Molecular pathology of renal chloride channels and calcium metabolism

Molecular pathology of renal chloride channels and calcium metabolism

Bibliografiska uppgifter
Huvudupphovsman:	Thakker, R
Materialtyp:	Conference item
Publicerad:	2003

Liknande verk

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Chloride channels in renal disease.
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Low molecular weight ('tubular') proteinuria in patients with mutations of the CLCN5 renal chloride channel gene.
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Renal chloride channel, CLCN5, mutations in Dent's disease.
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Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
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Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5.
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Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease.
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Renal ion channels: Function and regulation - Preface
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Modeling study of human renal chloride channel (hCLC-5) mutations suggests a structural-functional relationship.
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The Calcium-Activated Chloride Channel TMEM16A is Inhibitied by Liquiritigenin
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Gating the pore of the calcium-activated chloride channel TMEM16A
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Permeation Mechanisms in the TMEM16B Calcium-Activated Chloride Channels.
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ANO1: More Than Just Calcium-Activated Chloride Channel in Cancer
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Mechanism of pore opening in the calcium-activated chloride channel TMEM16A
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