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Patrick F Chinnery

Showing results (331-340 of 473) with videos related to

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Acta Neuropathologica|March 29, 2017
Amyloid-β accumulation in the CNS in human growth hormone recipients in the UKDiane L Ritchie, Peter Adlard, Alexander H Peden, et al.
Nature Communications|July 24, 2020
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Human Molecular Genetics|January 24, 2018
A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathiesMarina Bartsakoulia, Angela Pyle, Diego Troncoso-Chandía, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Neuroferritinopathy: a window on the role of iron in neurodegenerationDouglas E Crompton, Patrick F Chinnery, Constanze Fey, et al.
Human Genomics|February 2, 2019
A genome-wide association study of mitochondrial DNA copy number in two population-based cohortsAnna L Guyatt, Rebecca R Brennan, Kimberley Burrows, et al.
Annals of Neurology|February 6, 2015
Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial diseaseGráinne S Gorman, Andrew M Schaefer, Yi Ng, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Adult Onset Leigh Syndrome in the Intensive Care Setting: A Novel Presentation of a C12orf65 Related Mitochondrial DiseaseMaria Wesolowska, Grainne S Gorman, Charlotte L Alston, et al.
Nature Genetics|October 9, 2012
Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmissionChristoph Freyer, Lynsey M Cree, Arnaud Mourier, et al.
Annals of Neurology|August 9, 2007
Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's diseaseAn Goris, Caroline H Williams-Gray, Graeme R Clark, et al.
Molecular Cell|August 31, 2022
The human mitochondrial genome contains a second light strand promoterBenedict G Tan, Christian D Mutti, Yonghong Shi, et al.
Pageof 48

Showing results (331-340 of 473) with videos related to

Sort By:
Pageof 48
Acta Neuropathologica|March 29, 2017
Amyloid-β accumulation in the CNS in human growth hormone recipients in the UKDiane L Ritchie, Peter Adlard, Alexander H Peden, et al.
Nature Communications|July 24, 2020
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Human Molecular Genetics|January 24, 2018
A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathiesMarina Bartsakoulia, Angela Pyle, Diego Troncoso-Chandía, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Neuroferritinopathy: a window on the role of iron in neurodegenerationDouglas E Crompton, Patrick F Chinnery, Constanze Fey, et al.
Human Genomics|February 2, 2019
A genome-wide association study of mitochondrial DNA copy number in two population-based cohortsAnna L Guyatt, Rebecca R Brennan, Kimberley Burrows, et al.
Annals of Neurology|February 6, 2015
Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial diseaseGráinne S Gorman, Andrew M Schaefer, Yi Ng, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Adult Onset Leigh Syndrome in the Intensive Care Setting: A Novel Presentation of a C12orf65 Related Mitochondrial DiseaseMaria Wesolowska, Grainne S Gorman, Charlotte L Alston, et al.
Nature Genetics|October 9, 2012
Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmissionChristoph Freyer, Lynsey M Cree, Arnaud Mourier, et al.
Annals of Neurology|August 9, 2007
Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's diseaseAn Goris, Caroline H Williams-Gray, Graeme R Clark, et al.
Molecular Cell|August 31, 2022
The human mitochondrial genome contains a second light strand promoterBenedict G Tan, Christian D Mutti, Yonghong Shi, et al.
Pageof 48