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Showing results (131-140 of 173) with videos related to

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JCI Insight|September 6, 2019
Vincristine and bortezomib use distinct upstream mechanisms to activate a common SARM1-dependent axon degeneration programStefanie Geisler, Ryan A Doan, Galen C Cheng, et al.
Cell Reports|June 29, 2022
Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathyKelsey L Krus, Amy Strickland, Yurie Yamada, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 13, 2012
A model of toxic neuropathy in Drosophila reveals a role for MORN4 in promoting axonal degenerationMartha R C Bhattacharya, Josiah Gerdts, Sarah A Naylor, et al.
Elife|June 9, 2016
An evolutionarily conserved mechanism for cAMP elicited axonal regeneration involves direct activation of the dual leucine zipper kinase DLKYan Hao, Erin Frey, Choya Yoon, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 20, 2021
Multiple domain interfaces mediate SARM1 autoinhibitionChen Shen, Mihir Vohra, Pengfei Zhang, et al.
The Journal of Experimental Medicine|January 16, 2019
Gene therapy targeting SARM1 blocks pathological axon degeneration in miceStefanie Geisler, Shay X Huang, Amy Strickland, et al.
Experimental Neurology|February 23, 2020
cADPR is a gene dosage-sensitive biomarker of SARM1 activity in healthy, compromised, and degenerating axonsYo Sasaki, Thomas M Engber, Robert O Hughes, et al.
Biorxiv : the Preprint Server for Biology|December 15, 2025
Dysregulated lactate metabolism synergizes with ALS genetic risk factors to accelerate motor declineShweta Tendulkar, Tong Wu, Amy Strickland, et al.
Elife|August 17, 2022
Defining hierarchical protein interaction networks from spectral analysis of bacterial proteomesMark A Zaydman, Alexander S Little, Fidel Haro, et al.
Journal of Neuroinflammation|May 23, 2025
Diverse cell types establish a pathogenic immune environment in peripheral neuropathyJulie Choi, Amy Strickland, Hui Qi Loo, et al.
Pageof 18

Showing results (131-140 of 173) with videos related to

Sort By:
Pageof 18
JCI Insight|September 6, 2019
Vincristine and bortezomib use distinct upstream mechanisms to activate a common SARM1-dependent axon degeneration programStefanie Geisler, Ryan A Doan, Galen C Cheng, et al.
Cell Reports|June 29, 2022
Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathyKelsey L Krus, Amy Strickland, Yurie Yamada, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 13, 2012
A model of toxic neuropathy in Drosophila reveals a role for MORN4 in promoting axonal degenerationMartha R C Bhattacharya, Josiah Gerdts, Sarah A Naylor, et al.
Elife|June 9, 2016
An evolutionarily conserved mechanism for cAMP elicited axonal regeneration involves direct activation of the dual leucine zipper kinase DLKYan Hao, Erin Frey, Choya Yoon, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 20, 2021
Multiple domain interfaces mediate SARM1 autoinhibitionChen Shen, Mihir Vohra, Pengfei Zhang, et al.
The Journal of Experimental Medicine|January 16, 2019
Gene therapy targeting SARM1 blocks pathological axon degeneration in miceStefanie Geisler, Shay X Huang, Amy Strickland, et al.
Experimental Neurology|February 23, 2020
cADPR is a gene dosage-sensitive biomarker of SARM1 activity in healthy, compromised, and degenerating axonsYo Sasaki, Thomas M Engber, Robert O Hughes, et al.
Biorxiv : the Preprint Server for Biology|December 15, 2025
Dysregulated lactate metabolism synergizes with ALS genetic risk factors to accelerate motor declineShweta Tendulkar, Tong Wu, Amy Strickland, et al.
Elife|August 17, 2022
Defining hierarchical protein interaction networks from spectral analysis of bacterial proteomesMark A Zaydman, Alexander S Little, Fidel Haro, et al.
Journal of Neuroinflammation|May 23, 2025
Diverse cell types establish a pathogenic immune environment in peripheral neuropathyJulie Choi, Amy Strickland, Hui Qi Loo, et al.
Pageof 18