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Timothy J Hines

Showing results (1-10 of 14) with videos related to

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Frontiers in Cell and Developmental Biology|January 20, 2022
An Integrated Approach to Studying Rare Neuromuscular Diseases Using Animal and Human Cell-Based ModelsTimothy J Hines, Cathleen Lutz, Stephen A Murray, et al.
Journal of the Peripheral Nervous System : JPNS|August 20, 2025
SARM1 Inhibition in Three Mouse Models of Charcot-Marie-Tooth DiseaseAlaura D Rice, Abigail L D Tadenev, Timothy J Hines, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Testing SIPA1L2 as a modifier of CMT1A using mouse modelsGeorge C Murray, Timothy J Hines, Abigail L D Tadenev, et al.
Journal of Neuropathology and Experimental Neurology|March 13, 2024
Testing SIPA1L2 as a modifier of CMT1A using mouse modelsGeorge C Murray, Timothy J Hines, Abigail L D Tadenev, et al.
Biorxiv : the Preprint Server for Biology|March 27, 2026
A mouse model of autosomal dominant spastic ataxia and myopathy caused by a mutation in <i>Tuba4a</i>Timothy J Hines, Jonathan R Funke, Samia L Pratt, et al.
Human Molecular Genetics|August 11, 2024
Clinically relevant mouse models of severe spinal muscular atrophy with respiratory distress type 1Sarah E Holbrook, Amy N Hicks, Paige B Martin, et al.
Eneuro|February 7, 2018
An Essential Postdevelopmental Role for Lis1 in MiceTimothy J Hines, Xu Gao, Subhshri Sahu, et al.
Human Molecular Genetics|November 22, 2022
Clinically relevant mouse models of Charcot-Marie-Tooth type 2SPaige B Martin, Sarah E Holbrook, Amy N Hicks, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 17, 2026
LIS1 is critical for axon integrity in adult miceSamaneh Matoo, Anne M Ventrone, Shreena Patel, et al.
Biology|July 29, 2023
A Novel ENU-Induced <i>Mfn2</i> Mutation Causes Motor Deficits in Mice without Causing Peripheral NeuropathyTimothy J Hines, Janice Bailey, Hedi Liu, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Frontiers in Cell and Developmental Biology|January 20, 2022
An Integrated Approach to Studying Rare Neuromuscular Diseases Using Animal and Human Cell-Based ModelsTimothy J Hines, Cathleen Lutz, Stephen A Murray, et al.
Journal of the Peripheral Nervous System : JPNS|August 20, 2025
SARM1 Inhibition in Three Mouse Models of Charcot-Marie-Tooth DiseaseAlaura D Rice, Abigail L D Tadenev, Timothy J Hines, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Testing SIPA1L2 as a modifier of CMT1A using mouse modelsGeorge C Murray, Timothy J Hines, Abigail L D Tadenev, et al.
Journal of Neuropathology and Experimental Neurology|March 13, 2024
Testing SIPA1L2 as a modifier of CMT1A using mouse modelsGeorge C Murray, Timothy J Hines, Abigail L D Tadenev, et al.
Biorxiv : the Preprint Server for Biology|March 27, 2026
A mouse model of autosomal dominant spastic ataxia and myopathy caused by a mutation in <i>Tuba4a</i>Timothy J Hines, Jonathan R Funke, Samia L Pratt, et al.
Human Molecular Genetics|August 11, 2024
Clinically relevant mouse models of severe spinal muscular atrophy with respiratory distress type 1Sarah E Holbrook, Amy N Hicks, Paige B Martin, et al.
Eneuro|February 7, 2018
An Essential Postdevelopmental Role for Lis1 in MiceTimothy J Hines, Xu Gao, Subhshri Sahu, et al.
Human Molecular Genetics|November 22, 2022
Clinically relevant mouse models of Charcot-Marie-Tooth type 2SPaige B Martin, Sarah E Holbrook, Amy N Hicks, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 17, 2026
LIS1 is critical for axon integrity in adult miceSamaneh Matoo, Anne M Ventrone, Shreena Patel, et al.
Biology|July 29, 2023
A Novel ENU-Induced <i>Mfn2</i> Mutation Causes Motor Deficits in Mice without Causing Peripheral NeuropathyTimothy J Hines, Janice Bailey, Hedi Liu, et al.
Pageof 2