5’UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia

Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived Malignancy

(2016) Katarzyna Rojek et al.   BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION

Correspondence Regarding the Consensus Statement from the Worldwide Network for Blood and Marrow Transplantation Standing Committee on Donor Issues

(2016) Jane E. Churpek et al.   BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION

Acute Myeloid Leukemia

(2015) Hartmut Döhner et al.   NEW ENGLAND JOURNAL OF MEDICINE

Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation

(2014) Dominique Bluteau et al.   JOURNAL OF CLINICAL INVESTIGATION

ANKRD26-related thrombocytopenia and myeloid malignancies

(2013) P. Noris et al.   BLOOD

Mutations in the 5′ UTR of ANKRD26, the Ankirin Repeat Domain 26 Gene, Cause an Autosomal-Dominant Form of Inherited Thrombocytopenia, THC2

(2011) Tommaso Pippucci et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families

(2011) P. Noris et al.   BLOOD

Ankrd26Gene Disruption Enhances Adipogenesis of Mouse Embryonic Fibroblasts

(2011) Zhaoliang Fei et al.   JOURNAL OF BIOLOGICAL CHEMISTRY