Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia (Q34762614)

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18 December 2019

title

Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia (English)

1 reference

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18 December 2019

main subject

cystic fibrosis

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transmembrane protein

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author

Lynda S Ostedgaard

1

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18 December 2019

Christoph O Randak

2

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18 December 2019

author name string

Tatiana Rokhlina

3

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18 December 2019

Philip Karp

4

1 reference

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18 December 2019

Daniel Vermeer

5

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18 December 2019

Katherine J Ashbourne Excoffon

6

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18 December 2019

Michael J Welsh

7

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18 December 2019

language of work or name

English

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publication date

10 February 2003

1 reference

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18 December 2019

number of pages

6

1 reference

Proceedings of the National Academy of Sciences of the United States of America

inferred from page(s)

published in

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18 December 2019

volume

100

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18 December 2019

issue

4

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18 December 2019

page(s)

1937-1942

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PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator

18 December 2019

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1 reference

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7 July 2018

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7 July 2018

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CFTR with a partially deleted R domain corrects the cystic fibrosis chloride transport defect in human airway epithelia in vitro and in mouse nasal mucosa in vivo

7 July 2018

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7 July 2018

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A cluster of negative charges at the amino terminal tail of CFTR regulates ATP-dependent channel gating

7 July 2018

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COOH-terminal truncations promote proteasome-dependent degradation of mature cystic fibrosis transmembrane conductance regulator from post-Golgi compartments

7 July 2018

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PACS-1 binding to adaptors is required for acidic cluster motif-mediated protein traffic.

7 July 2018

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Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by its R domain

7 July 2018

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Multiple endocytic signals in the C-terminal tail of the cystic fibrosis transmembrane conductance regulator

7 July 2018

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A PDZ-binding motif is essential but not sufficient to localize the C terminus of CFTR to the apical membrane

7 July 2018

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Regulation of cystic fibrosis transmembrane conductance regulator single-channel gating by bivalent PDZ-domain-mediated interaction

7 July 2018

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Functional cystic fibrosis transmembrane conductance regulator tagged with an epitope of the vesicular stomatis virus glycoprotein can be addressed to the apical domain of polarized cells

7 July 2018

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Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity

7 July 2018

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Localization of sequences within the C-terminal domain of the cystic fibrosis transmembrane conductance regulator which impact maturation and stability

7 July 2018

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The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane

7 July 2018

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A PDZ-interacting domain in CFTR is an apical membrane polarization signal

7 July 2018

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C-terminal truncations destabilize the cystic fibrosis transmembrane conductance regulator without impairing its biogenesis. A novel class of mutation

7 July 2018

1 reference

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7 July 2018

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An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton

7 July 2018

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A C-terminal motif found in the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteins

7 July 2018

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Peptide binding consensus of the NHE-RF-PDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR)

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Processing of CFTR bearing the P574H mutation differs from wild-type and deltaF508-CFTR

26 October 2018

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12 December 2020

Gene therapy for cystic fibrosis

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12 December 2020

The coxsackie B virus and adenovirus receptor resides in a distinct membrane microdomain

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12 December 2020

Expression of cystic fibrosis transmembrane conductance regulator in a model epithelium

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12 December 2020

A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis

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12 December 2020

Efficient endocytosis of the cystic fibrosis transmembrane conductance regulator requires a tyrosine-based signal

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12 December 2020

Identifiers

DOI

10.1073/PNAS.2627982100

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12578973%20AND%20SRC:MED&resulttype=core&format=json

18 December 2019

0 references

1 reference

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18 December 2019

1 reference