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The mouse mutation "thrombocytopenia and cardiomyopathy" (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia.
Chase TH, Lyons BL, Bronson RT, Foreman O, Donahue LR, Burzenski LM, Gott B, Lane P, Harris B, Ceglarek U, Thiery J, Wittenburg H, Thon JN, Italiano JE Jr, Johnson KR, Shultz LD. Chase TH, et al. Among authors: shultz ld. Blood. 2010 Feb 11;115(6):1267-76. doi: 10.1182/blood-2009-05-219808. Epub 2009 Oct 21. Blood. 2010. PMID: 19846887 Free PMC article.
Mouse models of genetic diseases.
Leiter EH, Beamer WG, Shultz LD, Barker JE, Lane PW. Leiter EH, et al. Among authors: shultz ld. Birth Defects Orig Artic Ser. 1987;23(3):221-57. Birth Defects Orig Artic Ser. 1987. PMID: 3307936 Review. No abstract available.
The interleukin-12 beta subunit (p40) maps to mouse chromosome 11.
Noben-Trauth N, Schweitzer PA, Johnson KR, Wolf SF, Knowles BB, Shultz LD. Noben-Trauth N, et al. Among authors: shultz ld. Mamm Genome. 1996 May;7(5):392. doi: 10.1007/s003359900113. Mamm Genome. 1996. PMID: 8661733 No abstract available.
495 results