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C R Scriver

Showing results (131-140 of 317) with videos related to

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The Journal of Pediatrics|November 1, 1985
So-called thiamin-responsive maple syrup urine disease: 15-year follow-up of the original patientC R Scriver, C L Clow, H George
Science (New York, N.Y.)|January 24, 1998
The HUGO Mutation Database InitiativeR G Cotton, V McKusick, C R Scriver
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 26, 1982
Inorganic sulfate in cerebrospinal fluid from infants and childrenD E Cole, J Shafai, C R Scriver
Pediatric Research|August 1, 1982
Neonatal iminoglycinuria: evidence that the prolinuria originates in selective deficiency of transport activity in the proximal nephronC R Scriver, M F Arthus, M Bergeron
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1970
Ontogeny of iminoglycine transport in mammalian kidneyK E Baerlocher, C R Scriver, F Mohyuddin
The American Journal of Physiology|July 1, 1988
Decreased transport in renal basolateral membrane vesicles from hypertaurinuric miceS Mandla, C R Scriver, H S Tenenhouse
The Biochemical Journal|April 15, 1979
Taurine transport in renal brush-border-membrane vesiclesR Rozen, H S Tenenhouse, C R Scriver
Clinical Biochemistry|September 1, 1973
On the screening, diagnosis and investigation of hereditary aminoacidopathiesC R Scriver, C L Clow, P Lamm
Annual Review of Genetics|January 1, 1988
Mendelian hyperphenylalaninemiaC R Scriver, S Kaufman, S L Woo
Journal of Inherited Metabolic Disease|August 1, 2008
What we know that could influence future treatment of phenylketonuriaC N Sarkissian, A Gámez, C R Scriver
Pageof 32

Showing results (131-140 of 317) with videos related to

Sort By:
Pageof 32
The Journal of Pediatrics|November 1, 1985
So-called thiamin-responsive maple syrup urine disease: 15-year follow-up of the original patientC R Scriver, C L Clow, H George
Science (New York, N.Y.)|January 24, 1998
The HUGO Mutation Database InitiativeR G Cotton, V McKusick, C R Scriver
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 26, 1982
Inorganic sulfate in cerebrospinal fluid from infants and childrenD E Cole, J Shafai, C R Scriver
Pediatric Research|August 1, 1982
Neonatal iminoglycinuria: evidence that the prolinuria originates in selective deficiency of transport activity in the proximal nephronC R Scriver, M F Arthus, M Bergeron
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1970
Ontogeny of iminoglycine transport in mammalian kidneyK E Baerlocher, C R Scriver, F Mohyuddin
The American Journal of Physiology|July 1, 1988
Decreased transport in renal basolateral membrane vesicles from hypertaurinuric miceS Mandla, C R Scriver, H S Tenenhouse
The Biochemical Journal|April 15, 1979
Taurine transport in renal brush-border-membrane vesiclesR Rozen, H S Tenenhouse, C R Scriver
Clinical Biochemistry|September 1, 1973
On the screening, diagnosis and investigation of hereditary aminoacidopathiesC R Scriver, C L Clow, P Lamm
Annual Review of Genetics|January 1, 1988
Mendelian hyperphenylalaninemiaC R Scriver, S Kaufman, S L Woo
Journal of Inherited Metabolic Disease|August 1, 2008
What we know that could influence future treatment of phenylketonuriaC N Sarkissian, A Gámez, C R Scriver
Pageof 32