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J S Chamberlain

Showing results (81-90 of 93) with videos related to

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Genomics|February 15, 1996
Isolation of tetranucleotide repeat polymorphisms flanking the BRCA1 geneP E Bennett-Baker, S Kiousis, S C Chandrasekharappa, et al.
Human Molecular Genetics|March 11, 1999
Characterization of dystrophin and utrophin diversity in the mouseC N Lumeng, S F Phelps, J A Rafael, et al.
Biophysical Journal|February 18, 2010
Microarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscleO Friedrich, M Both, C Weber, et al.
Human Molecular Genetics|May 23, 1998
mdx muscle pathology is independent of nNOS perturbationR H Crosbie, V Straub, H Y Yun, et al.
Journal of the National Cancer Institute. Monographs|January 1, 1995
Genetic analysis of eight breast-ovarian cancer families with suspected BRCA1 mutationsF J Couch, J Garber, S Kiousis, et al.
Current Biology : CB|August 30, 2001
Activation of JNK1 contributes to dystrophic muscle pathogenesisS M Kolodziejczyk, G S Walsh, K Balazsi, et al.
American Journal of Human Genetics|April 1, 1993
BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysisJ S Chamberlain, M Boehnke, T S Frank, et al.
The Journal of Experimental Medicine|August 1, 1996
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophyD S Chao, J R Gorospe, J E Brenman, et al.
American Journal of Human Genetics|October 1, 1989
Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) geneE F Gillard, J S Chamberlain, E G Murphy, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 19, 2000
Analysis of muscle creatine kinase regulatory elements in recombinant adenoviral vectorsM A Hauser, A Robinson, D Hartigan-O'Connor, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Genomics|February 15, 1996
Isolation of tetranucleotide repeat polymorphisms flanking the BRCA1 geneP E Bennett-Baker, S Kiousis, S C Chandrasekharappa, et al.
Human Molecular Genetics|March 11, 1999
Characterization of dystrophin and utrophin diversity in the mouseC N Lumeng, S F Phelps, J A Rafael, et al.
Biophysical Journal|February 18, 2010
Microarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscleO Friedrich, M Both, C Weber, et al.
Human Molecular Genetics|May 23, 1998
mdx muscle pathology is independent of nNOS perturbationR H Crosbie, V Straub, H Y Yun, et al.
Journal of the National Cancer Institute. Monographs|January 1, 1995
Genetic analysis of eight breast-ovarian cancer families with suspected BRCA1 mutationsF J Couch, J Garber, S Kiousis, et al.
Current Biology : CB|August 30, 2001
Activation of JNK1 contributes to dystrophic muscle pathogenesisS M Kolodziejczyk, G S Walsh, K Balazsi, et al.
American Journal of Human Genetics|April 1, 1993
BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysisJ S Chamberlain, M Boehnke, T S Frank, et al.
The Journal of Experimental Medicine|August 1, 1996
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophyD S Chao, J R Gorospe, J E Brenman, et al.
American Journal of Human Genetics|October 1, 1989
Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) geneE F Gillard, J S Chamberlain, E G Murphy, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 19, 2000
Analysis of muscle creatine kinase regulatory elements in recombinant adenoviral vectorsM A Hauser, A Robinson, D Hartigan-O'Connor, et al.
Pageof 10