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Volumn 12, Issue 5, 2014, Pages 761-772

Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: Potential role for candidate RUNX1 targets

Author keywords

Blood platelet disorder; FPD AML; NF E2 transcription factor; Platelet function tests; Rab27B protein, human; RUNX1 protein

Indexed keywords

INTEGRIN; MYOSIN LIGHT CHAIN; MYOSIN LIGHT CHAIN 9; PADGEM PROTEIN; RNA; THROMBOSPONDIN 1; TRANSCRIPTION FACTOR NF E2 P45 SUBUNIT; TRANSCRIPTION FACTOR RUNX1; UNCLASSIFIED DRUG; ADENOSINE TRIPHOSPHATE; BETA3 INTEGRIN; GLYCOPROTEIN IIB; NFE2 PROTEIN, HUMAN; RUNX1 PROTEIN, HUMAN; TYROSINE;

EID: 84901196941     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/jth.12550     Document Type: Article
Times cited : (57)

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