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American Journal of Pathology, Vol 138, 721-726, Copyright © 1991 by American Society for Investigative Pathology
REGULAR ARTICLES |
MD Traystman, LH Chow, BM McManus, A Herskowitz, MN Nesbitt and KW Beisel
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha 68198-6495.
This study was undertaken to determine the genetic control of host susceptibility to coxsackievirus B3 (CVB3)-induced chronic myocarditis in a mouse model. An autosomal recessive autoimmune myocardial disease (amd) gene (possibly more than one gene), which determined susceptibility to CVB3-induced chronic myocarditis in the A/J and DBA/2J inbred mouse strains, was mapped to a segment of chromosome 14. Data from both the AXB/BXA recombinant inbred (RI) strains and the B10.D2(57N) H-8b congenic mice supported this linkage relationship. Analysis of the AXB/BXA RI strain distribution patterns suggested that amd maps distal to the Np-2, Tcr alpha, and Myhc alpha loci.
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