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C R Scriver

Showing results (171-180 of 317) with videos related to

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The New England Journal of Medicine|June 10, 1971
Management of hereditary metabolic disease. The role of allied health personnelC L Clow, T M Reade, C R Scriver
Pediatrics|December 1, 1981
Outcome of early and long-term management of classical maple syrup urine diseaseC L Clow, T M Reade, C R Scriver
The Biochemical Journal|August 15, 1983
Metabolism of ethylmalonate to mesaconate in the rat. Evidence for trans-dehydrogenation of methylsuccinateJ A Montgomery, O A Mamer, C R Scriver
Metabolism: Clinical and Experimental|August 1, 1980
Labile methyl group balances in the human: the role of sarcosineS H Mudd, M H Ebert, C R Scriver
Annals of the New York Academy of Sciences|January 1, 1985
Isolation and culture of murine renal proximal tubule cells: a system to study solute transport in mutantsC L Bell, H S Tenenhouse, C R Scriver
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 1, 1972
Primary hyperparathyroidism and hyperaminoaciduriaD C Cusworth, C E Dent, C R Scriver
Nucleic Acids Research|January 1, 1996
PAH Mutation Analysis Consortium Database: a database for disease-producing and other allelic variation at the human PAH locusL Hoang, S Byck, L Prevost, et al.
Canadian Medical Association Journal|November 16, 1974
Screening, counselling and treatment of hereditary metabolic disease; a survey of resources in CanadaJ C Haworth, J R Miller, C R Scriver
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|July 1, 1988
Initiation and characterization of primary mouse kidney epithelial culturesC L Bell, H S Tenenhouse, C R Scriver
American Journal of Human Genetics|September 1, 1988
Primary cultures of renal epithelial cells from X-linked hypophosphatemic (Hyp) mice express defects in phosphate transport and vitamin D metabolismC L Bell, H S Tenenhouse, C R Scriver
Pageof 32

Showing results (171-180 of 317) with videos related to

Sort By:
Pageof 32
The New England Journal of Medicine|June 10, 1971
Management of hereditary metabolic disease. The role of allied health personnelC L Clow, T M Reade, C R Scriver
Pediatrics|December 1, 1981
Outcome of early and long-term management of classical maple syrup urine diseaseC L Clow, T M Reade, C R Scriver
The Biochemical Journal|August 15, 1983
Metabolism of ethylmalonate to mesaconate in the rat. Evidence for trans-dehydrogenation of methylsuccinateJ A Montgomery, O A Mamer, C R Scriver
Metabolism: Clinical and Experimental|August 1, 1980
Labile methyl group balances in the human: the role of sarcosineS H Mudd, M H Ebert, C R Scriver
Annals of the New York Academy of Sciences|January 1, 1985
Isolation and culture of murine renal proximal tubule cells: a system to study solute transport in mutantsC L Bell, H S Tenenhouse, C R Scriver
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 1, 1972
Primary hyperparathyroidism and hyperaminoaciduriaD C Cusworth, C E Dent, C R Scriver
Nucleic Acids Research|January 1, 1996
PAH Mutation Analysis Consortium Database: a database for disease-producing and other allelic variation at the human PAH locusL Hoang, S Byck, L Prevost, et al.
Canadian Medical Association Journal|November 16, 1974
Screening, counselling and treatment of hereditary metabolic disease; a survey of resources in CanadaJ C Haworth, J R Miller, C R Scriver
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|July 1, 1988
Initiation and characterization of primary mouse kidney epithelial culturesC L Bell, H S Tenenhouse, C R Scriver
American Journal of Human Genetics|September 1, 1988
Primary cultures of renal epithelial cells from X-linked hypophosphatemic (Hyp) mice express defects in phosphate transport and vitamin D metabolismC L Bell, H S Tenenhouse, C R Scriver
Pageof 32