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Layne N Rodden

Showing results (1-10 of 12) with videos related to

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Expert Opinion on Emerging Drugs|October 25, 2021
Designing phase II clinical trials in Friedreich ataxiaLayne N Rodden, David R Lynch
Neurology. Genetics|May 27, 2022
Clinical Evidence for Variegated Silencing in Patients With Friedreich AtaxiaLayne N Rodden, Christian Rummey, Yi Na Dong, et al.
Neurodegenerative Disease Management|June 29, 2022
Friedreich ataxia: clinical features and new developmentsMedina Keita, Kellie McIntyre, Layne N Rodden, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2023
A Novel Metric for Predicting Severity of Disease Features in Friedreich's AtaxiaLayne N Rodden, Christian Rummey, Sudha Kessler, et al.
Frontiers in Neuroscience|December 13, 2021
Epigenetic Heterogeneity in Friedreich Ataxia Underlies Variable <i>FXN</i> ReactivationLayne N Rodden, Kaitlyn M Gilliam, Christina Lam, et al.
Journal of Medical Genetics|January 12, 2023
<i>FXN</i> gene methylation determines carrier status in Friedreich ataxiaChristina Lam, Kaitlyn M Gilliam, Layne N Rodden, et al.
Annals of Clinical and Translational Neurology|June 19, 2023
Retinal hypoplasia and degeneration result in vision loss in Friedreich ataxiaLayne N Rodden, Kellie McIntyre, Medina Keita, et al.
Frontiers in Neuroscience|April 11, 2022
Cerebellar Pathology in an Inducible Mouse Model of Friedreich AtaxiaElizabeth Mercado-Ayón, Nathan Warren, Sarah Halawani, et al.
Scientific Reports|March 24, 2022
DNA methylation in Friedreich ataxia silences expression of frataxin isoform ELayne N Rodden, Kaitlyn M Gilliam, Christina Lam, et al.
Human Molecular Genetics|January 12, 2021
Methylated and unmethylated epialleles support variegated epigenetic silencing in Friedreich ataxiaLayne N Rodden, Yogesh K Chutake, Kaitlyn Gilliam, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Expert Opinion on Emerging Drugs|October 25, 2021
Designing phase II clinical trials in Friedreich ataxiaLayne N Rodden, David R Lynch
Neurology. Genetics|May 27, 2022
Clinical Evidence for Variegated Silencing in Patients With Friedreich AtaxiaLayne N Rodden, Christian Rummey, Yi Na Dong, et al.
Neurodegenerative Disease Management|June 29, 2022
Friedreich ataxia: clinical features and new developmentsMedina Keita, Kellie McIntyre, Layne N Rodden, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2023
A Novel Metric for Predicting Severity of Disease Features in Friedreich's AtaxiaLayne N Rodden, Christian Rummey, Sudha Kessler, et al.
Frontiers in Neuroscience|December 13, 2021
Epigenetic Heterogeneity in Friedreich Ataxia Underlies Variable <i>FXN</i> ReactivationLayne N Rodden, Kaitlyn M Gilliam, Christina Lam, et al.
Journal of Medical Genetics|January 12, 2023
<i>FXN</i> gene methylation determines carrier status in Friedreich ataxiaChristina Lam, Kaitlyn M Gilliam, Layne N Rodden, et al.
Annals of Clinical and Translational Neurology|June 19, 2023
Retinal hypoplasia and degeneration result in vision loss in Friedreich ataxiaLayne N Rodden, Kellie McIntyre, Medina Keita, et al.
Frontiers in Neuroscience|April 11, 2022
Cerebellar Pathology in an Inducible Mouse Model of Friedreich AtaxiaElizabeth Mercado-Ayón, Nathan Warren, Sarah Halawani, et al.
Scientific Reports|March 24, 2022
DNA methylation in Friedreich ataxia silences expression of frataxin isoform ELayne N Rodden, Kaitlyn M Gilliam, Christina Lam, et al.
Human Molecular Genetics|January 12, 2021
Methylated and unmethylated epialleles support variegated epigenetic silencing in Friedreich ataxiaLayne N Rodden, Yogesh K Chutake, Kaitlyn Gilliam, et al.
Pageof 2