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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 mice
Anny 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 dementia
Carmelo 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 proteins
Sarah Mizielinska, Sebastian Grönke, Teresa Niccoli, et al.
Science Advances
|
July 22, 2021
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translation
Nicol 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 retention
Jack 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 expansion
Pietro 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 models
Anny 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 models
Anny 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 neurons
Carmelo Milioto, Mireia Carcolé, Ashling Giblin, et al.
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
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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 mice
Anny 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 dementia
Carmelo 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 proteins
Sarah Mizielinska, Sebastian Grönke, Teresa Niccoli, et al.
Science Advances
|
July 22, 2021
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translation
Nicol 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 retention
Jack 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 expansion
Pietro 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 models
Anny 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 models
Anny 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 neurons
Carmelo Milioto, Mireia Carcolé, Ashling Giblin, et al.
Page
of 2