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Literature DB >> 26372836

Twenty-five years of CLC chloride transport proteins.

Peying Fong¹.

Abstract

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Year: 2015 PMID： 26372836 PMCID： PMC4594284 DOI： 10.1113/JP271325

Source DB: PubMed Journal: J Physiol ISSN： 0022-3751 Impact factor: 5.182

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14 in total

1. X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity.

Authors: Raimund Dutzler; Ernest B Campbell; Martine Cadene; Brian T Chait; Roderick MacKinnon
Journal: Nature Date: 2002-01-17 Impact factor: 49.962

2. Secondary active transport mediated by a prokaryotic homologue of ClC Cl- channels.

Authors: Alessio Accardi; Christopher Miller
Journal: Nature Date: 2004-02-26 Impact factor: 49.962

3. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

Authors: D B Simon; R S Bindra; T A Mansfield; C Nelson-Williams; E Mendonca; R Stone; S Schurman; A Nayir; H Alpay; A Bakkaloglu; J Rodriguez-Soriano; J M Morales; S A Sanjad; C M Taylor; D Pilz; A Brem; H Trachtman; W Griswold; G A Richard; E John; R P Lifton
Journal: Nat Genet Date: 1997-10 Impact factor: 38.330

4. Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes.

Authors: T J Jentsch; K Steinmeyer; G Schwarz
Journal: Nature Date: 1990-12-06 Impact factor: 49.962

Review 5. In the beginning: a personal reminiscence on the origin and legacy of ClC-0, the 'Torpedo Cl(-) channel'.

Authors: Christopher Miller
Journal: J Physiol Date: 2015-01-05 Impact factor: 5.182

Review 6. Structure and gating of CLC channels and exchangers.

Authors: Alessio Accardi
Journal: J Physiol Date: 2015-07-28 Impact factor: 5.182

7. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.

Authors: R Birkenhäger; E Otto; M J Schürmann; M Vollmer; E M Ruf; I Maier-Lutz; F Beekmann; A Fekete; H Omran; D Feldmann; D V Milford; N Jeck; M Konrad; D Landau; N V Knoers; C Antignac; R Sudbrak; A Kispert; F Hildebrandt
Journal: Nat Genet Date: 2001-11 Impact factor: 38.330

Twenty-five years of CLC chloride transport proteins.

1. X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity.

2. Secondary active transport mediated by a prokaryotic homologue of ClC Cl- channels.

3. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

4. Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes.

Review 5. In the beginning: a personal reminiscence on the origin and legacy of ClC-0, the 'Torpedo Cl(-) channel'.

Review 6. Structure and gating of CLC channels and exchangers.

7. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.

8. Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion.

9. Two highly homologous members of the ClC chloride channel family in both rat and human kidney.

10. Open-state substructure of single chloride channels from Torpedo electroplax.

1. Dynamical model of the CLC-2 ion channel reveals conformational changes associated with selectivity-filter gating.