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

Angela Pyle

Showing results (41-50 of 119) with videos related to

Pageof 12
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society|April 11, 2017
metabolic profiling of Parkinson's disease and mild cognitive impairmentFlorence Burté, David Houghton, Hannah Lowes, et al.
Neuromuscular Disorders : NMD|August 24, 2010
Clinical and neuropathological findings in patients with TACO1 mutationsJürgen Seeger, Bertold Schrank, Angela Pyle, et al.
Brain : a Journal of Neurology|April 12, 2012
MFN2 mutations cause compensatory mitochondrial DNA proliferationKamil S Sitarz, Patrick Yu-Wai-Man, Angela Pyle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 18, 2020
The Human Coronavirus Receptor ANPEP (CD13) Is Overexpressed in Parkinson's DiseaseHannah Lowes, Fiona Robertson, Angela Pyle, et al.
Neuromuscular Disorders : NMD|April 23, 2015
Phenotypic variability of TRPV4 related neuropathiesTeresinha Evangelista, Boglarka Bansagi, Angela Pyle, et al.
Mitochondrion|October 5, 2010
Mitochondrial DNA does not contribute to the heritability of non-alcoholic fatty liver diseaseNimantha de Alwis, Guruprasad Aithal, Elizabetta Bugianesi, et al.
Neurology|September 21, 2012
OPA1 mutations induce mtDNA proliferation in leukocytes of patients with dominant optic atrophyKamil S Sitarz, Gitte J Almind, Rita Horvath, et al.
Scientific Reports|September 9, 2024
Variant load of mitochondrial DNA in single human mesenchymal stem cellsDaniel Hipps, Angela Pyle, Anna L R Porter, et al.
European Journal of Human Genetics : EJHG|June 2, 2021
Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1)Ana Töpf, Angela Pyle, Helen Griffin, et al.
Mitochondrion|March 19, 2013
Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMTVivienne C M Neeve, Angela Pyle, Veronika Boczonadi, et al.
Pageof 12

Showing results (41-50 of 119) with videos related to

Sort By:
Pageof 12
Movement Disorders : Official Journal of the Movement Disorder Society|April 11, 2017
metabolic profiling of Parkinson's disease and mild cognitive impairmentFlorence Burté, David Houghton, Hannah Lowes, et al.
Neuromuscular Disorders : NMD|August 24, 2010
Clinical and neuropathological findings in patients with TACO1 mutationsJürgen Seeger, Bertold Schrank, Angela Pyle, et al.
Brain : a Journal of Neurology|April 12, 2012
MFN2 mutations cause compensatory mitochondrial DNA proliferationKamil S Sitarz, Patrick Yu-Wai-Man, Angela Pyle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 18, 2020
The Human Coronavirus Receptor ANPEP (CD13) Is Overexpressed in Parkinson's DiseaseHannah Lowes, Fiona Robertson, Angela Pyle, et al.
Neuromuscular Disorders : NMD|April 23, 2015
Phenotypic variability of TRPV4 related neuropathiesTeresinha Evangelista, Boglarka Bansagi, Angela Pyle, et al.
Mitochondrion|October 5, 2010
Mitochondrial DNA does not contribute to the heritability of non-alcoholic fatty liver diseaseNimantha de Alwis, Guruprasad Aithal, Elizabetta Bugianesi, et al.
Neurology|September 21, 2012
OPA1 mutations induce mtDNA proliferation in leukocytes of patients with dominant optic atrophyKamil S Sitarz, Gitte J Almind, Rita Horvath, et al.
Scientific Reports|September 9, 2024
Variant load of mitochondrial DNA in single human mesenchymal stem cellsDaniel Hipps, Angela Pyle, Anna L R Porter, et al.
European Journal of Human Genetics : EJHG|June 2, 2021
Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1)Ana Töpf, Angela Pyle, Helen Griffin, et al.
Mitochondrion|March 19, 2013
Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMTVivienne C M Neeve, Angela Pyle, Veronika Boczonadi, et al.
Pageof 12