1. Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
- Author
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Brigitte Schlegelberger, Martijn P. T. Ernst, Charlotte M. Niemeyer, Andreas Flaum, Ayami Yoshimi, Miriam Erlacher, Melanie Decker, Thomas Illig, Tim Lammens, Nicolas Duployez, Alina Ferster, Doris Steinemann, Tim Ripperger, Marc H.G.P. Raaijmakers, and Hematology
- Subjects
Transcriptional Activation ,Cancer Research ,medicine.medical_specialty ,Cancer genetics ,Genetic testing ,Translational research ,Genetics research ,Letter ,Myeloid ,Platelet disorder ,MEDLINE ,HEMATOPOIESIS ,Bioinformatics ,Anesthésiologie ,Core Binding Factor beta Subunit ,chemistry.chemical_compound ,Text mining ,Internal medicine ,Medicine and Health Sciences ,Medicine ,Humans ,Genetic Predisposition to Disease ,Phosphorylation ,Hematology ,Myeloproliferative Disorders ,business.industry ,PREDISPOSITION ,Cancérologie ,Leukemia, Myeloid, Acute ,Anesthesiology and Pain Medicine ,medicine.anatomical_structure ,Oncology ,RUNX1 ,chemistry ,Core Binding Factor Alpha 2 Subunit ,Mutation ,Biological Assay ,Blood Platelet Disorders ,Leukemia, Erythroblastic, Acute ,business ,LEUKEMIA ,Hématologie - Abstract
SCOPUS: ar.j, info:eu-repo/semantics/published
- Published
- 2021