Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Patrick F. Chinnery

Showing results (81-90 of 370) with videos related to

Pageof 37
Sort By:
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
Clinical ManifestationsMd Shafiqur Rahman, Timothy Rittman, Brian D M Tom, et al.
Neurology|September 6, 2015
Prevalence of neurogenetic disorders in the North of EnglandDavid Bargiela, Patrick Yu-Wai-Man, Michael Keogh, et al.
Nucleic Acids Research|December 1, 2021
Single-molecule mitochondrial DNA sequencing shows no evidence of CpG methylation in human cells and tissuesIacopo Bicci, Claudia Calabrese, Zoe J Golder, et al.
Molecular Vision|November 5, 2004
Apolipoprotein E promoter polymorphisms do not have a major influence on the risk of developing primary open angle glaucomaThomas Ressiniotis, Philip G Griffiths, Michael Birch, et al.
BMC Ophthalmology|April 6, 2005
A polymorphism at codon 31 of gene p21 is not associated with primary open angle glaucoma in CaucasiansThomas Ressiniotis, Philip G Griffiths, Sharon M Keers, et al.
Seminars in Cell & Developmental Biology|October 16, 2019
Mitochondrial heteroplasmy beyond the oocyte bottleneckJelle van den Ameele, Andy Y Z Li, Hansong Ma, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 19, 2007
Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystoniaFriedrich Asmus, Anita Devlin, Marita Munz, et al.
Parkinsonism & Related Disorders|February 7, 2006
Allelic variation of a functional polymorphism in the serotonin transporter gene and depression in Parkinson's diseaseDavid J Burn, Watcharee Tiangyou, Liesl M Allcock, et al.
Science Advances|March 7, 2025
Origin and cell type specificity of mitochondrial DNA mutations in <i>C9ORF72</i> ALS-FTLD human brain organoidsYu Nie, Kornélia Szebényi, Lea M D Wenger, et al.
Human Genetics|December 16, 2004
Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigreeNeil Howell, Iwona Kubacka, Sharon M Keers, et al.
Pageof 37

Showing results (81-90 of 370) with videos related to

Sort By:
Pageof 37
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
Clinical ManifestationsMd Shafiqur Rahman, Timothy Rittman, Brian D M Tom, et al.
Neurology|September 6, 2015
Prevalence of neurogenetic disorders in the North of EnglandDavid Bargiela, Patrick Yu-Wai-Man, Michael Keogh, et al.
Nucleic Acids Research|December 1, 2021
Single-molecule mitochondrial DNA sequencing shows no evidence of CpG methylation in human cells and tissuesIacopo Bicci, Claudia Calabrese, Zoe J Golder, et al.
Molecular Vision|November 5, 2004
Apolipoprotein E promoter polymorphisms do not have a major influence on the risk of developing primary open angle glaucomaThomas Ressiniotis, Philip G Griffiths, Michael Birch, et al.
BMC Ophthalmology|April 6, 2005
A polymorphism at codon 31 of gene p21 is not associated with primary open angle glaucoma in CaucasiansThomas Ressiniotis, Philip G Griffiths, Sharon M Keers, et al.
Seminars in Cell & Developmental Biology|October 16, 2019
Mitochondrial heteroplasmy beyond the oocyte bottleneckJelle van den Ameele, Andy Y Z Li, Hansong Ma, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 19, 2007
Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystoniaFriedrich Asmus, Anita Devlin, Marita Munz, et al.
Parkinsonism & Related Disorders|February 7, 2006
Allelic variation of a functional polymorphism in the serotonin transporter gene and depression in Parkinson's diseaseDavid J Burn, Watcharee Tiangyou, Liesl M Allcock, et al.
Science Advances|March 7, 2025
Origin and cell type specificity of mitochondrial DNA mutations in <i>C9ORF72</i> ALS-FTLD human brain organoidsYu Nie, Kornélia Szebényi, Lea M D Wenger, et al.
Human Genetics|December 16, 2004
Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigreeNeil Howell, Iwona Kubacka, Sharon M Keers, et al.
Pageof 37