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CLC chloride channels: correlating structure with function
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scholarly article
1 reference
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Europe PubMed Central
PubMed ID
12163078
retrieved
4 August 2017
review article
1 reference
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Europe PubMed Central
title
CLC chloride channels: correlating structure with function
(English)
1 reference
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Europe PubMed Central
PubMed ID
12163078
retrieved
4 August 2017
author
Thomas Jentsch
object named as
Thomas J Jentsch
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2
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author name string
Raúl Estévez
series ordinal
1
1 reference
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Europe PubMed Central
PubMed ID
12163078
retrieved
4 August 2017
publication date
1 August 2002
1 reference
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Europe PubMed Central
PubMed ID
12163078
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4 August 2017
published in
Current Opinion in Structural Biology
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Europe PubMed Central
PubMed ID
12163078
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4 August 2017
volume
12
1 reference
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Europe PubMed Central
PubMed ID
12163078
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4 August 2017
issue
4
1 reference
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Europe PubMed Central
PubMed ID
12163078
retrieved
4 August 2017
page(s)
531-539
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Europe PubMed Central
PubMed ID
12163078
retrieved
4 August 2017
cites work
Molecular structure and physiological function of chloride channels
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7 January 2021
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The skeletal muscle chloride channel in dominant and recessive human myotonia
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Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
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Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion
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Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channel.
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Disruption of ClC-3, a chloride channel expressed on synaptic vesicles, leads to a loss of the hippocampus
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ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's disease.
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Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man
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A common molecular basis for three inherited kidney stone diseases
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Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
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Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene
1 reference
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X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity
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7 January 2021
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Dimeric structure of single chloride channels from Torpedo electroplax
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7 January 2021
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Completely functional double-barreled chloride channel expressed from a single Torpedo cDNA
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Purification, reconstitution, and subunit composition of a voltage-gated chloride channel from Torpedo electroplax
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Homodimeric architecture of a ClC-type chloride ion channel
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7 January 2021
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Two physically distinct pores in the dimeric ClC-0 chloride channel.
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7 January 2021
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Subunit stoichiometry of human muscle chloride channels
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7 January 2021
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Projection structure of a ClC-type chloride channel at 6.5 A resolution
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7 January 2021
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Heteromultimeric CLC chloride channels with novel properties
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7 January 2021
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Pores Formed by Single Subunits in Mixed Dimers of Different CLC Chloride Channels
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7 January 2021
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Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-440X%2802%2900358-5
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7 January 2021
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The muscle chloride channel ClC-1 has a double-barreled appearance that is differentially affected in dominant and recessive myotonia
1 reference
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7 January 2021
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Steady-state coupling of ion-channel conformations to a transmembrane ion gradient
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7 January 2021
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Gating of the voltage-dependent chloride channel CIC-0 by the permeant anion.
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7 January 2021
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Nonequilibrium gating and voltage dependence of the ClC-0 Cl- channel
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7 January 2021
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Permeation and block of the skeletal muscle chloride channel, ClC-1, by foreign anions
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7 January 2021
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Interaction of hydrophobic anions with the rat skeletal muscle chloride channel ClC-1: effects on permeation and gating
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Transmembrane topology of a CLC chloride channel
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7 January 2021
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Pore-forming segments in voltage-gated chloride channels
1 reference
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7 January 2021
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Pore stoichiometry of a voltage-gated chloride channel
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Residues lining the inner pore vestibule of human muscle chloride channels
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Reconstitution of functional voltage-gated chloride channels from complementary fragments of CLC-1.
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The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity
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7 January 2021
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Structure of the light-driven chloride pump halorhodopsin at 1.8 A resolution
1 reference
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7 January 2021
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Chemistry of ion coordination and hydration revealed by a K+ channel-Fab complex at 2.0 A resolution
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7 January 2021
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Identification of functionally important regions of the muscular chloride channel CIC-1 by analysis of recessive and dominant myotonic mutations
1 reference
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7 January 2021
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Functional and structural analysis of ClC-K chloride channels involved in renal disease.
