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F D Ledley

Showing results (61-70 of 136) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 1, 1987
Retroviral gene transfer into primary hepatocytes: implications for genetic therapy of liver-specific functionsF D Ledley, G J Darlington, T Hahn, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Localization of the murine methylmalonyl CoA mutase (Mut) locus on chromosome 17 by in situ hybridizationD W Threadgill, M Wilkmeyer, J E Womack, et al.
Human Gene Therapy|December 1, 1992
The challenge of follow-up for clinical trials of somatic gene therapyF D Ledley, B Brody, C A Kozinetz, et al.
The Journal of Clinical Investigation|February 1, 1992
Cloning and expression of a mutant methylmalonyl coenzyme A mutase with altered cobalamin affinity that causes mut- methylmalonic aciduriaA M Crane, R Jansen, E R Andrews, et al.
Human Genetics|May 1, 1992
Phenotype of disease in three patients with identical mutations in methylmalonyl CoA mutaseA M Crane, L S Martin, D Valle, et al.
American Journal of Medical Genetics|March 1, 1993
Varying neurological phenotypes among muto and mut- patients with methylmalonylCoA mutase deficiencyM I Shevell, N Matiaszuk, F D Ledley, et al.
Genomics|March 1, 1990
Mapping of the L-methylmalonyl-CoA mutase gene to mouse chromosome 17J Sertić, V Vincek, F D Ledley, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Molecular basis of phenylketonuria and potential somatic gene therapyS L Woo, A G DiLella, J Marvit, et al.
Gene Therapy|December 6, 2013
Why commercialization of gene therapy stalled; examining the life cycles of gene therapy technologiesF D Ledley, L M McNamee, V Uzdil, et al.
The Journal of Pediatrics|July 1, 1991
Ketoacidotic crisis as a presentation of mild ("benign") methylmalonic acidemiaS K Shapira, F D Ledley, D S Rosenblatt, et al.
Pageof 14

Showing results (61-70 of 136) with videos related to

Sort By:
Pageof 14
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1987
Retroviral gene transfer into primary hepatocytes: implications for genetic therapy of liver-specific functionsF D Ledley, G J Darlington, T Hahn, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Localization of the murine methylmalonyl CoA mutase (Mut) locus on chromosome 17 by in situ hybridizationD W Threadgill, M Wilkmeyer, J E Womack, et al.
Human Gene Therapy|December 1, 1992
The challenge of follow-up for clinical trials of somatic gene therapyF D Ledley, B Brody, C A Kozinetz, et al.
The Journal of Clinical Investigation|February 1, 1992
Cloning and expression of a mutant methylmalonyl coenzyme A mutase with altered cobalamin affinity that causes mut- methylmalonic aciduriaA M Crane, R Jansen, E R Andrews, et al.
Human Genetics|May 1, 1992
Phenotype of disease in three patients with identical mutations in methylmalonyl CoA mutaseA M Crane, L S Martin, D Valle, et al.
American Journal of Medical Genetics|March 1, 1993
Varying neurological phenotypes among muto and mut- patients with methylmalonylCoA mutase deficiencyM I Shevell, N Matiaszuk, F D Ledley, et al.
Genomics|March 1, 1990
Mapping of the L-methylmalonyl-CoA mutase gene to mouse chromosome 17J Sertić, V Vincek, F D Ledley, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Molecular basis of phenylketonuria and potential somatic gene therapyS L Woo, A G DiLella, J Marvit, et al.
Gene Therapy|December 6, 2013
Why commercialization of gene therapy stalled; examining the life cycles of gene therapy technologiesF D Ledley, L M McNamee, V Uzdil, et al.
The Journal of Pediatrics|July 1, 1991
Ketoacidotic crisis as a presentation of mild ("benign") methylmalonic acidemiaS K Shapira, F D Ledley, D S Rosenblatt, et al.
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