(Q48059067)

English

Function of Xenopus cystic fibrosis transmembrane conductance regulator (CFTR) Cl channels and use of human-Xenopus chimeras to investigate the pore properties of CFTR.

scientific article published in October 1996

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scholarly article

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

Function of Xenopus cystic fibrosis transmembrane conductance regulator (CFTR) Cl channels and use of human-Xenopus chimeras to investigate the pore properties of CFTR. (English)

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

cystic fibrosis

0 references

transmembrane protein

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author name string

Price MP

1

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

Ishihara H

2

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

Sheppard DN

3

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

Welsh MJ

4

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

language of work or name

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publication date

1 October 1996

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

Journal of Biological Chemistry

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

271

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

41

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

25184-25191

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

The cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Effects of vasopressin on single Cl- channels in the apical membrane of distal nephron cells (A6).

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

cAMP-activated apical membrane chloride channels in Necturus gallbladder epithelium. Conductance, selectivity, and block

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Identification and developmental expression of the Xenopus laevis cystic fibrosis transmembrane conductance regulator gene.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Cap-independent translation of mRNA conferred by encephalomyocarditis virus 5' sequence improves the performance of the vaccinia virus/bacteriophage T7 hybrid expression system

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Calcium and cAMP activate different chloride channels in the apical membrane of normal and cystic fibrosis epithelia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Novel pore-lining residues in CFTR that govern permeation and open-channel block

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Molecular analysis of the ovine cystic fibrosis transmembrane conductance regulator gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

The amino-terminal portion of CFTR forms a regulated Cl- channel.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Multi-ion pore behaviour in the CFTR chloride channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.41.25184

21 January 2018

Identifiers

10.1074/JBC.271.41.25184

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8810276

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