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Communications Biology
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August 24, 2024
Cell-specific expression of key mitochondrial enzymes limits OXPHOS in astrocytes of the adult human neocortex and hippocampal formation
Arpád Dobolyi, Melinda Cservenák, Attila G Bagó, et al.
Scientific Reports
|
December 19, 2025
Quantifying variability of mitochondrial markers in m3243A > G myopathy
Tiago M Bernardino Gomes, Jordan B Childs, Valeria Di Leo, et al.
Scientific Reports
|
February 21, 2019
Mitochondrial Haplogroup and the Risk of Acute Kidney Injury Following Cardiac Bypass Surgery
Nigel S Kanagasundaram, Simon V Baudouin, Sarah Rowling, et al.
Molecular Vision
|
January 5, 2011
Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy
Gavin Hudson, Patrick Yu-Wai-Man, Phillip G Griffiths, et al.
Mitochondrion
|
May 22, 2012
Unique mitochondrial DNA in highly inbred feral cattle
Gavin Hudson, Ian Wilson, Brendan I A Payne, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 18, 2020
The Human Coronavirus Receptor ANPEP (CD13) Is Overexpressed in Parkinson's Disease
Hannah Lowes, Fiona Robertson, Angela Pyle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 11, 2017
metabolic profiling of Parkinson's disease and mild cognitive impairment
Florence Burté, David Houghton, Hannah Lowes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 15, 2021
Astrocytic Changes in Mitochondrial Oxidative Phosphorylation Protein Levels in Parkinson's Disease
Chun Chen, Emily Mossman, Philippa Malko, et al.
Archives of Neurology
|
April 11, 2007
Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism
Gavin Hudson, Andrew M Schaefer, Robert W Taylor, et al.
Archives of Neurology
|
January 16, 2008
POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease
Timothy Harrower, Joanna D Stewart, Gavin Hudson, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 100) with videos related to
Sort By:
Page
of 10
Communications Biology
|
August 24, 2024
Cell-specific expression of key mitochondrial enzymes limits OXPHOS in astrocytes of the adult human neocortex and hippocampal formation
Arpád Dobolyi, Melinda Cservenák, Attila G Bagó, et al.
Scientific Reports
|
December 19, 2025
Quantifying variability of mitochondrial markers in m3243A > G myopathy
Tiago M Bernardino Gomes, Jordan B Childs, Valeria Di Leo, et al.
Scientific Reports
|
February 21, 2019
Mitochondrial Haplogroup and the Risk of Acute Kidney Injury Following Cardiac Bypass Surgery
Nigel S Kanagasundaram, Simon V Baudouin, Sarah Rowling, et al.
Molecular Vision
|
January 5, 2011
Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy
Gavin Hudson, Patrick Yu-Wai-Man, Phillip G Griffiths, et al.
Mitochondrion
|
May 22, 2012
Unique mitochondrial DNA in highly inbred feral cattle
Gavin Hudson, Ian Wilson, Brendan I A Payne, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 18, 2020
The Human Coronavirus Receptor ANPEP (CD13) Is Overexpressed in Parkinson's Disease
Hannah Lowes, Fiona Robertson, Angela Pyle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 11, 2017
metabolic profiling of Parkinson's disease and mild cognitive impairment
Florence Burté, David Houghton, Hannah Lowes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 15, 2021
Astrocytic Changes in Mitochondrial Oxidative Phosphorylation Protein Levels in Parkinson's Disease
Chun Chen, Emily Mossman, Philippa Malko, et al.
Archives of Neurology
|
April 11, 2007
Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism
Gavin Hudson, Andrew M Schaefer, Robert W Taylor, et al.
Archives of Neurology
|
January 16, 2008
POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease
Timothy Harrower, Joanna D Stewart, Gavin Hudson, et al.
Page
of 10