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 Yu

Showing results (101-110 of 183) with videos related to

Pageof 19
Sort By:
Scientific Reports|August 5, 2018
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cellsSelena Trifunov, Angela Pyle, Maria Lucia Valentino, et al.
Investigative Ophthalmology & Visual Science|March 4, 2009
Quality of life in patients with leber hereditary optic neuropathyMatthew Anthony Kirkman, Alex Korsten, Miriam Leonhardt, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular musclesPatrick Yu-Wai-Man, Joey Lai-Cheong, Gillian M Borthwick, et al.
Acta Neuropathologica Communications|February 13, 2025
Disruption of mitochondrial homeostasis and permeability transition pore opening in OPA1 iPSC-derived retinal ganglion cellsMichael Whitehead, Joshua P Harvey, Paul E Sladen, et al.
Frontiers in Neurology|December 18, 2023
Case report: Mutations in <i>DNAJC30</i> causing autosomal recessive Leber hereditary optic neuropathy are common amongst Eastern European individualsToby Charles Major, Eszter Sara Arany, Katherine Schon, et al.
Asian Spine Journal|September 7, 2017
Prevalence, Patterns, and Genetic Association Analysis of Modic Vertebral Endplate ChangesRishi Mugesh Kanna, Rajasekaran Shanmuganathan, Veera Ranjani Rajagopalan, et al.
Journal of Medical Genetics|May 19, 2021
WFS1 protein expression correlates with clinical progression of optic atrophy in patients with Wolfram syndromeKun Hu, Malgorzata Zatyka, Dewi Astuti, et al.
Progress in Retinal and Eye Research|May 4, 2024
Mitochondrial retinopathies and optic neuropathies: The impact of retinal imaging on modern understanding of pathogenesis, diagnosis, and managementEnrico Borrelli, Francesco Bandello, Camiel J F Boon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 22, 2021
Characterization of Retinal Architecture in Spinocerebellar Ataxia Type 3 and Correlation with Disease SeverityFlávio Moura Rezende Filho, Neringa Jurkute, João Brainer Clares de Andrade, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 2023
<i>OPA1</i> disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusionBenjamín Cartes-Saavedra, Daniel Lagos, Josefa Macuada, et al.
Pageof 19

Showing results (101-110 of 183) with videos related to

Sort By:
Pageof 19
Scientific Reports|August 5, 2018
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cellsSelena Trifunov, Angela Pyle, Maria Lucia Valentino, et al.
Investigative Ophthalmology & Visual Science|March 4, 2009
Quality of life in patients with leber hereditary optic neuropathyMatthew Anthony Kirkman, Alex Korsten, Miriam Leonhardt, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular musclesPatrick Yu-Wai-Man, Joey Lai-Cheong, Gillian M Borthwick, et al.
Acta Neuropathologica Communications|February 13, 2025
Disruption of mitochondrial homeostasis and permeability transition pore opening in OPA1 iPSC-derived retinal ganglion cellsMichael Whitehead, Joshua P Harvey, Paul E Sladen, et al.
Frontiers in Neurology|December 18, 2023
Case report: Mutations in <i>DNAJC30</i> causing autosomal recessive Leber hereditary optic neuropathy are common amongst Eastern European individualsToby Charles Major, Eszter Sara Arany, Katherine Schon, et al.
Asian Spine Journal|September 7, 2017
Prevalence, Patterns, and Genetic Association Analysis of Modic Vertebral Endplate ChangesRishi Mugesh Kanna, Rajasekaran Shanmuganathan, Veera Ranjani Rajagopalan, et al.
Journal of Medical Genetics|May 19, 2021
WFS1 protein expression correlates with clinical progression of optic atrophy in patients with Wolfram syndromeKun Hu, Malgorzata Zatyka, Dewi Astuti, et al.
Progress in Retinal and Eye Research|May 4, 2024
Mitochondrial retinopathies and optic neuropathies: The impact of retinal imaging on modern understanding of pathogenesis, diagnosis, and managementEnrico Borrelli, Francesco Bandello, Camiel J F Boon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 22, 2021
Characterization of Retinal Architecture in Spinocerebellar Ataxia Type 3 and Correlation with Disease SeverityFlávio Moura Rezende Filho, Neringa Jurkute, João Brainer Clares de Andrade, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 2023
<i>OPA1</i> disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusionBenjamín Cartes-Saavedra, Daniel Lagos, Josefa Macuada, et al.
Pageof 19