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Wilfried Rossoll

Showing results (41-50 of 49) with videos related to

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Biorxiv : the Preprint Server for Biology|April 28, 2025
Context-dependent Interactors Regulate TDP-43 Dysfunction in ALS/FTLDLongxin Xie, Yuehua Zhu, Bryan T Hurtle, et al.
Science Advances|August 7, 2024
Cell-specific cross-talk proteomics reveals cathepsin B signaling as a driver of glioblastoma malignancy near the subventricular zoneEmily S Norton, Lauren A Whaley, Vanessa K Jones, et al.
Biorxiv : the Preprint Server for Biology|September 4, 2023
Cell-specific crosstalk proteomics reveals cathepsin B signaling as a driver of glioblastoma malignancy near the subventricular zoneEmily S Norton, Lauren A Whaley, Vanessa K Jones, et al.
Cell Reports|May 7, 2020
Hexanucleotide Repeat Expansions in c9FTD/ALS and SCA36 Confer Selective Patterns of Neurodegeneration In VivoTiffany W Todd, Zachary T McEachin, Jeannie Chew, et al.
Cell|May 24, 2025
Intra-condensate demixing of TDP-43 inside stress granules generates pathological aggregatesXiao Yan, David Kuster, Priyesh Mohanty, et al.
Nature Neuroscience|January 10, 2018
TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTDChing-Chieh Chou, Yi Zhang, Mfon E Umoh, et al.
Molecular Neurodegeneration|December 9, 2022
Nuclear import receptors are recruited by FG-nucleoporins to rescue hallmarks of TDP-43 proteinopathyBilal Khalil, Deepak Chhangani, Melissa C Wren, et al.
Neuron|May 7, 2020
Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36Zachary T McEachin, Tania F Gendron, Nisha Raj, et al.
Nature|July 18, 2012
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosisChi-Hong Wu, Claudia Fallini, Nicola Ticozzi, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Biorxiv : the Preprint Server for Biology|April 28, 2025
Context-dependent Interactors Regulate TDP-43 Dysfunction in ALS/FTLDLongxin Xie, Yuehua Zhu, Bryan T Hurtle, et al.
Science Advances|August 7, 2024
Cell-specific cross-talk proteomics reveals cathepsin B signaling as a driver of glioblastoma malignancy near the subventricular zoneEmily S Norton, Lauren A Whaley, Vanessa K Jones, et al.
Biorxiv : the Preprint Server for Biology|September 4, 2023
Cell-specific crosstalk proteomics reveals cathepsin B signaling as a driver of glioblastoma malignancy near the subventricular zoneEmily S Norton, Lauren A Whaley, Vanessa K Jones, et al.
Cell Reports|May 7, 2020
Hexanucleotide Repeat Expansions in c9FTD/ALS and SCA36 Confer Selective Patterns of Neurodegeneration In VivoTiffany W Todd, Zachary T McEachin, Jeannie Chew, et al.
Cell|May 24, 2025
Intra-condensate demixing of TDP-43 inside stress granules generates pathological aggregatesXiao Yan, David Kuster, Priyesh Mohanty, et al.
Nature Neuroscience|January 10, 2018
TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTDChing-Chieh Chou, Yi Zhang, Mfon E Umoh, et al.
Molecular Neurodegeneration|December 9, 2022
Nuclear import receptors are recruited by FG-nucleoporins to rescue hallmarks of TDP-43 proteinopathyBilal Khalil, Deepak Chhangani, Melissa C Wren, et al.
Neuron|May 7, 2020
Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36Zachary T McEachin, Tania F Gendron, Nisha Raj, et al.
Nature|July 18, 2012
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosisChi-Hong Wu, Claudia Fallini, Nicola Ticozzi, et al.
Pageof 5