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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 therapy
M 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 activity
M 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 6
H 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 fibroblasts
M 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 disorders
F D Ledley, H L Levy, S L Woo
Genomics
|
December 1, 1990
Structure of the human methylmalonyl-CoA mutase (MUT) locus
S 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 DNA
J 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 adenovirus
R 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 transfer
S Cholin, H Tonoki, T N Hansen, et al.
Enzyme
|
January 1, 1987
Molecular basis of phenylketonuria and recombinant DNA strategies for its therapy
S L Woo, A G DiLella, J Marvit, et al.
Page
of 14
Search research articles
Search
Showing results (51-60 of 136) with videos related to
Sort By:
Page
of 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 therapy
M 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 activity
M 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 6
H 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 fibroblasts
M 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 disorders
F D Ledley, H L Levy, S L Woo
Genomics
|
December 1, 1990
Structure of the human methylmalonyl-CoA mutase (MUT) locus
S 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 DNA
J 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 adenovirus
R 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 transfer
S Cholin, H Tonoki, T N Hansen, et al.
Enzyme
|
January 1, 1987
Molecular basis of phenylketonuria and recombinant DNA strategies for its therapy
S L Woo, A G DiLella, J Marvit, et al.
Page
of 14