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Patrick F Chinnery

Showing results (111-120 of 473) with videos related to

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Journal of Inherited Metabolic Disease|March 25, 2021
Editorial: Mitochondrial medicine special issuePatrick F Chinnery, Marni J Falk, Vamsi K Mootha, et al.
American Journal of Human Genetics|March 15, 2006
The power to detect disease associations with mitochondrial DNA haplogroupsDavid C Samuels, Andrew D Carothers, Robin Horton, et al.
Annals of Neurology|March 26, 2013
Childhood presentation of "adult" polyglucosan body disease: normal GBE1 sequence with no glycogen branching enzyme activityDeborah Bathgate, Ralph Wigley, Grainne Gorman, et al.
Trends in Genetics : TIG|September 13, 2005
mtDNA mutations and common neurodegenerative disordersNeil Howell, Joanna L Elson, Patrick F Chinnery, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 30, 2015
Deep resequencing of mitochondrial DNABrendan A I Payne, Kristian Gardner, Jonathan Coxhead, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2010
Dramatic response of facial stereotype/tic to tetrabenazine in the first reported cases of neuroferritinopathy in the United StatesWilliam G Ondo, Octavian R Adam, Joseph Jankovic, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 11, 2010
Dissociation of duration-based and beat-based auditory timing in cerebellar degenerationManon Grube, Freya E Cooper, Patrick F Chinnery, et al.
Lancet (London, England)|November 5, 2002
Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?Patrick F Chinnery, David C Samuels, Joanna Elson, et al.
Brain : a Journal of Neurology|November 26, 2013
Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domainGerald Pfeffer, Helen Griffin, Angela Pyle, et al.
Plos Genetics|May 24, 2014
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseasesGavin Hudson, Aurora Gomez-Duran, Ian J Wilson, et al.
Pageof 48

Showing results (111-120 of 473) with videos related to

Sort By:
Pageof 48
Journal of Inherited Metabolic Disease|March 25, 2021
Editorial: Mitochondrial medicine special issuePatrick F Chinnery, Marni J Falk, Vamsi K Mootha, et al.
American Journal of Human Genetics|March 15, 2006
The power to detect disease associations with mitochondrial DNA haplogroupsDavid C Samuels, Andrew D Carothers, Robin Horton, et al.
Annals of Neurology|March 26, 2013
Childhood presentation of "adult" polyglucosan body disease: normal GBE1 sequence with no glycogen branching enzyme activityDeborah Bathgate, Ralph Wigley, Grainne Gorman, et al.
Trends in Genetics : TIG|September 13, 2005
mtDNA mutations and common neurodegenerative disordersNeil Howell, Joanna L Elson, Patrick F Chinnery, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 30, 2015
Deep resequencing of mitochondrial DNABrendan A I Payne, Kristian Gardner, Jonathan Coxhead, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2010
Dramatic response of facial stereotype/tic to tetrabenazine in the first reported cases of neuroferritinopathy in the United StatesWilliam G Ondo, Octavian R Adam, Joseph Jankovic, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 11, 2010
Dissociation of duration-based and beat-based auditory timing in cerebellar degenerationManon Grube, Freya E Cooper, Patrick F Chinnery, et al.
Lancet (London, England)|November 5, 2002
Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?Patrick F Chinnery, David C Samuels, Joanna Elson, et al.
Brain : a Journal of Neurology|November 26, 2013
Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domainGerald Pfeffer, Helen Griffin, Angela Pyle, et al.
Plos Genetics|May 24, 2014
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseasesGavin Hudson, Aurora Gomez-Duran, Ian J Wilson, et al.
Pageof 48