标题
Piezo channels: from structure to function
作者
关键词
Piezo1, Piezo2, Mechanotransduction, Channels, Touch, Pain, Somatosensation
出版物
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
Volume 467, Issue 1, Pages 95-99
出版商
Springer Nature
发表日期
2014-07-19
DOI
10.1007/s00424-014-1578-z
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5
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- Merkel Cells Transduce and Encode Tactile Stimuli to Drive Aβ-Afferent Impulses
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- Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
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- piezo2bRegulates Vertebrate Light Touch Response
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- Runx1 Controls Terminal Morphology and Mechanosensitivity of VGLUT3-expressing C-Mechanoreceptors
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- Xerocytosis is caused by mutations that alter the kinetics of the mechanosensitive channel PIEZO1
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- Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis
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- Piezo1 and Piezo2 Are Essential Components of Distinct Mechanically Activated Cation Channels
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- Hereditary stomatocytosis and cation leaky red cells — Recent developments
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- Integrin activation by Fam38A uses a novel mechanism of R-Ras targeting to the endoplasmic reticulum
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- p73 poses a barrier to malignant transformation by limiting anchorage-independent growth
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