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Nonsense-Mediated mRNA Decay and Ubiquitin–Proteasome System Regulate Cardiac Myosin-Binding Protein C Mutant Levels in Cardiomyopathic Mice

Circulation research, 2009-07, Vol.105 (3), p.239-248

2009

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Long-term efficacy of myoblast transplantation on regional structure and function after myocardial infarction

Circulation (New York, N.Y.), 2002-09, Vol.106 (12 Suppl 1), p.I131-I136

2002

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Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Nature genetics, 1999-03, Vol.21 (3), p.285-288

1999

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Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy

Journal of cell science, 2001-12, Vol.114 (Pt 24), p.4435-4445

2001

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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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Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

American journal of human genetics, 2000-04, Vol.66 (4), p.1407-1412

2000

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Comparison of the effects of fetal cardiomyocyte and skeletal myoblast transplantation on postinfarction left ventricular function

The Journal of thoracic and cardiovascular surgery, 2000-06, Vol.119 (6), p.1169-1175

2000

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Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy

Biochemical and biophysical research communications, 2007-05, Vol.357 (1), p.162-167

2007

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Genetic and molecular basis of cardiac arrhythmias : Impact on clinical management parts I and II

Circulation (New York, N.Y.), 1999-02, Vol.99 (4), p.518-528

1999

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Factors affecting functional outcome after autologous skeletal myoblast transplantation

The Annals of thoracic surgery, 2001-03, Vol.71 (3), p.844-851

2001

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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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Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene

Circulation (New York, N.Y.), 1998-06, Vol.97 (22), p.2230-2236

1998

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Organization and Sequence of Human Cardiac Myosin Binding Protein C Gene (MYBPC3) and Identification of Mutations Predicted to Produce Truncated Proteins in Familial Hypertrophic Cardiomyopathy

Circulation research, 1997-03, Vol.80 (3), p.427-434

1997

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Molecular basis of familial cardiomyopathies

Circulation (New York, N.Y.), 1995-01, Vol.91 (2), p.532-540

1995

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Characterization of a Unique Genetic Variant in the β1-adrenoceptor Gene and Evaluation of its Role in Idiopathic Dilated Cardiomyopathy

Journal of molecular and cellular cardiology, 1999-05, Vol.31 (5), p.1025-1032

1999

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Genetic and molecular basis of cardiac arrhythmias : Impact on clinical management. Part III

Circulation (New York, N.Y.), 1999-02, Vol.99 (5), p.674-681

1999

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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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Is Skeletal Myoblast Transplantation Clinically Relevant in the Era of Angiotensin-Converting Enzyme Inhibitors?

Circulation (New York, N.Y.), 2001-09, Vol.104 (suppl 1), p.I-223-I-228

2001

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COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes

Journal of molecular biology, 1999-11, Vol.294 (2), p.443-456

1999

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Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction

Journal of the American College of Cardiology, 2003-04, Vol.41 (7), p.1078-1083

2003

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Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

Circulation (New York, N.Y.), 2003-05, Vol.107 (17), p.2227-2232

2003

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Skeletal myoblast transplantation in ischemic heart failure : Long-term follow-up of the first phase I cohort of patients

Circulation (New York, N.Y.), 2006-07, Vol.114 (1), p.I108-I113

2006

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A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block

Neuromuscular disorders : NMD, 2001-09, Vol.11 (6), p.542-546

2001

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Skeletal Myoblast Transplantation in Ischemic Heart Failure

Circulation (New York, N.Y.), 2006-07, Vol.114 (1_supplement)

2006

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Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

Human molecular genetics, 2005-01, Vol.14 (1), p.155-169

2005

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Nonsense-Mediated mRNA Decay and Ubiquitin–Proteasome System Regulate Cardiac Myosin-Binding Protein C Mutant Levels in Cardiomyopathic Mice

Long-term efficacy of myoblast transplantation on regional structure and function after myocardial infarction

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy

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

Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

Comparison of the effects of fetal cardiomyocyte and skeletal myoblast transplantation on postinfarction left ventricular function

Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy

Genetic and molecular basis of cardiac arrhythmias : Impact on clinical management parts I and II

Factors affecting functional outcome after autologous skeletal myoblast transplantation

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

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene

Organization and Sequence of Human Cardiac Myosin Binding Protein C Gene (MYBPC3) and Identification of Mutations Predicted to Produce Truncated Proteins in Familial Hypertrophic Cardiomyopathy

Molecular basis of familial cardiomyopathies

Characterization of a Unique Genetic Variant in the β1-adrenoceptor Gene and Evaluation of its Role in Idiopathic Dilated Cardiomyopathy

Genetic and molecular basis of cardiac arrhythmias : Impact on clinical management. Part III

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

Is Skeletal Myoblast Transplantation Clinically Relevant in the Era of Angiotensin-Converting Enzyme Inhibitors?

COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes

Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction

Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

Skeletal myoblast transplantation in ischemic heart failure : Long-term follow-up of the first phase I cohort of patients

A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block

Skeletal Myoblast Transplantation in Ischemic Heart Failure

Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

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