Functional characterization of the human α-cardiac actin mutations Y166C and M305L involved in hypertrophic cardiomyopathy (Q47696386)

4 February 2018

title

Functional characterization of the human α-cardiac actin mutations Y166C and M305L involved in hypertrophic cardiomyopathy (English)

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4 February 2018

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4 February 2018

Stefan Raunser

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4 February 2018

Dietmar J. Manstein

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4 February 2018

Hans Georg Mannherz

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4 February 2018

Antonina Mazur

object named as

Antonina Joanna Mazur

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Mirco Müller

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4 February 2018

Ralph P Diensthuber

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4 February 2018

Michael B Radke

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4 February 2018

Zheng Qu

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4 February 2018

Christoph Littwitz

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4 February 2018

Cora-Ann Schoenenberger

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4 February 2018

publication date

29 May 2012

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4 February 2018

Cellular and Molecular Life Sciences

published in

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4 February 2018

volume

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4 February 2018

issue

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4 February 2018

page(s)

3457-3479

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4 February 2018

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

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Shared genetic causes of cardiac hypertrophy in children and adults

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Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy

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12 December 2020

An electrophoretic procedure for detecting proteins that bind actin monomers

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Mutations in the motor domain modulate myosin activity and myofibril organization

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Thermal unfolding of G-actin monitored with the DNase I-inhibition assay stabilities of actin isoforms

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Hypertrophic cardiomyopathy

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10.1007/S00018-012-1030-5

Identifiers

DOI

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4 February 2018

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4 February 2018