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Very mild muscular dystrophy associated with the deletion of 46% of dystrophin

Nature (London), 1990-01, Vol.343 (6254), p.180-182

1990

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The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

Nature (London), 1988-06, Vol.333 (6172), p.466-469

1988

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Age-Related Conversion of Dystrophin-Negative to -Positive Fiber Segments of Skeletal but not Cardiac Muscle Fibers in Heterozygote mdx Mice

Journal of neuropathology and experimental neurology, 1990-03, Vol.49 (2), p.96-105

1990

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Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophin

American journal of human genetics, 1991-02, Vol.48 (2), p.295-304

1991

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The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

Nature (London), 1988-06, Vol.333 (6172), p.466-469

1988

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Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantation

The American journal of pathology, 1989-07, Vol.135 (1), p.27-32

1989

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Molecular Cloning and Expression of cDNA Encoding the 53,000-Dalton Glycoprotein of Rabbit Skeletal Muscle Sarcoplasmic Reticulum

The Journal of biological chemistry, 1989-02, Vol.264 (6), p.3484-3493

1989

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Dystrophin is tightly associated with the sarcolemma of mammalian skeletal muscle fibers

Experimental cell research, 1991, Vol.192 (1), p.278-288

1991

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Myogenic regulation of dystrophin gene expression

British medical bulletin, 1989, Vol.45 (3), p.681-702

1989

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Immunohistochemical studies show truncated dystrophins in the myotubes of three fetuses at risk for Duchenne muscular dystrophy

Journal of medical genetics, 1991-08, Vol.28 (8), p.505-510

1991

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Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein

Journal of the neurological sciences, 1991-02, Vol.101 (2), p.141-147

1991

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Biosynthesis of intrinsic sarcoplasmic reticulum proteins during differentiation of the myogenic cell line L6

The Journal of biological chemistry, 1983-04, Vol.258 (7), p.4576-4581

1983

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Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminus

Neuromuscular disorders : NMD, 1991, Vol.1 (2), p.113-119

1991

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Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies

American journal of medical genetics, 1991-04, Vol.39 (1), p.38-41

1991

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Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical study

Muscle & nerve, 1990-05, Vol.13 (5), p.376-380

1990

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Calcium oxalate-loaded sarcoplasmic reticulum vesicles from developing skeletal muscle are highly differentiated

Progress in clinical and biological research, 1988, Vol.252, p.133

1988

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SARCOPLASMIC RETICULUM AND SARCOLEMMA DURING DEVELOPMENT

Plasticity of Muscle, 2019, p.209-224

Originally published 1980, 2019

Volltextzugriff (PDF)

Identification of dystrophin in cardiac sarcolemmal vesicles

Biochemical and biophysical research communications, 1990-06, Vol.169 (2), p.565-570

1990

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Studies on sarcoplasmic reticulum from slow-twitch muscle

Journal of muscle research and cell motility, 1982-06, Vol.3 (2), p.191-212

1982

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Identification of sarcoplasmic reticulum-like system in Physarum polycephalum

FEBS letters, 1979-11, Vol.107 (2), p.335-339

1979

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Monoclonal antibodies to the Ca2+ + Mg2+-dependent ATPase of sarcoplasmic reticulum identify polymorphic forms of the enzyme and indicate the presence in the enzyme of a classical high-affinity Ca2+ binding site

Journal of bioenergetics and biomembranes, 1984-12, Vol.16 (5-6), p.441-464

1984

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Assembly of the sarcoplasmic reticulum during muscle development

Current topics in membranes and transport, 1985, Vol.24, p.337-368

1985

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Genetic and biochemical determinations in the pre-transplant workup and in the post-transplant assessment period

Advances in experimental medicine and biology, 1990, Vol.280, p.219

1990

Volltextzugriff (PDF)

Immunofluorescence dystrophy study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal regiona of the protein

Journal of the neurological sciences, 1991, Vol.101 (2), p.141-147

1991

Volltextzugriff (PDF)

Immunological study of dystrophin in Duchenne fetus

The Lancet (British edition), 1989-11, Vol.2 (8673), p.1212-1213

1989

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Diseases Of Striated Muscles. Neuromuscular Diseases
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Very mild muscular dystrophy associated with the deletion of 46% of dystrophin

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

Age-Related Conversion of Dystrophin-Negative to -Positive Fiber Segments of Skeletal but not Cardiac Muscle Fibers in Heterozygote mdx Mice

Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophin

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantation

Molecular Cloning and Expression of cDNA Encoding the 53,000-Dalton Glycoprotein of Rabbit Skeletal Muscle Sarcoplasmic Reticulum

Dystrophin is tightly associated with the sarcolemma of mammalian skeletal muscle fibers

Myogenic regulation of dystrophin gene expression

Immunohistochemical studies show truncated dystrophins in the myotubes of three fetuses at risk for Duchenne muscular dystrophy

Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein

Biosynthesis of intrinsic sarcoplasmic reticulum proteins during differentiation of the myogenic cell line L6

Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminus

Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies

Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical study

Calcium oxalate-loaded sarcoplasmic reticulum vesicles from developing skeletal muscle are highly differentiated

SARCOPLASMIC RETICULUM AND SARCOLEMMA DURING DEVELOPMENT

Identification of dystrophin in cardiac sarcolemmal vesicles

Studies on sarcoplasmic reticulum from slow-twitch muscle

Identification of sarcoplasmic reticulum-like system in Physarum polycephalum

Monoclonal antibodies to the Ca2+ + Mg2+-dependent ATPase of sarcoplasmic reticulum identify polymorphic forms of the enzyme and indicate the presence in the enzyme of a classical high-affinity Ca2+ binding site

Assembly of the sarcoplasmic reticulum during muscle development

Genetic and biochemical determinations in the pre-transplant workup and in the post-transplant assessment period

Immunofluorescence dystrophy study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal regiona of the protein

Immunological study of dystrophin in Duchenne fetus

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