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Nature Communications|October 3, 2022
Chemical engineering of therapeutic siRNAs for allele-specific gene silencing in Huntington's disease modelsFaith Conroy, Rachael Miller, Julia F Alterman, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 13, 2023
Di-valent siRNA-mediated silencing of MSH3 blocks somatic repeat expansion in mouse models of Huntington's diseaseDaniel O'Reilly, Jillian Belgrad, Chantal Ferguson, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2026
WWOX contributes to DNA damage, but not somatic instability in Huntington's diseaseTiziana Petrozziello, Zachariah L McLean, Adel Boudi, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Transcriptomic profiling uncovers mis-splicing and gene fusions in amyotrophic lateral sclerosisHuilin Xu, Tiziana Petrozziello, Adel Boudi, et al.
Brain : a Journal of Neurology|September 22, 2018
A feedback loop between dipeptide-repeat protein, TDP-43 and karyopherin-α mediates C9orf72-related neurodegenerationDaniel A Solomon, Alan Stepto, Wing Hei Au, et al.
Journal of Huntington'S Disease|September 11, 2023
Age-Dependent Increase in Tau Phosphorylation at Serine 396 in Huntington's Disease Prefrontal CortexTiziana Petrozziello, Sommer S Huntress, Ayleen L Castillo-Torres, et al.
Medrxiv : the Preprint Server for Health Sciences|June 19, 2023
Age-dependent increase in tau phosphorylation at serine 396 in Huntington's disease pre-frontal cortexTiziana Petrozziello, Sommer S Huntress, Ayleen L Castillo-Torres, et al.
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