Homozygous missense N629D hERG (KCNH2) potassium channel mutation causes developmental defects in the right ventricle and its outflow tract and embryonic lethality. (Q30491532)

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English	Homozygous missense N629D hERG (KCNH2) potassium channel mutation causes developmental defects in the right ventricle and its outflow tract and embryonic lethality.	scientific article

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25 December 2019

Homozygous missense N629D hERG (KCNH2) potassium channel mutation causes developmental defects in the right ventricle and its outflow tract and embryonic lethality (English)

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25 December 2019

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25 December 2019

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25 December 2019

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Guo Qi Teng

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25 December 2019

Xian Zhao

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25 December 2019

James P Lees-Miller

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25 December 2019

F Russell Quinn

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25 December 2019

Pin Li

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25 December 2019

Derrick E Rancourt

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23 October 2008

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25 December 2019

Circulation Research

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25 December 2019

103

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25 December 2019

1483-1491

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25 December 2019

Doxazosin induces apoptosis of cells expressing hERG K+ channels.

1 reference

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Smad4 is required to regulate the fate of cranial neural crest cells

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Expression and significance of HERG protein in gastric cancer

1 reference

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Mesoderm progenitor cells of common origin contribute to the head musculature and the cardiac outflow tract

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A case of long QT syndrome associated with familial occurrence of persistent patency of the arterial duct

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Applications for multifrequency ultrasound biomicroscopy in mice from implantation to adulthood.

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Role of glycosylation in cell surface expression and stability of HERG potassium channels

1 reference

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Genotype and severity of long QT syndrome

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1 reference

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20 June 2018

Multiple different missense mutations in the pore region of HERG in patients with long QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774899

20 June 2018

HERG- and IRK-like inward rectifier currents are sequentially expressed during neuronal development of neural crest cells and their derivatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774899

20 June 2018

Two Isoforms of the Mouse Ether-a-go-go –Related Gene Coassemble to Form Channels With Properties Similar to the Rapidly Activating Component of the Cardiac Delayed Rectifier K + Current

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774899

20 June 2018

Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774899

20 June 2018

Developmental changes in the delayed rectifier K+ channels in mouse heart.

1 reference

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20 June 2018

Exogenous retinoic acid rapidly induces anterior ectopic expression of murine Hox-2 genes in vivo

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20 June 2018

Ca2+ influx-induced sarcoplasmic reticulum Ca2+ overload causes mitochondrial-dependent apoptosis in ventricular myocytes

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26 November 2018

Post-hoc diagnosis of congenital long QT syndrome in patients with tetralogy of Fallot

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Mutations in the HERG K+-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

1 reference

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[K(+)](o)-dependent change in conformation of the HERG1 long QT mutation N629D channel results in partial reversal of the in vitro disease phenotype

1 reference

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Novel gain-of-function mechanism in K(+) channel-related long-QT syndrome: altered gating and selectivity in the HERG1 N629D mutant

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[Autosomal dominant Mendelian midline complex. Secundum atrial septal defect associated with cardiac and facial-thoracic defects. A familial case]

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12 December 2020

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inferred from PubMed ID database lookup

Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children

1 reference

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Prolonged repolarization and triggered activity induced by adenoviral expression of HERG N629D in cardiomyocytes derived from stem cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18948620

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inferred from PubMed ID database lookup

Loss of Apaf-1 leads to partial rescue of the HAND2-null phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/18948620

12 December 2020

based on heuristic

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Polytherapy with hERG-blocking antiepileptic drugs: increased risk for embryonic cardiac arrhythmia and teratogenicity

1 reference

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1 reference

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Identifiers

10.1161/CIRCRESAHA.108.177055

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25 December 2019

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25 December 2019

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25 December 2019

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