1 reference
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7 January 2021
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Mutational analysis demonstrates that ClC-4 and ClC-5 directly mediate plasma membrane currents.
1 reference
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7 January 2021
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Analysis of a protein region involved in permeation and gating of the voltage-gated Torpedo chloride channel ClC-0
1 reference
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7 January 2021
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Inward rectification in ClC-0 chloride channels caused by mutations in several protein regions
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7 January 2021
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Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel
1 reference
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7 January 2021
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Temperature dependence of fast and slow gating relaxations of ClC-0 chloride channels
1 reference
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7 January 2021
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Myotonia caused by mutations in the muscle chloride channel gene CLCN1.
1 reference
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7 January 2021
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Identification of three cysteines as targets for the Zn2+ blockade of the human skeletal muscle chloride channel
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7 January 2021
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Elimination of the slow gating of ClC-0 chloride channel by a point mutation
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7 January 2021
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Extracellular zinc ion inhibits ClC-0 chloride channels by facilitating slow gating
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https://api.crossref.org/works/10.1016%2FS0959-440X%2802%2900358-5
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7 January 2021
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Determinants of slow gating in ClC-0, the voltage-gated chloride channel of Torpedo marmorata.
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-440X%2802%2900358-5
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7 January 2021
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Formation of CLC-0 chloride channels from separated transmembrane and cytoplasmic domains.
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7 January 2021
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The CLC chloride channel family
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7 January 2021
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An internalization signal in ClC-5, an endosomal Cl-channel mutated in dent's disease.
1 reference
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7 January 2021
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The structure of a domain common to archaebacteria and the homocystinuria disease protein
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7 January 2021
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Structure and mechanism of inosine monophosphate dehydrogenase in complex with the immunosuppressant mycophenolic acid
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7 January 2021
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Characteristics and crystal structure of bacterial inosine-5'-monophosphate dehydrogenase
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7 January 2021
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Golgi localization and functionally important domains in the NH2 and COOH terminus of the yeast CLC putative chloride channel Gef1p
1 reference
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7 January 2021
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Domain architecture of the heme-independent yeast cystathionine beta-synthase provides insights into mechanisms of catalysis and regulation
1 reference
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7 January 2021
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Mutations in the regulatory domain of cystathionine beta synthase can functionally suppress patient-derived mutations in cis.
1 reference
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7 January 2021
based on heuristic
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Relevance of the D13 region to the function of the skeletal muscle chloride channel, ClC-1.
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-440X%2802%2900358-5
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7 January 2021
based on heuristic
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High-level expression, functional reconstitution, and quaternary structure of a prokaryotic ClC-type chloride channel
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-440X%2802%2900358-5
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7 January 2021
based on heuristic
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Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-440X%2802%2900358-5
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7 January 2021
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Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-440X%2802%2900358-5
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7 January 2021
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Correction of disease-causing CBS mutations in yeast
1 reference
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7 January 2021
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Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-440X%2802%2900358-5
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7 January 2021
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Identification of a gene responsible for familial Wolff-Parkinson-White syndrome
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-440X%2802%2900358-5
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7 January 2021
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A mutation in PRKAG3 associated with excess glycogen content in pig skeletal muscle
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-440X%2802%2900358-5
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7 January 2021
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DOI
10.1016/S0959-440X(02)00358-5
1 reference
stated in
Europe PubMed Central
PubMed ID
12163078
retrieved
4 August 2017
Fatcat ID
release_3bqggn5fl5gw5osphivxlyqfge
1 reference
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Fatcat
reference URL
https://api.fatcat.wiki/v0/release/3bqggn5fl5gw5osphivxlyqfge
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24 November 2022
based on heuristic
mapped directly with Wikidata item
PubMed ID
12163078
1 reference
stated in
Europe PubMed Central
PubMed ID
12163078
retrieved
4 August 2017
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