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Gavin Hudson

Showing results (61-70 of 100) with videos related to

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Scientific Reports|September 9, 2024
Variant load of mitochondrial DNA in single human mesenchymal stem cellsDaniel Hipps, Angela Pyle, Anna L R Porter, et al.
Mitochondrion|October 5, 2010
Mitochondrial DNA does not contribute to the heritability of non-alcoholic fatty liver diseaseNimantha de Alwis, Guruprasad Aithal, Elizabetta Bugianesi, et al.
Investigative Ophthalmology & Visual Science|March 4, 2009
Quality of life in patients with leber hereditary optic neuropathyMatthew Anthony Kirkman, Alex Korsten, Miriam Leonhardt, et al.
Neurobiology of Aging|May 4, 2013
Frailty and mortality are not influenced by mitochondrial DNA haplotypes in the very oldJoanna Collerton, Deepthi Ashok, Carmen Martin-Ruiz, et al.
American Journal of Human Genetics|May 11, 2006
Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegiaMatthew J Longley, Susanna Clark, Cynthia Yu Wai Man, et al.
NPJ Parkinson'S Disease|January 20, 2024
Early-stage idiopathic Parkinson's disease is associated with reduced circular RNA expressionBenjamin J Whittle, Osagie G Izuogu, Hannah Lowes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2014
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutationsHelen R Griffin, Angela Pyle, Emma L Blakely, et al.
Journal of Neurology|April 21, 2010
Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG2Maggie C Walter, Birgit Czermin, Solvig Muller-Ziermann, et al.
NPJ Parkinson'S Disease|May 13, 2021
Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson's diseaseChun Chen, David McDonald, Alasdair Blain, et al.
Ophthalmology|April 27, 2010
The prevalence and natural history of dominant optic atrophy due to OPA1 mutationsPatrick Yu-Wai-Man, Philip G Griffiths, Ailbhe Burke, et al.
Pageof 10

Showing results (61-70 of 100) with videos related to

Sort By:
Pageof 10
Scientific Reports|September 9, 2024
Variant load of mitochondrial DNA in single human mesenchymal stem cellsDaniel Hipps, Angela Pyle, Anna L R Porter, et al.
Mitochondrion|October 5, 2010
Mitochondrial DNA does not contribute to the heritability of non-alcoholic fatty liver diseaseNimantha de Alwis, Guruprasad Aithal, Elizabetta Bugianesi, et al.
Investigative Ophthalmology & Visual Science|March 4, 2009
Quality of life in patients with leber hereditary optic neuropathyMatthew Anthony Kirkman, Alex Korsten, Miriam Leonhardt, et al.
Neurobiology of Aging|May 4, 2013
Frailty and mortality are not influenced by mitochondrial DNA haplotypes in the very oldJoanna Collerton, Deepthi Ashok, Carmen Martin-Ruiz, et al.
American Journal of Human Genetics|May 11, 2006
Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegiaMatthew J Longley, Susanna Clark, Cynthia Yu Wai Man, et al.
NPJ Parkinson'S Disease|January 20, 2024
Early-stage idiopathic Parkinson's disease is associated with reduced circular RNA expressionBenjamin J Whittle, Osagie G Izuogu, Hannah Lowes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2014
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutationsHelen R Griffin, Angela Pyle, Emma L Blakely, et al.
Journal of Neurology|April 21, 2010
Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG2Maggie C Walter, Birgit Czermin, Solvig Muller-Ziermann, et al.
NPJ Parkinson'S Disease|May 13, 2021
Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson's diseaseChun Chen, David McDonald, Alasdair Blain, et al.
Ophthalmology|April 27, 2010
The prevalence and natural history of dominant optic atrophy due to OPA1 mutationsPatrick Yu-Wai-Man, Philip G Griffiths, Ailbhe Burke, et al.
Pageof 10