MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.
about
Macrothrombocytopenia and dense granule deficiency associated with FLI1 variants: ultrastructural and pathogenic features.Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects.Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivationLessons in platelet production from inherited thrombocytopenias.Update on the causes of platelet disorders and functional consequences.Progress in understanding the diagnosis and molecular genetics of macrothrombocytopenias.Jacobsen syndrome: Advances in our knowledge of phenotype and genotype.Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.Inherited platelet dysfunction and hematopoietic transcription factor mutations.Germline variants in ETV6 underlie reduced platelet formation, platelet dysfunction and increased levels of circulating CD34+ progenitors.Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutation.Hematopoietic transcription factor mutations: important players in inherited platelet defects.FLI1 level during megakaryopoiesis affects thrombopoiesis and platelet biology.Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders.Life without double-headed non-muscle myosin II motor proteins.A role for RUNX1 in hematopoiesis and myeloid leukemia.Myelodysplastic syndromes and acute leukemia with genetic predispositions: a new challenge for hematologists.Gene of the issue: RUNX1 mutations and inherited bleeding.Successful use of eltrombopag for surgical preparation in a patient with ANKRD26-related thrombocytopenia.Challenges on the diagnostic approach of inherited platelet function disorders: Is a paradigm change necessary?
P2860
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P2860
MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
name
MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.
@ast
MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.
@en
type
label
MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.
@ast
MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.
@en
prefLabel
MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.
@ast
MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.
@en
P2093
P50
P1433
P1476
MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations
@en
P2093
Aline Renneville
Françoise Boehlen
Guy Leverger
Iléana Antony-Debré
Margot Morabito
Rémi Favier
Véronique Baccini
Yunhua Chang
P304
P356
10.1182/BLOOD-2012-04-422352
P407
P50
P577
2012-06-07T00:00:00Z