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Matthew A White

Showing results (1-10 of 8) with videos related to

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Current Opinion in Neurology|August 19, 2016
Amyotrophic lateral sclerosis: recent genetic highlightsMatthew A White, Jemeen Sreedharan
Development (Cambridge, England)|October 20, 2018
TWE-PRIL reverse signalling suppresses sympathetic axon growth and tissue innervationLaura Howard, Erin Wosnitzka, Darian Okakpu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|September 23, 2025
Quantitative Profiling of Nanoscopic Protein Aggregates Reveals Specific Fingerprint of TDP-43-Positive Assemblies in Motor Neuron DiseaseDezerae Cox, Melanie Burke, Sara Milani, et al.
Translational Psychiatry|November 5, 2020
Coexistence of perseveration and apathy in the TDP-43<sup>Q331K</sup> knock-in mouse model of ALS-FTDEosu Kim, Matthew A White, Benjamin U Phillips, et al.
Acta Neuropathologica Communications|October 30, 2019
Sarm1 deletion suppresses TDP-43-linked motor neuron degeneration and cortical spine lossMatthew A White, Ziqiang Lin, Eugene Kim, et al.
Brain Communications|June 17, 2021
MRI-guided histology of TDP-43 knock-in mice implicates parvalbumin interneuron loss, impaired neurogenesis and aberrant neurodevelopment in amyotrophic lateral sclerosis-frontotemporal dementiaZiqiang Lin, Eugene Kim, Mohi Ahmed, et al.
Nature Neuroscience|March 21, 2018
TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTDMatthew A White, Eosu Kim, Amanda Duffy, et al.
Nature Neuroscience|June 7, 2018
Publisher Correction: TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTDMatthew A White, Eosu Kim, Amanda Duffy, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Current Opinion in Neurology|August 19, 2016
Amyotrophic lateral sclerosis: recent genetic highlightsMatthew A White, Jemeen Sreedharan
Development (Cambridge, England)|October 20, 2018
TWE-PRIL reverse signalling suppresses sympathetic axon growth and tissue innervationLaura Howard, Erin Wosnitzka, Darian Okakpu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|September 23, 2025
Quantitative Profiling of Nanoscopic Protein Aggregates Reveals Specific Fingerprint of TDP-43-Positive Assemblies in Motor Neuron DiseaseDezerae Cox, Melanie Burke, Sara Milani, et al.
Translational Psychiatry|November 5, 2020
Coexistence of perseveration and apathy in the TDP-43<sup>Q331K</sup> knock-in mouse model of ALS-FTDEosu Kim, Matthew A White, Benjamin U Phillips, et al.
Acta Neuropathologica Communications|October 30, 2019
Sarm1 deletion suppresses TDP-43-linked motor neuron degeneration and cortical spine lossMatthew A White, Ziqiang Lin, Eugene Kim, et al.
Brain Communications|June 17, 2021
MRI-guided histology of TDP-43 knock-in mice implicates parvalbumin interneuron loss, impaired neurogenesis and aberrant neurodevelopment in amyotrophic lateral sclerosis-frontotemporal dementiaZiqiang Lin, Eugene Kim, Mohi Ahmed, et al.
Nature Neuroscience|March 21, 2018
TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTDMatthew A White, Eosu Kim, Amanda Duffy, et al.
Nature Neuroscience|June 7, 2018
Publisher Correction: TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTDMatthew A White, Eosu Kim, Amanda Duffy, et al.
Pageof 1