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J S Chamberlain

Showing results (71-80 of 93) with videos related to

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The Journal of Cell Biology|August 1, 1996
Transgenic mdx mice expressing dystrophin with a deletion in the actin-binding domain display a "mild Becker" phenotypeK Corrado, J A Rafael, P L Mills, et al.
American Journal of Human Genetics|November 1, 1990
Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophyD A Pillers, J A Towbin, J S Chamberlain, et al.
American Journal of Human Genetics|November 1, 1991
Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphismsP R Clemens, R G Fenwick, J S Chamberlain, et al.
Gene Therapy|November 9, 2002
Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene productK Yuasa, M Sakamoto, Y Miyagoe-Suzuki, et al.
Gene Therapy|March 11, 2005
Stable transduction of myogenic cells with lentiviral vectors expressing a minidystrophinS Li, E Kimura, B M Fall, et al.
Circulation|June 1, 1993
X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locusJ A Towbin, J F Hejtmancik, P Brink, et al.
Human Molecular Genetics|August 1, 1995
Expression of full-length and truncated dystrophin mini-genes in transgenic mdx miceS F Phelps, M A Hauser, N M Cole, et al.
Science (New York, N.Y.)|March 18, 1988
Expression of the murine Duchenne muscular dystrophy gene in muscle and brainJ S Chamberlain, J A Pearlman, D M Muzny, et al.
Genomics|December 1, 1994
Characterization of 10 new polymorphic dinucleotide repeats and generation of a high-density microsatellite-based physical map of the BRCA1 region of chromosome 17q21F J Couch, S Kiousis, L H Castilla, et al.
Nature|August 19, 1993
Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicityG A Cox, N M Cole, K Matsumura, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
The Journal of Cell Biology|August 1, 1996
Transgenic mdx mice expressing dystrophin with a deletion in the actin-binding domain display a "mild Becker" phenotypeK Corrado, J A Rafael, P L Mills, et al.
American Journal of Human Genetics|November 1, 1990
Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophyD A Pillers, J A Towbin, J S Chamberlain, et al.
American Journal of Human Genetics|November 1, 1991
Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphismsP R Clemens, R G Fenwick, J S Chamberlain, et al.
Gene Therapy|November 9, 2002
Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene productK Yuasa, M Sakamoto, Y Miyagoe-Suzuki, et al.
Gene Therapy|March 11, 2005
Stable transduction of myogenic cells with lentiviral vectors expressing a minidystrophinS Li, E Kimura, B M Fall, et al.
Circulation|June 1, 1993
X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locusJ A Towbin, J F Hejtmancik, P Brink, et al.
Human Molecular Genetics|August 1, 1995
Expression of full-length and truncated dystrophin mini-genes in transgenic mdx miceS F Phelps, M A Hauser, N M Cole, et al.
Science (New York, N.Y.)|March 18, 1988
Expression of the murine Duchenne muscular dystrophy gene in muscle and brainJ S Chamberlain, J A Pearlman, D M Muzny, et al.
Genomics|December 1, 1994
Characterization of 10 new polymorphic dinucleotide repeats and generation of a high-density microsatellite-based physical map of the BRCA1 region of chromosome 17q21F J Couch, S Kiousis, L H Castilla, et al.
Nature|August 19, 1993
Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicityG A Cox, N M Cole, K Matsumura, et al.
Pageof 10