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Alberto Brusati

Showing results (1-10 of 18) with videos related to

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Iscience|June 1, 2026
Global transcriptional changes across multiple isogenic <i>C9orf72</i> patient iPSC-derived neuronsAparna Sreeram, Desiree M Baron, Alberto Brusati, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 7, 2023
Exploration and Retrieval of Virus-Related Molecular Data Using ExTaxsI: The Monkeypox Use CaseAlberto Brusati, Giulia Agostinetto, Antonia Bruno, et al.
Gigascience|January 25, 2022
ExTaxsI: an exploration tool of biodiversity molecular dataGiulia Agostinetto, Alberto Brusati, Anna Sandionigi, et al.
Frontiers in Aging Neuroscience|July 14, 2022
Parkinsonian Syndromes in Motor Neuron Disease: A Clinical StudyJacopo Pasquini, Francesca Trogu, Claudia Morelli, et al.
Journal of the Neurological Sciences|April 18, 2025
Characterization of human healthy i<sup>3</sup> lower motor neurons exposed to CSF from ALS patients stratified by UNC13A and C9ORF72 genotypeValeria Casiraghi, Enrico Pellegrini, Alberto Brusati, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 15, 2023
Analysis of normal <i>C9orf72</i> repeat length as possible disease modifier in amyotrophic lateral sclerosisSilvia Peverelli, Alberto Brusati, Valeria Casiraghi, et al.
Human Molecular Genetics|September 2, 2024
NEK1 haploinsufficiency worsens DNA damage, but not defective ciliogenesis, in C9ORF72 patient-derived iPSC-motoneuronsSerena Santangelo, Sabrina Invernizzi, Marta Nice Sorce, et al.
Journal of the Neurological Sciences|September 6, 2024
Quantification of serum TDP-43 and neurofilament light chain in patients with amyotrophic lateral sclerosis stratified by UNC13A genotypeValeria Casiraghi, Ilaria Milone, Alberto Brusati, et al.
International Journal of Molecular Sciences|August 26, 2022
<i>TMEM106B</i> Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral SclerosisArianna Manini, Antonia Ratti, Alberto Brusati, et al.
Frontiers in Aging Neuroscience|December 13, 2023
Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association studyAlberto Brusati, Silvia Peverelli, Luciano Calzari, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Iscience|June 1, 2026
Global transcriptional changes across multiple isogenic <i>C9orf72</i> patient iPSC-derived neuronsAparna Sreeram, Desiree M Baron, Alberto Brusati, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 7, 2023
Exploration and Retrieval of Virus-Related Molecular Data Using ExTaxsI: The Monkeypox Use CaseAlberto Brusati, Giulia Agostinetto, Antonia Bruno, et al.
Gigascience|January 25, 2022
ExTaxsI: an exploration tool of biodiversity molecular dataGiulia Agostinetto, Alberto Brusati, Anna Sandionigi, et al.
Frontiers in Aging Neuroscience|July 14, 2022
Parkinsonian Syndromes in Motor Neuron Disease: A Clinical StudyJacopo Pasquini, Francesca Trogu, Claudia Morelli, et al.
Journal of the Neurological Sciences|April 18, 2025
Characterization of human healthy i<sup>3</sup> lower motor neurons exposed to CSF from ALS patients stratified by UNC13A and C9ORF72 genotypeValeria Casiraghi, Enrico Pellegrini, Alberto Brusati, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 15, 2023
Analysis of normal <i>C9orf72</i> repeat length as possible disease modifier in amyotrophic lateral sclerosisSilvia Peverelli, Alberto Brusati, Valeria Casiraghi, et al.
Human Molecular Genetics|September 2, 2024
NEK1 haploinsufficiency worsens DNA damage, but not defective ciliogenesis, in C9ORF72 patient-derived iPSC-motoneuronsSerena Santangelo, Sabrina Invernizzi, Marta Nice Sorce, et al.
Journal of the Neurological Sciences|September 6, 2024
Quantification of serum TDP-43 and neurofilament light chain in patients with amyotrophic lateral sclerosis stratified by UNC13A genotypeValeria Casiraghi, Ilaria Milone, Alberto Brusati, et al.
International Journal of Molecular Sciences|August 26, 2022
<i>TMEM106B</i> Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral SclerosisArianna Manini, Antonia Ratti, Alberto Brusati, et al.
Frontiers in Aging Neuroscience|December 13, 2023
Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association studyAlberto Brusati, Silvia Peverelli, Luciano Calzari, et al.
Pageof 2