Hu YC - Search Results

1

Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese population.

Wang L, Guo JF, Zhang WW, Xu Q, Zuo X, Shi CH, Luo LZ, Liu J, Hu L, Hu YC, She L, Jiang H, Yan XX, Xia K, Pan Q, Tang BS. Wang L, et al. Among authors: hu yc, hu l. Neurosci Lett. 2010 Apr 5;473(2):131-5. doi: 10.1016/j.neulet.2010.02.037. Epub 2010 Feb 21. Neurosci Lett. 2010. PMID: 20178831

2

Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1.

Du J, Hu YC, Tang BS, Chen C, Luo YY, Zhan ZX, Zhao GH, Jiang H, Xia K, Shen L. Du J, et al. Among authors: hu yc. Clin Neurol Neurosurg. 2011 Jul;113(6):480-2. doi: 10.1016/j.clineuro.2011.02.011. Epub 2011 Mar 17. Clin Neurol Neurosurg. 2011. PMID: 21419568

3

Variant in the 3' region of SNCA associated with Parkinson's disease and serum α-synuclein levels.

Hu Y, Tang B, Guo J, Wu X, Sun Q, Shi C, Hu L, Wang C, Wang L, Tan L, Shen L, Yan X, Zhang H. Hu Y, et al. J Neurol. 2012 Mar;259(3):497-504. doi: 10.1007/s00415-011-6209-4. Epub 2011 Aug 19. J Neurol. 2012. PMID: 21853288

4

Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s disease.

Wang L, Guo JF, Zhang WW, Xu Q, Zuo X, Shi CH, Luo LZ, Liu J, Hu L, Hu YC, Yan XX, Tang BS. Wang L, et al. Among authors: hu yc, hu l. J Clin Neurosci. 2011 Dec;18(12):1699-701. doi: 10.1016/j.jocn.2011.05.014. J Clin Neurosci. 2011. PMID: 22115759

5

Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease.

Tian JY, Guo JF, Wang L, Sun QY, Yao LY, Luo LZ, Shi CH, Hu YC, Yan XX, Tang BS. Tian JY, et al. Among authors: hu yc. Neurosci Lett. 2012 May 16;516(2):207-11. doi: 10.1016/j.neulet.2012.03.086. Epub 2012 Apr 5. Neurosci Lett. 2012. PMID: 22503729

6

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. PLoS One. 2013 Dec 2;8(12):e81884. doi: 10.1371/journal.pone.0081884. eCollection 2013. PLoS One. 2013. PMID: 24312598 Free PMC article.

7

Hypomethylation of SNCA in blood of patients with sporadic Parkinson's disease.

Ai SX, Xu Q, Hu YC, Song CY, Guo JF, Shen L, Wang CR, Yu RL, Yan XX, Tang BS. Ai SX, et al. Among authors: hu yc. J Neurol Sci. 2014 Feb 15;337(1-2):123-8. doi: 10.1016/j.jns.2013.11.033. Epub 2013 Dec 1. J Neurol Sci. 2014. PMID: 24326201

8

Polygenic determinants of Parkinson's disease in a Chinese population.

Guo JF, Li K, Yu RL, Sun QY, Wang L, Yao LY, Hu YC, Lv ZY, Luo LZ, Shen L, Jiang H, Yan XX, Pan Q, Xia K, Tang BS. Guo JF, et al. Among authors: hu yc. Neurobiol Aging. 2015 Apr;36(4):1765.e1-1765.e6. doi: 10.1016/j.neurobiolaging.2014.12.030. Epub 2015 Jan 6. Neurobiol Aging. 2015. PMID: 25623333

9

Involvement of Bcl-2-associated athanogene (BAG)-family proteins in the neuroprotection by rasagiline.

Guo JF, He S, Kang JF, Xu Q, Hu YC, Zhang HN, Wang CY, Yan XX, Tang BS. Guo JF, et al. Among authors: hu yc. Int J Clin Exp Med. 2015 Oct 15;8(10):18158-64. eCollection 2015. Int J Clin Exp Med. 2015. PMID: 26770414 Free PMC article.

10

Genome-wide analysis of DNA methylation during antagonism of DMOG to MnCl2-induced cytotoxicity in the mouse substantia nigra.

Yang N, Wei Y, Wang T, Guo J, Sun Q, Hu Y, Yan X, Zhu X, Tang B, Xu Q. Yang N, et al. Sci Rep. 2016 Jul 6;6:28933. doi: 10.1038/srep28933. Sci Rep. 2016. PMID: 27380887 Free PMC article.

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