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Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation

The New England journal of medicine, 2006-06, Vol.354 (25), p.2677-2688

2006

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A CRISPR/Cas9 zebrafish lamin A/C mutant model of muscular laminopathy

Developmental dynamics, 2022-04, Vol.251 (4), p.645-661

2022

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ACSL5 genotype influence on fatty acid metabolism: a cellular, tissue, and whole-body study

Metabolism, clinical and experimental, 2018-06, Vol.83, p.271-279

2018

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Lamin A/C and cardiac diseases

Current opinion in cardiology, 2006-05, Vol.21 (3), p.159-165

2006

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Cellular and Animal Models of Striated Muscle Laminopathies

Cells (Basel, Switzerland), 2019-03, Vol.8 (4), p.291

2019

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Lamin A/C mutants disturb sumo1 localization and sumoylation in vitro and in vivo

PloS one, 2012-09, Vol.7 (9), p.e45918-e45918

2012

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Decreased Mitochondrial Proton Leak and Reduced Expression of Uncoupling Protein 3 in Skeletal Muscle of Obese Diet-Resistant Women

Diabetes (New York, N.Y.), 2002-08, Vol.51 (8), p.2459-2466

2002

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Lamin A/C mutations in dilated cardiomyopathy

Cardiology journal, 2014-01, Vol.21 (4), p.331-342

2014

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The TaqIA RFLP is associated with attenuated intervention-induced body weight loss and increased carbohydrate intake in post-menopausal obese women

Appetite, 2013-01, Vol.60 (1), p.111-116

2013

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Can Circulating Cardiac Biomarkers Be Helpful in the Assessment of LMNA Mutation Carriers?

Journal of clinical medicine, 2020-05, Vol.9 (5), p.1443

2020

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Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle Laminopathies

Cells (Basel, Switzerland), 2020-11, Vol.9 (11), p.2388

2020

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Acyl-CoA synthetase long-chain 5 genotype is associated with body composition changes in response to lifestyle interventions in postmenopausal women with overweight and obesity: a genetic association study on cohorts Montréal-Ottawa New Emerging Team, and Complications Associated with Obesity

BMC medical genetics, 2016-08, Vol.17 (1), p.56-56, Article 56

2016

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Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption

Basic research in cardiology, 2010-05, Vol.105 (3), p.365-377

2010

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Peroxisome Proliferator-activated Receptor γ 2 and Acyl-CoA Synthetase 5 Polymorphisms Influence Diet Response

Obesity (Silver Spring, Md.), 2007-05, Vol.15 (5), p.1068-1075

2007

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Still Building on Candidate-Gene Strategy in Hypertension?

Hypertension (Dallas, Tex. 1979), 2007-10, Vol.50 (4), p.607-608

2007

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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

Journal of human genetics, 2011-01, Vol.56 (1), p.83-86

2011

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Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population

Circulation (New York, N.Y.), 1997-07, Vol.96 (1), p.214-219

1997

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Genotype-specific weight loss treatment advice: how close are we?

Applied physiology, nutrition, and metabolism, 2007-06, Vol.32 (3), p.351

2007

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Functional characterization of a promoter polymorphism that drives ACSL5 gene expression in skeletal muscle and associates with diet-induced weight loss

The FASEB journal, 2009-06, Vol.23 (6), p.1705-1709

2009

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Specific contribution of lamin A and lamin C in the development of laminopathies

Experimental cell research, 2008-08, Vol.314 (13), p.2362-2375

2008

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Effects of Exercise Training on Molecular Markers of Lipogenesis and Lipid Partitioning in Fructose-Induced Liver Fat Accumulation

Journal of nutrition and metabolism, 2012-01, Vol.2012, p.181687-10

2012

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Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation

Journal of the neurological sciences, 2008-08, Vol.271 (1), p.91-96

2008

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Sequence analysis of coding and 3' and 5' flanking regions of the epithelial sodium channel alpha, beta, and gamma genes in Dahl S versus R rats

BMC genetics, 2007-06, Vol.8, p.35

2007

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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Nature genetics, 1997-02, Vol.15 (2), p.186-189

1997

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Mutations in the laminin α2-chain gene ( LAMA2 ) cause merosin-deficient congenital muscular dystrophy

Nature genetics, 1995-10, Vol.11 (2), p.216-218

1995

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Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation

A CRISPR/Cas9 zebrafish lamin A/C mutant model of muscular laminopathy

ACSL5 genotype influence on fatty acid metabolism: a cellular, tissue, and whole-body study

Lamin A/C and cardiac diseases

Cellular and Animal Models of Striated Muscle Laminopathies

Lamin A/C mutants disturb sumo1 localization and sumoylation in vitro and in vivo

Decreased Mitochondrial Proton Leak and Reduced Expression of Uncoupling Protein 3 in Skeletal Muscle of Obese Diet-Resistant Women

Lamin A/C mutations in dilated cardiomyopathy

The TaqIA RFLP is associated with attenuated intervention-induced body weight loss and increased carbohydrate intake in post-menopausal obese women

Can Circulating Cardiac Biomarkers Be Helpful in the Assessment of LMNA Mutation Carriers?

Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle Laminopathies

Acyl-CoA synthetase long-chain 5 genotype is associated with body composition changes in response to lifestyle interventions in postmenopausal women with overweight and obesity: a genetic association study on cohorts Montréal-Ottawa New Emerging Team, and Complications Associated with Obesity

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption

Peroxisome Proliferator-activated Receptor γ 2 and Acyl-CoA Synthetase 5 Polymorphisms Influence Diet Response

Still Building on Candidate-Gene Strategy in Hypertension?

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

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population

Genotype-specific weight loss treatment advice: how close are we?

Functional characterization of a promoter polymorphism that drives ACSL5 gene expression in skeletal muscle and associates with diet-induced weight loss

Specific contribution of lamin A and lamin C in the development of laminopathies

Effects of Exercise Training on Molecular Markers of Lipogenesis and Lipid Partitioning in Fructose-Induced Liver Fat Accumulation

Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation

Sequence analysis of coding and 3' and 5' flanking regions of the epithelial sodium channel alpha, beta, and gamma genes in Dahl S versus R rats

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Mutations in the laminin α2-chain gene ( LAMA2 ) cause merosin-deficient congenital muscular dystrophy

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