-
1
-
-
0035189356
-
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
-
Birkenhäger R et al (2001) Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nat Med 29: 310-314
-
(2001)
Nat. Med.
, vol.29
, pp. 310-314
-
-
Birkenhäger, R.1
-
2
-
-
0037122805
-
X-ray structure of a CLC chloride channel at 3.0 Å reveals the molecular basis of anion selectivity
-
Dutzler R, Campbell EB, Cadene M, Chait BT, MacKinnon R (2002) X-ray structure of a CLC chloride channel at 3.0 Å reveals the molecular basis of anion selectivity. Nature 415: 287-294
-
(2002)
Nature
, vol.415
, pp. 287-294
-
-
Dutzler, R.1
Campbell, E.B.2
Cadene, M.3
Chait, B.T.4
MacKinnon, R.5
-
4
-
-
0345146920
-
Conservation of chloride channel structure revealed by an inhibitor binding site in CIC-1
-
Estévez R, Schroeder BC, Accardi A, Jentsch TJ, Pusch M (2003) Conservation of chloride channel structure revealed by an inhibitor binding site in CIC-1. Neuron 38: 47-59
-
(2003)
Neuron
, vol.38
, pp. 47-59
-
-
Estévez, R.1
Schroeder, B.C.2
Accardi, A.3
Jentsch, T.J.4
Pusch, M.5
-
5
-
-
0036083537
-
Molecular structure and physiological function of chloride channels
-
Jentsch TJ, Stein V, Weinreich F, Zdebik AA (2002) Molecular structure and physiological function of chloride channels. Physiol Rev 82: 503-568
-
(2002)
Physiol. Rev.
, vol.82
, pp. 503-568
-
-
Jentsch, T.J.1
Stein, V.2
Weinreich, F.3
Zdebik, A.A.4
-
6
-
-
0028360729
-
Two highly homologous members of the CIC chloride channel family in both rat and human kidney
-
Kieferle S, Fong P, Bens M, Vandewalle A, Jentsch TJ (1994) Two highly homologous members of the CIC chloride channel family in both rat and human kidney. Proc Natl Acad Sci USA 91: 6943-6947
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 6943-6947
-
-
Kieferle, S.1
Fong, P.2
Bens, M.3
Vandewalle, A.4
Jentsch, T.J.5
-
7
-
-
0034920817
-
Intrarenal and cellular localization of CLC-K2 protein in the mouse kidney
-
Kobayashi K, Uchida S, Mizutani S, Sasaki S, Marumo F (2001) Intrarenal and cellular localization of CLC-K2 protein in the mouse kidney. J Am Soc Nephrol 12:1327-1334
-
(2001)
J. Am. Soc. Nephrol.
, vol.12
, pp. 1327-1334
-
-
Kobayashi, K.1
Uchida, S.2
Mizutani, S.3
Sasaki, S.4
Marumo, F.5
-
8
-
-
0036073613
-
Molecular requisites for drug binding to muscle CLC-1 and renal CLC-K channel revealed by the use of phenoxy-alkyl derivatives of 2-(p-chlorophenoxy)propionic acid
-
Liantonio A et al (2002) Molecular requisites for drug binding to muscle CLC-1 and renal CLC-K channel revealed by the use of phenoxy-alkyl derivatives of 2-(p-chlorophenoxy)propionic acid. Mol Pharmacol 62: 265-271
-
(2002)
Mol. Pharmacol.
, vol.62
, pp. 265-271
-
-
Liantonio, A.1
-
9
-
-
9144241252
-
Investigations of pharmacologic properties of the renal CLC-K1 chloride channel co-expressed with barttin by the use of 2-(p-chlorophenoxy)propionic acid derivatives and other structurally unrelated chloride channels blockers
-
Liantonio A et al (2004) Investigations of pharmacologic properties of the renal CLC-K1 chloride channel co-expressed with barttin by the use of 2-(p-chlorophenoxy)propionic acid derivatives and other structurally unrelated chloride channels blockers. J Am Soc Nephrol 15: 13-20
-
(2004)
J. Am. Soc. Nephrol.
, vol.15
, pp. 13-20
-
-
Liantonio, A.1
-
10
-
-
0032947011
-
Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channel
-
Matsumura Y et al (1999) Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channel. Nat Genet 21: 95-98
-
(1999)
Nat. Genet.
, vol.21
, pp. 95-98
-
-
Matsumura, Y.1
-
11
-
-
4344666270
-
Molecular determinants of differential pore blocking of kidney CLC-K chloride channels
-
Picollo A, Liantonio A, Didonna MP, Elia L, Conte Camerino D, Pusch M (2004) Molecular determinants of differential pore blocking of kidney CLC-K chloride channels. EMBO Rep 5: 584-589
-
(2004)
EMBO Rep.
, vol.5
, pp. 584-589
-
-
Picollo, A.1
Liantonio, A.2
Didonna, M.P.3
Elia, L.4
Conte Camerino, D.5
Pusch, M.6
-
12
-
-
16944366243
-
Mutations in the chloride channel gene CLCNKB, cause Bartter's syndrome type III
-
Simon D et al (1997) Mutations in the chloride channel gene CLCNKB, cause Bartter's syndrome type III. Nat Genet 17: 171-178
-
(1997)
Nat. Genet.
, vol.17
, pp. 171-178
-
-
Simon, D.1
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