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D M Danks

Showing results (161-170 of 255) with videos related to

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The Biochemical Journal|June 15, 1979
Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) miceJ R Mann, J Camakaris, D M Danks, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Mutations in humans and animals which affect copper metabolismJ Camakaris, M Phillips, D M Danks, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Carrier detection in ornithine transcarbamylase deficiencyE A Haan, D M Danks, A Grimes, et al.
Birth Defects Original Article Series|January 1, 1974
Craniomandibular dermatodysostosisD M Danks, V Mayne, N B Wettenhall, 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.
The Journal of Pediatrics|August 1, 1981
Tertiary lactic acidosisJ G Rogers, R G Wilkinson, I Skelton, 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.
Methods in Enzymology|January 1, 1987
Use of naphthoquinone adsorbent for the isolation of human dihydropteridine reductaseF A Firgaira, R G Cotton, I Jennings, et al.
Pageof 26

Showing results (161-170 of 255) with videos related to

Sort By:
Pageof 26
The Biochemical Journal|June 15, 1979
Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) miceJ R Mann, J Camakaris, D M Danks, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Mutations in humans and animals which affect copper metabolismJ Camakaris, M Phillips, D M Danks, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Carrier detection in ornithine transcarbamylase deficiencyE A Haan, D M Danks, A Grimes, et al.
Birth Defects Original Article Series|January 1, 1974
Craniomandibular dermatodysostosisD M Danks, V Mayne, N B Wettenhall, 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.
The Journal of Pediatrics|August 1, 1981
Tertiary lactic acidosisJ G Rogers, R G Wilkinson, I Skelton, 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.
Methods in Enzymology|January 1, 1987
Use of naphthoquinone adsorbent for the isolation of human dihydropteridine reductaseF A Firgaira, R G Cotton, I Jennings, et al.
Pageof 26