(Q33292065)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Calnexin Delta 185-520 partially reverses the misprocessing of the Delta F508 cystic fibrosis transmembrane conductance regulator (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

main subject

cystic fibrosis

0 references

transmembrane protein

0 references

author

Tsukasa Okiyoneda

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Ikuo Wada

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

author name string

Hirofumi Jono

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Tsuyoshi Shuto

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Kazuhisa Yoshitake

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Nahoko Nakano

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Shin-ichi Nagayama

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Kazutsune Harada

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Yoichiro Isohama

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Takeshi Miyata

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Hirofumi Kai

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

language of work or name

English

0 references

publication date

1 August 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

volume

526

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

page(s)

87-92

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

issue

1-3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

Nucleoside triphosphates are required to open the CFTR chloride channel.

12 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

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%2802%2903134-4

Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

Identification of the cystic fibrosis gene: genetic analysis

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

Identification of the cystic fibrosis gene: chromosome walking and jumping

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

The spectrum of cystic fibrosis mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

The molecular biology of cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

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/10.1016%2FS0014-5793%2802%2903134-4

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%2802%2903134-4

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/10.1016%2FS0014-5793%2802%2903134-4

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%2802%2903134-4

Calcium-pump inhibitors induce functional surface expression of Delta F508-CFTR protein in cystic fibrosis epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

Setting the standards: quality control in the secretory pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

ER quality control: towards an understanding at the molecular level

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

Lectins as chaperones in glycoprotein folding

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

Calnexin discriminates between protein conformational states and functions as a molecular chaperone in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

The lectin chaperone calnexin utilizes polypeptide-based interactions to associate with many of its substrates in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

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%2802%2903134-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

Degradation of CFTR by the ubiquitin-proteasome pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

CFTR expression and chloride secretion in polarized immortal human bronchial epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

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/10.1016%2FS0014-5793%2802%2903134-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

The Structure of calnexin, an ER chaperone involved in quality control of protein folding

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

The LDL receptor locus in familial hypercholesterolemia: mutational analysis of a membrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

Naturally occurring mutations in intestinal sucrase-isomaltase provide evidence for the existence of an intracellular sorting signal in the isomaltase subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

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%2802%2903134-4

Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATP

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2903134-4

10.1016/S0014-5793(02)03134-4

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12208510%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference