(Q48930233)

16 February 2018

title

Characterization of mutations located in exon 18 of the CFTR gene. (English)

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16 February 2018

author name string

Vankeerberghen A

1

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16 February 2018

Wei L

2

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16 February 2018

Teng H

3

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16 February 2018

Jaspers M

4

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16 February 2018

Cassiman JJ

5

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16 February 2018

Nilius B

6

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16 February 2018

Cuppens H

7

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16 February 2018

language of work or name

English

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publication date

1 October 1998

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16 February 2018

published in

FEBS Letters

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16 February 2018

volume

437

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16 February 2018

issue

1-2

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16 February 2018

page(s)

1-4

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16 February 2018

Identification of the cystic fibrosis gene: chromosome walking and jumping

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1 reference

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

21 January 2018

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Identification of the cystic fibrosis gene: genetic analysis

21 January 2018

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Pyrophosphate stimulates wild-type and mutant cystic fibrosis transmembrane conductance regulator Cl- channels

21 January 2018

1 reference

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Intracellular loop between transmembrane segments IV and V of cystic fibrosis transmembrane conductance regulator is involved in regulation of chloride channel conductance state

21 January 2018

1 reference

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Disease-associated mutations in the fourth cytoplasmic loop of cystic fibrosis transmembrane conductance regulator compromise biosynthetic processing and chloride channel activity.

21 January 2018

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Cytoplasmic loop three of cystic fibrosis transmembrane conductance regulator contributes to regulation of chloride channel activity.

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901042-4

Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulator.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901042-4

Mutations in the putative pore‐forming domain of CFTR do not change anion selectivity of the cAMP activated Cl− conductance

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901042-4

Alternate translation initiation codons can create functional forms of cystic fibrosis transmembrane conductance regulator

21 January 2018

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Locating the anion-selectivity filter of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel.

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901042-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901042-4

Disease-Associated Mutations in Cytoplasmic Loops 1 and 2 of Cystic Fibrosis Transmembrane Conductance Regulator Impede Processing or Opening of the Channel†

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901042-4

Association of domains within the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901042-4

The two nucleotide-binding domains of cystic fibrosis transmembrane conductance regulator (CFTR) have distinct functions in controlling channel activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901042-4

10.1016/S0014-5793(98)01042-4

7 January 2021

Identifiers

DOI

1 reference

16 February 2018

1 reference

16 February 2018