Cardiac ion channel gene mutations in sudden infant death syndrome (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

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16 September 2017

Kazuki Kijima

2

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16 September 2017

Motoki Osawa

3

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16 September 2017

Kuniaki Ishii

4

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16 September 2017

Naomasa Makita

5

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16 September 2017

Ryoji Matoba

6

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

16 September 2017

cites work

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The sudden infant death syndrome gene: does it exist?

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

21 January 2018

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

21 January 2018

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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

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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

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

21 January 2018

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Altered cardiac repolarization in some victims of sudden infant death syndrome

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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

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

21 January 2018

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

21 January 2018

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

21 January 2018

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The inward rectification mechanism of the HERG cardiac potassium channel

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

21 January 2018

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

21 January 2018

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Pro: Newborn ECG screening to prevent sudden cardiac death

21 January 2018

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Con: Newborn screening to prevent sudden cardiac death?

21 January 2018

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

21 January 2018

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

21 January 2018

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Molecular diagnosis in a child with sudden infant death syndrome

21 January 2018

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

21 January 2018

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10.1203/PDR.0B013E3181841ECA

21 January 2018

Identifiers

DOI

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Dimensions Publication ID

16 September 2017

1017758578

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1 reference