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Items: 1 to 20 of 104

1.

The polymorphism of SREBF1 gene rs11868035 G/A is associated with susceptibility to Parkinson's disease in a Chinese population.

Lou F, Li M, Liu N, Li X, Ren Y, Luo X.

Int J Neurosci. 2019 Jul;129(7):660-665. doi: 10.1080/00207454.2018.1526796. Epub 2019 Feb 6.

PMID:
30231795
2.

Association analysis of SNP rs11868035 in SREBF1 with sporadic Parkinson's disease, sporadic amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.

Yuan X, Cao B, Wu Y, Chen Y, Wei Q, Ou R, Yang J, Chen X, Zhao B, Song W, Shang H.

Neurosci Lett. 2018 Jan 18;664:128-132. doi: 10.1016/j.neulet.2017.11.015. Epub 2017 Nov 8.

PMID:
29128630
3.

Association of sterol regulatory element-binding protein-1c gene polymorphism with type 2 diabetes mellitus, insulin resistance and blood lipid levels in Chinese population.

Liu JX, Liu J, Li PQ, Xie XD, Guo Q, Tian LM, Ma XQ, Zhang JP, Liu J, Gao JY.

Diabetes Res Clin Pract. 2008 Oct;82(1):42-7. doi: 10.1016/j.diabres.2008.06.017. Epub 2008 Aug 8.

PMID:
18692268
4.

[Association of sterol regulatory element binding protein-1c genetic polymorphisms rs2297508 and rs11868035 with type 2 diabetes mellitus in Gansu Han and Dongxiang population].

Liu JX, Liu J, Guo Q, Liu J.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Jun;29(3):328-33. doi: 10.3760/cma.j.issn.1003-9406.2012.03.018. Chinese.

PMID:
22678801
5.

SNCA rs356182 variant increases risk of sporadic Parkinson's disease in ethnic Chinese.

Cheng L, Wang L, Li NN, Yu WJ, Sun XY, Li JY, Zhou D, Peng R.

J Neurol Sci. 2016 Sep 15;368:231-4. doi: 10.1016/j.jns.2016.07.032. Epub 2016 Jul 14.

PMID:
27538639
6.

Association study between two novel single nucleotide polymorphisms and sporadic Parkinson's disease in Chinese Han population.

Li K, Tang BS, Yu RL, Lv ZY, Sun QY, Li Q, Xia K, Yan XX, Guo JF.

Neurosci Lett. 2012 May 23;517(1):56-9. doi: 10.1016/j.neulet.2012.04.024. Epub 2012 Apr 15.

PMID:
22531747
7.

The single nucleotide polymorphism Rs12817488 is associated with Parkinson's disease in the Chinese population.

Yu RL, Guo JF, Wang YQ, Liu ZH, Sun ZF, Su L, Zhang Y, Yan XX, Tang BS.

J Clin Neurosci. 2015 Jun;22(6):1002-4. doi: 10.1016/j.jocn.2014.11.024. Epub 2015 Mar 26.

PMID:
25818163
8.

Association analysis of NUCKS1 and INPP5K polymorphism with Parkinson's disease.

Zhu W, Luo X, Adnan A, Yu P, Zhang S, Huo Z, Xu Q, Pang H.

Genes Genet Syst. 2018 Sep 15;93(2):59-64. doi: 10.1266/ggs.17-00038. Epub 2018 Mar 30.

9.

Association analysis of single-nucleotide polymorphisms of USP24 and USP40 with Parkinson's disease in the Han Chinese population.

Zhao B, Song W, Chen YP, Huang R, Chen K, Cao B, Yang Y, Shang HF.

Eur Neurol. 2012;68(3):181-4. Epub 2012 Aug 24.

PMID:
22923019
10.

Case-control study of the UCH-L1 S18Y variant in sporadic Parkinson's disease in the Chinese population.

Wang L, Guo JF, Nie LL, Luo L, Zuo X, Shen L, Jiang H, Yan XX, Xia K, Pan Q, Tang BS.

J Clin Neurosci. 2011 Apr;18(4):541-4. doi: 10.1016/j.jocn.2010.07.142. Epub 2011 Feb 18.

PMID:
21315600
11.

SNP rs356219 of the α-synuclein (SNCA) gene is associated with Parkinson's disease in a Chinese Han population.

Pan F, Dong H, Ding H, Ye M, Liu W, Wu Y, Zhang X, Chen Z, Luo Y, Ding X.

Parkinsonism Relat Disord. 2012 Jun;18(5):632-4. doi: 10.1016/j.parkreldis.2012.01.025. Epub 2012 Feb 19.

PMID:
22349157
12.

[Association of the ubiquitin carboxy-terminal hydrolase-L1 genetic polymorphism with the susceptibility of Parkinson's disease].

Xiao Y, Zhang B.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Oct;25(5):586-7. Chinese.

PMID:
18841579
13.

Lack of evidence for association of a UCH-L1 S18Y polymorphism with Parkinson's disease in a Han-Chinese population.

Zhang ZJ, Burgunder JM, An XK, Wu Y, Chen WJ, Zhang JH, Wang YC, Xu YM, Gou YR, Yuan GG, Mao XY, Peng R.

Neurosci Lett. 2008 Sep 19;442(3):200-2. doi: 10.1016/j.neulet.2008.07.012. Epub 2008 Jul 10.

PMID:
18638528
14.

GWAS-linked GAK locus in Parkinson's disease in Han Chinese and meta-analysis.

Li NN, Chang XL, Mao XY, Zhang JH, Zhao DM, Tan EK, Peng R.

Hum Genet. 2012 Jul;131(7):1089-93. doi: 10.1007/s00439-011-1133-3. Epub 2011 Dec 24.

PMID:
22198721
15.

P268S in NOD2 associates with susceptibility to Parkinson's disease in Chinese population.

Ma Q, An X, Li Z, Zhang H, Huang W, Cai L, Hu P, Lin Q, Tzeng CM.

Behav Brain Funct. 2013 May 7;9:19. doi: 10.1186/1744-9081-9-19.

16.

[Association analysis of the parkin gene in patients with sporadic Parkinson's disease from a Han population of Sichuan province].

Peng R, Chen WJ, Wu Y, Liu M, Lai XH, Zhang JH, Yuan GG, Gou YR, Li T, Wang YC.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Feb;24(1):38-41. Chinese.

PMID:
17285542
17.

Association of polymorphism in rs2736990 of the α-synuclein gene with Parkinson's disease in a Chinese population.

Pan F, Ding H, Dong H, Ye M, Liu W, Cui G, Chen J, Wu Y, Wang H, Dai X, Shi H, Ding X.

Neurol India. 2013 Jul-Aug;61(4):360-4. doi: 10.4103/0028-3886.117595.

18.

Ubiquitin specific proteases USP24 and USP40 and ubiquitin thiolesterase UCHL1 polymorphisms have synergic effect on the risk of Parkinson's disease among Taiwanese.

Wu YR, Chen CM, Chen YC, Chao CY, Ro LS, Fung HC, Hsiao YC, Hu FJ, Lee-Chen GJ.

Clin Chim Acta. 2010 Jul 4;411(13-14):955-8. doi: 10.1016/j.cca.2010.03.013. Epub 2010 Mar 17.

PMID:
20302855
19.
20.

Correlation between LRRK2 gene G2385R polymorphisms and Parkinson's disease.

Yan H, Ma Q, Yang X, Wang Y, Yao Y, Li H.

Mol Med Rep. 2012 Oct;6(4):879-83. doi: 10.3892/mmr.2012.1008. Epub 2012 Jul 26.

PMID:
22842796

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