Showing results (51-60 of 99) with videos related to

Sort By:
Pageof 10
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cellsW Günther, A Lüchow, F Cluzeaud, et al.
The Journal of Biological Chemistry|June 17, 1998
Golgi localization and functionally important domains in the NH2 and COOH terminus of the yeast CLC putative chloride channel Gef1pB Schwappach, S Stobrawa, M Hechenberger, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1991
Completely functional double-barreled chloride channel expressed from a single Torpedo cDNAC K Bauer, K Steinmeyer, J R Schwarz, et al.
The Journal of Biological Chemistry|December 29, 1995
Cloning and functional expression of rat CLC-5, a chloride channel related to kidney diseaseK Steinmeyer, B Schwappach, M Bens, et al.
The EMBO Journal|February 15, 1994
Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen)K Steinmeyer, C Lorenz, M Pusch, et al.
Experimental Eye Research|August 1, 1985
Response of the intracellular potentials of cultured bovine lens cells to ions and inhibitorsT J Jentsch, B von der Haar, S K Keller, et al.
Nature|December 1, 2000
ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's diseaseN Piwon, W Günther, M Schwake, et al.
The Journal of Biological Chemistry|September 15, 1986
The regulation of intracellular pH in monkey kidney epithelial cells (BSC-1). Roles of Na+/H+ antiport, Na+-HCO3(-)-(NaCO3-) symport, and Cl-/HCO3- exchangeT J Jentsch, I Janicke, D Sorgenfrei, et al.
The Journal of Biological Chemistry|May 19, 2000
KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currentsB C Schroeder, M Hechenberger, F Weinreich, et al.
Human Molecular Genetics|June 1, 1994
Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotoniaC Lorenz, C Meyer-Kleine, K Steinmeyer, et al.
Pageof 10