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Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin)

The Journal of biological chemistry, 1993-11, Vol.268 (32), p.23739-23742

1993

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Cloning and Tissue-Specific Expression of Five Voltage-Gated Potassium Channel cDNAs Expressed in Rat Heart

Proceedings of the National Academy of Sciences - PNAS, 1991-03, Vol.88 (5), p.1798-1802

1991

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Time-, voltage-, and state-dependent block by quinidine of a cloned human cardiac potassium channel

Molecular pharmacology, 1992-02, Vol.41 (2), p.322-330

1992

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Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Nature genetics, 1995-06, Vol.10 (2), p.243-245

1995

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Disruption of the dystrophin-glycoprotein complex in the cardiomyopathic hamster

The Journal of biological chemistry, 1993-06, Vol.268 (16), p.11496-11499

1993

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Clustering and Immobilization of Acetylcholine Receptors by the 43-kD Protein: A Possible Role for Dystrophin-Related Protein

The Journal of cell biology, 1993-11, Vol.123 (3), p.729-740

1993

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Disease mechanisms revealed by transcription profiling in SOD1-G93A transgenic mouse spinal cord

Annals of neurology, 2001-12, Vol.50 (6), p.730-740

2001

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A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy

Human molecular genetics, 1995-07, Vol.4 (7), p.1163-1167

1995

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Non-Muscle α-Dystroglycan Is Involved in Epithelial Development

The Journal of cell biology, 1995-07, Vol.130 (1), p.79-91

1995

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A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering

Cell, 1994-06, Vol.77 (5), p.663-674

1994

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A cluster of novel serotonin receptor 3-like genes on human chromosome 3

Gene, 2003-11, Vol.319, p.137-148

2003

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Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

Cell, 1994-08, Vol.78 (4), p.625-633

1994

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Rapsyn may function as a link between the acetylcholine receptor and the agrin-binding dystrophin-associated glycoprotein complex

Neuron (Cambridge, Mass.), 1995-07, Vol.15 (1), p.115-126

1995

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Ultrastructural localization of adhalin, alpha-dystroglycan and merosin in normal and dystrophic muscle

Neuropathology and applied neurobiology, 1996-02, Vol.22 (1), p.30-37, Article 30

1996

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Functional characterization of RK5, a voltage-gated K + channel cloned from the rat cardiovascular system

FEBS letters, 1991-12, Vol.295 (1), p.211-213

1991

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Developmental expression of cloned cardiac potassium channels

FEBS letters, 1991-06, Vol.284 (2), p.152-154

1991

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Adhalin gene polymorphism

Human molecular genetics, 1994-12, Vol.3 (12), p.2269-2269

1994

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The Expression of Dystrophin-associated Glycoproteins During Skeletal Muscle Degeneration and Regeneration. An Immunofluorescence Study

Journal of neuropathology and experimental neurology, 1995-07, Vol.54 (4), p.557-569

1995

Volltextzugriff (PDF)

CLINICAL AND MOLECULAR PATHOLOGICAL FEATURES OF SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY IN SAUDI ARABIA

Developmental medicine and child neurology, 1996-03, Vol.38 (3), p.262-270

1996

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Laminin abnormality in severe childhood autosomal recessive muscular dystrophy

Laboratory investigation, 1995-06, Vol.72 (6), p.715

1995

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Expression of deletion-containing dystrophins in mdx muscle : implications for gene therapy and dystrophin function

Pediatric research, 1995-06, Vol.37 (6), p.693-700

1995

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Applying genomics tools to identify therapeutic targets for asthma

Expert opinion on investigational drugs, 1998-08, Vol.7 (8), p.1301-1312

Roberds, Steven L

1998

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A 5′ Dystrophin Duplication Mutation Causes Membrane Deficiency of α-Dystroglycan in a Family with X-linked Cardiomyopathy

Journal of molecular and cellular cardiology, 1997-12, Vol.29 (12), p.3175-3188

1997

Volltextzugriff (PDF)

Molecular Biology of the Voltage-Gated Potassium Channels of the Cardiovascular System

Journal of cardiovascular electrophysiology, 1993-02, Vol.4 (1), p.68-80

1993

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BACE knockout mice are healthy despite lacking the primary β-secretase activity in brain: implications for Alzheimer's disease therapeutics

Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin)

Cloning and Tissue-Specific Expression of Five Voltage-Gated Potassium Channel cDNAs Expressed in Rat Heart

Time-, voltage-, and state-dependent block by quinidine of a cloned human cardiac potassium channel

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Disruption of the dystrophin-glycoprotein complex in the cardiomyopathic hamster

Clustering and Immobilization of Acetylcholine Receptors by the 43-kD Protein: A Possible Role for Dystrophin-Related Protein

Disease mechanisms revealed by transcription profiling in SOD1-G93A transgenic mouse spinal cord

A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy

Non-Muscle α-Dystroglycan Is Involved in Epithelial Development

A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering

A cluster of novel serotonin receptor 3-like genes on human chromosome 3

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

Rapsyn may function as a link between the acetylcholine receptor and the agrin-binding dystrophin-associated glycoprotein complex

Ultrastructural localization of adhalin, alpha-dystroglycan and merosin in normal and dystrophic muscle

Functional characterization of RK5, a voltage-gated K + channel cloned from the rat cardiovascular system

Developmental expression of cloned cardiac potassium channels

Adhalin gene polymorphism

The Expression of Dystrophin-associated Glycoproteins During Skeletal Muscle Degeneration and Regeneration. An Immunofluorescence Study

CLINICAL AND MOLECULAR PATHOLOGICAL FEATURES OF SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY IN SAUDI ARABIA

Laminin abnormality in severe childhood autosomal recessive muscular dystrophy

Expression of deletion-containing dystrophins in mdx muscle : implications for gene therapy and dystrophin function

Applying genomics tools to identify therapeutic targets for asthma

A 5′ Dystrophin Duplication Mutation Causes Membrane Deficiency of α-Dystroglycan in a Family with X-linked Cardiomyopathy

Molecular Biology of the Voltage-Gated Potassium Channels of the Cardiovascular System

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