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Scientific Reports|March 11, 2017
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohortHui Guo, Yu Peng, Zhengmao Hu, et al.
Molecular Neurodegeneration|December 2, 2023
MLKL deficiency alleviates neuroinflammation and motor deficits in the α-synuclein transgenic mouse model of Parkinson's diseaseLu Geng, Wenqing Gao, Hexige Saiyin, et al.
Nature Structural & Molecular Biology|January 4, 2024
Aurora kinase A-mediated phosphorylation triggers structural alteration of Rab1A to enhance ER complexity during mitosisWei Zhang, Zijian Zhang, Yun Xiang, et al.
Nature Communications|November 9, 2016
De novo genic mutations among a Chinese autism spectrum disorder cohortTianyun Wang, Hui Guo, Bo Xiong, et al.
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