Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5

Author:

Jouret François,Igarashi Takashi,Gofflot Françoise,Wilson Patricia D.,Karet Fiona E.,Thakker Rajesh V.,Devuyst Olivier

Publisher

Elsevier BV

Subject

Nephrology

Reference35 articles.

1. Molecular structure and physiological function of chloride channels;Jentsch;Physiol Rev,2002

2. Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis);Fisher;Hum Mol Genet,1994

3. A common molecular basis for three inherited kidney stone diseases;Lloyd;Nature,1996

4. X-linked hypercalciuric nephrolithiasis: Clinical syndromes and chloride channel mutations;Scheinman;Kidney Int,1998

5. ClC-5, the chloride channel mutated in Dent's disease, co-localizes with the proton pump in endocytotically active kidney cells;Günther;Proc Natl Acad Sci USA,1998

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