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Cell Stem Cell|February 4, 2017
Revealing the Hidden Powers that Fuel Adult NeurogenesisWeijun Feng, Hai-Kun LiuProgress in Neuro-Psychopharmacology & Biological Psychiatry|May 25, 2017
CRISPR-engineered genome editing for the next generation neurological disease modelingWeijun Feng, Hai-Kun Liu, Daisuke KawauchiFrontiers in Molecular Neuroscience|October 17, 2017
Versatile Roles of the Chromatin Remodeler CHD7 during Brain Development and DiseaseWeijun Feng, Chunxuan Shao, Hai-Kun LiuGenesis (New York, N.Y. : 2000)|November 22, 2023
Generation and characterization of Chd7-iCreERT2-tdTomato miceZi'ang Han, Ze Wang, Zhuxi Huang, et al.Molecular Cell|August 21, 2007
Activation of RNA polymerase I transcription by cockayne syndrome group B protein and histone methyltransferase G9aXuejun Yuan, Weijun Feng, Axel Imhof, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 17, 2024
A spectrum of AKT3 activating mutations cause focal malformations of cortical development (FMCDs) in cortical organoidsYing Xu, Rongrong Lu, Hao Li, et al.Nature Structural & Molecular Biology|March 9, 2010
PHF8 activates transcription of rRNA genes through H3K4me3 binding and H3K9me1/2 demethylationWeijun Feng, Masato Yonezawa, Jing Ye, et al.Environmental Pollution (Barking, Essex : 1987)|November 3, 2024
Lead exposure leads to premature neural differentiation via inhibiting Wnt signalingJun Li, Meixin Hu, Yingying Liu, et al.Human Genetics|April 8, 2025
Histone H3K36 methyltransferases NSD1 and SETD2 are required for brain developmentBo Chen, Chenyang Zhang, Huanwen Rui, et al.Journal of Molecular Neuroscience : MN|December 27, 2024
Identifying the Pathogenicity of a Novel NPRL3 Missense Mutation Using Personalized Cortical Organoid Model of Focal Cortical DysplasiaRongrong Lu, Ying Xu, Hao Li, et al.Pageof 3