Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies

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Bibliographic Details
Published in:Leukemia 2021-11, Vol.35 (11), p.3304-3308
Main Authors: Decker, Melanie, Lammens, Tim, Ferster, Alina, Erlacher, Miriam, Yoshimi, Ayami, Niemeyer, Charlotte M., Ernst, Martijn P. T., Raaijmakers, Marc H. G. P., Duployez, Nicolas, Flaum, Andreas, Steinemann, Doris, Schlegelberger, Brigitte, Illig, Thomas, Ripperger, Tim
Format: Article
Language:English
Subjects:
13/95
42/70
631/208/2489/144/68
631/208/68
692/308/2056
692/308/575
692/420/2489/1512
82/1
96/109
96/33
96/35
96/44
Biochemical assays
Biological Assay
Blood platelet disorders
Blood Platelet Disorders - genetics
Blood Platelet Disorders - metabolism
Blood Platelet Disorders - pathology
Cancer
Cancer Research
Classification
Core Binding Factor Alpha 2 Subunit - classification
Core Binding Factor Alpha 2 Subunit - genetics
Core Binding Factor Alpha 2 Subunit - metabolism
Core Binding Factor beta Subunit - genetics
Core Binding Factor beta Subunit - metabolism
Critical Care Medicine
Familial diseases
Genetic aspects
Genetic Predisposition to Disease
Genetic variation
Hematology
Humans
Intensive
Internal Medicine
Investigations
Letter
Leukemia
Leukemia, Erythroblastic, Acute - genetics
Leukemia, Erythroblastic, Acute - metabolism
Leukemia, Erythroblastic, Acute - pathology
Leukemia, Myeloid, Acute - genetics
Leukemia, Myeloid, Acute - metabolism
Leukemia, Myeloid, Acute - pathology
Medicine
Medicine & Public Health
Mutation
Myelodysplastic syndromes
Myeloproliferative Disorders - genetics
Myeloproliferative Disorders - metabolism
Myeloproliferative Disorders - pathology
Oncology
Oncology, Experimental
Pediatrics
Phosphorylation
Risk factors
Runx1 protein
Transcriptional Activation
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ISSN:0887-6924
1476-5551
DOI:10.1038/s41375-021-01200-w