(Q81198197)

English

Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms

scientific article published on 10 September 2005

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16155735%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms (English)

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6 January 2020

high-performance liquid chromatography

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corrigendum / erratum

Erratum to: Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms

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1

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6 January 2020

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6 January 2020

Jyh-Ming Jimmy Juang

5

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6 January 2020

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6 January 2020

14

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Meng-Huan Lei

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6 January 2020

Hsuan-Ming Tsao

15

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Hsuan-Ming Tsao

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6 January 2020

21

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Jiunn-Lee Lin

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6 January 2020

6

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Yen-Bin Liu

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6 January 2020

9

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San-Jou Yeh

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6 January 2020

13

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Kwo-Chang Ueng

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6 January 2020

Shoei K Stephen Huang

20

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Shoei K Stephen Huang

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6 January 2020

author name string

Yi-Ning Su

2

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6 January 2020

Fon-Jou Hsieh

3

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6 January 2020

Wen-Jone Chen

8

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6 January 2020

Chun-Chieh Wang

10

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6 January 2020

Yu-Lin Ko

11

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6 January 2020

Tsu-Juey Wu

12

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6 January 2020

Shih-Ann Chen

16

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6 January 2020

Tin-Kwang Lin

17

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6 January 2020

Mei-Hwan Wu

18

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6 January 2020

Huey-Ming Lo

19

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Europe PubMed Central

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6 January 2020

publication date

10 September 2005

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6 January 2020

Journal of Human Genetics

1 reference

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6 January 2020

50

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6 January 2020

9

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Europe PubMed Central

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6 January 2020

490-496

1 reference

Europe PubMed Central

PubMed publication ID

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6 January 2020

https://scigraph.springernature.com/pub.10.1007/s10038-005-0283-3

0 references

Clinical profile and genetic basis of Brugada syndrome in the Chinese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel missense mutation (G601S) of HERG in a Japanese long QT syndrome family

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: different incidences in familial and sporadic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DHPLC analysis of potassium ion channel genes in congenital long QT syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism of the gene encoding a human minimal potassium ion channel (minK)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nucleotide changes in the translated region of SCN5A from Japanese patients with Brugada syndrome and control subjects.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited arrhythmogenic diseases: the complexity beyond monogenic disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stilbenes and fenamates rescue the loss of I(KS) channel function induced by an LQT5 mutation and other IsK mutants

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single nucleotide polymorphisms of the SCN5A gene in Han Chinese and their relation with Brugada syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Denaturing high-performance liquid chromatography: A review

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/16155735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-005-0283-3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16155735%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16155735%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

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