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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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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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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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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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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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Mutational analysis of the PEX gene in patients with X-linked hypophosphatemic rickets

American journal of human genetics, 1997-04, Vol.60 (4), p.790-797

1997

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Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11

The Journal of biological chemistry, 1992-05, Vol.267 (13), p.9281-9288

1992

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Dystrophin: The protein product of the duchenne muscular dystrophy locus

Cell, 1987-12, Vol.51 (6), p.919-928

1987

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The Subcellular Distribution of Dystrophin in Mouse Skeletal, Cardiac, and Smooth Muscle

The Journal of cell biology, 1991-10, Vol.115 (2), p.411-421

1991

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Reversal of neurobehavioral social deficits in dystrophic mice using inhibitors of phosphodiesterases PDE5A and PDE9A

Translational psychiatry, 2016-09, Vol.6 (9), p.e901-e901

2016

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Systemic Delivery of Human Microdystrophin to Regenerating Mouse Dystrophic Muscle by Muscle Progenitor Cells

Proceedings of the National Academy of Sciences - PNAS, 2004-03, Vol.101 (10), p.3581-3586

2004

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Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder

Translational psychiatry, 2013-05, Vol.3 (5), p.e262-e262

2013

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Minimal Haplotype Tagging

Proceedings of the National Academy of Sciences - PNAS, 2003-08, Vol.100 (17), p.9900-9905

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

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

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

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

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

Mutational analysis of the PEX gene in patients with X-linked hypophosphatemic rickets

Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11

Dystrophin: The protein product of the duchenne muscular dystrophy locus

The Subcellular Distribution of Dystrophin in Mouse Skeletal, Cardiac, and Smooth Muscle

Reversal of neurobehavioral social deficits in dystrophic mice using inhibitors of phosphodiesterases PDE5A and PDE9A

Systemic Delivery of Human Microdystrophin to Regenerating Mouse Dystrophic Muscle by Muscle Progenitor Cells

Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder

Minimal Haplotype Tagging

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