(Q28374793)

English

Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome. Pharmacological and temperature effects

scientific article

In more languages

Statements

scholarly article

0 references

Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome. Pharmacological and temperature effects (English)

0 references

1 reference

based on heuristic

inferred from title

0 references

author name string

Z Zhou

1

0 references

Q Gong

2

0 references

C T January

3

0 references

language of work or name

0 references

publication date

29 October 1999

0 references

Journal of Biological Chemistry

0 references

274

0 references

31123-6

0 references

44

0 references

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

A family of potassium channel genes related to eag in Drosophila and mammals

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

HERG, a human inward rectifier in the voltage-gated potassium channel family

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Properties of HERG channels stably expressed in HEK 293 cells studied at physiological temperature

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Block of HERG potassium channels by the antihistamine astemizole and its metabolites desmethylastemizole and norastemizole

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

The inward rectification mechanism of the HERG cardiac potassium channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

A receptor-mediated pathway for cholesterol homeostasis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Water channels encoded by mutant aquaporin-2 genes in nephrogenic diabetes insipidus are impaired in their cellular routing

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Defective protein folding as a basis of human disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Quality control in the secretory pathway: the role of calreticulin, calnexin and BiP in the retention of glycoproteins with C-terminal truncations

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Novel mechanism associated with an inherited cardiac arrhythmia: defective protein trafficking by the mutant HERG (G601S) potassium channel.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Correction of Defective Protein Kinesis of Human P-glycoprotein Mutants by Substrates and Modulators

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.44.31123

21 January 2018

Identifiers

10.1074/JBC.274.44.31123

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

release_iukfxm62eva7tha3oc7t2zr5ku

1 reference

https://api.fatcat.wiki/v0/release/iukfxm62eva7tha3oc7t2zr5ku

24 November 2022

based on heuristic

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28374793&oldid=1979983337"