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Y H Edwards

Showing results (91-100 of 98) with videos related to

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Human Molecular Genetics|May 1, 1992
Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cellsD J Blake, D R Love, J Tinsley, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 1995
G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brainD J Blake, J N Schofield, R A Zuellig, et al.
Human Molecular Genetics|May 1, 1996
Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifidaK Morrison, C Papapetrou, J Attwood, 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.
Genomics|July 8, 1998
Cloning and mapping of human chromosome 6q26-q27 deleted in B-cell non-Hodgkin lymphoma and multiple tumor typesR S Hauptschein, B Gamberi, P H Rao, 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.
American Journal of Medical Genetics|May 19, 2000
Association between historically high frequencies of neural tube defects and the human T homologue of mouse T (Brachyury)D C Shields, D Ramsbottom, C Donoghue, et al.
Cytogenetic and Genome Research|June 26, 2004
Cloning and characterization of an inversion breakpoint at 6q23.3 suggests a role for Map7 in sacral dysgenesisR Sood, P I Bader, M C Speer, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
Human Molecular Genetics|May 1, 1992
Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cellsD J Blake, D R Love, J Tinsley, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 1995
G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brainD J Blake, J N Schofield, R A Zuellig, et al.
Human Molecular Genetics|May 1, 1996
Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifidaK Morrison, C Papapetrou, J Attwood, 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.
Genomics|July 8, 1998
Cloning and mapping of human chromosome 6q26-q27 deleted in B-cell non-Hodgkin lymphoma and multiple tumor typesR S Hauptschein, B Gamberi, P H Rao, 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.
American Journal of Medical Genetics|May 19, 2000
Association between historically high frequencies of neural tube defects and the human T homologue of mouse T (Brachyury)D C Shields, D Ramsbottom, C Donoghue, et al.
Cytogenetic and Genome Research|June 26, 2004
Cloning and characterization of an inversion breakpoint at 6q23.3 suggests a role for Map7 in sacral dysgenesisR Sood, P I Bader, M C Speer, et al.
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