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Journal of Inherited Metabolic Disease|January 1, 1989
Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome)K Hayasaka, G K Brown, D M Danks, et al.The American Journal of Physiology|June 1, 1990
Role of albumin's copper binding site in copper uptake by mouse hepatocytesH J McArdle, S M Gross, D M Danks, et al.Biochemical and Molecular Medicine|April 1, 1995
Normal metallothionein synthesis in fibroblasts obtained from children with Indian childhood cirrhosis or copper-associated childhood cirrhosisS H Hahn, M S Tanner, D M Danks, et al.The Biochemical Journal|June 1, 1986
A study of the role of metallothionein in the inherited copper toxicosis of dogsD M Hunt, S A Wake, J F Mercer, et al.The Biochemical Journal|August 1, 1979
Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuriaK H Choo, R G Cotton, D M Danks, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 1987
Stability of protein and mRNA in human postmortem liver--analysis by two-dimensional gel electrophoresisJ M Finger, J F Mercer, R G Cotton, et al.The Biochemical Journal|October 15, 1987
Uptake and efflux of copper-64 in Menkes'-disease and normal continuous lymphoid cell linesS M Herd, J Camakaris, R Christofferson, et al.Biochemical and Molecular Medicine|October 1, 1995
mtDNA deletion in a patient with symptoms of mitochondrial cytopathy but without ragged red fibersR B Blok, D R Thorburn, D M Danks, et al.Journal of Inorganic Biochemistry|December 2, 1998
Analysis of the distribution of Cu, Fe and Zn and other elements in brindled mouse kidney using a scanning proton microprobeB J Kirby, D M Danks, G J Legge, et al.Bioscience Reports|October 1, 1981
Copper induction of translatable metallothionein messenger RNAJ F Mercer, I Lazdins, T Stevenson, et al.Pageof 19