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P F Chinnery

Showing results (131-140 of 152) with videos related to

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Neurology|July 26, 2000
Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodiesP F Chinnery, G A Taylor, N Howell, et al.
Human Reproduction Update|March 30, 2012
PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspringD M E I Hellebrekers, R Wolfe, A T M Hendrickx, et al.
Neurology|November 26, 2008
OPA1 in multiple mitochondrial DNA deletion disordersJ D Stewart, G Hudson, P Yu-Wai-Man, et al.
Neurology|August 29, 2007
Homoplasmy, heteroplasmy, and mitochondrial dystoniaR McFarland, P F Chinnery, E L Blakely, et al.
Brain : a Journal of Neurology|February 8, 2013
Persistence of the treatment effect of idebenone in Leber's hereditary optic neuropathyT Klopstock, G Metz, P Yu-Wai-Man, et al.
American Journal of Human Genetics|April 17, 1999
An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathyK M Clark, R W Taylor, M A Johnson, et al.
Neurology|March 24, 2012
No consistent evidence for association between mtDNA variants and Alzheimer diseaseG Hudson, R Sims, D Harold, et al.
Mitochondrion|September 28, 2011
Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distributionA M Voets, B J C van den Bosch, A P Stassen, et al.
Neuropathology and Applied Neurobiology|May 29, 2020
Neuropathological and biochemical investigation of Hereditary Ferritinopathy cases with ferritin light chain mutation: Prominent protein aggregation in the absence of major mitochondrial or oxidative stressM Kurzawa-Akanbi, M Keogh, E Tsefou, et al.
Translational Psychiatry|February 3, 2016
Exome sequencing in dementia with Lewy bodiesM J Keogh, M Kurzawa-Akanbi, H Griffin, et al.
Pageof 16

Showing results (131-140 of 152) with videos related to

Sort By:
Pageof 16
Neurology|July 26, 2000
Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodiesP F Chinnery, G A Taylor, N Howell, et al.
Human Reproduction Update|March 30, 2012
PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspringD M E I Hellebrekers, R Wolfe, A T M Hendrickx, et al.
Neurology|November 26, 2008
OPA1 in multiple mitochondrial DNA deletion disordersJ D Stewart, G Hudson, P Yu-Wai-Man, et al.
Neurology|August 29, 2007
Homoplasmy, heteroplasmy, and mitochondrial dystoniaR McFarland, P F Chinnery, E L Blakely, et al.
Brain : a Journal of Neurology|February 8, 2013
Persistence of the treatment effect of idebenone in Leber's hereditary optic neuropathyT Klopstock, G Metz, P Yu-Wai-Man, et al.
American Journal of Human Genetics|April 17, 1999
An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathyK M Clark, R W Taylor, M A Johnson, et al.
Neurology|March 24, 2012
No consistent evidence for association between mtDNA variants and Alzheimer diseaseG Hudson, R Sims, D Harold, et al.
Mitochondrion|September 28, 2011
Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distributionA M Voets, B J C van den Bosch, A P Stassen, et al.
Neuropathology and Applied Neurobiology|May 29, 2020
Neuropathological and biochemical investigation of Hereditary Ferritinopathy cases with ferritin light chain mutation: Prominent protein aggregation in the absence of major mitochondrial or oxidative stressM Kurzawa-Akanbi, M Keogh, E Tsefou, et al.
Translational Psychiatry|February 3, 2016
Exome sequencing in dementia with Lewy bodiesM J Keogh, M Kurzawa-Akanbi, H Griffin, et al.
Pageof 16