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B H Robinson

Showing results (81-90 of 257) with videos related to

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Biochimica Et Biophysica Acta|April 18, 1998
Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIcN Lee, C Morin, G Mitchell, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findingsS Pitkänen, A Feigenbaum, R Laframboise, et al.
Critical Care Medicine|January 6, 1999
Lactic acidemia and bradyarrhythmia in a child sedated with propofolS H Cray, B H Robinson, P N Cox
Journal of Inherited Metabolic Disease|January 1, 1996
Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complexB H Robinson, N MacKay, K Chun, et al.
Canadian Journal of Biochemistry|June 1, 1976
Properties of the citrate transporter in rat heart: implications for regulation of glycolysis by cytosolic citrateS Cheema-Dhadli, B H Robinson, M L Halperin
Molecular and Cellular Endocrinology|April 1, 2006
Pyruvate dehydrogenase phosphatase deficiency: orphan disease or an under-diagnosed condition?M C Maj, J M Cameron, B H Robinson
The Journal of Biological Chemistry|May 25, 1983
[3H]biotin-labeled proteins in cultured human skin fibroblasts from patients with pyruvate carboxylase deficiencyB H Robinson, J Oei, M Saunders, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Brain amino acid abnormalities in pyruvate carboxylase deficiencyT L Perry, J C Haworth, B H Robinson
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1972
Effects of palmitoyl CoA on citrate and malate transport by rat liver mitochondriaM L Halperin, B H Robinson, I B Fritz
Cytometry|November 21, 2000
Simultaneous detection of mitochondrial respiratory chain activity and reactive oxygen in digitonin-permeabilized cells using flow cytometryN A Pham, B H Robinson, D W Hedley
Pageof 26

Showing results (81-90 of 257) with videos related to

Sort By:
Pageof 26
Biochimica Et Biophysica Acta|April 18, 1998
Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIcN Lee, C Morin, G Mitchell, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findingsS Pitkänen, A Feigenbaum, R Laframboise, et al.
Critical Care Medicine|January 6, 1999
Lactic acidemia and bradyarrhythmia in a child sedated with propofolS H Cray, B H Robinson, P N Cox
Journal of Inherited Metabolic Disease|January 1, 1996
Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complexB H Robinson, N MacKay, K Chun, et al.
Canadian Journal of Biochemistry|June 1, 1976
Properties of the citrate transporter in rat heart: implications for regulation of glycolysis by cytosolic citrateS Cheema-Dhadli, B H Robinson, M L Halperin
Molecular and Cellular Endocrinology|April 1, 2006
Pyruvate dehydrogenase phosphatase deficiency: orphan disease or an under-diagnosed condition?M C Maj, J M Cameron, B H Robinson
The Journal of Biological Chemistry|May 25, 1983
[3H]biotin-labeled proteins in cultured human skin fibroblasts from patients with pyruvate carboxylase deficiencyB H Robinson, J Oei, M Saunders, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Brain amino acid abnormalities in pyruvate carboxylase deficiencyT L Perry, J C Haworth, B H Robinson
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1972
Effects of palmitoyl CoA on citrate and malate transport by rat liver mitochondriaM L Halperin, B H Robinson, I B Fritz
Cytometry|November 21, 2000
Simultaneous detection of mitochondrial respiratory chain activity and reactive oxygen in digitonin-permeabilized cells using flow cytometryN A Pham, B H Robinson, D W Hedley
Pageof 26