Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?

Related Experiment Video

Updated: Apr 19, 2026

A Simple Composite Phenotype Scoring System for Evaluating Mouse Models of Cerebellar Ataxia
07:33

A Simple Composite Phenotype Scoring System for Evaluating Mouse Models of Cerebellar Ataxia

Published on: May 21, 2010

37.6K

Brent L Fogel1, Sonya M Hanson, Esther B E Becker

  • 1Program in Neurogenetics, Department of Neurology David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.

Movement Disorders : Official Journal of the Movement Disorder Society
|December 6, 2014
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Cerebellar Regional Dissection for Molecular Analysis
08:51

Cerebellar Regional Dissection for Molecular Analysis

Published on: December 5, 2020

5.5K
Expression and Purification of the Human Lipid-sensitive Cation Channel TRPC3 for Structural Determination by Single-particle Cryo-electron Microscopy
08:27

Expression and Purification of the Human Lipid-sensitive Cation Channel TRPC3 for Structural Determination by Single-particle Cryo-electron Microscopy

Published on: January 7, 2019

10.1K

Related Experiment Videos

Last Updated: Apr 19, 2026

A Simple Composite Phenotype Scoring System for Evaluating Mouse Models of Cerebellar Ataxia
07:33

A Simple Composite Phenotype Scoring System for Evaluating Mouse Models of Cerebellar Ataxia

Published on: May 21, 2010

37.6K
Cerebellar Regional Dissection for Molecular Analysis
08:51

Cerebellar Regional Dissection for Molecular Analysis

Published on: December 5, 2020

5.5K
Expression and Purification of the Human Lipid-sensitive Cation Channel TRPC3 for Structural Determination by Single-particle Cryo-electron Microscopy
08:27

Expression and Purification of the Human Lipid-sensitive Cation Channel TRPC3 for Structural Determination by Single-particle Cryo-electron Microscopy

Published on: January 7, 2019

10.1K

Related Concept Videos

Translation01:31

Translation

162.8K
Lesson: Translation
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of...
162.8K
Translation01:31

Translation

23.4K
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life
Proteins are...
23.4K

Articles linked to this work by shared authors, journal, and citation graph.

Deep Learning-based Modeling Enhances Efficacy of Natural Ligand CAR Binders Targeting CD70.

bioRxiv : the preprint server for biology·2026

The CAHRA Challenge: A Community-Wide Assessment of Cryo-EM Heterogeneous Reconstruction Algorithms.

bioRxiv : the preprint server for biology·2026

Correction: Study of Protein-Protein Interactions in Septin Assembly: Multiple amphipathic helix domains cooperate in binding to the lipid membrane.

PLoS computational biology·2026

seekrflow: Towards an End-to-End Automated Simulation Pipeline with Machine-Learned Force Fields for Accelerated Drug-Target Kinetic and Thermodynamic Predictions.

Journal of chemical theory and computation·2026

Frequency of ZFHX3-Mediated Spinocerebellar Ataxia 4 in a US Undiagnosed Ataxia Cohort.

Movement disorders : official journal of the Movement Disorder Society·2026

Study of Protein-Protein Interactions in Septin Assembly: Multiple amphipathic helix domains cooperate in binding to the lipid membrane.

PLoS computational biology·2026

Genetic Analysis of the SLC38A6 Gene in Chinese Patients with Essential Tremor: Not Causative, But Rather an Additional Susceptibility Gene?

Movement disorders : official journal of the Movement Disorder Society·2026

Neuromelanin-Sensitive MRI as a Marker of Clinical Severity and Disease Burden in Parkinson's Disease: A Systematic Review and Meta-analysis.

Movement disorders : official journal of the Movement Disorder Society·2026

Reduced Sensory Attenuation Scales with Tic Severity in Tourette Syndrome.

Movement disorders : official journal of the Movement Disorder Society·2026

Longitudinal Real-Time Quaking-Induced Conversion Analysis of Misfolded α-Synuclein in Idiopathic Rapid Eye Movement Sleep Behavior Disorder Patients with Baseline Cerebrospinal Fluid Negativity.

Movement disorders : official journal of the Movement Disorder Society·2026

Mortality in People with Action Tremor: Findings from Three Population-Based Cohort Studies.

Movement disorders : official journal of the Movement Disorder Society·2026

Focused Ultrasound for Essential Tremor in Denmark: Results After 1 Year of Follow-Up.

Movement disorders : official journal of the Movement Disorder Society·2026
See all related articles
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
Jove
Visualize
Contact Us