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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
June 15, 1988
The problem of Duchenne muscular dystrophy
R 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 densitometry
D 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 gene
H 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 infant
M J Huggins, J R Smith, K Chun, et al.
Genomics
|
April 1, 1989
Molecular structure of the human asparagine synthetase gene
Y 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 mutations
S Yano, B Baskin, A Bagheri, et al.
FEBS Letters
|
October 12, 2000
Alternative splicing regulates the nuclear or cytoplasmic localization of dystrophin Dp71
E González, C Montañez, P N Ray, et al.
Human Molecular Genetics
|
May 1, 1995
A novel dystrophin isoform is required for normal retinal electrophysiology
V 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 mice
G 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 implantation
G Karpati, Y Pouliot, E Zubrzycka-Gaarn, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 110) with videos related to
Sort By:
Page
of 11
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
June 15, 1988
The problem of Duchenne muscular dystrophy
R 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 densitometry
D 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 gene
H 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 infant
M J Huggins, J R Smith, K Chun, et al.
Genomics
|
April 1, 1989
Molecular structure of the human asparagine synthetase gene
Y 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 mutations
S Yano, B Baskin, A Bagheri, et al.
FEBS Letters
|
October 12, 2000
Alternative splicing regulates the nuclear or cytoplasmic localization of dystrophin Dp71
E González, C Montañez, P N Ray, et al.
Human Molecular Genetics
|
May 1, 1995
A novel dystrophin isoform is required for normal retinal electrophysiology
V 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 mice
G 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 implantation
G Karpati, Y Pouliot, E Zubrzycka-Gaarn, et al.
Page
of 11