Constitutive phosphorylation of Akt/PKB protein in acute myeloid leukemia: its significance as a prognostic variable
Leukemia, 2003•nature.com
1 Shurtleff SA, Buijs A, Behm FG, Rubnitz JE, Raimondi SC, Hancock ML et al. TEL/AML1
fusion resulting from a cryptic t (12; 21) is the most common genetic lesion in pediatric ALL
and defines a subgroup of patients with an excellent prognosis. Leukemia 1995; 9: 1985–
1989. 2 Borkhardt A, Cazzaniga G, Viehmann S, Valsecchi MG, Ludwig WD, Burci L et al.
Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute
lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials …
fusion resulting from a cryptic t (12; 21) is the most common genetic lesion in pediatric ALL
and defines a subgroup of patients with an excellent prognosis. Leukemia 1995; 9: 1985–
1989. 2 Borkhardt A, Cazzaniga G, Viehmann S, Valsecchi MG, Ludwig WD, Burci L et al.
Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute
lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials …
1 Shurtleff SA, Buijs A, Behm FG, Rubnitz JE, Raimondi SC, Hancock ML et al. TEL/AML1 fusion resulting from a cryptic t (12; 21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis. Leukemia 1995; 9: 1985–1989. 2 Borkhardt A, Cazzaniga G, Viehmann S, Valsecchi MG, Ludwig WD, Burci L et al. Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials. Associazione Italiana Ematologia Oncologia Pediatrica and the Berlin–Frankfurt–Munster Study Group. Blood 1997; 90: 571–577.
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