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Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice

Human molecular genetics, 2009-02, Vol.18 (4), p.607-620

2009

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β-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

Nature genetics, 1995-11, Vol.11 (3), p.266-273

1995

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Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy

Science (American Association for the Advancement of Science), 1995-11, Vol.270 (5237), p.819-822

1995

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Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex

Journal of cell science, 2000-07, Vol.113 ( Pt 14) (14), p.2535-2544

2000

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Muscle Degeneration without Mechanical Injury in Sarcoglycan Deficiency

Proceedings of the National Academy of Sciences - PNAS, 1999-09, Vol.96 (19), p.10723-10728

1999

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Caveolin-3 in Muscular Dystrophy

Human molecular genetics, 1998-05, Vol.7 (5), p.871-877

1998

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Muscle-specific promoters may be necessary for adeno-associated virus-mediated gene transfer in the treatment of muscular dystrophies

Human gene therapy, 2001-01, Vol.12 (2), p.205-215

2001

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Myoferlin, a candidate gene and potential modifier of muscular dystrophy

Human molecular genetics, 2000-01, Vol.9 (2), p.217-226

2000

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Mild and severe muscular dystrophy caused by a single γ-sarcoglycan mutation

American journal of human genetics, 1996-11, Vol.59 (5), p.1040-1047

1996

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The Sarcoglycan Complex in the Six Autosomal Recessive Limb-Girdle Muscular Dystrophies

Human molecular genetics, 1996-12, Vol.5 (12), p.1963-1969

1996

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Corrosion Performance of Friction Stir Linear Lap Welded AM60B Joints

JOM (1989), 2017-11, Vol.69 (11), p.2335-2344

2017

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Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21

American journal of human genetics, 1997-04, Vol.60 (4), p.891-895

1997

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Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23

American journal of human genetics, 1997-10, Vol.61 (4), p.909-917

1997

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Using interviews to construct and disseminate knowledge of oral health policy

International journal of dental hygiene, 2012-05, Vol.10 (2), p.91-97

2012

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Mutations That Disrupt the Carboxyl-Terminus of γ-Sarcoglycan Cause Muscular Dystrophy

Human molecular genetics, 1996-11, Vol.5 (11), p.1841-1847

1996

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Calcium-sensitive Phospholipid Binding Properties of Normal and Mutant Ferlin C2 Domains

The Journal of biological chemistry, 2002-06, Vol.277 (25), p.22883-22888

2002

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Genomic Screening for β-Sarcoglycan Gene Mutations: Missense Mutations May Cause Severe Limb-girdle Muscular Dystrophy Type 2E (LGMD 2E)

Human molecular genetics, 1996-12, Vol.5 (12), p.1953-1961

1996

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Hormonal Modulation of a Gene Injected into Rat Heart in vivo

Proceedings of the National Academy of Sciences - PNAS, 1991-05, Vol.88 (10), p.4138-4142

1991

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Filamin 2 (FLN2): A Muscle-Specific Sarcoglycan Interacting Protein

The Journal of cell biology, 2000-01, Vol.148 (1), p.115-126

2000

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Dominant negative myostatin produces hypertrophy without hyperplasia in muscle

FEBS letters, 2000-05, Vol.474 (1), p.71-75

2000

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NOVEL NESPRIN-1 MUTATIONS DISRUPT NE ORGANIZATION AND INDUCE DILATED CARDIOMYOPATHY

Heart (British Cardiac Society), 2014-12, Vol.100 (Suppl 4), p.A19-A19

2014

Volltextzugriff (PDF)

Human Adhalin is Alternatively Spliced and the Gene is Located on Chromosome 17q21

Proceedings of the National Academy of Sciences - PNAS, 1994-10, Vol.91 (21), p.9690-9694

1994

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Dysferlin protein analysis in limb-girdle muscular dystrophies

Journal of molecular neuroscience, 2001-08, Vol.17 (1), p.71-80

2001

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ζ-Sarcoglycan, a novel component of the sarcoglycan complex, is reduced in muscular dystrophy

Human molecular genetics, 2002-09, Vol.11 (18), p.2147-2154

2002

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Repairing the tears: dysferlin in muscle membrane repair

Trends in molecular medicine, 2003-08, Vol.9 (8), p.327-330

2003

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Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice

β-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy

Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex

Muscle Degeneration without Mechanical Injury in Sarcoglycan Deficiency

Caveolin-3 in Muscular Dystrophy

Muscle-specific promoters may be necessary for adeno-associated virus-mediated gene transfer in the treatment of muscular dystrophies

Myoferlin, a candidate gene and potential modifier of muscular dystrophy

Mild and severe muscular dystrophy caused by a single γ-sarcoglycan mutation

The Sarcoglycan Complex in the Six Autosomal Recessive Limb-Girdle Muscular Dystrophies

Corrosion Performance of Friction Stir Linear Lap Welded AM60B Joints

Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21

Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23

Using interviews to construct and disseminate knowledge of oral health policy

Mutations That Disrupt the Carboxyl-Terminus of γ-Sarcoglycan Cause Muscular Dystrophy

Calcium-sensitive Phospholipid Binding Properties of Normal and Mutant Ferlin C2 Domains

Genomic Screening for β-Sarcoglycan Gene Mutations: Missense Mutations May Cause Severe Limb-girdle Muscular Dystrophy Type 2E (LGMD 2E)

Hormonal Modulation of a Gene Injected into Rat Heart in vivo

Filamin 2 (FLN2): A Muscle-Specific Sarcoglycan Interacting Protein

Dominant negative myostatin produces hypertrophy without hyperplasia in muscle

NOVEL NESPRIN-1 MUTATIONS DISRUPT NE ORGANIZATION AND INDUCE DILATED CARDIOMYOPATHY

Human Adhalin is Alternatively Spliced and the Gene is Located on Chromosome 17q21

Dysferlin protein analysis in limb-girdle muscular dystrophies

ζ-Sarcoglycan, a novel component of the sarcoglycan complex, is reduced in muscular dystrophy

Repairing the tears: dysferlin in muscle membrane repair

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