(Q48891110)

16 February 2018

title

Suppressive interactions between mutations located in the two nucleotide binding domains of CFTR. (English)

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16 February 2018

author name string

Wei L

1

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16 February 2018

Vankeerberghen A

2

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16 February 2018

Jaspers M

3

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16 February 2018

Cassiman J

4

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16 February 2018

Nilius B

5

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16 February 2018

Cuppens H

6

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16 February 2018

language of work or name

English

0 references

publication date

1 May 2000

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16 February 2018

published in

FEBS Letters

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16 February 2018

volume

473

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16 February 2018

issue

2

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16 February 2018

page(s)

149-153

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16 February 2018

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

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21 January 2018

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Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents

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CFTR as a cAMP-dependent regulator of sodium channels

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Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance.

21 January 2018

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Detection of 98.5% of the mutations in 200 Belgian cystic fibrosis alleles by reverse dot-blot and sequencing of the complete coding region and exon/intron junctions of the CFTR gene

21 January 2018

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21 January 2018

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Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels

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

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10.1016/S0014-5793(00)01519-2

7 January 2021

Identifiers

DOI

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16 February 2018

1 reference

16 February 2018