Guo Y - Search Results

1

Identification of a GNE homozygous mutation in a Han-Chinese family with GNE myopathy.

Wu Y, Yuan L, Guo Y, Lu A, Zheng W, Xu H, Yang Y, Hu P, Gu S, Wang B, Deng H. Wu Y, et al. Among authors: guo y. J Cell Mol Med. 2018 Nov;22(11):5533-5538. doi: 10.1111/jcmm.13827. Epub 2018 Aug 29. J Cell Mol Med. 2018. PMID: 30160005 Free PMC article.

2

Small interfering RNA targeting the PINK1 induces apoptosis in dopaminergic cells SH-SY5Y.

Deng H, Jankovic J, Guo Y, Xie W, Le W. Deng H, et al. Among authors: guo y. Biochem Biophys Res Commun. 2005 Dec 2;337(4):1133-8. doi: 10.1016/j.bbrc.2005.09.178. Epub 2005 Oct 6. Biochem Biophys Res Commun. 2005. PMID: 16226715

3

Heterogeneous phenotype in a family with compound heterozygous parkin gene mutations.

Deng H, Le WD, Hunter CB, Ondo WG, Guo Y, Xie WJ, Jankovic J. Deng H, et al. Among authors: guo y. Arch Neurol. 2006 Feb;63(2):273-7. doi: 10.1001/archneur.63.2.273. Arch Neurol. 2006. PMID: 16476817

4

Genetic analysis of LRRK2 mutations in patients with Parkinson disease.

Deng H, Le W, Guo Y, Hunter CB, Xie W, Huang M, Jankovic J. Deng H, et al. Among authors: guo y. J Neurol Sci. 2006 Dec 21;251(1-2):102-6. doi: 10.1016/j.jns.2006.09.017. Epub 2006 Nov 9. J Neurol Sci. 2006. PMID: 17097110

5

GIGYF2 Asn56Ser and Asn457Thr mutations in Parkinson disease patients.

Guo Y, Jankovic J, Zhu S, Le W, Song Z, Xie W, Liao D, Yang H, Deng H. Guo Y, et al. Neurosci Lett. 2009 May 1;454(3):209-11. doi: 10.1016/j.neulet.2009.03.039. Epub 2009 Mar 16. Neurosci Lett. 2009. PMID: 19429085

6

LINGO1 rs9652490 variant in Parkinson disease patients.

Guo Y, Jankovic J, Song Z, Yang H, Zheng W, Le W, Tang X, Deng X, Yang Y, Deng S, Luo Z, Deng H. Guo Y, et al. Neurosci Lett. 2011 Jan 7;487(2):174-6. doi: 10.1016/j.neulet.2010.10.016. Epub 2010 Oct 15. Neurosci Lett. 2011. PMID: 20951767

7

Systematic genetic analysis of the PITX3 gene in patients with Parkinson disease.

Guo Y, Le WD, Jankovic J, Yang HR, Xu HB, Xie WJ, Song Z, Deng H. Guo Y, et al. Mov Disord. 2011 Aug 1;26(9):1729-32. doi: 10.1002/mds.23693. Epub 2011 Apr 5. Mov Disord. 2011. PMID: 21469209

8

HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease.

Guo Y, Deng X, Zheng W, Xu H, Song Z, Liang H, Lei J, Jiang X, Luo Z, Deng H. Guo Y, et al. Neurosci Lett. 2011 Sep 1;501(3):185-7. doi: 10.1016/j.neulet.2011.05.245. Epub 2011 Jul 20. Neurosci Lett. 2011. PMID: 21791235

9

Genetic analysis of IREB2, FAM13A and XRCC5 variants in Chinese Han patients with chronic obstructive pulmonary disease.

Guo Y, Lin H, Gao K, Xu H, Deng X, Zhang Q, Luo Z, Sun S, Deng H. Guo Y, et al. Biochem Biophys Res Commun. 2011 Nov 18;415(2):284-7. doi: 10.1016/j.bbrc.2011.10.042. Epub 2011 Oct 18. Biochem Biophys Res Commun. 2011. PMID: 22027142

10

Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD.

Guo Y, Deng X, Zhang J, Su L, Xu H, Luo Z, Deng H. Guo Y, et al. Neurosci Lett. 2012 May 23;517(1):18-20. doi: 10.1016/j.neulet.2012.03.097. Epub 2012 Apr 9. Neurosci Lett. 2012. PMID: 22507240

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