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The Journal of Biological Chemistry|December 18, 2008
SGK1 phosphorylation of IkappaB Kinase alpha and p300 Up-regulates NF-kappaB activity and increases N-Methyl-D-aspartate receptor NR2A and NR2B expressionDerek J C Tai, Chia-Chen Su, Yun-Li Ma, et al.Scientific Reports|January 25, 2020
Restoring Wnt6 signaling ameliorates behavioral deficits in MeCP2 T158A mouse model of Rett syndromeWei-Lun Hsu, Yun-Li Ma, Yen-Chen Liu, et al.The EMBO Journal|November 25, 2010
Novel role and mechanism of protein inhibitor of activated STAT1 in spatial learningDerek J C Tai, Wei L Hsu, Yen C Liu, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 18, 2014
CREB SUMOylation by the E3 ligase PIAS1 enhances spatial memoryYan-Chu Chen, Wei-Lun Hsu, Yun-Li Ma, et al.Nature Communications|February 5, 2016
MeCP2 SUMOylation rescues Mecp2-mutant-induced behavioural deficits in a mouse model of Rett syndromeDerek J C Tai, Yen C Liu, Wei L Hsu, et al.Cell Reports Methods|December 13, 2023
Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR librariesXander Nuttle, Nicholas D Burt, Benjamin Currall, et al.Nature Communications|May 19, 2021
16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitroMaria Sundberg, Hannah Pinson, Richard S Smith, et al.Biorxiv : the Preprint Server for Biology|March 18, 2024
Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editingDahlia Rohm, Joshua B Black, Sean R McCutcheon, et al.Cell Genomics|February 13, 2025
Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editingDahlia Rohm, Joshua B Black, Sean R McCutcheon, et al.American Journal of Medical Genetics. Part A|October 22, 2019
Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndromePhilip M Boone, Scott Paterson, Kiana Mohajeri, et al.Pageof 3