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Molecular Neurodegeneration|May 26, 2020
Interleukin-6 deficiency exacerbates Huntington's disease model phenotypesMary H Wertz, S Sebastian Pineda, Hyeseung Lee, et al.Biorxiv : the Preprint Server for Biology|April 10, 2026
Scn4b Modulates Huntington's Disease Phenotype Severity in vivoSuphinya Sathitloetsakun, Vanessa Farrell, S Sebastian Pineda, et al.Proceedings of the National Academy of Sciences of the United States of America|August 22, 2022
A partnership between the lipid scramblase XK and the lipid transfer protein VPS13A at the plasma membraneAndrés Guillén-Samander, Yumei Wu, S Sebastian Pineda, et al.Biorxiv : the Preprint Server for Biology|July 9, 2025
Sideroflexins enable mitochondrial transport of polar neutral amino acidsSamuel Block, Fangtao Chi, Paul C Rosen, et al.Neuron|July 19, 2020
Cell Type-Specific Transcriptomics Reveals that Mutant Huntingtin Leads to Mitochondrial RNA Release and Neuronal Innate Immune ActivationHyeseung Lee, Robert J Fenster, S Sebastian Pineda, et al.Neuron|February 1, 2020
Genome-wide In Vivo CNS Screening Identifies Genes that Modify CNS Neuronal Survival and mHTT ToxicityMary H Wertz, Mollie R Mitchem, S Sebastian Pineda, et al.Cell|March 23, 2024
Single-cell dissection of the human motor and prefrontal cortices in ALS and FTLDS Sebastian Pineda, Hyeseung Lee, Maria J Ulloa-Navas, et al.Pageof 1