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Patrick F. Chinnery

Showing results (111-120 of 370) with videos related to

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Neurology|November 8, 2013
Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutationsGerald Pfeffer, Ailbhe Burke, Patrick Yu-Wai-Man, et al.
Acta Ophthalmologica|December 12, 2007
Investigation of auditory dysfunction in Leber hereditary optic neuropathyPatrick Yu-Wai-Man, Clive Elliott, Philip G Griffiths, et al.
Science Advances|October 25, 2023
High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout lifeAngelos Glynos, Lyuba V Bozhilova, Michele Frison, et al.
Human Molecular Genetics|October 10, 2023
CHCHD10 mutations induce tissue-specific mitochondrial DNA deletions with a distinct signatureMario K Shammas, Yu Nie, Alexandra Gilsrud, et al.
Neurobiology of Aging|July 29, 2011
No evidence of substantia nigra telomere shortening in Parkinson's diseaseGavin Hudson, David Faini, Andrea Stutt, et al.
Molecular Genetics and Metabolism|April 15, 2014
Valproic acid triggers increased mitochondrial biogenesis in POLG-deficient fibroblastsKamil S Sitarz, Hannah R Elliott, Betül S Karaman, et al.
Annals of Neurology|February 14, 2014
Mitochondrial DNA and traumatic brain injuryHarry Bulstrode, James A R Nicoll, Gavin Hudson, et al.
Neuromuscular Disorders : NMD|January 22, 2014
A new disease allele for the p.C30071R mutation in titin causing hereditary myopathy with early respiratory failureGerald Pfeffer, Nyamkhishig Sambuughin, Montse Olivé, et al.
Progress in Neurobiology|May 15, 2020
Epigenetic regulation in the pathophysiology of Lewy body dementiaLeonidas Chouliaras, Gautham S Kumar, Alan J Thomas, et al.
BMJ Neurology Open|June 11, 2024
Evidence for sodium valproate toxicity in mitochondrial diseases: a systematic analysisThiloka E Ratnaike, Nour Elkhateeb, Angela Lochmüller, et al.
Pageof 37

Showing results (111-120 of 370) with videos related to

Sort By:
Pageof 37
Neurology|November 8, 2013
Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutationsGerald Pfeffer, Ailbhe Burke, Patrick Yu-Wai-Man, et al.
Acta Ophthalmologica|December 12, 2007
Investigation of auditory dysfunction in Leber hereditary optic neuropathyPatrick Yu-Wai-Man, Clive Elliott, Philip G Griffiths, et al.
Science Advances|October 25, 2023
High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout lifeAngelos Glynos, Lyuba V Bozhilova, Michele Frison, et al.
Human Molecular Genetics|October 10, 2023
CHCHD10 mutations induce tissue-specific mitochondrial DNA deletions with a distinct signatureMario K Shammas, Yu Nie, Alexandra Gilsrud, et al.
Neurobiology of Aging|July 29, 2011
No evidence of substantia nigra telomere shortening in Parkinson's diseaseGavin Hudson, David Faini, Andrea Stutt, et al.
Molecular Genetics and Metabolism|April 15, 2014
Valproic acid triggers increased mitochondrial biogenesis in POLG-deficient fibroblastsKamil S Sitarz, Hannah R Elliott, Betül S Karaman, et al.
Annals of Neurology|February 14, 2014
Mitochondrial DNA and traumatic brain injuryHarry Bulstrode, James A R Nicoll, Gavin Hudson, et al.
Neuromuscular Disorders : NMD|January 22, 2014
A new disease allele for the p.C30071R mutation in titin causing hereditary myopathy with early respiratory failureGerald Pfeffer, Nyamkhishig Sambuughin, Montse Olivé, et al.
Progress in Neurobiology|May 15, 2020
Epigenetic regulation in the pathophysiology of Lewy body dementiaLeonidas Chouliaras, Gautham S Kumar, Alan J Thomas, et al.
BMJ Neurology Open|June 11, 2024
Evidence for sodium valproate toxicity in mitochondrial diseases: a systematic analysisThiloka E Ratnaike, Nour Elkhateeb, Angela Lochmüller, et al.
Pageof 37