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D M Kirby

Showing results (11-20 of 21) with videos related to

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The Journal of Pediatrics|March 4, 1999
Respiratory chain complex III [correction of complex] in deficiency with pruritus: a novel vitamin responsive clinical featureD Mowat, D M Kirby, K R Kamath, et al.
Neurology|April 24, 1999
Respiratory chain complex I deficiency: an underdiagnosed energy generation disorderD M Kirby, M Crawford, M A Cleary, et al.
The Journal of Pediatrics|March 1, 1997
Mitochondrial electron transport chain defect presenting as hypoglycemiaM L Freckmann, D R Thorburn, D M Kirby, et al.
FEBS Letters|June 30, 1997
HIV-1 protein Vpr causes gross mitochondrial dysfunction in the yeast Saccharomyces cerevisiaeI G Macreadie, D R Thorburn, D M Kirby, et al.
The Journal of Pediatrics|June 1, 1991
Continuous venovenous hemofiltration in the management of acute decompensation in inborn errors of metabolismG N Thompson, W W Butt, F A Shann, et al.
European Journal of Pediatrics|January 1, 1988
"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosisG K Brown, E A Haan, D M Kirby, et al.
The Journal of Pediatrics|January 1, 1997
Mitochondrial myopathy with tRNA(Leu(UUR)) mutation and complex I deficiency responsive to riboflavinR F Ogle, J Christodoulou, E Fagan, et al.
Annals of Neurology|March 1, 1996
Leigh syndrome: clinical features and biochemical and DNA abnormalitiesS Rahman, R B Blok, H H Dahl, et al.
The EMBO Journal|June 9, 2007
Human CIA30 is involved in the early assembly of mitochondrial complex I and mutations in its gene cause diseaseC J R Dunning, M McKenzie, C Sugiana, et al.
Cell Proliferation|June 26, 2009
Transmitochondrial embryonic stem cells containing pathogenic mtDNA mutations are compromised in neuronal differentiationD M Kirby, K J Rennie, T K Smulders-Srinivasan, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
The Journal of Pediatrics|March 4, 1999
Respiratory chain complex III [correction of complex] in deficiency with pruritus: a novel vitamin responsive clinical featureD Mowat, D M Kirby, K R Kamath, et al.
Neurology|April 24, 1999
Respiratory chain complex I deficiency: an underdiagnosed energy generation disorderD M Kirby, M Crawford, M A Cleary, et al.
The Journal of Pediatrics|March 1, 1997
Mitochondrial electron transport chain defect presenting as hypoglycemiaM L Freckmann, D R Thorburn, D M Kirby, et al.
FEBS Letters|June 30, 1997
HIV-1 protein Vpr causes gross mitochondrial dysfunction in the yeast Saccharomyces cerevisiaeI G Macreadie, D R Thorburn, D M Kirby, et al.
The Journal of Pediatrics|June 1, 1991
Continuous venovenous hemofiltration in the management of acute decompensation in inborn errors of metabolismG N Thompson, W W Butt, F A Shann, et al.
European Journal of Pediatrics|January 1, 1988
"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosisG K Brown, E A Haan, D M Kirby, et al.
The Journal of Pediatrics|January 1, 1997
Mitochondrial myopathy with tRNA(Leu(UUR)) mutation and complex I deficiency responsive to riboflavinR F Ogle, J Christodoulou, E Fagan, et al.
Annals of Neurology|March 1, 1996
Leigh syndrome: clinical features and biochemical and DNA abnormalitiesS Rahman, R B Blok, H H Dahl, et al.
The EMBO Journal|June 9, 2007
Human CIA30 is involved in the early assembly of mitochondrial complex I and mutations in its gene cause diseaseC J R Dunning, M McKenzie, C Sugiana, et al.
Cell Proliferation|June 26, 2009
Transmitochondrial embryonic stem cells containing pathogenic mtDNA mutations are compromised in neuronal differentiationD M Kirby, K J Rennie, T K Smulders-Srinivasan, et al.
Pageof 3