(Q36594740)

English

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

scientific article published on October 1993

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

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

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

cystic fibrosis

0 references

transmembrane protein

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4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

author name string

Y Yang

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

S Janich

2

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

J A Cohn

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

language of work or name

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publication date

1 October 1993

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Europe PubMed Central

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23 October 2019

number of pages

5

1 reference

based on heuristic

inferred from page(s)

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

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

90

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

20

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

9480-9484

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

The nucleotide sequence of the chick cytoplasmic β-actin gene

1 reference

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9 September 2017

Effect of weak bases on the intralysosomal pH in mouse peritoneal macrophages

1 reference

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9 September 2017

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

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9 September 2017

Identification of the cystic fibrosis gene: genetic analysis

1 reference

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9 September 2017

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

1 reference

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9 September 2017

Requirement for hsp70 in the mitochondrial matrix for translocation and folding of precursor proteins

1 reference

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9 September 2017

Protein folding in the cell

1 reference

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The mechanism of Z alpha 1-antitrypsin accumulation in the liver

1 reference

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9 September 2017

Examining the function and regulation of hsp 70 in cells subjected to metabolic stress

1 reference

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9 September 2017

Cystic fibrosis: molecular biology and therapeutic implications

1 reference

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9 September 2017

Characterization of the cystic fibrosis transmembrane conductance regulator in a colonocyte cell line

1 reference

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9 September 2017

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

1 reference

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9 September 2017

Immunoglobulin heavy chain-binding protein binds to misfolded mutant insulin receptors with mutations in the extracellular domain

1 reference

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30 September 2017

70K heat shock related proteins stimulate protein translocation into microsomes

1 reference

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28 June 2018

Posttranslational association of immunoglobulin heavy chain binding protein with nascent heavy chains in nonsecreting and secreting hybridomas

1 reference

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28 June 2018

A very strong enhancer is located upstream of an immediate early gene of human cytomegalovirus

1 reference

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28 June 2018

Uncoating ATPase is a member of the 70 kilodalton family of stress proteins.

1 reference

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28 June 2018

Immunocytochemical localization of BiP to the rough endoplasmic reticulum: evidence for protein sorting by selective retention

1 reference

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28 June 2018

Interaction of Hsp 70 with newly synthesized proteins: implications for protein folding and assembly.

1 reference

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28 June 2018

Heavy chain binding protein recognizes incompletely disulfide-bonded forms of vesicular stomatitis virus G protein

1 reference

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28 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47592

28 June 2018

Defective acidification of intracellular organelles in cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47592

28 June 2018

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer

1 reference

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28 June 2018

Interaction of heat-shock protein 70 with p53 translated in vitro: evidence for interaction with dimeric p53 and for a role in the regulation of p53 conformation

1 reference

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28 June 2018

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

1 reference

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28 June 2018

Regulation of plasma membrane recycling by CFTR.

1 reference

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28 June 2018

In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium

1 reference

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28 June 2018

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

1 reference

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20 September 2018

Submucosal glands are the predominant site of CFTR expression in the human bronchus

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Lebanese allele at the low density lipoprotein receptor locus. Nonsense mutation produces truncated receptor that is retained in endoplasmic reticulum

1 reference

https://pubmed.ncbi.nlm.nih.gov/7692448

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cystic fibrosis transmembrane conductance regulator. Effects of the most common cystic fibrosis-causing mutation on the secondary structure and stability of a synthetic peptide

1 reference

https://pubmed.ncbi.nlm.nih.gov/7692448

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland

1 reference

https://pubmed.ncbi.nlm.nih.gov/7692448

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.90.20.9480

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1993PNAS...90.9480Y

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7692448%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

ResearchGate publication ID

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