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Christopher A Reid

Showing results (121-130 of 131) with videos related to

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Annals of Clinical and Translational Neurology|September 5, 2015
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsyMichael S Hildebrand, Rick Tankard, Elena V Gazina, et al.
Circulation|August 21, 2023
Improved Cardiac Function in Postischemic Rats Using an Optimized Cardiac Reprogramming Cocktail Delivered in a Single Novel Adeno-Associated VirusHuanyu Zhou, Jin Yang, Chetan Srinath, et al.
Brain : a Journal of Neurology|April 22, 2026
Collapse of feed-forward inhibition underpins hyperexcitability in GABAA gain-of-function epilepsyChaseley E McKenzie, Khaing Phyu Aung, Altair Brito Dos Santos, et al.
Nature Communications|March 4, 2025
AAV9-mediated MYBPC3 gene therapy with optimized expression cassette enhances cardiac function and survival in MYBPC3 cardiomyopathy modelsAmara Greer-Short, Anna Greenwood, Elena C Leon, et al.
Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Nature Communications|August 7, 2024
Male autism spectrum disorder is linked to brain aromatase disruption by prenatal BPA in multimodal investigations and 10HDA ameliorates the related mouse phenotypeChristos Symeonides, Kristina Vacy, Sarah Thomson, et al.
Brain : a Journal of Neurology|November 17, 2023
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40Angela T Morgan, Thomas S Scerri, Adam P Vogel, et al.
Annals of Neurology|June 5, 2025
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell ModelsClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Mono and biallelic variants in <i>HCN2</i> cause severe neurodevelopmental disordersClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
The Journal of Clinical Investigation|November 25, 2025
Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessiveKatrine M Johannesen, Khaing Phyu Aung, Vivian Wy Liao, et al.
Pageof 14

Showing results (121-130 of 131) with videos related to

Sort By:
Pageof 14
Annals of Clinical and Translational Neurology|September 5, 2015
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsyMichael S Hildebrand, Rick Tankard, Elena V Gazina, et al.
Circulation|August 21, 2023
Improved Cardiac Function in Postischemic Rats Using an Optimized Cardiac Reprogramming Cocktail Delivered in a Single Novel Adeno-Associated VirusHuanyu Zhou, Jin Yang, Chetan Srinath, et al.
Brain : a Journal of Neurology|April 22, 2026
Collapse of feed-forward inhibition underpins hyperexcitability in GABAA gain-of-function epilepsyChaseley E McKenzie, Khaing Phyu Aung, Altair Brito Dos Santos, et al.
Nature Communications|March 4, 2025
AAV9-mediated MYBPC3 gene therapy with optimized expression cassette enhances cardiac function and survival in MYBPC3 cardiomyopathy modelsAmara Greer-Short, Anna Greenwood, Elena C Leon, et al.
Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Nature Communications|August 7, 2024
Male autism spectrum disorder is linked to brain aromatase disruption by prenatal BPA in multimodal investigations and 10HDA ameliorates the related mouse phenotypeChristos Symeonides, Kristina Vacy, Sarah Thomson, et al.
Brain : a Journal of Neurology|November 17, 2023
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40Angela T Morgan, Thomas S Scerri, Adam P Vogel, et al.
Annals of Neurology|June 5, 2025
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell ModelsClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Mono and biallelic variants in <i>HCN2</i> cause severe neurodevelopmental disordersClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
The Journal of Clinical Investigation|November 25, 2025
Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessiveKatrine M Johannesen, Khaing Phyu Aung, Vivian Wy Liao, et al.
Pageof 14