Showing results (11-20 of 24) with videos related to
Sort By:
Pageof 3
Cell Reports Methods|August 3, 2023
A structured evaluation of cryopreservation in generating single-cell transcriptomes from cerebrospinal fluidHanane Touil, Tina Roostaei, Daniela Calini, et al.Neuron|January 30, 2022
Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosis susceptibilityMandy Meijer, Eneritz Agirre, Mukund Kabbe, et al.Neurobiology of Aging|July 6, 2013
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosisDaniela Calini, Lucia Corrado, Roberto Del Bo, et al.Neuron|December 21, 2024
snRNA-seq stratifies multiple sclerosis patients into distinct white matter glial responsesWill Macnair, Daniela Calini, Eneritz Agirre, et al.Biorxiv : the Preprint Server for Biology|October 9, 2023
Disease-specific selective vulnerability and neuroimmune pathways in dementia revealed by single cell genomicsJessica E Rexach, Yuyan Cheng, Lawrence Chen, et al.Cell Reports. Medicine|March 19, 2025
T-bet+ CXCR3+ B cells drive hyperreactive B-T cell interactions in multiple sclerosisIvan Jelcic, Reza Naghavian, Imran Fanaswala, et al.Neurobiology of Aging|July 7, 2012
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effectAntonia Ratti, Lucia Corrado, Barbara Castellotti, et al.Cell|September 12, 2024
Cross-disorder and disease-specific pathways in dementia revealed by single-cell genomicsJessica E Rexach, Yuyan Cheng, Lawrence Chen, et al.Neurobiology of Aging|October 16, 2012
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementiaCinzia Tiloca, Nicola Ticozzi, Viviana Pensato, et al.Human Mutation|July 18, 2017
The role of de novo mutations in the development of amyotrophic lateral sclerosisPerry T C van Doormaal, Nicola Ticozzi, Jochen H Weishaupt, et al.Pageof 3