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International Journal of Biological Macromolecules|December 8, 2025
UBA5 missense variants disrupt UFM1 activation: Structural, dynamic, and functional dissectionLiqiang Ai, Wenbo Han, Shengwei Xiao, et al.
Neuron|August 19, 2007
Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndromePeng Jin, Ranhui Duan, Abrar Qurashi, et al.
Cell & Bioscience|April 26, 2026
Integrator subunit IntS11 orchestrates the temporal dynamics of neural lineage progression in DrosophilaQiao Xiao, Liqiang Ai, Boquan Jia, et al.
Clinical Chemistry|September 28, 2022
Comprehensive Analysis of Fragile X Syndrome: Full Characterization of the FMR1 Locus by Long-Read SequencingQiaowei Liang, Yingdi Liu, Yaning Liu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 11, 2022
The exploration of genetic aetiology and diagnostic strategy for 321 Chinese individuals with intellectual disabilityHongyun Zhang, Xin Chen, Hu Tan, et al.
Cell Death & Disease|July 31, 2024
Eg5 UFMylation promotes spindle organization during mitosisGuangxu Li, Yuanjiang Huang, Wenbo Han, et al.
Frontiers in Neurology|June 30, 2023
Characteristics of autonomic dysfunction in neuronal intranuclear inclusion diseaseLu Zhou, Yun Tian, Sizhe Zhang, et al.
Neurobiology of Disease|June 10, 2019
Amyotrophic Lateral Sclerosis-associated GGGGCC repeat expansion promotes Tau phosphorylation and toxicityHua He, Wen Huang, Ruoxi Wang, et al.
Plos One|February 13, 2016
UBA5 Mutations Cause a New Form of Autosomal Recessive Cerebellar AtaxiaRanhui Duan, Yuting Shi, Li Yu, et al.
Human Molecular Genetics|October 9, 2012
Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellumTao Wang, Qian Pan, Li Lin, et al.
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