A cytoplasmic domain mutation in ClC-Kb affects long-distance communication across the membrane (Q30845345)

14 September 2017

A cytoplasmic domain mutation in ClC-Kb affects long-distance communication across the membrane (English)

1 reference

14 September 2017

Gilbert Q Martinez

1

1 reference

14 September 2017

Merritt Maduke

series ordinal

2

1 reference

14 September 2017

language of work or name

English

0 references

publication date

23 July 2008

1 reference

14 September 2017

1 reference

14 September 2017

3

1 reference

14 September 2017

7

1 reference

14 September 2017

e2746

1 reference

Creative Commons Attribution 4.0 International

14 September 2017

start time

23 July 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Biochemical and Structural Characterization of a Novel Family of Cystathionine β-Synthase Domain Proteins Fused to a Zn Ribbon-Like Domain

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CLC chloride channels and transporters: a biophysical and physiological perspective

14 July 2018

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The CLC 'chloride channel' family: revelations from prokaryotes

14 July 2018

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The structure of the cytoplasmic domain of the chloride channel ClC-Ka reveals a conserved interaction interface

14 July 2018

1 reference

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Structure of a CBS-domain pair from the regulatory gamma1 subunit of human AMPK in complex with AMP and ZMP

14 July 2018

1 reference

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Nucleotide recognition by the cytoplasmic domain of the human chloride transporter ClC-5

14 July 2018

1 reference

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Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6.

14 July 2018

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Crystal structure of the cytoplasmic domain of the chloride channel ClC-0.

14 July 2018

1 reference

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CBS domains: structure, function, and pathology in human proteins

14 July 2018

1 reference

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Cysteine accessibility in ClC-0 supports conservation of the ClC intracellular vestibule

14 July 2018

1 reference

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Physiological functions of CLC Cl- channels gleaned from human genetic disease and mouse models

14 July 2018

1 reference

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Function of chloride channels in the kidney

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Novel mutations of the chloride channel Kb gene in two Japanese patients clinically diagnosed as Bartter syndrome with hypocalciuria

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

CLCN2 and idiopathic generalized epilepsy

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Functional evaluation of human ClC-2 chloride channel mutations associated with idiopathic generalized epilepsies

14 July 2018

1 reference

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A role for CBS domain 2 in trafficking of chloride channel CLC-5

14 July 2018

1 reference

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14 July 2018

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Probing the pore of ClC-0 by substituted cysteine accessibility method using methane thiosulfonate reagents

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Molecular mechanisms of Bartter syndrome caused by mutations in the BSND gene

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

The ClC-5 chloride channel knock-out mouse - an animal model for Dent's disease.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Functional analysis of mutations in the gamma 2 subunit of AMP-activated protein kinase associated with cardiac hypertrophy and Wolff-Parkinson-White syndrome.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

CLC chloride channels: correlating structure with function

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Myotonia caused by mutations in the muscle chloride channel gene CLCN1.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Molecular structure and physiological function of chloride channels

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Regulation of human cystathionine beta-synthase by S-adenosyl-L-methionine: evidence for two catalytically active conformations involving an autoinhibitory domain in the C-terminal region

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Characteristics and crystal structure of bacterial inosine-5'-monophosphate dehydrogenase

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependence.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Golgi localization and functionally important domains in the NH2 and COOH terminus of the yeast CLC putative chloride channel Gef1p

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Determinants of slow gating in ClC-0, the voltage-gated chloride channel of Torpedo marmorata.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Reconstitution of functional voltage-gated chloride channels from complementary fragments of CLC-1.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

The structure of a domain common to archaebacteria and the homocystinuria disease protein

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Molecular basis for decreased muscle chloride conductance in the myotonic goat

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

A common molecular basis for three inherited kidney stone diseases

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Localization and functional characterization of rat kidney-specific chloride channel, ClC-K1

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Myotonias due to CLC-1 chloride channel mutations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

Effect of Ca2+ on Cl- transport in thin ascending limb of Henle's loop.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

The skeletal muscle chloride channel in dominant and recessive human myotonia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447174

CLC Chloride Channels and Transporters: From Genes to Protein Structure, Pathology and Physiology

14 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

Mice lacking renal chloride channel, CLC-5, are a model for Dent's disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

Functional and structural conservation of CBS domains from CLC chloride channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

Coexpression of complementary fragments of ClC-5 and restoration of chloride channel function in a Dent's disease mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

Formation of CLC-0 chloride channels from separated transmembrane and cytoplasmic domains.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

Functional and structural analysis of ClC-K chloride channels involved in renal disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

Crystal structure of a tandem cystathionine-beta-synthase (CBS) domain protein (TM0935) from Thermotoga maritima at 1.87 A resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

Association between activating mutations of calcium-sensing receptor and Bartter's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002746

Renal Chloride Channel, CLCN5, Mutations in Dent's Disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18648499

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Renal interstitial Ca(2+)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18648499

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Functional Characterization of a Calcium-Sensing Receptor Mutation in Severe Autosomal Dominant Hypocalcemia with a Bartter-Like Syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18648499

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0002746

1 reference

14 September 2017

0 references

1 reference

14 September 2017

PubMed publication ID

18648499

1 reference