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Molecular Psychiatry|June 16, 2025
Functional defects in FOXG1 variants predict the severity of brain anomalies in FOXG1 syndromeTsai-Yu Lin, Lee-Chin Wong, Pei-Shan Hou, et al.Stem Cell Reports|February 15, 2014
Suppression of the SOX2 neural effector gene by PRDM1 promotes human germ cell fate in embryonic stem cellsI-Ying Lin, Feng-Lan Chiu, Chen-Hsiang Yeang, et al.Stem Cells and Development|September 11, 2009
PiggyBac transposon-mediated, reversible gene transfer in human embryonic stem cellsYou-Tzung Chen, Kenryo Furushima, Pei-Shan Hou, et al.Development (Cambridge, England)|December 27, 2023
A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain developmentMeng-Han Tsai, Wan-Cian Lin, Shih-Ying Chen, et al.Nature Communications|March 10, 2026
Epilepsy-associated FOXJ3 variants link a transcriptional program of the PTEN-mTOR pathway to neuronal specification and cortical laminationHaw-Yuan Cheng, Chen Liu, Chiao-Wen Nien, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|July 15, 2025
TRPML2 channel modulation by PI(3,5)P₂ and small-molecule agonists controls endosomal vesicle dynamicsZi-Qi Gu, Hsuan-Ti Wang, Yanfen Li, et al.Pageof 3