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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

Volltextzugriff (PDF)

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

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

1998

Volltextzugriff (PDF)

Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia

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

1990

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Genetics of Duchenne Muscular Dystrophy

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

1988

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Dystrophin isoforms Dp71 and Dp427 have distinct roles in myogenic cells

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

1999

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Localization of the mdx mutation within the mouse dystrophin gene

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

1988

Volltextzugriff (PDF)

On Discovery, Genomes, The Society, and Society

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

Worton, Ronald G.

2001

Volltextzugriff (PDF)

Dystrophin in frameshift deletion patients with Becker muscular dystrophy

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

1992

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Myoblast transfer in duchenne muscular dystrophy

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

1993

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Dystrophin: the long and short of it

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

Worton, R G

1994

Volltextzugriff (PDF)

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

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

1996

Volltextzugriff (PDF)

A canadian collaborative study of mosaicism in amniotic fluid cell cultures

Prenatal diagnosis, 1984-01, Vol.4 (7), p.131-144

1984

Volltextzugriff (PDF)

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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

A canadian collaborative study of mosaicism in amniotic fluid cell cultures

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