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157 related items for PubMed ID: 21524731
21. Association study between SNP rs150689919 in the DNA demethylation gene, TET1, and Parkinson's disease in Chinese Han population. Liao XX, Zhan ZX, Luo YY, Li K, Wang JL, Guo JF, Yan XX, Xia K, Tang BS, Shen L. BMC Neurol; 2013 Dec 11; 13():196. PubMed ID: 24325350 [Abstract] [Full Text] [Related]
22. Assessment of RIT2 rs12456492 association with Parkinson's disease in Mainland China. Liu ZH, Guo JF, Wang YQ, Li K, Sun QY, Xu Q, Yan XX, Xu CS, Tang BS. Neurobiol Aging; 2015 Mar 11; 36(3):1600.e9-11. PubMed ID: 25559334 [Abstract] [Full Text] [Related]
23. 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. PubMed ID: 27538639 [Abstract] [Full Text] [Related]
24. Decreased NURR1 and PITX3 gene expression in Chinese patients with Parkinson's disease. Liu H, Wei L, Tao Q, Deng H, Ming M, Xu P, Le W. Eur J Neurol; 2012 Jun 15; 19(6):870-5. PubMed ID: 22309633 [Abstract] [Full Text] [Related]
25. 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. PubMed ID: 22531747 [Abstract] [Full Text] [Related]
26. 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 May 23; 61(4):360-4. PubMed ID: 24005725 [Abstract] [Full Text] [Related]
27. Evaluation of the relationship between SORL1 gene polymorphism and Parkinson's disease in the Chinese population. Wang Y, Luan M, Xue L, Jin J, Xie A. Neurosci Lett; 2022 May 01; 778():136602. PubMed ID: 35364126 [Abstract] [Full Text] [Related]
28. 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. PubMed ID: 29607885 [Abstract] [Full Text] [Related]
29. The association between TLR3 rs3775290 polymorphism and sporadic Parkinson's disease in Chinese Han population. Wang J, Liu Y, Liu Y, Zhu K, Xie A. Neurosci Lett; 2020 May 29; 728():135005. PubMed ID: 32335220 [Abstract] [Full Text] [Related]
31. GLIS1 rs797906: an increased risk factor for late-onset Parkinson's disease in the Han Chinese population. Song W, Chen YP, Huang R, Chen K, Pan PL, Li J, Yang Y, Shang HF. Eur Neurol; 2012 Apr 29; 68(2):89-92. PubMed ID: 22759478 [Abstract] [Full Text] [Related]
33. Vitamin D receptor rs2228570 polymorphism and Parkinson's disease risk in a Chinese population. Hu W, Wang L, Chen B, Wang X. Neurosci Lett; 2020 Jan 19; 717():134722. PubMed ID: 31877334 [Abstract] [Full Text] [Related]
34. 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 Jan 19; 68(3):181-4. PubMed ID: 22923019 [Abstract] [Full Text] [Related]
36. Association of RAGE gene polymorphisms with sporadic Parkinson's disease in Chinese Han population. Gao J, Teng J, Liu H, Han X, Chen B, Xie A. Neurosci Lett; 2014 Jan 24; 559():158-62. PubMed ID: 24304868 [Abstract] [Full Text] [Related]
37. Genetic analysis of FGF20 in Chinese patients with Parkinson's disease. Sun XY, Wang L, Cheng L, Li NN, Lu ZJ, Li JY, Peng R. Neurol Sci; 2017 May 24; 38(5):887-891. PubMed ID: 28238162 [Abstract] [Full Text] [Related]
38. Association of VEGF gene polymorphisms with sporadic Parkinson's disease in Chinese Han population. Wu Y, Zhang Y, Han X, Li X, Xue L, Xie A. Neurol Sci; 2016 Dec 24; 37(12):1923-1929. PubMed ID: 27481110 [Abstract] [Full Text] [Related]
39. Association between epidermal growth factor receptor gene polymorphisms and susceptibility to Parkinson's disease. Jin J, Xue L, Bai X, Zhang X, Tian Q, Xie A. Neurosci Lett; 2020 Sep 25; 736():135273. PubMed ID: 32712352 [Abstract] [Full Text] [Related]