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Gavin Hudson

Showing results (31-40 of 100) with videos related to

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Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|June 20, 2008
Leber hereditary optic neuropathy presenting in a 75-year-old manPatrick Yu-Wai-Man, David E Bateman, Gavin Hudson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 19, 2016
Reduced mitochondrial DNA is not a biomarker of depression in Parkinson's diseaseAngela Pyle, Hannah Lowes, Rebecca Brennan, et al.
Brain : a Journal of Neurology|April 18, 2007
The A467T and W748S POLG substitutions are a rare cause of adult-onset ataxia in EuropeKate Craig, Gianfrancesco Ferrari, Watcharee Tiangyou, et al.
Mitochondrion|August 12, 2018
Assessing mitochondrial heteroplasmy using next generation sequencing: A note of cautionMauro Santibanez-Koref, Helen Griffin, Douglass M Turnbull, 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.
Nature Communications|May 30, 2023
The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticismCharley Xia, Sarah J Pickett, David C M Liewald, et al.
Brain : a Journal of Neurology|October 31, 2007
Does mitochondrial DNA predispose to neuromyelitis optica (Devic's disease)?Gavin Hudson, Catherine Mowbray, Joanna L Elson, et al.
Annals of Neurology|February 14, 2014
Mitochondrial DNA and traumatic brain injuryHarry Bulstrode, James A R Nicoll, Gavin Hudson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 27, 2009
No association between common POLG1 variants and sporadic idiopathic Parkinson's diseaseGavin Hudson, Watcharee Tiangyou, Andrea Stutt, et al.
Analytical and Bioanalytical Chemistry|March 2, 2022
A subcellular cookie cutter for spatial genomics in human tissueAlexander G Bury, Angela Pyle, Fabio Marcuccio, et al.
Pageof 10

Showing results (31-40 of 100) with videos related to

Sort By:
Pageof 10
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|June 20, 2008
Leber hereditary optic neuropathy presenting in a 75-year-old manPatrick Yu-Wai-Man, David E Bateman, Gavin Hudson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 19, 2016
Reduced mitochondrial DNA is not a biomarker of depression in Parkinson's diseaseAngela Pyle, Hannah Lowes, Rebecca Brennan, et al.
Brain : a Journal of Neurology|April 18, 2007
The A467T and W748S POLG substitutions are a rare cause of adult-onset ataxia in EuropeKate Craig, Gianfrancesco Ferrari, Watcharee Tiangyou, et al.
Mitochondrion|August 12, 2018
Assessing mitochondrial heteroplasmy using next generation sequencing: A note of cautionMauro Santibanez-Koref, Helen Griffin, Douglass M Turnbull, 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.
Nature Communications|May 30, 2023
The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticismCharley Xia, Sarah J Pickett, David C M Liewald, et al.
Brain : a Journal of Neurology|October 31, 2007
Does mitochondrial DNA predispose to neuromyelitis optica (Devic's disease)?Gavin Hudson, Catherine Mowbray, Joanna L Elson, et al.
Annals of Neurology|February 14, 2014
Mitochondrial DNA and traumatic brain injuryHarry Bulstrode, James A R Nicoll, Gavin Hudson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 27, 2009
No association between common POLG1 variants and sporadic idiopathic Parkinson's diseaseGavin Hudson, Watcharee Tiangyou, Andrea Stutt, et al.
Analytical and Bioanalytical Chemistry|March 2, 2022
A subcellular cookie cutter for spatial genomics in human tissueAlexander G Bury, Angela Pyle, Fabio Marcuccio, et al.
Pageof 10