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Robert Adalbert

Showing results (21-30 of 30) with videos related to

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Nature Communications|October 31, 2023
Microglia-mediated demyelination protects against CD8<sup>+</sup> T cell-driven axon degeneration in mice carrying PLP defectsJanos Groh, Tassnim Abdelwahab, Yogita Kattimani, et al.
Brain : a Journal of Neurology|January 13, 2005
The slow Wallerian degeneration gene, WldS, inhibits axonal spheroid pathology in gracile axonal dystrophy miceWeiqian Mi, Bogdan Beirowski, Thomas H Gillingwater, et al.
The European Journal of Neuroscience|January 19, 2005
A rat model of slow Wallerian degeneration (WldS) with improved preservation of neuromuscular synapsesRobert Adalbert, Thomas H Gillingwater, Jane E Haley, et al.
Molecular and Cellular Neurosciences|May 13, 2008
VCP binding influences intracellular distribution of the slow Wallerian degeneration protein, Wld(S)Anna L Wilbrey, Jane E Haley, Thomas M Wishart, et al.
The Journal of Cell Biology|February 25, 2009
Wld S protein requires Nmnat activity and a short N-terminal sequence to protect axons in miceLaura Conforti, Anna Wilbrey, Giacomo Morreale, et al.
Molecular Biology of the Cell|December 24, 2005
The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleusHeike Laser, Laura Conforti, Giacomo Morreale, et al.
JCI Insight|April 10, 2020
Human endogenous retrovirus HERV-K(HML-2) RNA causes neurodegeneration through Toll-like receptorsPaul Dembny, Andrew G Newman, Manvendra Singh, 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.
Science (New York, N.Y.)|June 9, 2012
dSarm/Sarm1 is required for activation of an injury-induced axon death pathwayJeannette M Osterloh, Jing Yang, Timothy M Rooney, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Nature Communications|October 31, 2023
Microglia-mediated demyelination protects against CD8<sup>+</sup> T cell-driven axon degeneration in mice carrying PLP defectsJanos Groh, Tassnim Abdelwahab, Yogita Kattimani, et al.
Brain : a Journal of Neurology|January 13, 2005
The slow Wallerian degeneration gene, WldS, inhibits axonal spheroid pathology in gracile axonal dystrophy miceWeiqian Mi, Bogdan Beirowski, Thomas H Gillingwater, et al.
The European Journal of Neuroscience|January 19, 2005
A rat model of slow Wallerian degeneration (WldS) with improved preservation of neuromuscular synapsesRobert Adalbert, Thomas H Gillingwater, Jane E Haley, et al.
Molecular and Cellular Neurosciences|May 13, 2008
VCP binding influences intracellular distribution of the slow Wallerian degeneration protein, Wld(S)Anna L Wilbrey, Jane E Haley, Thomas M Wishart, et al.
The Journal of Cell Biology|February 25, 2009
Wld S protein requires Nmnat activity and a short N-terminal sequence to protect axons in miceLaura Conforti, Anna Wilbrey, Giacomo Morreale, et al.
Molecular Biology of the Cell|December 24, 2005
The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleusHeike Laser, Laura Conforti, Giacomo Morreale, et al.
JCI Insight|April 10, 2020
Human endogenous retrovirus HERV-K(HML-2) RNA causes neurodegeneration through Toll-like receptorsPaul Dembny, Andrew G Newman, Manvendra Singh, 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.
Science (New York, N.Y.)|June 9, 2012
dSarm/Sarm1 is required for activation of an injury-induced axon death pathwayJeannette M Osterloh, Jing Yang, Timothy M Rooney, et al.
Pageof 3