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R W TAYLOR

Showing results (191-200 of 254) with videos related to

Pageof 26
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Leukemia|October 3, 2003
Somatic mitochondrial DNA mutations in adult-onset leukaemiaL He, L Luo, S J Proctor, et al.
Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.
Pediatric Obesity|August 28, 2025
The Impact of Sleep Loss on Screen Time in Children: Secondary Analyses of a Randomised Crossover Trial Using Objective Measures of Screen TimeR F Jackson, K A Meredith-Jones, J J Haszard, et al.
Neuropediatrics|July 30, 2009
Two cases with progressive cystic leukoencephalopathyZ Yapici, G Benbir, S Saltik, et al.
Lancet (London, England)|August 6, 1994
Apolipoprotein E and familial non-insulin-dependent diabetes mellitusR W Taylor, M W Stewart, P J Avery, et al.
Diabetes Care|February 1, 1995
Insulin sensitivity and mitochondrial gene mutationM Walker, R W Taylor, M W Stewart, et al.
Neuroreport|March 14, 2003
Investigation of mitochondrial function in hereditary spastic paraparesisC J McDermott, R W Taylor, C Hayes, et al.
Advanced Drug Delivery Reviews|May 30, 2001
An antigenomic strategy for treating heteroplasmic mtDNA disordersR W Taylor, T M Wardell, P M Smith, et al.
Journal of Medical Genetics|February 6, 2004
Mitochondrial DNA deletion in "identical" twin brothersE L Blakely, L He, R W Taylor, et al.
Biochemical Society Transactions|August 1, 1993
Defects of oxidative phosphorylation in manR W Taylor, M A Birch-Machin, S Lowerson, et al.
Pageof 26

Showing results (191-200 of 254) with videos related to

Sort By:
Pageof 26
Leukemia|October 3, 2003
Somatic mitochondrial DNA mutations in adult-onset leukaemiaL He, L Luo, S J Proctor, et al.
Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.
Pediatric Obesity|August 28, 2025
The Impact of Sleep Loss on Screen Time in Children: Secondary Analyses of a Randomised Crossover Trial Using Objective Measures of Screen TimeR F Jackson, K A Meredith-Jones, J J Haszard, et al.
Neuropediatrics|July 30, 2009
Two cases with progressive cystic leukoencephalopathyZ Yapici, G Benbir, S Saltik, et al.
Lancet (London, England)|August 6, 1994
Apolipoprotein E and familial non-insulin-dependent diabetes mellitusR W Taylor, M W Stewart, P J Avery, et al.
Diabetes Care|February 1, 1995
Insulin sensitivity and mitochondrial gene mutationM Walker, R W Taylor, M W Stewart, et al.
Neuroreport|March 14, 2003
Investigation of mitochondrial function in hereditary spastic paraparesisC J McDermott, R W Taylor, C Hayes, et al.
Advanced Drug Delivery Reviews|May 30, 2001
An antigenomic strategy for treating heteroplasmic mtDNA disordersR W Taylor, T M Wardell, P M Smith, et al.
Journal of Medical Genetics|February 6, 2004
Mitochondrial DNA deletion in "identical" twin brothersE L Blakely, L He, R W Taylor, et al.
Biochemical Society Transactions|August 1, 1993
Defects of oxidative phosphorylation in manR W Taylor, M A Birch-Machin, S Lowerson, et al.
Pageof 26