Associated Papers
Functional Characterization of Cardiac Actin Mutants Causing Hypertrophic (p.A295S) and Dilated Cardiomyopathy (p.R312H and p.E361G).
Hassoun R et al.
International Journal of Molecular Sciences, 2022
35457283 (PubMed )
Supplement: ijms-23-04465-s001.zip › ijms-1693968-supplementary.pdf
Classifying Cardiac Actin Mutations Associated With Hypertrophic Cardiomyopathy.
Despond EA et al.
Frontiers in Physiology, 2018
Cryo-EM structure of a human cytoplasmic actomyosin complex at near-atomic resolution.
von der Ecken J et al.
Nature, 2016
Using baculovirus/insect cell expressed recombinant actin to study the molecular pathogenesis of HCM caused by actin mutation A331P.
Bai F et al.
Journal of Molecular and Cellular Cardiology, 2014
Regulation of actin by ion-linked equilibria.
Kang H et al.
Biophysical Journal, 2013
Functional characterization of the human α-cardiac actin mutations Y166C and M305L involved in hypertrophic cardiomyopathy.
Müller M et al.
Cellular and Molecular Life Sciences : Cmls, 2012
Subdomain location of mutations in cardiac actin correlate with type of functional change.
Mundia MM et al.
Plos One, 2012
Functional consequences of a mutation in an expressed human alpha-cardiac actin at a site implicated in familial hypertrophic cardiomyopathy.
Bookwalter CS et al.
The Journal of Biological Chemistry, 2006
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