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Article

Slower Piezo1 inactivation in dehydrated hereditary stomatocytosis (xerocytosis).

Biophysical journal - 20 Aug 2013

Demolombe Sophie, Duprat Fabrice, Honoré Eric, Patel Amanda

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Share to Anemia, Hemolytic, Congenital
Share to Dehydration
Share to Hydrops Fetalis
Share to Ion Channels

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 23972832
DOI: 10.1016/j.bpj.2013.07.018
PMCID: PMC3752110

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Related research

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Slower Piezo1 inactivation in dehydrated hereditary stomatocytosis (xerocytosis).PMID 23972832Read ↗

PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis.Semantic proximity Read ↗

Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels.Semantic proximity Read ↗

Variant spectrum of PIEZO1 and KCNN4 in Japanese patients with dehydrated hereditary stomatocytosisSemantic proximity Read ↗

Hereditary dehydrated stomatocytosis with splicing site mutation of PIEZO1 mimicking myelodysplastic syndrome diagnosed by targeted next-generation sequencing.Semantic proximity Read ↗

Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia.Semantic proximity Read ↗

Recent advances in the pathophysiology of PIEZO1 ‐related hereditary xerocytosisSemantic proximity Read ↗

PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood CellsSemantic proximity Read ↗

Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients.Semantic proximity Read ↗

Dehydrated stomatocytic anemia due to the heterozygous mutation R2456H in the mechanosensitive cation channel PIEZO1: a case report.Semantic proximity Read ↗

Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)Semantic proximity Read ↗

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.Semantic proximity Read ↗

Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutations.Semantic proximity Read ↗

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