Related references
Note: Only part of the references are listed.Does p. Q247X in TRIM63 Cause Human Hypertrophic Cardiomyopathy?
Rafal Ploski et al.
CIRCULATION RESEARCH (2014)
Rare Variants in Genes Encoding MuRF1 and MuRF2 Are Modifiers of Hypertrophic Cardiomyopathy
Ming Su et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2014)
Myosinopathies: pathology and mechanisms
Homa Tajsharghi et al.
ACTA NEUROPATHOLOGICA (2013)
Skeletal muscle alpha-actin diseases (actinopathies): pathology and mechanisms
Kristen J. Nowak et al.
ACTA NEUROPATHOLOGICA (2013)
Myofibrillar myopathies: new developments
Montse Olive et al.
CURRENT OPINION IN NEUROLOGY (2013)
Inherited Cardiomyopathies Molecular Genetics and Clinical Genetic Testing in the Postgenomic Era
Polakit Teekakirikul et al.
JOURNAL OF MOLECULAR DIAGNOSTICS (2013)
Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathy
A. Maerkens et al.
JOURNAL OF PROTEOMICS (2013)
A Combined Laser Microdissection and Mass Spectrometry Approach Reveals New Disease Relevant Proteins Accumulating in Aggregates of Filaminopathy Patients
Rudolf A. Kley et al.
MOLECULAR & CELLULAR PROTEOMICS (2013)
Human Molecular Genetic and Functional Studies Identify TRIM63, Encoding Muscle RING Finger Protein 1, as a Novel Gene for Human Hypertrophic Cardiomyopathy
Suet Nee Chen et al.
CIRCULATION RESEARCH (2012)
Recent advances in the biology and therapy of muscle wasting
David Glass et al.
MOLECULAR AND INTEGRATIVE PHYSIOLOGY OF THE MUSCULOSKELETAL SYSTEM (2010)
Brief Report: Glycogenin-1 Deficiency and Inactivated Priming of Glycogen Synthesis.
Ali-Reza Moslemi et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
Sarcomere Formation Occurs by the Assembly of Multiple Latent Protein Complexes
Yanning Rui et al.
PLOS GENETICS (2010)
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study
Kristl G. Claeys et al.
ACTA NEUROPATHOLOGICA (2009)
Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy
Lucie Gueneau et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Muscle ring finger 1 mediates cardiac atrophy in vivo
Monte S. Willis et al.
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY (2009)
MINI-SYMPOSIUM: Protein Aggregate Myopathies Introduction
Hans H. Goebel
BRAIN PATHOLOGY (2009)
Cardiac Muscle Ring Finger-1 Increases Susceptibility to Heart Failure In Vivo
Monte S. Willis et al.
CIRCULATION RESEARCH (2009)
An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1
Christian Windpassinger et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Atypical ubiquitin chains: new molecular signals - 'Protein modifications: Beyond the usual suspects' review series
Fumiyo Ikeda et al.
EMBO REPORTS (2008)
Cooperative control of striated muscle mass and metabolism by MuRF1 and MuRF2
Christian C. Witt et al.
EMBO JOURNAL (2008)
The E3 ligase MuRF1 degrades myosin heavy chain protein in dexamethasone-treated skeletal muscle
Brian A. Clarke et al.
CELL METABOLISM (2007)
Myosin storage myopathy with cardiomyopathy
H. Tajsharghi et al.
NEUROMUSCULAR DISORDERS (2007)
Myosin accumulation and striated muscle myopathy result from the loss of muscle RING finger 1 and 3
Jens Fielitz et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Loss of muscle-specific RING-finger 3 predisposes the heart to cardiac rupture after myocardial infarction
Jens Fielitz et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Microtubule-dependent transport and organization of sarcomeric myosin during skeletal muscle differentiation
V Pizon et al.
EMBO JOURNAL (2005)
MURF-1 and MURF-2 target a specific subset of myofibrillar proteins redundantly: Towards understanding MURF-dependent muscle ubiquitination
SH Witt et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
Myosin storage myopathy associated with a heterozygous missense mutation in MYH7
H Tajsharghi et al.
ANNALS OF NEUROLOGY (2003)
Muscle-specific RING finger-1 interacts with titin to regulate sarcomeric M-line and thick filament structure and may have nuclear functions via its interaction with glucocorticoid modulatory element binding protein-1
AS McElhinny et al.
JOURNAL OF CELL BIOLOGY (2002)
Identification of ubiquitin ligases required for skeletal muscle atrophy
SC Bodine et al.
SCIENCE (2001)
Regulation of microtubule dynamics and myogenic differentiation by MURF, a striated muscle RING-finger protein
JA Spencer et al.
JOURNAL OF CELL BIOLOGY (2000)
Ubiquitination: RING for destruction?
PS Freemont
CURRENT BIOLOGY (2000)
Acute quadriplegia and loss of muscle myosin in patients treated with nondepolarizing neuromuscular blocking agents and corticosteroids: Mechanisms at the cellular and molecular levels
L Larsson et al.
CRITICAL CARE MEDICINE (2000)