Rescue of NBD2 mutants N1303K and S1235R of CFTR by small-molecule correctors and transcomplementation (Q28544842)

3

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Liudmila Cebotaru

6

object named as

Liudmila Cebotaru

0 references

William B Guggino

5

object named as

William B Guggino

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author name string

Daniele Rapino

1

0 references

Inna Sabirzhanova

2

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Rahul Grover

Creative Commons Attribution 4.0 International

4

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language of work or name

English

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publication date

2015

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published in

PLOS One

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volume

10

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issue

3

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page(s)

e0119796

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copyright license

start time

23 March 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Transcomplementation by a truncation mutant of cystic fibrosis transmembrane conductance regulator (CFTR) enhances ΔF508 processing through a biomolecular interaction

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The cystic fibrosis-causing mutation deltaF508 affects multiple steps in cystic fibrosis transmembrane conductance regulator biogenesis.

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Strict coupling between CFTR's catalytic cycle and gating of its Cl- ion pore revealed by distributions of open channel burst durations.

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Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis

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CFTR expression and activity from the human CFTR locus in BAC vectors, with regulatory regions, isolated by a single-step procedure

21 January 2018

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CFTR genotypes in patients with normal or borderline sweat chloride levels

21 January 2018

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Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene

21 January 2018

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Bilateral spontaneous pneumothorax in a newborn with N1303K mutation of cystic fibrosis (CFTR) gene

21 January 2018

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12 December 2020

E-64 [L-trans-epoxysuccinyl-leucyl-amido(4-guanidino)butane] and related epoxides as inhibitors of cysteine proteinases

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12 December 2020

[CFTR gene analyis in 207 patients with cystic fibrosis in southwest France: high frequency of N1303K and 1811+1.6bA>G mutations]

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12 December 2020

Co- and posttranslational translocation mechanisms direct cystic fibrosis transmembrane conductance regulator N terminus transmembrane assembly

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12 December 2020

The Delta F508 mutation shortens the biochemical half-life of plasma membrane CFTR in polarized epithelial cells

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12 December 2020

The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells

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12 December 2020

10.1371/JOURNAL.PONE.0119796

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3677285

ADS bibcode

2015PLoSO..1019796R

0 references

OpenCitations bibliographic resource ID

3677285

1 reference