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Items: 1 to 20 of 418

1.

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.

2.

Association between NOD2/CARD15 gene polymorphisms and Crohn's disease in Chinese Zhuang patients.

Long WY, Chen L, Zhang CL, Nong RM, Lin MJ, Zhan LL, Lv XP.

World J Gastroenterol. 2014 Apr 28;20(16):4737-44. doi: 10.3748/wjg.v20.i16.4737.

3.

CARD15 variants in patients with sporadic Parkinson's disease.

Bialecka M, Kurzawski M, Klodowska-Duda G, Opala G, Juzwiak S, Kurzawski G, Tan EK, Drozdzik M.

Neurosci Res. 2007 Mar;57(3):473-6. Epub 2006 Dec 14.

PMID:
17174426
5.

Association of mitochondrial DNA polymerase γ gene POLG1 polymorphisms with parkinsonism in Chinese populations.

Gui YX, Xu ZP, Lv W, Liu HM, Zhao JJ, Hu XY.

PLoS One. 2012;7(12):e50086. doi: 10.1371/journal.pone.0050086. Epub 2012 Dec 10.

6.

Variation at NOD2/CARD15 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish population.

Zhou Z, Lin XY, Akolkar PN, Gulwani-Akolkar B, Levine J, Katz S, Silver J.

Am J Gastroenterol. 2002 Dec;97(12):3095-101.

PMID:
12492195
8.

HLA-DRB1 alleles are associated with the susceptibility to sporadic Parkinson's disease in Chinese Han population.

Sun C, Wei L, Luo F, Li Y, Li J, Zhu F, Kang P, Xu R, Xiao L, Liu Z, Xu P.

PLoS One. 2012;7(11):e48594. doi: 10.1371/journal.pone.0048594. Epub 2012 Nov 6.

9.

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
10.

Confirmation of three inflammatory bowel disease susceptibility loci in a Chinese cohort.

Lv C, Yang X, Zhang Y, Zhao X, Chen Z, Long J, Zhang Y, Zhong C, Zhi J, Yao G, Jiang B, Zhi F.

Int J Colorectal Dis. 2012 Nov;27(11):1465-72. doi: 10.1007/s00384-012-1450-6. Epub 2012 Mar 20.

PMID:
22426692
11.

Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan.

Bonen DK, Ogura Y, Nicolae DL, Inohara N, Saab L, Tanabe T, Chen FF, Foster SJ, Duerr RH, Brant SR, Cho JH, Nuñez G.

Gastroenterology. 2003 Jan;124(1):140-6.

PMID:
12512038
12.

Crohn disease: frequency and nature of CARD15 mutations in Ashkenazi and Sephardi/Oriental Jewish families.

Tukel T, Shalata A, Present D, Rachmilewitz D, Mayer L, Grant D, Risch N, Desnick RJ.

Am J Hum Genet. 2004 Apr;74(4):623-36. Epub 2004 Mar 5.

13.

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
14.

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
15.

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.

16.

NOD2/CARD15 polymorphism in patients with rectal cancer.

Szeliga J, Sondka Z, Jackowski M, Jarkiewicz-Tretyn J, Tretyn A, Malenczyk M.

Med Sci Monit. 2008 Sep;14(9):CR480-4.

PMID:
18758419
17.

Lack of replication of a previously reported association between polymorphism in the 3'UTR of the alpha-synuclein gene and Parkinson's disease in Chinese subjects.

Hu FY, Hu WB, Liu L, Yu LH, Xi J, He XH, Zhu MR, Liu ZL, Xu YM.

Neurosci Lett. 2010 Jul 19;479(1):31-3. doi: 10.1016/j.neulet.2010.05.022. Epub 2010 May 15.

PMID:
20478361
18.

Polymorphisms of NOD2 and the risk of tuberculosis: a validation study in the Chinese population.

Pan H, Dai Y, Tang S, Wang J.

Int J Immunogenet. 2012 Jun;39(3):233-40. doi: 10.1111/j.1744-313X.2011.01079.x. Epub 2012 Jan 2.

PMID:
22212192
19.
20.

Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson's disease in a Han-Chinese population in south-eastern China.

Cai J, Lin Y, Chen W, Lin Q, Cai B, Wang N, Zheng W.

Neurol Sci. 2013 Nov;34(11):2001-6. doi: 10.1007/s10072-013-1436-3. Epub 2013 Apr 30.

PMID:
23624603

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