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Proceedings of the National Academy of Sciences of the United States of America|August 5, 1998
Hepatocyte injury in tyrosinemia type 1 is induced by fumarylacetoacetate and is inhibited by caspase inhibitorsS Kubo, M Sun, M Miyahara, et al.Human Gene Therapy|January 1, 1997
In vivo correction with recombinant adenovirus of 4-hydroxyphenylpyruvic acid dioxygenase deficiencies in strain III miceS Kubo, K Kiwaki, H Awata, et al.Brain & Development|January 1, 1988
Neonatal onset of medium-chain acyl-CoA dehydrogenase deficiency in two siblingsY Nobukuni, T Yokoo, Y Ohtani, et al.Neuroscience Letters|May 21, 1999
Immunohistochemical determination of the Wilson Copper-transporting P-type ATPase in the brain tissues of the ratT Saito, M Okabe, T Hosokawa, et al.Human Cell|March 1, 1989
[An usage of cultured human cell lines in studies of inherited metabolic disease]I MatsudaNihon Rinsho. Japanese Journal of Clinical Medicine|February 24, 2001
[Perspectives on postgenome medicine: Inborn error of metabolism]I MatsudaHepatology (Baltimore, Md.)|March 21, 1998
Intracellular distribution of the Wilson's disease gene product (ATPase7B) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's diseaseK Nagano, K Nakamura, K I Urakami, et al.Nihon Rinsho. Japanese Journal of Clinical Medicine|July 1, 1992
[Inborn errors of imino acid metabolism]F EndoMolecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.Genes to Cells : Devoted to Molecular & Cellular Mechanisms|February 17, 1999
Human ubiquitin-protein ligase Nedd4: expression, subcellular localization and selective interaction with ubiquitin-conjugating enzymesT Anan, Y Nagata, H Koga, et al.Pageof 50