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Scientific Reports
|
August 5, 2018
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells
Selena Trifunov, Angela Pyle, Maria Lucia Valentino, et al.
Investigative Ophthalmology & Visual Science
|
March 4, 2009
Quality of life in patients with leber hereditary optic neuropathy
Matthew 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 muscles
Patrick 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 cells
Michael 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 individuals
Toby 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 Changes
Rishi 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 syndrome
Kun 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 management
Enrico 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 Severity
Flávio 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 fusion
Benjamín Cartes-Saavedra, Daniel Lagos, Josefa Macuada, et al.
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Search research articles
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Showing results (101-110 of 183) with videos related to
Sort By:
Page
of 19
Scientific Reports
|
August 5, 2018
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells
Selena Trifunov, Angela Pyle, Maria Lucia Valentino, et al.
Investigative Ophthalmology & Visual Science
|
March 4, 2009
Quality of life in patients with leber hereditary optic neuropathy
Matthew 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 muscles
Patrick 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 cells
Michael 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 individuals
Toby 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 Changes
Rishi 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 syndrome
Kun 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 management
Enrico 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 Severity
Flávio 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 fusion
Benjamín Cartes-Saavedra, Daniel Lagos, Josefa Macuada, et al.
Page
of 19