(Q44790624)

English

Additional disruption of the ClC-2 Cl(-) channel does not exacerbate the cystic fibrosis phenotype of cystic fibrosis transmembrane conductance regulator mouse models

scientific article published on 7 March 2004

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scholarly article

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Europe PubMed Central

PubMed publication ID

6 December 2017

Additional disruption of the ClC-2 Cl(-) channel does not exacerbate the cystic fibrosis phenotype of cystic fibrosis transmembrane conductance regulator mouse models (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

cystic fibrosis

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transmembrane protein

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5

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

object named as

Marko Bertog

3

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author name string

Anselm A Zdebik

1

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

John E Cuffe

2

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Christoph Korbmacher

4

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

language of work or name

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publication date

7 March 2004

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Europe PubMed Central

PubMed publication ID

6 December 2017

number of pages

8

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based on heuristic

inferred from page(s)

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

279

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Europe PubMed Central

PubMed publication ID

6 December 2017

21

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Europe PubMed Central

PubMed publication ID

6 December 2017

22276-22283

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Europe PubMed Central

PubMed publication ID

6 December 2017

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

CFTR as a cAMP-dependent regulator of sodium channels

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

The cystic fibrosis transmembrane conductance regulator attenuates the endogenous Ca2+ activated Cl- conductance of Xenopus oocytes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

An animal model for cystic fibrosis made by gene targeting

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

A mouse model for the delta F508 allele of cystic fibrosis.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Amelioration of intestinal disease severity in cystic fibrosis mice is associated with improved chloride secretory capacity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Molecular structure and physiological function of chloride channels

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

The skeletal muscle chloride channel in dominant and recessive human myotonia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

A common molecular basis for three inherited kidney stone diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

A chloride channel widely expressed in epithelial and non-epithelial cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

CIC-2: a developmentally dependent chloride channel expressed in the fetal lung and downregulated after birth.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Molecular dissection of gating in the ClC-2 chloride channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Analysis of ClC-2 channels as an alternative pathway for chloride conduction in cystic fibrosis airway cells.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Regions involved in the opening of CIC-2 chloride channel by voltage and cell volume

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Male germ cells and photoreceptors, both dependent on close cell-cell interactions, degenerate upon ClC-2 Cl(-) channel disruption

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Loss of hyperpolarization-activated Cl(-) current in salivary acinar cells from Clcn2 knockout mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Basolateral PAR-2 receptors mediate KCl secretion and inhibition of Na+ absorption in the mouse distal colon

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

A constitutively open potassium channel formed by KCNQ1 and KCNE3

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Cystic fibrosis and the salt controversy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Distribution of ClC-2 chloride channel in rat and human epithelial tissues

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Inward-rectifying anion channels are expressed in the epithelial cells of choroid plexus isolated from ClC-2 'knock-out' mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Role of airway surface liquid and submucosal glands in cystic fibrosis lung disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Expression of cystic fibrosis transmembrane regulator Cl- channels in heart

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309899200

21 January 2018

Identifiers

10.1074/JBC.M309899200

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

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