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Journal of Inherited Metabolic Disease|January 1, 1982
Carrier detection in ornithine transcarbamylase deficiencyE A Haan, D M Danks, A Grimes, et al.Science (New York, N.Y.)|March 16, 1973
Menkes' kinky hair disease: further definition of the defect in copper transportD M Danks, E Cartwright, B J Stevens, et al.European Journal of Biochemistry|September 17, 1984
Cloning and sequencing of a sheep metallothionein cDNAM G Peterson, I Lazdins, D M Danks, et al.European Journal of Pediatrics|February 1, 1981
Familial occurrence of meconium ileusJ L Allan, M Robbie, P D Phelan, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|March 1, 1979
Urinary dihydroxanthopterin in the diagnosis of malignant hyperphenylalaninemia and phenylketonuriaP Schlesinger, B M Watson, R G Cotton, et al.The Journal of Nutrition|November 1, 1990
Effects of cellular copper content on copper uptake and metallothionein and ceruloplasmin mRNA levels in mouse hepatocytesH J McArdle, J F Mercer, A M Sargeson, et al.Journal of Inherited Metabolic Disease|January 1, 1980
Observations indicating the nature of the mutation in phenylketonuriaK H Choo, R G Cotton, I G Jennings, et al.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.Pageof 19