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Comparative RNA editing in autistic and neurotypical cerebella

Molecular psychiatry, 2013-09, Vol.18 (9), p.1041-1048

2013

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MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation

Cell death and differentiation, 2013-09, Vol.20 (9), p.1194-1208

2013

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Loss of FilaminC (FLNc) Results in Severe Defects in Myogenesis and Myotube Structure

Molecular and Cellular Biology, 2006-09, Vol.26 (17), p.6522-6534

2006

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Dystrophin expression in the mdx mouse restored by stem cell transplantation

Nature (London), 1999-09, Vol.401 (6751), p.390-394

1999

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Molecular profiles of inflammatory myopathies

Neurology, 2002-10, Vol.59 (8), p.1170-1182

2002

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The dystrophin associated protein complex in zebrafish

Human molecular genetics, 2003-03, Vol.12 (6), p.601-615

2003

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A Genome-Wide Scan for Linkage to Human Exceptional Longevity Identifies a Locus on Chromosome 4

Proceedings of the National Academy of Sciences - PNAS, 2001-08, Vol.98 (18), p.10505-10508

2001

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Gene Expression Comparison of Biopsies from Duchenne Muscular Dystrophy (DMD) and Normal Skeletal Muscle

Proceedings of the National Academy of Sciences - PNAS, 2002-11, Vol.99 (23), p.15000-15005

2002

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Peripheral blood gene expression signature differentiates children with autism from unaffected siblings

Neurogenetics, 2013-05, Vol.14 (2), p.143-152

2013

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Stable Expression of Calpain 3 from a Muscle Transgene in vivo: Immature Muscle in Transgenic Mice Suggests a Role for Calpain 3 in Muscle Maturation

Proceedings of the National Academy of Sciences - PNAS, 2002-06, Vol.99 (13), p.8874-8879

2002

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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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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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The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

Cell, 1988-04, Vol.53 (2), p.219-228

1988

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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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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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Caveolin-3 in Muscular Dystrophy

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

1998

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Cloning and Characterization of the Human Homologue of a Dystrophin Related Phosphoprotein Found at the Torpedo Electric Organ Post-Synaptic Membrane

Human molecular genetics, 1996-04, Vol.5 (4), p.489-496

1996

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Dp140: a novel 140 kDa CNS transcript from the dystrophin locus

Human molecular genetics, 1995-03, Vol.4 (3), p.329-335

1995

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Syntrophin Binds to an Alternatively Spliced Exon of Dystrophin

The Journal of cell biology, 1995-02, Vol.128 (3), p.363-371

1995

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Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

Cell, 1987-07, Vol.50 (3), p.509-517

1987

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Side Population cells isolated from different tissues share transcriptome signatures and express tissue-specific markers

Experimental cell research, 2005-02, Vol.303 (2), p.360-374

2005

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Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts

Nature (London), 1989-01, Vol.337 (6203), p.176-179

1989

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Identification of FLRT1, FLRT2, and FLRT3: A Novel Family of Transmembrane Leucine-Rich Repeat Proteins

Genomics (San Diego, Calif.), 1999-12, Vol.62 (3), p.417-426

1999

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Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics

Nature genetics, 1998-09, Vol.20 (1), p.83-86

1998

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Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscle

Journal of the neurological sciences, 2003-01, Vol.206 (1), p.71-78

2003

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Comparative RNA editing in autistic and neurotypical cerebella

MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation

Loss of FilaminC (FLNc) Results in Severe Defects in Myogenesis and Myotube Structure

Dystrophin expression in the mdx mouse restored by stem cell transplantation

Molecular profiles of inflammatory myopathies

The dystrophin associated protein complex in zebrafish

A Genome-Wide Scan for Linkage to Human Exceptional Longevity Identifies a Locus on Chromosome 4

Gene Expression Comparison of Biopsies from Duchenne Muscular Dystrophy (DMD) and Normal Skeletal Muscle

Peripheral blood gene expression signature differentiates children with autism from unaffected siblings

Stable Expression of Calpain 3 from a Muscle Transgene in vivo: Immature Muscle in Transgenic Mice Suggests a Role for Calpain 3 in Muscle Maturation

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

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

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

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

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

Caveolin-3 in Muscular Dystrophy

Cloning and Characterization of the Human Homologue of a Dystrophin Related Phosphoprotein Found at the Torpedo Electric Organ Post-Synaptic Membrane

Dp140: a novel 140 kDa CNS transcript from the dystrophin locus

Syntrophin Binds to an Alternatively Spliced Exon of Dystrophin

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

Side Population cells isolated from different tissues share transcriptome signatures and express tissue-specific markers

Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts

Identification of FLRT1, FLRT2, and FLRT3: A Novel Family of Transmembrane Leucine-Rich Repeat Proteins

Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics

Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscle

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