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Anny Devoy

Showing results (11-20 of 19) with videos related to

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Brain : a Journal of Neurology|October 21, 2017
Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in 'FUSDelta14' knockin miceAnny Devoy, Bernadett Kalmar, Michelle Stewart, et al.
Brain Communications|March 26, 2026
<i>C9orf72</i> poly(glycine-alanine) knock-in mice exhibit mild rotarod and proteomic changes consistent with amyotrophic lateral sclerosis/frontotemporal dementiaCarmelo Milioto, Mireia Carcolé, Matteo Zanovello, et al.
Science (New York, N.Y.)|August 9, 2014
C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteinsSarah Mizielinska, Sebastian Grönke, Teresa Niccoli, et al.
Science Advances|July 22, 2021
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translationNicol Birsa, Agnieszka M Ule, Maria Giovanna Garone, et al.
Nucleic Acids Research|June 2, 2020
FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retentionJack Humphrey, Nicol Birsa, Carmelo Milioto, et al.
Neurobiology of Aging|September 3, 2014
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansionPietro Fratta, James M Polke, Jia Newcombe, et al.
Iscience|January 6, 2022
Generation and analysis of innovative genomically humanized knockin <i>SOD1</i>, <i>TARDBP</i> (TDP-43), and <i>FUS</i> mouse modelsAnny Devoy, Georgia Price, Francesca De Giorgio, et al.
Iscience|March 17, 2022
Erratum: Generation and analysis of innovative genomically humanized knockin <i>SOD1</i>, <i>TARDBP</i> (TDP-43), and <i>FUS</i> mouse modelsAnny Devoy, Georgia Price, Francesca De Giorgio, et al.
Nature Neuroscience|February 29, 2024
PolyGR and polyPR knock-in mice reveal a conserved neuroprotective extracellular matrix signature in C9orf72 ALS/FTD neuronsCarmelo Milioto, Mireia Carcolé, Ashling Giblin, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Brain : a Journal of Neurology|October 21, 2017
Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in 'FUSDelta14' knockin miceAnny Devoy, Bernadett Kalmar, Michelle Stewart, et al.
Brain Communications|March 26, 2026
<i>C9orf72</i> poly(glycine-alanine) knock-in mice exhibit mild rotarod and proteomic changes consistent with amyotrophic lateral sclerosis/frontotemporal dementiaCarmelo Milioto, Mireia Carcolé, Matteo Zanovello, et al.
Science (New York, N.Y.)|August 9, 2014
C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteinsSarah Mizielinska, Sebastian Grönke, Teresa Niccoli, et al.
Science Advances|July 22, 2021
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translationNicol Birsa, Agnieszka M Ule, Maria Giovanna Garone, et al.
Nucleic Acids Research|June 2, 2020
FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retentionJack Humphrey, Nicol Birsa, Carmelo Milioto, et al.
Neurobiology of Aging|September 3, 2014
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansionPietro Fratta, James M Polke, Jia Newcombe, et al.
Iscience|January 6, 2022
Generation and analysis of innovative genomically humanized knockin <i>SOD1</i>, <i>TARDBP</i> (TDP-43), and <i>FUS</i> mouse modelsAnny Devoy, Georgia Price, Francesca De Giorgio, et al.
Iscience|March 17, 2022
Erratum: Generation and analysis of innovative genomically humanized knockin <i>SOD1</i>, <i>TARDBP</i> (TDP-43), and <i>FUS</i> mouse modelsAnny Devoy, Georgia Price, Francesca De Giorgio, et al.
Nature Neuroscience|February 29, 2024
PolyGR and polyPR knock-in mice reveal a conserved neuroprotective extracellular matrix signature in C9orf72 ALS/FTD neuronsCarmelo Milioto, Mireia Carcolé, Ashling Giblin, et al.
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