(Q47406703)

15 January 2018

title

Rescue of functional DeltaF508-CFTR channels by co-expression with truncated CFTR constructs in COS-1 cells (English)

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15 January 2018

3

Bernd Nilius

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15 January 2018

1

Grzegorz Owsianik

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15 January 2018

Lishuang Cao

2

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15 January 2018

language of work or name

English

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publication date

1 November 2003

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15 January 2018

published in

FEBS Letters

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15 January 2018

volume

554

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15 January 2018

issue

1-2

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15 January 2018

page(s)

173-178

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15 January 2018

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

cites work

1 reference

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

21 January 2018

1 reference

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Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

21 January 2018

1 reference

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

21 January 2018

1 reference

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The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

The molecular chaperone Hsc70 assists the in vitro folding of the N-terminal nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein

21 January 2018

1 reference

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Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

21 January 2018

1 reference

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Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast

21 January 2018

1 reference

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Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene

21 January 2018

1 reference

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Mutations in the nucleotide binding domain 1 signature motif region rescue processing and functional defects of cystic fibrosis transmembrane conductance regulator delta f508.

21 January 2018

1 reference

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A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels

21 January 2018

1 reference

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Severed molecules functionally define the boundaries of the cystic fibrosis transmembrane conductance regulator's NH(2)-terminal nucleotide binding domain

21 January 2018

1 reference

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Site-directed mutagenesis by overlap extension using the polymerase chain reaction

21 January 2018

1 reference

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Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

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%2803%2901162-1

Multiple proteolytic systems, including the proteasome, contribute to CFTR processing.

21 January 2018

1 reference

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Traffic pattern of cystic fibrosis transmembrane regulator through the early exocytic pathway

21 January 2018

1 reference

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A principal role for the proteasome in endoplasmic reticulum-associated degradation of misfolded intracellular cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

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Degradation of CFTR by the ubiquitin-proteasome pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Expression of human pICln and ClC-6 in Xenopus oocytes induces an identical endogenous chloride conductance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

21 January 2018

ER Export: Call 14-3-3

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Removal of multiple arginine-framed trafficking signals overcomes misprocessing of delta F508 CFTR present in most patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Use of a bicistronic GFP-expression vector to characterise ion channels after transfection in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Inhibition of volume-regulated anion channels by expression of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Functional characterization of the CFTR R domain using CFTR/MDR1 hybrid and deletion constructs

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Functional analysis of CFTR chloride channel activity in cells with elevated MDR1 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Biosynthesis and degradation of CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

The human DnaJ homologue (Hdj)-1/heat-shock protein (Hsp) 40 co-chaperone is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

Mechanisms of renal tubular cell hypertrophy: mitogen-induced suppression of proteolysis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

A Cystic Fibrosis Bronchial Epithelial Cell Line: Immortalization by Adeno-12-SV40 Infection

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

The chloride current induced by expression of the protein pICln in Xenopus oocytes differs from the endogenous volume-sensitive chloride current.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2901162-1

10.1016/S0014-5793(03)01162-1

7 January 2021

Identifiers

DOI

1 reference

15 January 2018

PubMed ID

14596935

1 reference

15 January 2018