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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 functions
F 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 hybridization
D 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 therapy
F 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 aciduria
A 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 mutase
A 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 deficiency
M I Shevell, N Matiaszuk, F D Ledley, et al.
Genomics
|
March 1, 1990
Mapping of the L-methylmalonyl-CoA mutase gene to mouse chromosome 17
J 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 therapy
S 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 technologies
F 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 acidemia
S K Shapira, F D Ledley, D S Rosenblatt, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 136) with videos related to
Sort By:
Page
of 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 functions
F 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 hybridization
D 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 therapy
F 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 aciduria
A 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 mutase
A 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 deficiency
M I Shevell, N Matiaszuk, F D Ledley, et al.
Genomics
|
March 1, 1990
Mapping of the L-methylmalonyl-CoA mutase gene to mouse chromosome 17
J 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 therapy
S 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 technologies
F 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 acidemia
S K Shapira, F D Ledley, D S Rosenblatt, et al.
Page
of 14