These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
193 related articles for article (PubMed ID: 34944443)
1. SNCA 3' UTR Genetic Variants in Patients with Parkinson's Disease. Blažeković A; Jerčić KG; Borovečki F Biomolecules; 2021 Nov; 11(12):. PubMed ID: 34944443 [TBL] [Abstract][Full Text] [Related]
2. A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease. Cardo LF; Coto E; de Mena L; Ribacoba R; Lorenzo-Betancor O; Pastor P; Samaranch L; Mata IF; Díaz M; Moris G; Menéndez M; Corao AI; Alvarez V J Mol Neurosci; 2012 Jul; 47(3):425-30. PubMed ID: 22076805 [TBL] [Abstract][Full Text] [Related]
3. SNCA 3'UTR genetic variants in patients with Parkinson's disease and REM sleep behavior disorder. Toffoli M; Dreussi E; Cecchin E; Valente M; Sanvilli N; Montico M; Gagno S; Garziera M; Polano M; Savarese M; Calandra-Buonaura G; Placidi F; Terzaghi M; Toffoli G; Gigli GL Neurol Sci; 2017 Jul; 38(7):1233-1240. PubMed ID: 28409245 [TBL] [Abstract][Full Text] [Related]
4. Variants in the 3'UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression. Schmitt I; Wüllner U; van Rooyen JP; Khazneh H; Becker J; Volk A; Kubisch C; Becker T; Kostic VS; Klein C; Ramirez A Eur J Hum Genet; 2012 Dec; 20(12):1265-9. PubMed ID: 22617348 [TBL] [Abstract][Full Text] [Related]
6. Genetic analysis of α-synuclein 3' untranslated region and its corresponding microRNAs in relation to Parkinson's disease compared to dementia with Lewy bodies. Tagliafierro L; Glenn OC; Zamora ME; Beach TG; Woltjer RL; Lutz MW; Chiba-Falek O Alzheimers Dement; 2017 Nov; 13(11):1237-1250. PubMed ID: 28431219 [TBL] [Abstract][Full Text] [Related]
7. [SNCA rs356219 AND rs356165 VARIANTS ARE ASSOCIATED WITH PARKINSON'S DISEASE AND INCREASED ALPHA-SYNUCLEIN GENE EXPRESSION IN THE CD45(+)-BLOOD CELLS]. Emelyanov AK; Andoskin PA; Miliukhina IV; Timofeeva AA; Yakimovskii AF; Senkevich KA; Nikolaev MA; Pchelina SN Tsitologiia; 2016; 58(2):99-104. PubMed ID: 27228655 [TBL] [Abstract][Full Text] [Related]
8. Genetic variants of SNCA and LRRK2 genes are associated with sporadic PD susceptibility: a replication study in a Taiwanese cohort. Wu-Chou YH; Chen YT; Yeh TH; Chang HC; Weng YH; Lai SC; Huang CL; Chen RS; Huang YZ; Chen CC; Hung J; Chuang WL; Lin WY; Chen CH; Lu CS Parkinsonism Relat Disord; 2013 Feb; 19(2):251-5. PubMed ID: 23182315 [TBL] [Abstract][Full Text] [Related]
9. Assessment of risk factor variants of LRRK2, MAPT, SNCA and TCEANC2 genes in Hungarian sporadic Parkinson's disease patients. Boros FA; Török R; Vágvölgyi-Sümegi E; Pesei ZG; Klivényi P; Vécsei L Neurosci Lett; 2019 Jul; 706():140-145. PubMed ID: 31085292 [TBL] [Abstract][Full Text] [Related]
10. Multiple alpha-synuclein gene polymorphisms are associated with Parkinson's disease in a Norwegian population. Myhre R; Toft M; Kachergus J; Hulihan MM; Aasly JO; Klungland H; Farrer MJ Acta Neurol Scand; 2008 Nov; 118(5):320-7. PubMed ID: 18485051 [TBL] [Abstract][Full Text] [Related]
11. Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population. Chen Y; Wei QQ; Ou R; Cao B; Chen X; Zhao B; Guo X; Yang Y; Chen K; Wu Y; Song W; Shang HF PLoS One; 2015; 10(7):e0133776. PubMed ID: 26208350 [TBL] [Abstract][Full Text] [Related]
12. Familial genes in sporadic disease: common variants of alpha-synuclein gene associate with Parkinson's disease. Ross OA; Gosal D; Stone JT; Lincoln SJ; Heckman MG; Irvine GB; Johnston JA; Gibson JM; Farrer MJ; Lynch T Mech Ageing Dev; 2007; 128(5-6):378-82. PubMed ID: 17531291 [TBL] [Abstract][Full Text] [Related]
13. 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; 479(1):31-3. PubMed ID: 20478361 [TBL] [Abstract][Full Text] [Related]
14. 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; 368():231-4. PubMed ID: 27538639 [TBL] [Abstract][Full Text] [Related]
15. Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations. Rudakou U; Yu E; Krohn L; Ruskey JA; Asayesh F; Dauvilliers Y; Spiegelman D; Greenbaum L; Fahn S; Waters CH; Dupré N; Rouleau GA; Hassin-Baer S; Fon EA; Alcalay RN; Gan-Or Z Brain; 2021 Mar; 144(2):462-472. PubMed ID: 33349842 [TBL] [Abstract][Full Text] [Related]
17. Alpha-synuclein gene polymorphism affects risk of dementia in Han Chinese with Parkinson's disease. Zheng J; Zang Q; Hu F; Wei H; Ma J; Xu Y Neurosci Lett; 2019 Jul; 706():146-150. PubMed ID: 31102707 [TBL] [Abstract][Full Text] [Related]
18. Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease. Benitez BA; Davis AA; Jin SC; Ibanez L; Ortega-Cubero S; Pastor P; Choi J; Cooper B; Perlmutter JS; Cruchaga C Mol Neurodegener; 2016 Apr; 11():29. PubMed ID: 27094865 [TBL] [Abstract][Full Text] [Related]
19. alpha-Synuclein and Parkinson disease susceptibility. Winkler S; Hagenah J; Lincoln S; Heckman M; Haugarvoll K; Lohmann-Hedrich K; Kostic V; Farrer M; Klein C Neurology; 2007 Oct; 69(18):1745-50. PubMed ID: 17872362 [TBL] [Abstract][Full Text] [Related]
20. The rs3756063 polymorphism is associated with SNCA methylation in the Chinese Han population. Wei Y; Yang N; Xu Q; Sun Q; Guo J; Li K; Liu Z; Yan X; Zhu X; Tang B J Neurol Sci; 2016 Aug; 367():11-4. PubMed ID: 27423554 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]