Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression
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Title
Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression
Authors
Keywords
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Journal
BLOOD
Volume 120, Issue 13, Pages 2708-2718
Publisher
American Society of Hematology
Online
2012-08-17
DOI
10.1182/blood-2012-04-422337
References
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Related references
Note: Only part of the references are listed.- MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations
- (2012) I. Antony-Debre et al. BLOOD
- Microtubule and cortical forces determine platelet size during vascular platelet production
- (2012) Jonathan N Thon et al. Nature Communications
- RUNX1-induced silencing of non-muscle myosin heavy chain IIB contributes to megakaryocyte polyploidization
- (2012) Larissa Lordier et al. Nature Communications
- Myosin regulatory light chains are required to maintain the stability of myosin II and cellular integrity
- (2011) Inju Park et al. BIOCHEMICAL JOURNAL
- Down-regulation of the RUNX1-target gene NR4A3 contributes to hematopoiesis deregulation in familial platelet disorder/acute myelogenous leukemia
- (2011) D. Bluteau et al. BLOOD
- Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A
- (2011) Y. Zhang et al. BLOOD
- Aurora B is dispensable for megakaryocyte polyploidization, but contributes to the endomitotic process
- (2010) L. Lordier et al. BLOOD
- RUNX1/core binding factor A2 regulates platelet 12-lipoxygenase gene (ALOX12): studies in human RUNX1 haplodeficiency
- (2010) G. Kaur et al. BLOOD
- Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency
- (2010) G. Jalagadugula et al. BLOOD
- Proplatelet formation deficit and megakaryocyte death contribute to thrombocytopenia in Myh9 knockout mice
- (2010) A. ECKLY et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- Mechanism of platelet factor 4 (PF4) deficiency with RUNX1 haplodeficiency: RUNX1 is a transcriptional regulator of PF4
- (2010) K. ANEJA et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- MAL/SRF complex is involved in platelet formation and megakaryocyte migration by regulating MYL9 (MLC2) and MMP9
- (2009) L. Gilles et al. BLOOD
- High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder
- (2009) C. Preudhomme et al. BLOOD
- Integrative analysis of RUNX1 downstream pathways and target genes
- (2009) Joëlle Michaud et al. BMC GENOMICS
- P19INK4D links endomitotic arrest and megakaryocyte maturation and is regulated by AML-1
- (2008) L. Gilles et al. BLOOD
- Abnormal megakaryocyte morphology and proplatelet formation in mice with megakaryocyte-restricted MYH9 inactivation
- (2008) A. Eckly et al. BLOOD
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