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P N Ray

Showing results (61-70 of 110) with videos related to

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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 15, 1988
The problem of Duchenne muscular dystrophyR G Worton, P N Ray, S Bodrug, et al.
American Journal of Medical Genetics|February 5, 1998
Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometryD J Allingham-Hawkins, L K McGlynn-Steele, C A Brown, et al.
Human Molecular Genetics|October 1, 1996
Identification of a transcriptional enhancer within muscle intron 1 of the human dystrophin geneH J Klamut, L O Bosnoyan-Collins, R G Worton, et al.
American Journal of Medical Genetics|June 9, 1999
Achondroplasia-hypochondroplasia complex in a newborn infantM J Huggins, J R Smith, K Chun, et al.
Genomics|April 1, 1989
Molecular structure of the human asparagine synthetase geneY P Zhang, M A Lambert, A E Cairney, et al.
Clinical Genetics|October 19, 2010
Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutationsS Yano, B Baskin, A Bagheri, et al.
FEBS Letters|October 12, 2000
Alternative splicing regulates the nuclear or cytoplasmic localization of dystrophin Dp71E González, C Montañez, P N Ray, et al.
Human Molecular Genetics|May 1, 1995
A novel dystrophin isoform is required for normal retinal electrophysiologyV N D'Souza, T M Nguyen, G E Morris, et al.
Journal of Neuropathology and Experimental Neurology|March 1, 1990
Age-related conversion of dystrophin-negative to -positive fiber segments of skeletal but not cardiac muscle fibers in heterozygote mdx miceG Karpati, E E Zubrzycka-Gaarn, S Carpenter, et al.
The American Journal of Pathology|July 1, 1989
Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantationG Karpati, Y Pouliot, E Zubrzycka-Gaarn, et al.
Pageof 11

Showing results (61-70 of 110) with videos related to

Sort By:
Pageof 11
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 15, 1988
The problem of Duchenne muscular dystrophyR G Worton, P N Ray, S Bodrug, et al.
American Journal of Medical Genetics|February 5, 1998
Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometryD J Allingham-Hawkins, L K McGlynn-Steele, C A Brown, et al.
Human Molecular Genetics|October 1, 1996
Identification of a transcriptional enhancer within muscle intron 1 of the human dystrophin geneH J Klamut, L O Bosnoyan-Collins, R G Worton, et al.
American Journal of Medical Genetics|June 9, 1999
Achondroplasia-hypochondroplasia complex in a newborn infantM J Huggins, J R Smith, K Chun, et al.
Genomics|April 1, 1989
Molecular structure of the human asparagine synthetase geneY P Zhang, M A Lambert, A E Cairney, et al.
Clinical Genetics|October 19, 2010
Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutationsS Yano, B Baskin, A Bagheri, et al.
FEBS Letters|October 12, 2000
Alternative splicing regulates the nuclear or cytoplasmic localization of dystrophin Dp71E González, C Montañez, P N Ray, et al.
Human Molecular Genetics|May 1, 1995
A novel dystrophin isoform is required for normal retinal electrophysiologyV N D'Souza, T M Nguyen, G E Morris, et al.
Journal of Neuropathology and Experimental Neurology|March 1, 1990
Age-related conversion of dystrophin-negative to -positive fiber segments of skeletal but not cardiac muscle fibers in heterozygote mdx miceG Karpati, E E Zubrzycka-Gaarn, S Carpenter, et al.
The American Journal of Pathology|July 1, 1989
Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantationG Karpati, Y Pouliot, E Zubrzycka-Gaarn, et al.
Pageof 11