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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.
Journal of Microbiology & Biology Education|January 10, 2015
Positioning genomics in biology education: content mapping of undergraduate biology textbooksNaomi L B Wernick, Eric Ndung'u, Dominique Haughton, et al.
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.
Catheterization and Cardiovascular Diagnosis|August 1, 1994
Internal mammary artery collateral to the external iliac artery: an angiographic consideration prior to coronary bypass surgeryD K Parashara, M N Kotler, G S Ledley, et al.
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