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注意:仅列出部分参考文献,下载原文获取全部文献信息。PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis
Immacolata Andolfo et al.
HAEMATOLOGICA (2018)
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Mechanical stretch triggers rapid epithelial cell division through Piezo1
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PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus
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Piezo1-dependent regulation of urinary osmolarity
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Dehydrated stomatocytic anemia due to the heterozygous mutation R2456H in the mechanosensitive cation channel PIEZO1: a case report
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Hereditary xerocytosis and familial haemolysis due to mutation in the PIEZO1 gene: a simple diagnostic approach
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Piezol integration of vascular architecture with physiological force
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Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
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Xerocytosis is caused by mutations that alter the kinetics of the mechanosensitive channel PIEZO1
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Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels
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Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis
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