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D R Love

Showing results (71-80 of 85) with videos related to

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Human Molecular Genetics|March 1, 1993
Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2E Gardner, L Papi, D F Easton, et al.
Nature|May 4, 1989
An autosomal transcript in skeletal muscle with homology to dystrophinD R Love, D F Hill, G Dickson, et al.
Human Molecular Genetics|April 1, 1992
Human dystrophin expression corrects the myopathic phenotype in transgenic mdx miceD J Wells, K E Wells, F S Walsh, et al.
Nature|December 10, 1992
Primary structure of dystrophin-related proteinJ M Tinsley, D J Blake, A Roche, et al.
Nature|June 3, 1993
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2AL M Mulligan, J B Kwok, C S Healey, et al.
Human Molecular Genetics|November 1, 1992
A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genesA P Walker, J Chelly, D R Love, et al.
American Journal of Medical Genetics|September 1, 1990
Characterization of deletions in the dystrophin gene giving mild phenotypesD R Love, T J Flint, R F Marsden, et al.
Nature|January 11, 1990
Very mild muscular dystrophy associated with the deletion of 46% of dystrophinS B England, L V Nicholson, M A Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1991
Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouseD R Love, G E Morris, J M Ellis, et al.
Genomics|May 1, 1991
Sequences of junction fragments in the deletion-prone region of the dystrophin geneD R Love, S B England, A Speer, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|March 1, 1993
Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2E Gardner, L Papi, D F Easton, et al.
Nature|May 4, 1989
An autosomal transcript in skeletal muscle with homology to dystrophinD R Love, D F Hill, G Dickson, et al.
Human Molecular Genetics|April 1, 1992
Human dystrophin expression corrects the myopathic phenotype in transgenic mdx miceD J Wells, K E Wells, F S Walsh, et al.
Nature|December 10, 1992
Primary structure of dystrophin-related proteinJ M Tinsley, D J Blake, A Roche, et al.
Nature|June 3, 1993
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2AL M Mulligan, J B Kwok, C S Healey, et al.
Human Molecular Genetics|November 1, 1992
A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genesA P Walker, J Chelly, D R Love, et al.
American Journal of Medical Genetics|September 1, 1990
Characterization of deletions in the dystrophin gene giving mild phenotypesD R Love, T J Flint, R F Marsden, et al.
Nature|January 11, 1990
Very mild muscular dystrophy associated with the deletion of 46% of dystrophinS B England, L V Nicholson, M A Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1991
Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouseD R Love, G E Morris, J M Ellis, et al.
Genomics|May 1, 1991
Sequences of junction fragments in the deletion-prone region of the dystrophin geneD R Love, S B England, A Speer, et al.
Pageof 9