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J S Chamberlain

Showing results (51-60 of 93) with videos related to

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Neurology|April 1, 1989
Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophiesL L Baumbach, J S Chamberlain, P A Ward, et al.
Molecular Biology of the Cell|October 1, 1994
Myotubes from transgenic mdx mice expressing full-length dystrophin show normal calcium regulationW F Denetclaw, F W Hopf, G A Cox, et al.
Molecular and Cellular Biology|August 1, 1986
Transcriptional regulation of the muscle creatine kinase gene and regulated expression in transfected mouse myoblastsJ B Jaynes, J S Chamberlain, J N Buskin, et al.
Annals of Neurology|October 1, 1991
Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophyE P Hoffman, C A Garcia, J S Chamberlain, et al.
The Journal of Cell Biology|July 1, 1996
Forced expression of dystrophin deletion constructs reveals structure-function correlationsJ A Rafael, G A Cox, K Corrado, et al.
Biochemistry|August 7, 1998
An epitope structure for the C-terminal domain of dystrophin and utrophinG E Morris, S G Sedgwick, J M Ellis, et al.
Human Molecular Genetics|October 1, 1994
Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoformJ A Rafael, Y Sunada, N M Cole, et al.
Nucleic Acids Research|April 11, 1992
Human and murine dystrophin mRNA transcripts are differentially expressed during skeletal muscle, heart, and brain developmentR D Bies, S F Phelps, M D Cortez, et al.
Genomics|June 1, 1993
Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20C N Ting, D L Burgess, J S Chamberlain, et al.
Human Molecular Genetics|July 1, 1993
Tetranucleotide repeat polymorphism at D17S846 maps within 40 kb of GAS at 17q12-q22W L Flejter, J F Kukowska-Latallo, S Kiousis, et al.
Pageof 10

Showing results (51-60 of 93) with videos related to

Sort By:
Pageof 10
Neurology|April 1, 1989
Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophiesL L Baumbach, J S Chamberlain, P A Ward, et al.
Molecular Biology of the Cell|October 1, 1994
Myotubes from transgenic mdx mice expressing full-length dystrophin show normal calcium regulationW F Denetclaw, F W Hopf, G A Cox, et al.
Molecular and Cellular Biology|August 1, 1986
Transcriptional regulation of the muscle creatine kinase gene and regulated expression in transfected mouse myoblastsJ B Jaynes, J S Chamberlain, J N Buskin, et al.
Annals of Neurology|October 1, 1991
Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophyE P Hoffman, C A Garcia, J S Chamberlain, et al.
The Journal of Cell Biology|July 1, 1996
Forced expression of dystrophin deletion constructs reveals structure-function correlationsJ A Rafael, G A Cox, K Corrado, et al.
Biochemistry|August 7, 1998
An epitope structure for the C-terminal domain of dystrophin and utrophinG E Morris, S G Sedgwick, J M Ellis, et al.
Human Molecular Genetics|October 1, 1994
Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoformJ A Rafael, Y Sunada, N M Cole, et al.
Nucleic Acids Research|April 11, 1992
Human and murine dystrophin mRNA transcripts are differentially expressed during skeletal muscle, heart, and brain developmentR D Bies, S F Phelps, M D Cortez, et al.
Genomics|June 1, 1993
Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20C N Ting, D L Burgess, J S Chamberlain, et al.
Human Molecular Genetics|July 1, 1993
Tetranucleotide repeat polymorphism at D17S846 maps within 40 kb of GAS at 17q12-q22W L Flejter, J F Kukowska-Latallo, S Kiousis, et al.
Pageof 10