Search research articles
Contact Us
Filters
Showing results (71-80 of 100) with videos related to
Page
of 10
Sort By:
NPJ Parkinson'S Disease
|
August 8, 2023
Parkinson's disease neurons exhibit alterations in mitochondrial quality control proteins
Chun Chen, David McDonald, Alasdair Blain, et al.
Human Genomics
|
February 2, 2019
A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts
Anna L Guyatt, Rebecca R Brennan, Kimberley Burrows, et al.
Brain : a Journal of Neurology
|
December 11, 2007
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance
Gavin Hudson, Patrizia Amati-Bonneau, Emma L Blakely, et al.
American Journal of Human Genetics
|
December 29, 2005
Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder
Gavin Hudson, Sharon Keers, Patrick Yu-Wai-Man, et al.
Neurology
|
May 7, 2013
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
Gavin Hudson, Mike Nalls, Jonathan R Evans, et al.
Nature Cell Biology
|
December 15, 2022
Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos
Vasileios I Floros, Angela Pyle, Sabine Dietmann, et al.
Nature Cell Biology
|
January 17, 2018
Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos
Vasileios I Floros, Angela Pyle, Sabine Dietmann, et al.
Nature Cell Biology
|
April 21, 2018
Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos
Vasileios I Floros, Angela Pyle, Sabine Dietmann, et al.
Plos Genetics
|
April 1, 2022
Heteroplasmic mitochondrial DNA variants in cardiovascular diseases
Claudia Calabrese, Angela Pyle, Helen Griffin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 22, 2011
Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome
Sophie E Winder-Rhodes, Pablo Garcia-Reitböck, Maria Ban, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 100) with videos related to
Sort By:
Page
of 10
NPJ Parkinson'S Disease
|
August 8, 2023
Parkinson's disease neurons exhibit alterations in mitochondrial quality control proteins
Chun Chen, David McDonald, Alasdair Blain, et al.
Human Genomics
|
February 2, 2019
A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts
Anna L Guyatt, Rebecca R Brennan, Kimberley Burrows, et al.
Brain : a Journal of Neurology
|
December 11, 2007
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance
Gavin Hudson, Patrizia Amati-Bonneau, Emma L Blakely, et al.
American Journal of Human Genetics
|
December 29, 2005
Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder
Gavin Hudson, Sharon Keers, Patrick Yu-Wai-Man, et al.
Neurology
|
May 7, 2013
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
Gavin Hudson, Mike Nalls, Jonathan R Evans, et al.
Nature Cell Biology
|
December 15, 2022
Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos
Vasileios I Floros, Angela Pyle, Sabine Dietmann, et al.
Nature Cell Biology
|
January 17, 2018
Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos
Vasileios I Floros, Angela Pyle, Sabine Dietmann, et al.
Nature Cell Biology
|
April 21, 2018
Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos
Vasileios I Floros, Angela Pyle, Sabine Dietmann, et al.
Plos Genetics
|
April 1, 2022
Heteroplasmic mitochondrial DNA variants in cardiovascular diseases
Claudia Calabrese, Angela Pyle, Helen Griffin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 22, 2011
Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome
Sophie E Winder-Rhodes, Pablo Garcia-Reitböck, Maria Ban, et al.
Page
of 10