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The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally spliced

Nature genetics, 1995-02, Vol.9 (2), p.184-190

1995

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Condensation of plasmid DNA with polylysine improves liposome-mediated gene transfer into established and primary muscle cells

Gene therapy, 1996-05, Vol.3 (5), p.396

1996

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Transfection of cultured myoblasts in high serum concentration with DODAC:DOPE liposomes

Gene therapy, 1998-10, Vol.5 (10), p.1306-1313

1998

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Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia

Nature (London), 1990-02, Vol.343 (6258), p.559-561

1990

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A substitution of cysteine for arginine 614 in the ryanodine receptor is potentially causative of human malignant hyperthermia

Genomics (San Diego, Calif.), 1991-11, Vol.11 (3), p.751-755

1991

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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 and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy gene

Molecular and Cellular Biology, 1990-01, Vol.10 (1), p.193-205

1990

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Frame-Shift Deletions in Patients with Duchenne and Becker Muscular Dystrophy

Science (American Association for the Advancement of Science), 1988-11, Vol.242 (4879), p.755-759

1988

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Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene

American journal of human genetics, 1989-10, Vol.45 (4), p.507-520

1989

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Genetics of Duchenne Muscular Dystrophy

Annual review of genetics, 1988-01, Vol.22 (1), p.601-629

1988

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Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotype/genotype correlation

American journal of human genetics, 1990-04, Vol.46 (4), p.682-695

1990

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Polymorphisms and deduced amino acid substitutions in the coding sequence of the ryanodine receptor ( RYR1) gene in individuals with malignant hyperthermia

Genomics (San Diego, Calif.), 1992-08, Vol.13 (4), p.1247-1254

1992

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Dystrophin isoforms Dp71 and Dp427 have distinct roles in myogenic cells

Muscle & nerve, 1999-01, Vol.22 (1), p.16-27

1999

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Mechanisms of tandem duplication in the Duchenne muscular dystrophy gene include both homologous and nonhomologous intrachromosomal recombination

The EMBO journal, 1991-09, Vol.10 (9), p.2471-2477

1991

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Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy

Nature (London), 1985-01, Vol.318 (6047), p.672-675

1985

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Localization of the mdx mutation within the mouse dystrophin gene

The EMBO journal, 1988-10, Vol.7 (10), p.3017-3021

1988

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On Discovery, Genomes, The Society, and Society

American journal of human genetics, 2001-04, Vol.68 (4), p.819-825

Worton, Ronald G.

2001

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Dystrophin in frameshift deletion patients with Becker muscular dystrophy

American journal of human genetics, 1992-09, Vol.51 (3), p.562-570

1992

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A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifs

Nucleic acids research, 1997-04, Vol.25 (8), p.1618

1997

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Myoblast transfer in duchenne muscular dystrophy

Annals of neurology, 1993-07, Vol.34 (1), p.8-17

1993

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Identification of a Transcriptional Enhancer Within Muscle Intron 1 of the Human Dystrophin Gene

Human molecular genetics, 1996-10, Vol.5 (10), p.1599-1606

1996

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Human Ribosomal RNA Genes: Orientation of the Tandem Array and Conservation of the 5$^{\prime}$ End

Science (American Association for the Advancement of Science), 1988-01, Vol.239 (4835), p.64-68

1988

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Dystrophin: the long and short of it

The Journal of clinical investigation, 1994-01, Vol.93 (1), p.4-4

Worton, R G

1994

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Expression of the dystrophin isoform Dp71 in differentiating human fetal myogenic cultures

Human molecular genetics, 1996-10, Vol.5 (10), p.1559-1566

1996

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Partial gene duplication in Duchenne and Becker muscular dystrophies

Journal of medical genetics, 1988-06, Vol.25 (6), p.369-376

1988

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The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally spliced

Condensation of plasmid DNA with polylysine improves liposome-mediated gene transfer into established and primary muscle cells

Transfection of cultured myoblasts in high serum concentration with DODAC:DOPE liposomes

Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia

A substitution of cysteine for arginine 614 in the ryanodine receptor is potentially causative of human malignant hyperthermia

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

Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy gene

Frame-Shift Deletions in Patients with Duchenne and Becker Muscular Dystrophy

Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene

Genetics of Duchenne Muscular Dystrophy

Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotype/genotype correlation

Polymorphisms and deduced amino acid substitutions in the coding sequence of the ryanodine receptor ( RYR1) gene in individuals with malignant hyperthermia

Dystrophin isoforms Dp71 and Dp427 have distinct roles in myogenic cells

Mechanisms of tandem duplication in the Duchenne muscular dystrophy gene include both homologous and nonhomologous intrachromosomal recombination

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy

Localization of the mdx mutation within the mouse dystrophin gene

On Discovery, Genomes, The Society, and Society

Dystrophin in frameshift deletion patients with Becker muscular dystrophy

A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifs

Myoblast transfer in duchenne muscular dystrophy

Identification of a Transcriptional Enhancer Within Muscle Intron 1 of the Human Dystrophin Gene

Human Ribosomal RNA Genes: Orientation of the Tandem Array and Conservation of the 5$^{\prime}$ End

Dystrophin: the long and short of it

Expression of the dystrophin isoform Dp71 in differentiating human fetal myogenic cultures

Partial gene duplication in Duchenne and Becker muscular dystrophies

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