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    The iddm4 locus segregates with diabetes susceptibility in congenic WF.iddm4 rats

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    Authors
    Mordes, John P.
    Leif, Jean H.
    Novak, Stephen
    DeScipio, Cheryl
    Greiner, Dale L.
    Blankenhorn, Elizabeth P.
    UMass Chan Affiliations
    Department of Pathology
    Department of Medicine, Diabetes Division
    Document Type
    Journal Article
    Publication Date
    2002-10-29
    Keywords
    Adoptive Transfer
    Alleles
    Animals
    *Chromosome Mapping
    Diabetes Mellitus, Type 1
    Disease Models, Animal
    Genetic Markers
    Genetic Predisposition to Disease
    Homozygote
    Islets of Langerhans
    Pancreatic Diseases
    Rats
    Rats, Mutant Strains
    Life Sciences
    Medicine and Health Sciences
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    Link to Full Text
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4034451/
    Abstract
    Viral antibody-free BBDR and WF rats never develop spontaneous diabetes. BBDR rats, however, develop autoimmune diabetes after perturbation of the immune system, e.g., by viral infection. We previously identified a disease-susceptibility locus in the BBDR rat, iddm4, which is associated with the development of autoimmune diabetes after treatment with polyinosinic:polycytidylic acid and an antibody that depletes ART2(+) regulatory cells. We have now developed lines of congenic WF.iddm4 rats and report that in an intercross of N5 generation WF.iddm4 rats, approximately 70% of animals either homozygous or heterozygous for the BBDR origin allele of iddm4 became hyperglycemic after treatment to induce diabetes. Fewer than 20% of rats expressing the WF origin allele of iddm4 became diabetic. Testing the progeny of various recombinant N5 WF.iddm4 congenic rats for susceptibility to diabetes suggests that iddm4 is centered on a small segment of chromosome 4 bounded by the proximal marker D4Rat135 and the distal marker D4Got51, an interval of
    Source

    Diabetes. 2002 Nov;51(11):3254-62.

    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/42027
    PubMed ID
    12401717
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