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D R Thorburn

Showing results (51-60 of 69) with videos related to

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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.
American Journal of Human Genetics|July 27, 1999
Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993S L White, V R Collins, R Wolfe, et al.
Human Reproduction (Oxford, England)|March 14, 2019
Public attitudes towards novel reproductive technologies: a citizens' jury on mitochondrial donationA J Newson, S de Lacey, D K Dowling, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variationS L White, S Shanske, J J McGill, 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.
Neuropediatrics|November 10, 2004
Nemaline rods and complex I deficiency in three infants with hypotonia, motor delay and failure to thriveP J Lamont, D R Thorburn, V Fabian, 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.
Trends in Genetics : TIG|November 14, 2000
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?P F Chinnery, D R Thorburn, D C Samuels, et al.
Biochemical Pharmacology|June 1, 1997
Serine protease inhibition and mitochondrial dysfunction associated with cisplatin resistance in human tumor cell lines: targets for therapyY Dong, S J Berners-Price, D R Thorburn, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
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.
American Journal of Human Genetics|July 27, 1999
Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993S L White, V R Collins, R Wolfe, et al.
Human Reproduction (Oxford, England)|March 14, 2019
Public attitudes towards novel reproductive technologies: a citizens' jury on mitochondrial donationA J Newson, S de Lacey, D K Dowling, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variationS L White, S Shanske, J J McGill, 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.
Neuropediatrics|November 10, 2004
Nemaline rods and complex I deficiency in three infants with hypotonia, motor delay and failure to thriveP J Lamont, D R Thorburn, V Fabian, 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.
Trends in Genetics : TIG|November 14, 2000
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?P F Chinnery, D R Thorburn, D C Samuels, et al.
Biochemical Pharmacology|June 1, 1997
Serine protease inhibition and mitochondrial dysfunction associated with cisplatin resistance in human tumor cell lines: targets for therapyY Dong, S J Berners-Price, D R Thorburn, et al.
Pageof 7