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In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis.
Michaud J, Wu F, Osato M, Cottles GM, Yanagida M, Asou N, Shigesada K, Ito Y, Benson KF, Raskind WH, Rossier C, Antonarakis SE, Israels S, McNicol A, Weiss H, Horwitz M, Scott HS. Michaud J, et al. Among authors: ito y. Blood. 2002 Feb 15;99(4):1364-72. doi: 10.1182/blood.v99.4.1364. Blood. 2002. PMID: 11830488 Free article.
Heterozygous PU.1 mutations are associated with acute myeloid leukemia.
Mueller BU, Pabst T, Osato M, Asou N, Johansen LM, Minden MD, Behre G, Hiddemann W, Ito Y, Tenen DG. Mueller BU, et al. Among authors: ito y. Blood. 2002 Aug 1;100(3):998-1007. doi: 10.1182/blood.v100.3.998. Blood. 2002. PMID: 12130514 Free article.
Heterozygous PU.1 mutations are associated with acute myeloid leukemia.
Mueller BU, Pabst T, Osato M, Asou N, Johansen LM, Minden MD, Behre G, Hiddemann W, Ito Y, Tenen DG. Mueller BU, et al. Among authors: ito y. Blood. 2003 Mar 1;101(5):2074. doi: 10.1182/blood-2002-12-3903. Blood. 2003. PMID: 12584148 Free article. No abstract available.
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