Neuronal differentiation and activity drive nucleocytoplasmic shuttling of the intellectual disability kinase TLK2神经元分化和活动驱动智力障碍激酶TLK2的核质穿梭Frontiers in Cellular NeuroscienceIF42026-04-070OAAI
Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptomeNATURE MEDICINEIF502017-09-1898OAAI
Elevating expression of MeCP2 T158M rescues DNA binding and Rett syndrome-like phenotypesJOURNAL OF CLINICAL INVESTIGATIONIF13.62017-04-1046OA
Loss of MeCP2 function is associated with distinct gene expression changes in the striatumNEUROBIOLOGY OF DISEASEIF5.62013-11-0153OAAI
Loss of CDKL5 disrupts kinome profile and event-related potentials leading to autistic-like phenotypes in micePROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAIF9.12012-12-10169OAAI
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