New cardiac and skeletal protein aggregate myopathy associated with combined MuRF1 and MuRF3 mutations

Does p.Q247X in TRIM63 Cause Human Hypertrophic Cardiomyopathy?

(2014) Rafał Płoski et al.   CIRCULATION RESEARCH

Rare Variants in Genes Encoding MuRF1 and MuRF2 Are Modifiers of Hypertrophic Cardiomyopathy

(2014) Ming Su et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Myofibrillar myopathies

(2013) Montse Olivé et al.   CURRENT OPINION IN NEUROLOGY

Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathy

(2013) A. Maerkens et al.   Journal of Proteomics

Myosinopathies: pathology and mechanisms

(2012) Homa Tajsharghi et al.   ACTA NEUROPATHOLOGICA

Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms

(2012) Kristen J. Nowak et al.   ACTA NEUROPATHOLOGICA

Human Molecular Genetic and Functional Studies Identify TRIM63 , Encoding Muscle RING Finger Protein 1, as a Novel Gene for Human Hypertrophic Cardiomyopathy

(2012) Suet Nee Chen et al.   CIRCULATION RESEARCH

Inherited Cardiomyopathies

(2012) Polakit Teekakirikul et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

A Combined Laser Microdissection and Mass Spectrometry Approach Reveals New Disease Relevant Proteins Accumulating in Aggregates of Filaminopathy Patients

(2012) Rudolf A. Kley et al.   MOLECULAR & CELLULAR PROTEOMICS

Recent advances in the biology and therapy of muscle wasting

(2010) David Glass et al.   Annals of the New York Academy of Sciences

Glycogenin-1 Deficiency and Inactivated Priming of Glycogen Synthesis

(2010) Ali-Reza Moslemi et al.   NEW ENGLAND JOURNAL OF MEDICINE

Sarcomere Formation Occurs by the Assembly of Multiple Latent Protein Complexes

(2010) Yanning Rui et al.   PLoS Genetics

Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study

(2009) Kristl G. Claeys et al.   ACTA NEUROPATHOLOGICA

Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

(2009) Lucie Gueneau et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Muscle ring finger 1 mediates cardiac atrophy in vivo

(2009) Monte S. Willis et al.   AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY

Introduction

(2009) Hans H. Goebel   BRAIN PATHOLOGY

Cardiac Muscle Ring Finger-1 Increases Susceptibility to Heart Failure In Vivo

(2009) Monte S. Willis et al.   CIRCULATION RESEARCH

An X-Linked Myopathy with Postural Muscle Atrophy and Generalized Hypertrophy, Termed XMPMA, Is Caused by Mutations in FHL1

(2008) Christian Windpassinger et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Atypical ubiquitin chains: new molecular signals. ‘Protein Modifications: Beyond the Usual Suspects’ Review Series

(2008) Fumiyo Ikeda et al.   EMBO REPORTS