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Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene

British heart journal, 2002-03, Vol.87 (3), p.270-275

2002

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α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere

Cell, 1994-06, Vol.77 (5), p.701-712

1994

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A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation

Cell, 1990-09, Vol.62 (5), p.999-1006

1990

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Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

Nature genetics, 1995-12, Vol.11 (4), p.438-440

1995

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A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance

Circulation (New York, N.Y.), 2000-03, Vol.101 (12), p.1396-1402

2000

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Instability of short-sequence DNA repeats of pear pathogenic Erwinia strains from Japan and Erwinia amylovora fruit tree and raspberry strains

Molecular genetics and genomics : MGG, 2003-03, Vol.268 (6), p.739-749

2003

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A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated β-myosin heavy chain genes

Human genetics, 1998-03, Vol.102 (3), p.299-304

1998

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Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin Gene

Journal of the American College of Cardiology, 1997-03, Vol.29 (3), p.635-640

1997

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A molecular basis for familial hypertrophic cardiomyopathy : an α/β cardiac myosin heavy chain hybrid gene

Cell, 1990-09, Vol.62 (5), p.991-998

1990

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DNA topoisomerases: enzymes that control DNA conformation

Current topics in microbiology and immunology, 1985, Vol.114, p.19

Vosberg, H P

1985

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The polymerase chain reaction: an improved method for the analysis of nucleic acids

Human genetics, 1989-08, Vol.83 (1), p.1-15

VOSBERG, H.-P

1989

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Genomic structure and fine mapping of the two human filamin gene paralogues FLNB and FLNC and comparative analysis of the filamin gene family

Human genetics, 2000-12, Vol.107 (6), p.597-611

2000

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A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12

American journal of human genetics, 1990-09, Vol.47 (3), p.389-394

1990

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Inhibition of calf thymus type II DNA topoisomerase by poly(ADP‐ribosylation)

The EMBO journal, 1985-08, Vol.4 (8), p.2129-2134

1985

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Exclusion of Cardiac Myosin Heavy Chain and Actin Gene Involvement in Hypertrophic Cardiomyopathy of Several French Families

Circulation research, 1992-07, Vol.71 (1), p.3-8

1992

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Identification of Gene Defects by Linkage Analysis: Use in Inherited Cardiomyopathies

European heart journal, 1994-12, Vol.15 (suppl-D), p.20-23

Vosberg, H P

1994

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Regulation of myosin heavy chain expression in the hearts of hypertensive rats by testosterone

Circulation research, 1990-06, Vol.66 (6), p.1585-1590

1990

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Scl 70 autoantibodies from scleroderma patients recognize a 95 kDa protein identified as DNA topoisomerase I

Chromosoma, 1986-01, Vol.94 (2), p.132-138

1986

Volltextzugriff (PDF)

Direct sequencing of polymerase chain reaction amplified DNA fragments through the incorporation of deoxynucleoside α-thiotriphosphates

Nucleic acids research, 1988-11, Vol.16 (21), p.9947-9959

1988

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Myosin mutations in hypertrophic cardiomyopathy and functional implications

Herz, 1994-04, Vol.19 (2), p.75-83

Vosberg, H P

1994

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Mapping of the Actomyosin Interfaces

Proceedings of the National Academy of Sciences - PNAS, 1994-03, Vol.91 (7), p.2772-2776

1994

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A polymorphism of the MYH7 gene

Nucleic acids research, 1990-10, Vol.18 (20), p.6173-6173

1990

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Gene symbol: MYBPC3. Disease: Hypertrophic cardiomyopathy

Human genetics, 2004-03, Vol.114 (4), p.406-406

2004

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Effect of deoxynucleoside phosphorothioates incorporated in DNA on cleavage by restriction enzymes

The Journal of biological chemistry, 1982-06, Vol.257 (11), p.6595-6599

1982

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The regulation of the human beta myosin heavy-chain gene

Basic research in cardiology, 1992, Vol.87 Suppl 1, p.161-173

1992

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Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene

α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere

A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance

Instability of short-sequence DNA repeats of pear pathogenic Erwinia strains from Japan and Erwinia amylovora fruit tree and raspberry strains

A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated β-myosin heavy chain genes

Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin Gene

A molecular basis for familial hypertrophic cardiomyopathy : an α/β cardiac myosin heavy chain hybrid gene

DNA topoisomerases: enzymes that control DNA conformation

The polymerase chain reaction: an improved method for the analysis of nucleic acids

Genomic structure and fine mapping of the two human filamin gene paralogues FLNB and FLNC and comparative analysis of the filamin gene family

A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12

Inhibition of calf thymus type II DNA topoisomerase by poly(ADP‐ribosylation)

Exclusion of Cardiac Myosin Heavy Chain and Actin Gene Involvement in Hypertrophic Cardiomyopathy of Several French Families

Identification of Gene Defects by Linkage Analysis: Use in Inherited Cardiomyopathies

Regulation of myosin heavy chain expression in the hearts of hypertensive rats by testosterone

Scl 70 autoantibodies from scleroderma patients recognize a 95 kDa protein identified as DNA topoisomerase I

Direct sequencing of polymerase chain reaction amplified DNA fragments through the incorporation of deoxynucleoside α-thiotriphosphates

Myosin mutations in hypertrophic cardiomyopathy and functional implications

Mapping of the Actomyosin Interfaces

A polymorphism of the MYH7 gene

Gene symbol: MYBPC3. Disease: Hypertrophic cardiomyopathy

Effect of deoxynucleoside phosphorothioates incorporated in DNA on cleavage by restriction enzymes

The regulation of the human beta myosin heavy-chain gene

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