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J S Chamberlain

Showing results (21-30 of 93) with videos related to

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Brain Research|June 3, 1999
Expression of the 71 kDa dystrophin isoform (Dp71) evaluated by gene targetingC N Lumeng, M Hauser, V Brown, et al.
Human Molecular Genetics|May 1, 1993
Dinucleotide repeat polymorphism at D21S49 (21q22.3)I N Bespalova, S Kiousis, J S Chamberlain, et al.
The Journal of Cell Biology|October 23, 1997
Animal models for muscular dystrophy show different patterns of sarcolemmal disruptionV Straub, J A Rafael, J S Chamberlain, et al.
Journal of Muscle Research and Cell Motility|April 20, 2002
Tibialis anterior muscles in mdx mice are highly susceptible to contraction-induced injuryC Dellorusso, R W Crawford, J S Chamberlain, et al.
Nature Genetics|December 1, 1994
Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophyG A Cox, Y Sunada, K P Campbell, et al.
Molecular Biology & Medicine|December 1, 1989
Detection of new mutation disease in man and mouseM Grompe, R A Gibbs, J S Chamberlain, et al.
Human Molecular Genetics|October 13, 2000
Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophyA Ahmad, M Brinson, B L Hodges, et al.
Nature Genetics|May 1, 1993
New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophinG A Cox, S F Phelps, V M Chapman, et al.
Nature|January 24, 1991
Expression of recombinant dystrophin and its localization to the cell membraneC C Lee, J A Pearlman, J S Chamberlain, et al.
The Journal of Biological Chemistry|November 10, 1995
Identification and characterization of the dystrophin anchoring site on beta-dystroglycanD Jung, B Yang, J Meyer, et al.
Pageof 10

Showing results (21-30 of 93) with videos related to

Sort By:
Pageof 10
Brain Research|June 3, 1999
Expression of the 71 kDa dystrophin isoform (Dp71) evaluated by gene targetingC N Lumeng, M Hauser, V Brown, et al.
Human Molecular Genetics|May 1, 1993
Dinucleotide repeat polymorphism at D21S49 (21q22.3)I N Bespalova, S Kiousis, J S Chamberlain, et al.
The Journal of Cell Biology|October 23, 1997
Animal models for muscular dystrophy show different patterns of sarcolemmal disruptionV Straub, J A Rafael, J S Chamberlain, et al.
Journal of Muscle Research and Cell Motility|April 20, 2002
Tibialis anterior muscles in mdx mice are highly susceptible to contraction-induced injuryC Dellorusso, R W Crawford, J S Chamberlain, et al.
Nature Genetics|December 1, 1994
Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophyG A Cox, Y Sunada, K P Campbell, et al.
Molecular Biology & Medicine|December 1, 1989
Detection of new mutation disease in man and mouseM Grompe, R A Gibbs, J S Chamberlain, et al.
Human Molecular Genetics|October 13, 2000
Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophyA Ahmad, M Brinson, B L Hodges, et al.
Nature Genetics|May 1, 1993
New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophinG A Cox, S F Phelps, V M Chapman, et al.
Nature|January 24, 1991
Expression of recombinant dystrophin and its localization to the cell membraneC C Lee, J A Pearlman, J S Chamberlain, et al.
The Journal of Biological Chemistry|November 10, 1995
Identification and characterization of the dystrophin anchoring site on beta-dystroglycanD Jung, B Yang, J Meyer, et al.
Pageof 10