Early remodeling of repolarizing K+ currents in the αMHC403/+ mouse model of familial hypertrophic cardiomyopathy.

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Early remodeling of repolarizing K+ currents in the αMHC403/+ mouse model of familial hypertrophic cardiomyopathy.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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Early remodeling of repolarizi ...... l hypertrophic cardiomyopathy.

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Early remodeling of repolarizi ...... l hypertrophic cardiomyopathy.

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label

Early remodeling of repolarizi ...... l hypertrophic cardiomyopathy.

@en

Early remodeling of repolarizi ...... l hypertrophic cardiomyopathy.

@nl

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Early remodeling of repolarizi ...... l hypertrophic cardiomyopathy.

@en

Early remodeling of repolarizi ...... l hypertrophic cardiomyopathy.

@nl

P1476

Early remodeling of repolarizi ...... l hypertrophic cardiomyopathy.

@en

P2093

Adam Adenwala

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Christine E Seidman

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Jeanne M Nerbonne

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Jonathan G Seidman

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Rebecca L Mellor

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Rocco Hueneke

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P2860

A defect in the Kv channel-interacting protein 2 (KChIP2) gene leads to a complete loss of I(to) and confers susceptibility to ventricular tachycardia

Familial hypertrophic cardiomyopathy: from mutations to functional defects

QT dispersion in alpha-myosin heavy-chain familial hypertrophic cardiomyopathy mice

A mouse model of familial hypertrophic cardiomyopathy

Diastolic dysfunction and altered energetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy

Electrophysiological abnormalities and arrhythmias in alpha MHC mutant familial hypertrophic cardiomyopathy mice

Animal models of hypertrophic cardiomyopathy.

Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia.

The consequences of disrupting cardiac inwardly rectifying K(+) current (I(K1)) as revealed by the targeted deletion of the murine Kir2.1 and Kir2.2 genes.

Prevalence and clinical correlates of QT prolongation in patients with hypertrophic cardiomyopathy.

P304

93-101

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P31

scholarly article

P356

10.1016/J.YJMCC.2017.01.006

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P478

103

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P577

2017-01-12T00:00:00Z

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P698

28089740

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P932

5398411

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