Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia
A-K Eisfeld(The Ohio State University), Clara D. Bloomfield(North Shore University Hospital), Christopher J. Walker(Ohio University), Shelley Orwick(St. Jude Children's Research Hospital), Maria R. Baer(University of Maryland, Baltimore), Jessica Kohlschmidt(The Ohio State University), Albert de la Chapelle(Université Claude Bernard Lyon 1), Jonathan E. Kolitz(Memorial Sloan Kettering Cancer Center), Richard M. Stone(Dana-Farber Cancer Institute), Andrew J. Carroll(University of Alabama at Birmingham), Krzysztof Mrózek(The Ohio State University), Chandni Shah(The Ohio State University), James S. Blachly(The Ohio State University Wexner Medical Center), Maryam A. Bainazar(The Ohio State University), Deedra Nicolet(The Ohio State University), Karl Kroll(The Ohio State University), John C. Byrd(University of Cincinnati), Bayard L. Powell(Atrium Health Wake Forest Baptist), Sebastian Schwind
Cited by 67
Related Papers
Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling
|Nature|2000|10k
PD-1 Blockade in Tumors with Mismatch-Repair Deficiency
|New England Journal of Medicine|2015|9.4k
Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel
|Blood|2016|5.9k