(Q44200339)

30 November 2017

Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation (English)

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30 November 2017

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9

Gérard Lenoir

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30 November 2017

Isabelle Sermet-Gaudelus

1

object named as

Isabelle Sermet-Gaudelus

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30 November 2017

6

Anne Fajac

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30 November 2017

11

Aleksander Edelman

1 reference

30 November 2017

Benoit Vallée

2

1 reference

30 November 2017

Ilse Urbin

3

1 reference

30 November 2017

Tania Torossi

4

1 reference

30 November 2017

Rémi Marianovski

5

1 reference

30 November 2017

Marie-Noëlle Feuillet

7

1 reference

30 November 2017

Jean-Louis Bresson

8

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30 November 2017

Jean François Bernaudin

10

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30 November 2017

language of work or name

English

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publication date

1 November 2002

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30 November 2017

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30 November 2017

52

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30 November 2017

5

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30 November 2017

628-635

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https://scigraph.springernature.com/pub.10.1203/00006450-200211000-00005

30 November 2017

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cites work

Identification of the cystic fibrosis gene: genetic analysis

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

The diagnosis of cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

Aspirin and some other nonsteroidal anti-inflammatory drugs inhibit cystic fibrosis transmembrane conductance regulator protein gene expression in T-84 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

In vivo activation of the cystic fibrosis transmembrane conductance regulator mutant deltaF508 in murine nasal epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

Activation of chloride channels in normal and cystic fibrosis airway epithelial cells by multifunctional calcium/calmodulin-dependent protein kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

Modifier genes and variation in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

Lack of correlation between CFTR expression, CFTR Cl- currents, amiloride-sensitive Na+ conductance, and cystic fibrosis phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200211000-00005

10.1203/00006450-200211000-00005

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

30 November 2017

1022202101

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Fatcat ID

release_whucxsyfszbhnhaw3vaj25uuuy

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/whucxsyfszbhnhaw3vaj25uuuy

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference