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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 gene
Matthias 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 Disease
Louise 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 Neuronopathy
David 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 myopathy
Rita 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 tumorigenesis
Anna 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 tumorigenesis
Anna 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 neuropathy
Carla 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 Traits
Aldi T Kraja, Chunyu Liu, Jessica L Fetterman, et al.
Page
of 10
Search research articles
Search
Showing results (91-100 of 100) with videos related to
Sort By:
Page
of 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 gene
Matthias 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 Disease
Louise 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 Neuronopathy
David 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 myopathy
Rita 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 tumorigenesis
Anna 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 tumorigenesis
Anna 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 neuropathy
Carla 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 Traits
Aldi T Kraja, Chunyu Liu, Jessica L Fetterman, et al.
Page
of 10