MYH9related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype
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Nonmuscle myosin-2: mix and matchRenal manifestations of patients with MYH9-related disorders.Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias.The abnormal proplatelet formation in MYH9-related macrothrombocytopenia results from an increased actomyosin contractility and is rescued by myosin IIA inhibition.MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.Congenital macrothrombocytopenia is a heterogeneous disorder in India.Life without double-headed non-muscle myosin II motor proteins.The role of vertebrate nonmuscle Myosin II in development and human disease.
P2860
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P2860
MYH9related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована у квітні 2010
@uk
name
MYH9related disease: four nove ...... with a mild clinical phenotype
@en
MYH9related disease: four nove ...... with a mild clinical phenotype
@nl
type
label
MYH9related disease: four nove ...... with a mild clinical phenotype
@en
MYH9related disease: four nove ...... with a mild clinical phenotype
@nl
prefLabel
MYH9related disease: four nove ...... with a mild clinical phenotype
@en
MYH9related disease: four nove ...... with a mild clinical phenotype
@nl
P2093
P50
P1476
MYH9related disease: four nove ...... with a mild clinical phenotype
@en
P2093
Annalisa Pastore
Carlo L. Balduini
Carmelo Paparo
Luigi Podda
Nuria Pujol-Moix
P304
P356
10.1111/J.1600-0609.2009.01398.X
P577
2010-04-01T00:00:00Z