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F D Ledley

Showing results (51-60 of 136) with videos related to

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Somatic Cell and Molecular Genetics|November 1, 1992
Propionate metabolism in cultured human cells after overexpression of recombinant methylmalonyl CoA mutase: implications for somatic gene therapyM Wilkemeyer, J Stankovics, T Foy, et al.
The Biochemical Journal|December 15, 1993
Genomic structure of murine methylmalonyl-CoA mutase: evidence for genetic and epigenetic mechanisms determining enzyme activityM F Wilkemeyer, E R Andrews, F D Ledley
Genomics|November 1, 1988
Linkage relationships of the human methylmalonyl CoA mutase to the HLA and D6S4 loci on chromosome 6H Y Zoghbi, W E O'Brien, F D Ledley
The Journal of Clinical Investigation|March 1, 1991
Differential diagnosis of mut and cbl methylmalonic aciduria by DNA-mediated gene transfer in primary fibroblastsM F Wilkemeyer, A M Crane, F D Ledley
The New England Journal of Medicine|May 15, 1986
Molecular analysis of the inheritance of phenylketonuria and mild hyperphenylalaninemia in families with both disordersF D Ledley, H L Levy, S L Woo
Genomics|December 1, 1990
Structure of the human methylmalonyl-CoA mutase (MUT) locusS U Nham, M F Wilkemeyer, F D Ledley
Human Gene Therapy|May 1, 1995
Gene transfer to synovial cells by intra-articular administration of plasmid DNAJ Yovandich, B O'Malley, M Sikes, et al.
Journal of Virology|March 1, 1995
Infection by retroviral vectors outside of their host range in the presence of replication-defective adenovirusR M Adams, M Wang, D Steffen, et al.
Biochemical Medicine and Metabolic Biology|February 1, 1993
Expression of recombinant human glutathione reductase in eukaryotic cells after DNA-mediated gene transferS Cholin, H Tonoki, T N Hansen, et al.
Enzyme|January 1, 1987
Molecular basis of phenylketonuria and recombinant DNA strategies for its therapyS L Woo, A G DiLella, J Marvit, et al.
Pageof 14

Showing results (51-60 of 136) with videos related to

Sort By:
Pageof 14
Somatic Cell and Molecular Genetics|November 1, 1992
Propionate metabolism in cultured human cells after overexpression of recombinant methylmalonyl CoA mutase: implications for somatic gene therapyM Wilkemeyer, J Stankovics, T Foy, et al.
The Biochemical Journal|December 15, 1993
Genomic structure of murine methylmalonyl-CoA mutase: evidence for genetic and epigenetic mechanisms determining enzyme activityM F Wilkemeyer, E R Andrews, F D Ledley
Genomics|November 1, 1988
Linkage relationships of the human methylmalonyl CoA mutase to the HLA and D6S4 loci on chromosome 6H Y Zoghbi, W E O'Brien, F D Ledley
The Journal of Clinical Investigation|March 1, 1991
Differential diagnosis of mut and cbl methylmalonic aciduria by DNA-mediated gene transfer in primary fibroblastsM F Wilkemeyer, A M Crane, F D Ledley
The New England Journal of Medicine|May 15, 1986
Molecular analysis of the inheritance of phenylketonuria and mild hyperphenylalaninemia in families with both disordersF D Ledley, H L Levy, S L Woo
Genomics|December 1, 1990
Structure of the human methylmalonyl-CoA mutase (MUT) locusS U Nham, M F Wilkemeyer, F D Ledley
Human Gene Therapy|May 1, 1995
Gene transfer to synovial cells by intra-articular administration of plasmid DNAJ Yovandich, B O'Malley, M Sikes, et al.
Journal of Virology|March 1, 1995
Infection by retroviral vectors outside of their host range in the presence of replication-defective adenovirusR M Adams, M Wang, D Steffen, et al.
Biochemical Medicine and Metabolic Biology|February 1, 1993
Expression of recombinant human glutathione reductase in eukaryotic cells after DNA-mediated gene transferS Cholin, H Tonoki, T N Hansen, et al.
Enzyme|January 1, 1987
Molecular basis of phenylketonuria and recombinant DNA strategies for its therapyS L Woo, A G DiLella, J Marvit, et al.
Pageof 14