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FHOD3 gene

Known as: FORMIN HOMOLOGY-2 DOMAIN-CONTAINING PROTEIN 3, KIAA1695, FHOS2 
National Institutes of Health

Papers overview

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Review
2019
Review
2019
54 Novel formin homology 2 domain containing 3 (FHOD3) mutations associated with the pathogenesis of hypertrophic cardiomyopathy (HCM) in an irish population
Background The genetic cause of hypertrophic cardiomyopathy (HCM) remains unexplained in a substantial proportion of cases… 
2017
2017
Crucial Role of ROCK 2-Mediated Phosphorylation and Upregulation of FHOD 3 in the Pathogenesis of Angiotensin II – Induced Cardiac Hypertrophy
2015
2015
Distribution of formins in cardiac muscle: FHOD1 is a component of intercalated discs and costameres.
2014
2014
Circulation: Cardiovascular Genetics 2013 Editors’ Picks
Summary— Hypertrophic cardiomyopathy (HCM) is characterized by excessive thickening and enlargement of the heart muscle, causing… 
2004
2004
Identification and characterization of human FHOD3 gene in silico.
Formin homology proteins are actin regulators with scaffold function, which are implicated in organogenesis, normal tissue… 
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