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C R Scriver

Showing results (121-130 of 317) with videos related to

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American Journal of Human Genetics|February 1, 1995
Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparisonE Treacy, B Childs, C R Scriver
Human Genomics|April 6, 2006
Human mutation databasesRichard G H Cotton, C R Scriver
American Journal of Medical Genetics|November 1, 1984
Genetic causes of chronic musculoskeletal disease in childhood are commonD Gregory, P Kaplan, C R Scriver
Pediatrics|July 1, 1970
Histidinemia discovered by urine screening after renal transplantationD Rosenblatt, F Mohyuddin, C R Scriver
Human Mutation|May 25, 1999
Guidelines and recommendations for content, structure, and deployment of mutation databasesC R Scriver, P M Nowacki, H Lehväslaiho
Canadian Journal of Physiology and Pharmacology|May 1, 1980
Tubular reabsorption of alpha-aminoisobutyric acid in the pre-steady-state. Evidence for a cell-to-lumen fluxR R McInnes, F Mohyuddin, C R Scriver
Connective Tissue Research|January 1, 1983
Secreted collagen ratios in normal human and osteogenesis imperfecta skin fibroblastsJ Fraser, G A Lancaster, C R Scriver
Human Genetics|December 1, 1988
Lysinuric protein intolerance mutation is not expressed in the plasma membrane of erythrocytesD W Smith, C R Scriver, O Simell
Biochimica Et Biophysica Acta|December 3, 1971
The ontogeny of amino acid transport in rat kidney. II. Kinetics of uptake and effect of anoxiaK E Baerlocher, C R Scriver, F Mohyuddin
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1975
Role of epithelial architecture and intracellular metabolism in proline uptake and transtubular reclamation in PRO/re mouse kidneyC R Scriver, R R McInnes, F Mohyuddin
Pageof 32

Showing results (121-130 of 317) with videos related to

Sort By:
Pageof 32
American Journal of Human Genetics|February 1, 1995
Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparisonE Treacy, B Childs, C R Scriver
Human Genomics|April 6, 2006
Human mutation databasesRichard G H Cotton, C R Scriver
American Journal of Medical Genetics|November 1, 1984
Genetic causes of chronic musculoskeletal disease in childhood are commonD Gregory, P Kaplan, C R Scriver
Pediatrics|July 1, 1970
Histidinemia discovered by urine screening after renal transplantationD Rosenblatt, F Mohyuddin, C R Scriver
Human Mutation|May 25, 1999
Guidelines and recommendations for content, structure, and deployment of mutation databasesC R Scriver, P M Nowacki, H Lehväslaiho
Canadian Journal of Physiology and Pharmacology|May 1, 1980
Tubular reabsorption of alpha-aminoisobutyric acid in the pre-steady-state. Evidence for a cell-to-lumen fluxR R McInnes, F Mohyuddin, C R Scriver
Connective Tissue Research|January 1, 1983
Secreted collagen ratios in normal human and osteogenesis imperfecta skin fibroblastsJ Fraser, G A Lancaster, C R Scriver
Human Genetics|December 1, 1988
Lysinuric protein intolerance mutation is not expressed in the plasma membrane of erythrocytesD W Smith, C R Scriver, O Simell
Biochimica Et Biophysica Acta|December 3, 1971
The ontogeny of amino acid transport in rat kidney. II. Kinetics of uptake and effect of anoxiaK E Baerlocher, C R Scriver, F Mohyuddin
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1975
Role of epithelial architecture and intracellular metabolism in proline uptake and transtubular reclamation in PRO/re mouse kidneyC R Scriver, R R McInnes, F Mohyuddin
Pageof 32