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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 VIc
N 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 findings
S Pitkänen, A Feigenbaum, R Laframboise, et al.
Critical Care Medicine
|
January 6, 1999
Lactic acidemia and bradyarrhythmia in a child sedated with propofol
S H Cray, B H Robinson, P N Cox
Journal of Inherited Metabolic Disease
|
January 1, 1996
Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complex
B 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 citrate
S 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 deficiency
B H Robinson, J Oei, M Saunders, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
Brain amino acid abnormalities in pyruvate carboxylase deficiency
T 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 mitochondria
M 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 cytometry
N A Pham, B H Robinson, D W Hedley
Page
of 26
Search research articles
Search
Showing results (81-90 of 257) with videos related to
Sort By:
Page
of 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 VIc
N 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 findings
S Pitkänen, A Feigenbaum, R Laframboise, et al.
Critical Care Medicine
|
January 6, 1999
Lactic acidemia and bradyarrhythmia in a child sedated with propofol
S H Cray, B H Robinson, P N Cox
Journal of Inherited Metabolic Disease
|
January 1, 1996
Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complex
B 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 citrate
S 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 deficiency
B H Robinson, J Oei, M Saunders, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
Brain amino acid abnormalities in pyruvate carboxylase deficiency
T 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 mitochondria
M 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 cytometry
N A Pham, B H Robinson, D W Hedley
Page
of 26