(Q39966006)

16 September 2017

title

Cardiac ion channel gene mutations in sudden infant death syndrome (English)

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16 September 2017

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Tesshu Otagiri

1

1 reference

16 September 2017

Kazuki Kijima

2

1 reference

16 September 2017

Motoki Osawa

3

1 reference

16 September 2017

Kuniaki Ishii

4

1 reference

16 September 2017

Naomasa Makita

5

1 reference

16 September 2017

Ryoji Matoba

6

1 reference

16 September 2017

Kazuo Umetsu

7

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16 September 2017

Kiyoshi Hayasaka

8

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16 September 2017

language of work or name

English

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publication date

1 November 2008

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16 September 2017

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16 September 2017

volume

64

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16 September 2017

issue

5

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16 September 2017

page(s)

482-487

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https://scigraph.springernature.com/pub.10.1203/pdr.0b013e3181841eca

16 September 2017

exact match

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cites work

Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Annual summary of vital statistics--2003.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

The sudden infant death syndrome gene: does it exist?

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

IL-10 gene polymorphisms are associated with infectious cause of sudden infant death

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Serotonin transporter gene variation is a risk factor for sudden infant death syndrome in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Sudden infant death syndrome is not associated with the mutation of PHOX2B gene, a major causative gene of congenital central hypoventilation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Sensitive detection of polyalanine expansions in PHOX2B by polymerase chain reaction using bisulfite-converted DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Altered cardiac repolarization in some victims of sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

A molecular link between the sudden infant death syndrome and the long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

De novo mutation in the SCN5A gene associated with early onset of sudden infant death

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Sudden death associated with short-QT syndrome linked to mutations in HERG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Cross-talk between beta(1)-adrenoceptors and ET(A) receptors in modulation of the slow component of delayed rectifier K(+) currents

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Dissociation of E-4031 from the HERG channel caused by mutations of an amino acid results in greater block at high stimulation frequency

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Drug-induced long-QT syndrome associated with a subclinical SCN5A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

The inward rectification mechanism of the HERG cardiac potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Molecular physiology and pharmacology of HERG. Single-channel currents and block by dofetilide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Novel C-terminus frameshift mutation, 1122fs/147, of HERG in LQT2: additional amino acids generated by frameshift cause accelerated inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Characterization of S818L mutation in HERG C-terminus in LQT2. Modification of activation-deactivation gating properties.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Pro: Newborn ECG screening to prevent sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Con: Newborn screening to prevent sudden cardiac death?

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Sudden infant death syndrome: how significant are the cardiac channelopathies?

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Molecular diagnosis in a child with sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

Cost-effectiveness of neonatal ECG screening for the long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181841ECA

10.1203/PDR.0B013E3181841ECA

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

16 September 2017

1017758578

0 references

1 reference