The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR. (Q41565014)

3 October 2017

The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR. (English)

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3 October 2017

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Li C

1

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3 October 2017

Ramjeesingh M

2

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3 October 2017

Reyes E

3

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3 October 2017

Jensen T

4

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3 October 2017

Chang X

5

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3 October 2017

Rommens JM

6

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3 October 2017

Bear CE

7

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3 October 2017

language of work or name

English

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publication date

1 April 1993

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3 October 2017

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3 October 2017

3

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3 October 2017

4

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3 October 2017

311-316

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https://scigraph.springernature.com/pub.10.1038/ng0493-311

3 October 2017

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cites work

Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene

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Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

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Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation

21 January 2018

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Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

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Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2

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Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia

21 January 2018

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Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

21 January 2018

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Nucleoside triphosphates are required to open the CFTR chloride channel.

21 January 2018

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A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein

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Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport

21 January 2018

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Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

21 January 2018

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Identification of the cystic fibrosis gene: genetic analysis

21 January 2018

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7 January 2021

Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland

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7 January 2021

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

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7 January 2021

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance

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7 January 2021

Synthesis of the membrane fusion and hemagglutinin proteins of measles virus, using a novel baculovirus vector containing the beta-galactosidase gene

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7 January 2021

cAMP-activated chloride conductance in the colonic cell line, Caco-2

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7 January 2021

Nystatin-induced liposome fusion. A versatile approach to ion channel reconstitution into planar bilayers

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7 January 2021

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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7 January 2021

A simplification of the protein assay method of Lowry et al. which is more generally applicable

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https://api.crossref.org/works/10.1038%2FNG0493-311

7 January 2021

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

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7 January 2021

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

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7 January 2021

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

1 reference

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7 January 2021

Identifiers

DOI

10.1038/NG0493-311

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Dimensions Publication ID

3 October 2017

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