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  • 1
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    Infection-specific particle from the unconventional slow virus diseases (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-07-27
    Description: Scrapie-associated fibrils, first observed in brains of scrapie-infected mice, were also observed in scrapie-infected hamsters and monkeys, in humans with Creutzfeldt-Jakob disease, and in kuru-infected monkeys. These fibrils were not found in a comprehensive series of control brains from humans and animals affected with central nervous system disorders resulting in histopathologies, ultrastructural features, or disease symptoms similar to those of scrapie, kuru, and Creutzfeldt-Jakob disease. These fibrils are also found in preclinical scrapie and in the spleens of scrapie-infected mice; they are a specific marker for the "unconventional" slow virus diseases, and may be the etiological agent.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Merz, P A -- Rohwer, R G -- Kascsak, R -- Wisniewski, H M -- Somerville, R A -- Gibbs, C J Jr -- Gajdusek, D C -- AGO4220/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 1984 Jul 27;225(4660):437-40.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6377496" target="_blank"〉PubMed〈/a〉
    Keywords: Alzheimer Disease/pathology ; Amyloid/metabolism ; Amyotrophic Lateral Sclerosis/pathology ; Animals ; Brain/drug effects/ultrastructure ; Creutzfeldt-Jakob Syndrome/pathology ; Cricetinae ; Cuprizone/pharmacology ; Humans ; Kuru/pathology ; Mice ; Mice, Inbred C57BL ; Parkinson Disease/pathology ; Saimiri ; Scrapie/pathology ; Sheep ; Slow Virus Diseases/*pathology ; Spleen/ultrastructure ; Triethyltin Compounds/pharmacology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 2
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    Measles virus nucleotide sequences: detection by hybridization in situ (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-05-08
    Description: A tritium-labeled probe that detects measles virus nucleotide sequences was hybridized in situ to cells infected with measles virus and to sections of brain tissue from patients with subacute sclerosing panencephalitis and from patients with multiple sclerosis. The measles virus genome was detected in many cells in subacute sclerosing panencephalitis where this virus would have been missed by methods such as immunofluorescence. Measles virus sequences were also found in two foci in one of four cases of multiple sclerosis. This refined method of hybridization in situ, which can be useful in the search for covert virus infections of man, provides evidence that viruses may be involved in multiple sclerosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Haase, A T -- Ventura, P -- Gibbs, C J Jr -- Tourtellotte, W W -- New York, N.Y. -- Science. 1981 May 8;212(4495):672-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7221554" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Brain/microbiology ; Child ; Child, Preschool ; Female ; Humans ; Male ; Measles virus/*genetics ; Middle Aged ; Multiple Sclerosis/*microbiology ; Nucleic Acid Hybridization ; RNA, Viral/genetics ; Subacute Sclerosing Panencephalitis/*microbiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 3
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    Autoantibodies against axonal neurofilaments in patients with Kuru and Creutzfeldt-Jakob disease (1980)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1980-10-10
    Description: The serums of some patients with subacute spongiform encephalopathies contain an autoantibody in higher titer against a normal fibrillar protein within the axon of mature central neurons in culture. The morphological features of this neurofilament, as demonstrated by immunofluorescence and immunoperoxidase staining, and the partial characterization of the antibody are described. The detection of this hetero-specific autoantibody is the first evidence of an immune reaction in the spongiform encephalopathies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sotelo, J -- Gibbs, C J Jr -- Gajdusek, D C -- New York, N.Y. -- Science. 1980 Oct 10;210(4466):190-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6997994" target="_blank"〉PubMed〈/a〉
    Keywords: Antibody Specificity ; Autoantibodies/*analysis ; Autoimmune Diseases/immunology ; Axons/immunology ; Creutzfeldt-Jakob Syndrome/*immunology ; Cytoskeleton/*immunology ; Fluorescent Antibody Technique ; Humans ; Kuru/*immunology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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