbiology ; Retroviridae/isolation & purification ; Viruses/isolation & purification
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 1982-12-24
    Description: An influenza A reassortant virus that contained the hemagglutinin and neuraminidase genes of a virulent human virus, A/Udorn/72 (H3N2), and the six other influenza A virus genome segments from an avirulent avian virus, A/Mallard/New York/6750/78 (H2N2), was evaluated for its level of replication is squirrel monkeys and hamsters. In monkeys, the reassortant virus was as attenuated and as restricted in its level of replication in the upper and lower respiratory tract as its avian influenza virus parent. Nonetheless, infection with the reassortant induced significant resistant to challenge with virulent human influenza virus. In hamsters, the reassortant virus replicated to a level intermediate between that of its parents. These findings suggest that the nonsurface antigen genes of the avian parental virus are the primary determinants of restriction of replication of the reassortant virus in monkeys. Attenuation of the reassortant virus for primates is achieved by inefficient functioning of the avian influenza genes in primate cells, while antigenic specificity of the human influenza virus is provided by the neuraminidase and hemagglutinin genes derived from the human virus. This approach could lead to the development of a live influenza A virus vaccine that is attenuated for man if the avian influenza genes are similarly restricted in human cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Murphy, B R -- Sly, D L -- Tierney, E L -- Hosier, N T -- Massicot, J G -- London, W T -- Chanock, R M -- Webster, R G -- Hinshaw, V S -- CA 21765/CA/NCI NIH HHS/ -- N01-AI-02649/AI/NIAID NIH HHS/ -- N01-NS-7-2375/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1982 Dec 24;218(4579):1330-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6183749" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens, Surface/genetics ; Cricetinae ; Epitopes/genetics/immunology ; Hemagglutinins/genetics/immunology ; Influenza A virus/*genetics ; Influenza Vaccines/*immunology ; Neuraminidase/genetics/immunology ; Saimiri ; Vaccines, Attenuated/immunology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 1978-09-29
    Description: Owl monkeys were inoculated intracerebrally, subcutaneously, and intravenously with JC, BK, or SV40 virus. Two of four adult owl monkeys inoculated with JC virus, a human polyomavirus, developed brain tumors at 16 and 25 months after inoculation, respectively. A grade 3 to grade 4 astrocytoma (resembling a human glioblastoma multiforme) was found in the left cerebral hemisphere and brainstem of one monkey. The second monkey developed a malignant tumor in the left cerebral hemisphere containing both glial and neuronal cell types. Impression smears prepared from unfixed tissue of this tumor showed cells that contained polyomavirus T antigen. Virion antigens were not detected. Tumor cells cultured in vitro also contained T antigen but were negative for virion antigen. Infectious virus was not isolated from extracts of this tumor.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉London, W T -- Houff, S A -- Madden, D L -- Fuccillo, D A -- Gravell, M -- Wallen, W C -- Palmer, A E -- Sever, J L -- Padgett, B L -- Walker, D L -- ZuRhein, G M -- Ohashi, T -- New York, N.Y. -- Science. 1978 Sep 29;201(4362):1246-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/211583" target="_blank"〉PubMed〈/a〉
    Keywords: Antibodies, Viral/analysis ; Antigens, Viral/analysis ; Brain Neoplasms/*etiology/pathology ; Immunosuppression ; Neoplasms, Experimental/etiology/pathology ; *Polyomavirus/immunology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 1987-06-26
    Description: Malaria parasites are haploid for most of their life cycle, with zygote formation and meiosis occurring during the mosquito phase of development. The parasites can be analyzed genetically by transmitting mixtures of cloned parasites through mosquitoes to permit cross-fertilization of gametes to occur. A cross was made between two clones of Plasmodium falciparum differing in enzymes, drug sensitivity, antigens, and chromosome patterns. Parasites showing recombination between the parent clone markers were detected at a high frequency. Novel forms of certain chromosomes, detected by pulsed-field gradient gel electrophoresis, were produced readily, showing that extensive rearrangements occur in the parasite genome after cross-fertilization. Since patients are frequently infected with mixtures of genetically distinct parasites, mosquito transmission is likely to provide the principal mechanisms for generating parasites with novel genotypes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Walliker, D -- Quakyi, I A -- Wellems, T E -- McCutchan, T F -- Szarfman, A -- London, W T -- Corcoran, L M -- Burkot, T R -- Carter, R -- New York, N.Y. -- Science. 1987 Jun 26;236(4809):1661-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3299700" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Deaminase/genetics ; Animals ; Anopheles/parasitology ; Antigens, Protozoan/genetics ; Chromosomes ; Clone Cells ; Crosses, Genetic ; Insect Vectors ; Malaria/parasitology ; Pan troglodytes ; Plasmodium falciparum/*genetics ; Pyrimethamine/pharmacology ; Recombination, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Thalassaemia patients receive transfusions beginning early in life and are exposed to many serum proteins and other blood constituents which are different from their own. Seven years ago, Vierucci and his colleagues started a systematic study of thalassaemia patients from Ferrara and other sections ...
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 226 (1970), S. 172-173 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Twenty-four adult, female, New Zealand white rabbits without rubella haemagglutination inhibiting antibody were used8. They were individually mated and then housed separately in isolation chambers. On the second day of gestation, twelve animals were inoculated intravenously with 1.0 ml. of tissue ...
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  • 9
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 255 (1975), S. 483-484 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] We inoculated the virus directly into the foetus, rather than into the mother, to ensure maximum opportunity for the virus to infect the foetus and cause damage8. Fourteen pregnant rhesus monkeys (Macaca mulatta), serologically negative for influenza A virus antibody, were subjected to laparotomy ...
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  • 10
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