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Gavin Hudson

Showing results (91-100 of 100) with videos related to

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Annals of Neurology|December 26, 2009
Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease geneMatthias Elstner, Christopher M Morris, Katharina Heim, et al.
The New England Journal of Medicine|July 17, 2025
Mitochondrial Donation and Preimplantation Genetic Testing for mtDNA DiseaseLouise A Hyslop, Emma L Blakely, Magomet Aushev, et al.
American Journal of Human Genetics|May 5, 2018
Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor NeuronopathyDavid T Burns, Sandra Donkervoort, Juliane S Müller, et al.
Brain : a Journal of Neurology|September 2, 2009
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathyRita Horvath, John P Kemp, Helen A L Tuppen, et al.
Brain : a Journal of Neurology|December 20, 2012
What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?Vivienne C M Neeve, David C Samuels, Laurence A Bindoff, et al.
Nature Cancer|October 19, 2020
Age-associated mitochondrial DNA mutations cause metabolic remodelling that contributes to accelerated intestinal tumorigenesisAnna Lm Smith, Julia C Whitehall, Carla Bradshaw, et al.
Nature Cancer|February 5, 2022
Author Correction: Age-associated mitochondrial DNA mutations cause metabolic remodeling that contributes to accelerated intestinal tumorigenesisAnna L M Smith, Julia C Whitehall, Carla Bradshaw, et al.
Brain : a Journal of Neurology|December 27, 2013
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathyCarla Giordano, Luisa Iommarini, Luca Giordano, et al.
Human Molecular Genetics|November 4, 2010
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21, , Chris C A Spencer, et al.
American Journal of Human Genetics|January 1, 2019
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic TraitsAldi T Kraja, Chunyu Liu, Jessica L Fetterman, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
Annals of Neurology|December 26, 2009
Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease geneMatthias Elstner, Christopher M Morris, Katharina Heim, et al.
The New England Journal of Medicine|July 17, 2025
Mitochondrial Donation and Preimplantation Genetic Testing for mtDNA DiseaseLouise A Hyslop, Emma L Blakely, Magomet Aushev, et al.
American Journal of Human Genetics|May 5, 2018
Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor NeuronopathyDavid T Burns, Sandra Donkervoort, Juliane S Müller, et al.
Brain : a Journal of Neurology|September 2, 2009
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathyRita Horvath, John P Kemp, Helen A L Tuppen, et al.
Brain : a Journal of Neurology|December 20, 2012
What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?Vivienne C M Neeve, David C Samuels, Laurence A Bindoff, et al.
Nature Cancer|October 19, 2020
Age-associated mitochondrial DNA mutations cause metabolic remodelling that contributes to accelerated intestinal tumorigenesisAnna Lm Smith, Julia C Whitehall, Carla Bradshaw, et al.
Nature Cancer|February 5, 2022
Author Correction: Age-associated mitochondrial DNA mutations cause metabolic remodeling that contributes to accelerated intestinal tumorigenesisAnna L M Smith, Julia C Whitehall, Carla Bradshaw, et al.
Brain : a Journal of Neurology|December 27, 2013
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathyCarla Giordano, Luisa Iommarini, Luca Giordano, et al.
Human Molecular Genetics|November 4, 2010
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21, , Chris C A Spencer, et al.
American Journal of Human Genetics|January 1, 2019
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic TraitsAldi T Kraja, Chunyu Liu, Jessica L Fetterman, et al.
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