(Q40488178)

21 September 2017

1 reference

title

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis (English)

1 reference

21 September 2017

0 references

1

M. J. Welsh

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7686820

18 August 2024

author name string

A. E. Smith

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7686820

18 August 2024

language of work or name

English

0 references

publication date

1 July 1993

1 reference

21 September 2017

2 July 1993

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7686820

full work available at URL

18 August 2024

https://doi.org/10.1016/0092-8674(93)90353-r

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7686820

https://api.elsevier.com/content/article/PII:009286749390353R?httpAccept=text/xml

18 August 2024

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

https://api.elsevier.com/content/article/PII:009286749390353R?httpAccept=text/plain

18 August 2024

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

18 August 2024

1 reference

21 September 2017

volume

73

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21 September 2017

issue

7

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21 September 2017

page(s)

1251-1254

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Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains

21 September 2017

cites work

1

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

Defective acidification of intracellular organelles in cystic fibrosis

18 August 2024

3

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

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

18 August 2024

5

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

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

18 August 2024

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1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

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

18 August 2024

7

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

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

18 August 2024

8

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

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

18 August 2024

9

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene

18 August 2024

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1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

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

18 August 2024

11

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis

18 August 2024

12

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland

18 August 2024

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1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

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

18 August 2024

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Cystic fibrosis: a disease in electrolyte transport.

18 August 2024

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

18 August 2024

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

18 August 2024

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https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels

18 August 2024

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Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast

18 August 2024

20

1 reference

https://api.crossref.org/works/10.1016/0092-8674(93)90353-R

Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: A report from the cystic fibrosis genetic analysis consortium

18 August 2024

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

18 August 2024

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1 reference

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18 August 2024

Identifiers

1 reference

21 September 2017

1 reference