Induction of HSP70 promotes DeltaF508 CFTR trafficking (Q40798928)

23 September 2017

Induction of HSP70 promotes DeltaF508 CFTR trafficking (English)

1 reference

23 September 2017

Choo-Kang LR

1

1 reference

PubMed ID

11404246

23 September 2017

Zeitlin PL

series ordinal

2

1 reference

23 September 2017

1 July 2001

1 reference

American Journal of Physiology - Lung Cellular and Molecular Physiology

23 September 2017

1 reference

23 September 2017

281

1 reference

23 September 2017

1

1 reference

23 September 2017

L58-68

1 reference

Antisense oligonucleotide to the 70-kDa heat shock cognate protein inhibits synthesis of myelin basic protein

23 September 2017

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Direct activation of cystic fibrosis transmembrane conductance regulator channels by 8-cyclopentyl-1,3-dipropylxanthine (CPX) and 1,3-diallyl-8-cyclohexylxanthine (DAX).

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Strategies for correcting the delta F508 CFTR protein-folding defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

The constitutive and stress inducible forms of hsp 70 exhibit functional similarities and interact with one another in an ATP-dependent fashion

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Chemical chaperones mediate increased secretion of mutant alpha 1-antitrypsin (alpha 1-AT) Z: A potential pharmacological strategy for prevention of liver injury and emphysema in alpha 1-AT deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Functional activation of the cystic fibrosis trafficking mutant delta F508-CFTR by overexpression

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Effect of enteral glutamine on intestinal permeability and bacterial translocation after abdominal radiation injury in rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Immunocytochemical localization of the cystic fibrosis gene product CFTR

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Structure and expression of a human gene coding for a 71 kd heat shock 'cognate' protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

The consequences of expressing hsp70 in Drosophila cells at normal temperatures

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Post-translational disruption of the delta F508 cystic fibrosis transmembrane conductance regulator (CFTR)-molecular chaperone complex with geldanamycin stabilizes delta F508 CFTR in the rabbit reticulocyte lysate.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Delta F508 CFTR localizes in the endoplasmic reticulum-Golgi intermediate compartment in cystic fibrosis cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Surface expression of the cystic fibrosis transmembrane conductance regulator mutant DeltaF508 is markedly upregulated by combination treatment with sodium butyrate and low temperature

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Identification of the cystic fibrosis gene: genetic analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Correlation between synthesis of heat shock proteins and development of thermotolerance in Chinese hamster fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

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/10.1152%2FAJPLUNG.2001.281.1.L58

Cystic fibrosis gene and protein expression during fetal lung development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

The Hdj-2/Hsc70 chaperone pair facilitates early steps in CFTR biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Characterization of the thermotolerant cell. I. Effects on protein synthesis activity and the regulation of heat-shock protein 70 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Analysis by confocal microscopy of the behavior of heat shock protein 70 within the nucleus and of a nuclear matrix polypeptide during prolonged heat shock response in HeLa cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Alteration of the cystic fibrosis transmembrane conductance regulator folding pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Glutamine is a powerful effector of heat shock protein expression inDrosophila Kc cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Glutamine metabolism by the intestinal tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

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/10.1152%2FAJPLUNG.2001.281.1.L58

An evolutionarily conserved family of Hsp70/Hsc70 molecular chaperone regulators

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

The cystic fibrosis transmembrane conductance regulator gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Glutamine protects intestinal epithelial cells: role of inducible HSP70.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

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/10.1152%2FAJPLUNG.2001.281.1.L58

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

Butyrate increases apical membrane CFTR but reduces chloride secretion in MDCK cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.1.L58

10.1152/AJPLUNG.2001.281.1.L58

21 January 2018

Identifiers

DOI

0 references

PubMed ID

11404246

1 reference

PubMed ID

11404246