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Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.
Wang JL, Cao L, Li XH, Hu ZM, Li JD, Zhang JG, Liang Y, San-A, Li N, Chen SQ, Guo JF, Jiang H, Shen L, Zheng L, Mao X, Yan WQ, Zhou Y, Shi YT, Ai SX, Dai MZ, Zhang P, Xia K, Chen SD, Tang BS. Wang JL, et al. Among authors: li xh, li n, li jd. Brain. 2011 Dec;134(Pt 12):3493-3501. doi: 10.1093/brain/awr289. Epub 2011 Nov 26. Brain. 2011. PMID: 22120146 Free PMC article.
MicroRNA profiling in the serums of SCA3/MJD patients.
Shi Y, Huang F, Tang B, Li J, Wang J, Shen L, Xia K, Jiang H. Shi Y, et al. Int J Neurosci. 2014 Feb;124(2):97-101. doi: 10.3109/00207454.2013.827679. Epub 2013 Aug 22. Int J Neurosci. 2014. PMID: 23879331
miR-25 alleviates polyQ-mediated cytotoxicity by silencing ATXN3.
Huang F, Zhang L, Long Z, Chen Z, Hou X, Wang C, Peng H, Wang J, Li J, Duan R, Xia K, Chuang DM, Tang B, Jiang H. Huang F, et al. FEBS Lett. 2014 Dec 20;588(24):4791-8. doi: 10.1016/j.febslet.2014.11.013. Epub 2014 Nov 20. FEBS Lett. 2014. PMID: 25451224 Free PMC article.
Identification of CHIP as a novel causative gene for autosomal recessive cerebellar ataxia.
Shi Y, Wang J, Li JD, Ren H, Guan W, He M, Yan W, Zhou Y, Hu Z, Zhang J, Xiao J, Su Z, Dai M, Wang J, Jiang H, Guo J, Zhou Y, Zhang F, Li N, Du J, Xu Q, Hu Y, Pan Q, Shen L, Wang G, Xia K, Zhang Z, Tang B. Shi Y, et al. Among authors: li n, li jd. PLoS One. 2013 Dec 2;8(12):e81884. doi: 10.1371/journal.pone.0081884. eCollection 2013. PLoS One. 2013. PMID: 24312598 Free PMC article.
630 results