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Nature|August 23, 2011
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementiaHan-Xiang Deng, Wenjie Chen, Seong-Tshool Hong, et al.The Journal of Pathology|December 9, 2004
Systematic identification and molecular characterization of genes differentially expressed in breast and ovarian cancerEdgar Dahl, Ariane Sadr-Nabavi, Eva Klopocki, et al.Acta Pharmacologica Sinica|February 12, 2025
METTL14-mediated m6A methylation of pri-miR-5099 to facilitate cardiomyocyte pyroptosis in myocardial infarctionHang Yu, Qing-Sui Li, Jun-Nan Guo, et al.Nature Genetics|June 9, 2016
Identification of TMEM230 mutations in familial Parkinson's diseaseHan-Xiang Deng, Yong Shi, Yi Yang, et al.Acta Neuropathologica|May 22, 2010
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degenerationHazel Urwin, Keith A Josephs, Jonathan D Rohrer, et al.Pageof 21