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Gavin Hudson

Showing results (41-50 of 100) with videos related to

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Annals of Neurology|November 18, 2017
Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson diseaseAlexander G Bury, Angela Pyle, Joanna L Elson, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 11, 2011
Genetic variations within the OPA1 gene are not associated with neuromyelitis opticaKamil S Sitarz, Patrick Yu-Wai-Man, Gavin Hudson, et al.
Mitochondrion|March 15, 2011
Variation in MAPT is not a contributing factor to the incomplete penetrance in LHONGavin Hudson, Patrick Yu-Wai-Man, Philip G Griffiths, et al.
Neurobiology of Aging|August 5, 2015
Inherited mtDNA variations are not strong risk factors in human prion diseaseGavin Hudson, James Uphill, Holger Hummerich, et al.
Plos Genetics|May 15, 2015
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in HumansAngela Pyle, Gavin Hudson, Ian J Wilson, et al.
Neuromuscular Disorders : NMD|May 30, 2008
Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathyEmma Blakely, Langping He, Julie L Gardner, et al.
Annals of Neurology|September 8, 2015
Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's diseaseAngela Pyle, Rebecca Brennan, Marzena Kurzawa-Akanbi, et al.
Neuroscience Letters|May 25, 2010
Genetic variation of CHRNA4 does not modulate attention in Parkinson's diseaseGavin Hudson, Andrea Stutt, Martin Eccles, et al.
EMBO Reports|August 17, 2023
Feasibility and impact of haplogroup matching for mitochondrial replacement treatmentYuko Takeda, Louise Hyslop, Meenakshi Choudhary, et al.
Mitochondrion|September 1, 2024
Relationships of mitochondrial DNA mutations and select clinical diagnoses in perinatally HIV- and ART-exposed uninfected childrenGreg S Gojanovich, Carmen J Marsit, Deborah Kacanek, et al.
Pageof 10

Showing results (41-50 of 100) with videos related to

Sort By:
Pageof 10
Annals of Neurology|November 18, 2017
Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson diseaseAlexander G Bury, Angela Pyle, Joanna L Elson, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 11, 2011
Genetic variations within the OPA1 gene are not associated with neuromyelitis opticaKamil S Sitarz, Patrick Yu-Wai-Man, Gavin Hudson, et al.
Mitochondrion|March 15, 2011
Variation in MAPT is not a contributing factor to the incomplete penetrance in LHONGavin Hudson, Patrick Yu-Wai-Man, Philip G Griffiths, et al.
Neurobiology of Aging|August 5, 2015
Inherited mtDNA variations are not strong risk factors in human prion diseaseGavin Hudson, James Uphill, Holger Hummerich, et al.
Plos Genetics|May 15, 2015
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in HumansAngela Pyle, Gavin Hudson, Ian J Wilson, et al.
Neuromuscular Disorders : NMD|May 30, 2008
Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathyEmma Blakely, Langping He, Julie L Gardner, et al.
Annals of Neurology|September 8, 2015
Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's diseaseAngela Pyle, Rebecca Brennan, Marzena Kurzawa-Akanbi, et al.
Neuroscience Letters|May 25, 2010
Genetic variation of CHRNA4 does not modulate attention in Parkinson's diseaseGavin Hudson, Andrea Stutt, Martin Eccles, et al.
EMBO Reports|August 17, 2023
Feasibility and impact of haplogroup matching for mitochondrial replacement treatmentYuko Takeda, Louise Hyslop, Meenakshi Choudhary, et al.
Mitochondrion|September 1, 2024
Relationships of mitochondrial DNA mutations and select clinical diagnoses in perinatally HIV- and ART-exposed uninfected childrenGreg S Gojanovich, Carmen J Marsit, Deborah Kacanek, et al.
Pageof 10