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Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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P N Ray

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American Journal of Human Genetics|April 1, 1990

Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlationX Y Hu, P N Ray, E G Murphy, et al.

Gene|August 1, 1989

Fine structure analysis of the Chinese hamster AS gene encoding asparagine synthetaseI L Andrulis, M Shotwell, S Evans-Blackler, et al.

Human Molecular Genetics|September 1, 1995

Cloning and characterization of alternatively spliced isoforms of Dp71R C Austin, P L Howard, V N D'Souza, et al.

Nature|July 5, 1987

A cDNA clone from the Duchenne/Becker muscular dystrophy geneA H Burghes, C Logan, X Hu, et al.

Human Molecular Genetics|May 1, 1993

Genomic organization of exons 22 to 25 of the dystrophin geneK G Bebchuk, D E Bulman, V N D'Souza, et al.

Genomics|June 1, 1991

Point mutation in the human dystrophin gene: identification through western blot analysisD E Bulman, S B Gangopadhyay, K G Bebchuck, et al.

Journal of Medical Genetics|June 27, 2001

A missense mutation in the SEDL gene results in delayed onset of X linked spondyloepiphyseal dysplasia in a large pedigreeE Grunebaum, E Arpaia, J J MacKenzie, et al.

American Journal of Human Genetics|June 1, 1989

Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy geneX Y Hu, A H Burghes, D E Bulman, et al.

Muscle & Nerve|May 1, 1990

Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical studyS Carpenter, G Karpati, E Zubrzycka-Gaarn, et al.

American Journal of Human Genetics|February 1, 1991

Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophinD E Bulman, E G Murphy, E E Zubrzycka-Gaarn, et al.

Pageof 11

Search research articles

Showing results (51-60 of 110) with videos related to

Sort By:

Pageof 11

American Journal of Human Genetics|April 1, 1990

Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlationX Y Hu, P N Ray, E G Murphy, et al.

Gene|August 1, 1989

Fine structure analysis of the Chinese hamster AS gene encoding asparagine synthetaseI L Andrulis, M Shotwell, S Evans-Blackler, et al.

Human Molecular Genetics|September 1, 1995

Cloning and characterization of alternatively spliced isoforms of Dp71R C Austin, P L Howard, V N D'Souza, et al.

Nature|July 5, 1987

A cDNA clone from the Duchenne/Becker muscular dystrophy geneA H Burghes, C Logan, X Hu, et al.

Human Molecular Genetics|May 1, 1993

Genomic organization of exons 22 to 25 of the dystrophin geneK G Bebchuk, D E Bulman, V N D'Souza, et al.

Genomics|June 1, 1991

Point mutation in the human dystrophin gene: identification through western blot analysisD E Bulman, S B Gangopadhyay, K G Bebchuck, et al.

Journal of Medical Genetics|June 27, 2001

A missense mutation in the SEDL gene results in delayed onset of X linked spondyloepiphyseal dysplasia in a large pedigreeE Grunebaum, E Arpaia, J J MacKenzie, et al.

American Journal of Human Genetics|June 1, 1989

Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy geneX Y Hu, A H Burghes, D E Bulman, et al.

Muscle & Nerve|May 1, 1990

Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical studyS Carpenter, G Karpati, E Zubrzycka-Gaarn, et al.

American Journal of Human Genetics|February 1, 1991

Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophinD E Bulman, E G Murphy, E E Zubrzycka-Gaarn, et al.

Pageof 11