Related references
Note: Only part of the references are listed.DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death
Anne T. Bertrand et al.
HUMAN MOLECULAR GENETICS (2012)
A truncated lamin A in the Lmna-/- mouse line Implications for the understanding of laminopathies
Daniel Jahn et al.
NUCLEUS-AUSTIN (2012)
The ubiquitin-proteasome system in cardiomyopathies
Saskia Schlossarek et al.
CURRENT OPINION IN CARDIOLOGY (2011)
Update 2011: Clinical and Genetic Issues in Familial Dilated Cardiomyopathy
Ray E. Hershberger et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2011)
A laminopathic mutation disrupting lamin filament assembly causes disease-like phenotypes in Caenorhabditis elegans
Erin M. Bank et al.
MOLECULAR BIOLOGY OF THE CELL (2011)
Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption
Pallavi Gupta et al.
BASIC RESEARCH IN CARDIOLOGY (2010)
Effects of Mechanical Stress and Carvedilol in Lamin A/C-Deficient Dilated Cardiomyopathy
Suchitra Chandar et al.
CIRCULATION RESEARCH (2010)
Development of a Drug Screening Platform Based on Engineered Heart Tissue
Arne Hansen et al.
CIRCULATION RESEARCH (2010)
Quantitative Proteomics Reveals Subset-Specific Viral Recognition in Dendritic Cells
Christian A. Luber et al.
IMMUNITY (2010)
The Role of Ubiquitin in NF-kappa B Regulatory Pathways
Brian Skaug et al.
ANNUAL REVIEW OF BIOCHEMISTRY (2009)
Nonsense-Mediated mRNA Decay and Ubiquitin-Proteasome System Regulate Cardiac Myosin-Binding Protein C Mutant Levels in Cardiomyopathic Mice
Nicolas Vignier et al.
CIRCULATION RESEARCH (2009)
Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA gene
Sebastian Kandert et al.
EUROPEAN JOURNAL OF CELL BIOLOGY (2009)
De novo LMNA mutations cause a new form of congenital muscular dystrophy
Susana Quijano-Roy et al.
ANNALS OF NEUROLOGY (2008)
Elevated p53 expression is associated with dysregulation of the ubiquitin-proteasome system in dilated cardiomyopathy
Emma J. Birks et al.
CARDIOVASCULAR RESEARCH (2008)
Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease
Cordula M. Wolf et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2008)
Long-term outcome and risk stratification in dilated cardiolaminopathies
Michele Pasotti et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2008)
MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification
Juergen Cox et al.
NATURE BIOTECHNOLOGY (2008)
Decreased expression of the mitochondrial matrix proteases Lon and ClpP in cells from a patient with hereditary spastic paraplegia (SPG13)
J. Hansen et al.
NEUROSCIENCE (2008)
Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C gene
J. Peter van Tintelen et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2007)
Proteins that associate with lamins: many faces, many functions
Eric C. Schirmer et al.
EXPERIMENTAL CELL RESEARCH (2007)
Laminopathies: A wide spectrum of human diseases
Howard J. Worman et al.
EXPERIMENTAL CELL RESEARCH (2007)
Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips
Juri Rappsilber et al.
NATURE PROTOCOLS (2007)
Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy
Yuexia Wang et al.
HUMAN MOLECULAR GENETICS (2006)
Nuclear lamins: Laminopathies and their role in premature ageing
J. L. V. Broers et al.
PHYSIOLOGICAL REVIEWS (2006)
In-gel digestion for mass spectrometric characterization of proteins and proteomes
Andrej Shevchenko et al.
NATURE PROTOCOLS (2006)
Long-term expression and repeated administration of AAV type 1, 2 and 5 vectors in skeletal muscle of immunocompetent adult mice
C. Riviere et al.
GENE THERAPY (2006)
Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies
T Arimura et al.
HUMAN MOLECULAR GENETICS (2005)
Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice
V Nikolova et al.
JOURNAL OF CLINICAL INVESTIGATION (2004)
Desmin-related cardiomyopathy in transgenic mice: A cardiac amyloidosis
A Sanbe et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
A transgenic mouse model of the ubiquitin/proteasome system
K Lindsten et al.
NATURE BIOTECHNOLOGY (2003)
Hypertrophic cardiomyopathy - Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
P Richard et al.
CIRCULATION (2003)
Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy
C Favreau et al.
EXPERIMENTAL CELL RESEARCH (2003)
Regulation of receptor fate by ubiquitination of activated β2-adrenergic receptor and β-arrestin
SK Shenoy et al.
SCIENCE (2001)
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation
HM Bécane et al.
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY (2000)
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)
A Muchir et al.
HUMAN MOLECULAR GENETICS (2000)
Share Paper
