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Patrick F Chinnery

Showing results (201-210 of 473) with videos related to

Pageof 48
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Neurology|October 27, 2015
SCP2 mutations and neurodegeneration with brain iron accumulationRita Horvath, David Lewis-Smith, Konstantinos Douroudis, et al.
Investigative Ophthalmology & Visual Science|May 16, 2009
Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophyPatrick Yu-Wai-Man, Vanessa J Davies, Malgorzata J Piechota, et al.
Science Advances|November 12, 2025
The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagyLaura S Kremer, Zoe Golder, Tom Barton-Owen, et al.
Journal of Medical Genetics|September 5, 2006
Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutationAngela Pyle, Robert W Taylor, Steve E Durham, et al.
Neurobiology of Aging|August 5, 2015
Inherited mtDNA variations are not strong risk factors in human prion diseaseGavin Hudson, James Uphill, Holger Hummerich, et al.
Human Molecular Genetics|July 2, 2013
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiencyVeronika Boczonadi, Paul M Smith, Angela Pyle, et al.
Plos Genetics|May 15, 2015
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in HumansAngela Pyle, Gavin Hudson, Ian J Wilson, et al.
Muscle & Nerve|November 26, 2003
Late-onset mitochondrial disorder with electromyographic evidence of myotoniaMathew L P Howse, Theresa M Wardell, Christopher J Fisher, et al.
JAMA Neurology|May 12, 2015
Clinical and pathological features of mitochondrial DNA deletion disease following antiretroviral treatmentBrendan A I Payne, Kristian Gardner, Emma L Blakely, et al.
Neurology|August 12, 2016
Cardiac involvement in hereditary myopathy with early respiratory failure: A cohort studyHannah E Steele, Elizabeth Harris, Rita Barresi, et al.
Pageof 48

Showing results (201-210 of 473) with videos related to

Sort By:
Pageof 48
Neurology|October 27, 2015
SCP2 mutations and neurodegeneration with brain iron accumulationRita Horvath, David Lewis-Smith, Konstantinos Douroudis, et al.
Investigative Ophthalmology & Visual Science|May 16, 2009
Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophyPatrick Yu-Wai-Man, Vanessa J Davies, Malgorzata J Piechota, et al.
Science Advances|November 12, 2025
The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagyLaura S Kremer, Zoe Golder, Tom Barton-Owen, et al.
Journal of Medical Genetics|September 5, 2006
Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutationAngela Pyle, Robert W Taylor, Steve E Durham, et al.
Neurobiology of Aging|August 5, 2015
Inherited mtDNA variations are not strong risk factors in human prion diseaseGavin Hudson, James Uphill, Holger Hummerich, et al.
Human Molecular Genetics|July 2, 2013
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiencyVeronika Boczonadi, Paul M Smith, Angela Pyle, et al.
Plos Genetics|May 15, 2015
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in HumansAngela Pyle, Gavin Hudson, Ian J Wilson, et al.
Muscle & Nerve|November 26, 2003
Late-onset mitochondrial disorder with electromyographic evidence of myotoniaMathew L P Howse, Theresa M Wardell, Christopher J Fisher, et al.
JAMA Neurology|May 12, 2015
Clinical and pathological features of mitochondrial DNA deletion disease following antiretroviral treatmentBrendan A I Payne, Kristian Gardner, Emma L Blakely, et al.
Neurology|August 12, 2016
Cardiac involvement in hereditary myopathy with early respiratory failure: A cohort studyHannah E Steele, Elizabeth Harris, Rita Barresi, et al.
Pageof 48