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

Puneet Opal

Showing results (31-40 of 63) with videos related to

Pageof 7
Sort By:
The Journal of Biological Chemistry|June 17, 2003
Mapmodulin/leucine-rich acidic nuclear protein binds the light chain of microtubule-associated protein 1B and modulates neuritogenesisPuneet Opal, Jesus J Garcia, Friedrich Propst, et al.
Human Molecular Genetics|March 6, 2014
The histone deacetylase HDAC3 is essential for Purkinje cell function, potentially complicating the use of HDAC inhibitors in SCA1Anand Venkatraman, Yuan-Shih Hu, Alessandro Didonna, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Intrafamilial phenotypic variability of the DYT1 dystonia: from asymptomatic TOR1A gene carrier status to dystonic stormPuneet Opal, Ron Tintner, Joseph Jankovic, et al.
Neurology|April 29, 2022
Clinical Reasoning: A 77-Year-Old Man With Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive ComplaintsToni Qian Cao, Glenn R Harris, Christina M Lineback, et al.
Human Molecular Genetics|December 28, 2018
Loss of the dystonia gene Thap1 leads to transcriptional deficits that converge on common pathogenic pathways in dystonic syndromesNatalie M Frederick, Parth V Shah, Alessandro Didonna, et al.
Molecular Biology of the Cell|November 1, 2016
The role of gigaxonin in the degradation of the glial-specific intermediate filament protein GFAPNi-Hsuan Lin, Yu-Shan Huang, Puneet Opal, et al.
Cerebellum (London, England)|May 27, 2023
Standards of Fluid Biomarker Collection and Pre-analytical Processes in Humans and Mice: Recommendations by the Ataxia Global Initiative Working Group on BiomarkersFilippo M Santorelli, Hayley S McLoughlin, Justin M Wolter, et al.
Neurobiology of Disease|April 4, 2024
Phenotypical, genotypical and pathological characterization of the moonwalker mouse, a model of ataxiaGabriella Sekerková, Sumeyra Kilic, Yen-Hsin Cheng, et al.
Neurology|February 16, 2026
Pearls & Oy-sters: SCA27B as an Elusive Genetic Cause of Episodic Neurologic Symptoms in Later AdulthoodJacob Yomtoob, Lucy Morse, Ignacio Juan Keller Sarmiento, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 3, 2014
An investigation of diffusion imaging techniques in the evaluation of spinocerebellar ataxia and multisystem atrophyMichael N Rozenfeld, Alexander J Nemeth, Matthew T Walker, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
The Journal of Biological Chemistry|June 17, 2003
Mapmodulin/leucine-rich acidic nuclear protein binds the light chain of microtubule-associated protein 1B and modulates neuritogenesisPuneet Opal, Jesus J Garcia, Friedrich Propst, et al.
Human Molecular Genetics|March 6, 2014
The histone deacetylase HDAC3 is essential for Purkinje cell function, potentially complicating the use of HDAC inhibitors in SCA1Anand Venkatraman, Yuan-Shih Hu, Alessandro Didonna, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Intrafamilial phenotypic variability of the DYT1 dystonia: from asymptomatic TOR1A gene carrier status to dystonic stormPuneet Opal, Ron Tintner, Joseph Jankovic, et al.
Neurology|April 29, 2022
Clinical Reasoning: A 77-Year-Old Man With Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive ComplaintsToni Qian Cao, Glenn R Harris, Christina M Lineback, et al.
Human Molecular Genetics|December 28, 2018
Loss of the dystonia gene Thap1 leads to transcriptional deficits that converge on common pathogenic pathways in dystonic syndromesNatalie M Frederick, Parth V Shah, Alessandro Didonna, et al.
Molecular Biology of the Cell|November 1, 2016
The role of gigaxonin in the degradation of the glial-specific intermediate filament protein GFAPNi-Hsuan Lin, Yu-Shan Huang, Puneet Opal, et al.
Cerebellum (London, England)|May 27, 2023
Standards of Fluid Biomarker Collection and Pre-analytical Processes in Humans and Mice: Recommendations by the Ataxia Global Initiative Working Group on BiomarkersFilippo M Santorelli, Hayley S McLoughlin, Justin M Wolter, et al.
Neurobiology of Disease|April 4, 2024
Phenotypical, genotypical and pathological characterization of the moonwalker mouse, a model of ataxiaGabriella Sekerková, Sumeyra Kilic, Yen-Hsin Cheng, et al.
Neurology|February 16, 2026
Pearls & Oy-sters: SCA27B as an Elusive Genetic Cause of Episodic Neurologic Symptoms in Later AdulthoodJacob Yomtoob, Lucy Morse, Ignacio Juan Keller Sarmiento, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 3, 2014
An investigation of diffusion imaging techniques in the evaluation of spinocerebellar ataxia and multisystem atrophyMichael N Rozenfeld, Alexander J Nemeth, Matthew T Walker, et al.
Pageof 7