Related references
Note: Only part of the references are listed.Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene
Antoine Muchir et al.
CARDIOVASCULAR RESEARCH (2012)
Nuclear lamina at the crossroads of the cytoplasm and nucleus
Larry Gerace et al.
JOURNAL OF STRUCTURAL BIOLOGY (2012)
Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers A European Cohort Study
Ingrid A. W. van Rijsingen et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2012)
Variants of the Lamin A/C (LMNA) Gene in Non-Valvular Atrial Fibrillation Patients A Possible Pathogenic Role of the Thr528Met Mutation
Michal Saj et al.
MOLECULAR DIAGNOSIS & THERAPY (2012)
CARDIAC INVOLVEMENT IN PATIENTS WITH LAMIN A/C GENE MUTATIONS: A COHORT OBSERVATION
Nicola Carboni et al.
MUSCLE & NERVE (2012)
Lamin A/C Mutants Disturb Sumo1 Localization and Sumoylation in Vitro and in Vivo
Emilie Boudreau et al.
PLOS ONE (2012)
Clinical and genetic heterogeneity in laminopathies
Anne T. Bertrand et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2011)
Novel LMNA Mutations in Patients With Emery-Dreifuss Muscular Dystrophy and Functional Characterization of Four LMNA Mutations
Juergen Scharner et al.
HUMAN MUTATION (2011)
A new c.1621 C > G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype-phenotype correlation
Lukasz A. Malek et al.
JOURNAL OF HUMAN GENETICS (2011)
Lamin A and lamin C form homodimers and coexist in higher complex forms both in the nucleoplasmic fraction and in the lamina of cultured human cells
Thorsten Kolb et al.
NUCLEUS (2011)
The genetics of dilated cardiomyopathy
Lisa Dellefave et al.
CURRENT OPINION IN CARDIOLOGY (2010)
Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals
Ray E. Hershberger et al.
GENETICS IN MEDICINE (2010)
Dilated cardiomyopathy with profound segmental wall motion abnormalities and ventricular arrhythmia caused by the R541C mutation in the LMNA gene
Michal Saj et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2010)
The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy
Daniel Vega Moller et al.
EUROPEAN JOURNAL OF HEART FAILURE (2009)
Laminopathies and the long strange trip from basic cell biology to therapy
Howard J. Worman et al.
JOURNAL OF CLINICAL INVESTIGATION (2009)
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
Sharie B. Parks et al.
AMERICAN HEART JOURNAL (2008)
Specific contribution of lamin A and lamin C in the development of laminopathies
Nicolas Sylvius et al.
EXPERIMENTAL CELL RESEARCH (2008)
Long-term outcome and risk stratification in dilated cardiolaminopathies
Michele Pasotti et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2008)
Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases
Perry Elliott et al.
EUROPEAN HEART JOURNAL (2008)
Clustal W and clustal X version 2.0
M. A. Larkin et al.
BIOINFORMATICS (2007)
Quantitative analysis of localization and nuclear aggregate formation induced by GFP-lamin a mutant proteins in living HeLa cells
S. Hubner et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2006)
Lamin A/C and cardiac diseases
Nicolas Sylvius et al.
CURRENT OPINION IN CARDIOLOGY (2006)
In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients
N Sylvius et al.
JOURNAL OF MEDICAL GENETICS (2005)
Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization
JLV Broers et al.
EXPERIMENTAL CELL RESEARCH (2005)
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations
A Muchir et al.
MUSCLE & NERVE (2004)
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations
MRG Taylor et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (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)
Loss of lamin A/C expression revealed by immuno-electron microscopy in dilated cardiomyopathy with atrioventricular block caused by LMNA gene defects
L Verga et al.
VIRCHOWS ARCHIV (2003)
PIRA PCR designer for restriction analysis of single nucleotide polymorphisms
XY Ke et al.
BIOINFORMATICS (2001)
Share Paper
