251 related articles for article (PubMed ID: 28017238)
1. Association of glutathione S-transferase omega polymorphism and spinocerebellar ataxia type 2.
Almaguer-Mederos LE; Almaguer-Gotay D; Aguilera-Rodríguez R; González-Zaldívar Y; Cuello-Almarales D; Laffita-Mesa J; Vázquez-Mojena Y; Zayas-Feria P; Rodríguez-Labrada R; Velázquez-Pérez L; MacLeod P
J Neurol Sci; 2017 Jan; 372():324-328. PubMed ID: 28017238
[TBL] [Abstract][Full Text] [Related]
2. Concomitance of Polymorphisms in Glutathione Transferase Omega Genes Is Associated with Risk of Clear Cell Renal Cell Carcinoma.
Radic TM; Coric VM; Pljesa-Ercegovac MS; Basta-Jovanovic GM; Radojevic-Skodric SM; Dragicevic DP; Matic MG; Bogdanovic LM; Dzamic ZM; Simic TP; Savic-Radojevic AR
Tohoku J Exp Med; 2018 Sep; 246(1):35-44. PubMed ID: 30224590
[TBL] [Abstract][Full Text] [Related]
3. One‑carbon metabolism factor MTHFR variant is associated with saccade latency in Spinocerebellar Ataxia type 2.
Almaguer-Mederos LE; Jorge-Sainz Y; Almaguer-Gotay D; Aguilera-Rodríguez R; Rodríguez-Labrada R; Velázquez-Pérez L; González-Zaldívar Y; Cuello-Almarales D; Vázquez-Mojena Y; Canales-Ochoa N; Aguiar-Santiago J; Auburger G; MacLeod P
J Neurol Sci; 2020 Feb; 409():116586. PubMed ID: 31812845
[TBL] [Abstract][Full Text] [Related]
4. Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors.
Monte TL; Pereira FS; Reckziegel EDR; Augustin MC; Locks-Coelho LD; Santos ASP; Pedroso JL; Barsottini O; Vargas FR; Saraiva-Pereira ML; Jardim LB;
Parkinsonism Relat Disord; 2017 Sep; 42():54-60. PubMed ID: 28648514
[TBL] [Abstract][Full Text] [Related]
5. Glutathione S-transferase omega-2 polymorphism Asn142Asp modifies the risk of age-related cataract in smokers and subjects exposed to ultraviolet irradiation.
Stamenkovic M; Radic T; Stefanovic I; Coric V; Sencanic I; Pljesa-Ercegovac M; Matic M; Jaksic V; Simic T; Savic-Radojevic A
Clin Exp Ophthalmol; 2014 Apr; 42(3):277-83. PubMed ID: 23927022
[TBL] [Abstract][Full Text] [Related]
6. Role of glutathione S-transferases in the spinocerebellar ataxia type 2 clinical phenotype.
Almaguer-Gotay D; Almaguer-Mederos LE; Aguilera-Rodríguez R; Estupiñán-Rodríguez A; González-Zaldivar Y; Cuello-Almarales D; Laffita-Mesa JM; Vázquez-Mojena Y
J Neurol Sci; 2014 Jun; 341(1-2):41-5. PubMed ID: 24780439
[TBL] [Abstract][Full Text] [Related]
7. Glutathione S-Transferase Omega 1 variation does not influence age at onset of Huntington's disease.
Arning L; Jagiello P; Wieczorek S; Saft C; Andrich J; Epplen JT
BMC Med Genet; 2004 Mar; 5():7. PubMed ID: 15040808
[TBL] [Abstract][Full Text] [Related]
8. Polymorphisms in glutathione S-transferase omega-1 gene and increased risk of sporadic Alzheimer disease.
Capurso C; Panza F; Seripa D; Frisardi V; Imbimbo BP; Verdile G; Vendemiale G; Pilotto A; Solfrizzi V
Rejuvenation Res; 2010 Dec; 13(6):645-52. PubMed ID: 20818931
[TBL] [Abstract][Full Text] [Related]
9. Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
Jacobi H; du Montcel ST; Bauer P; Giunti P; Cook A; Labrum R; Parkinson MH; Durr A; Brice A; Charles P; Marelli C; Mariotti C; Nanetti L; Panzeri M; Rakowicz M; Sulek A; Sobanska A; Schmitz-Hübsch T; Schöls L; Hengel H; Baliko L; Melegh B; Filla A; Antenora A; Infante J; Berciano J; van de Warrenburg BP; Timmann D; Szymanski S; Boesch S; Kang JS; Pandolfo M; Schulz JB; Molho S; Diallo A; Klockgether T
Lancet Neurol; 2015 Nov; 14(11):1101-8. PubMed ID: 26377379
[TBL] [Abstract][Full Text] [Related]
10. GSTO1*C/GSTO2*G haplotype is associated with risk of transitional cell carcinoma of urinary bladder.
Djukic T; Simic T; Radic T; Matic M; Pljesa-Ercegovac M; Suvakov S; Coric V; Pekmezovic T; Novakovic I; Dragicevic D; Savic-Radojevic A
Int Urol Nephrol; 2015 Apr; 47(4):625-30. PubMed ID: 25716313
[TBL] [Abstract][Full Text] [Related]
11. SCA2 in the Indian population: Unified haplotype and variable phenotypic patterns in a large case series.
Sonakar AK; Shamim U; Srivastava MP; Faruq M; Srivastava AK
Parkinsonism Relat Disord; 2021 Aug; 89():139-145. PubMed ID: 34298214
[TBL] [Abstract][Full Text] [Related]
12. GSTO1*E155del polymorphism associated with increased risk for late-onset Alzheimer's disease: association hypothesis for an uncommon genetic variant.
Piacentini S; Polimanti R; Squitti R; Mariani S; Migliore S; Vernieri F; Rossini PM; Manfellotto D; Fuciarelli M
Neurosci Lett; 2012 Jan; 506(2):203-7. PubMed ID: 22100662
[TBL] [Abstract][Full Text] [Related]
13. Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.
Pulst SM; Santos N; Wang D; Yang H; Huynh D; Velazquez L; Figueroa KP
Brain; 2005 Oct; 128(Pt 10):2297-303. PubMed ID: 16000334
[TBL] [Abstract][Full Text] [Related]
14. GSTA1, GSTO1 and GSTO2 gene polymorphisms in Italian asthma patients.
Polimanti R; Piacentini S; Moscatelli B; Pellicciotti L; Manfellotto D; Fuciarelli M
Clin Exp Pharmacol Physiol; 2010 Aug; 37(8):870-2. PubMed ID: 20374258
[TBL] [Abstract][Full Text] [Related]
15. Can ataxin-2 be down-regulated by allele-specific de novo DNA methylation in SCA2 patients?
Bauer PO; Zumrova A; Matoska V; Mitsui K; Goetz P
Med Hypotheses; 2004; 63(6):1018-23. PubMed ID: 15504570
[TBL] [Abstract][Full Text] [Related]
16. Association between arsenic metabolism gene polymorphisms and arsenic-induced skin lesions in individuals exposed to high-dose inorganic arsenic in northwest China.
Luo L; Li Y; Gao Y; Zhao L; Feng H; Wei W; Qiu C; He Q; Zhang Y; Fu S; Sun D
Sci Rep; 2018 Jan; 8(1):413. PubMed ID: 29323258
[TBL] [Abstract][Full Text] [Related]
17. ATXN2-AS, a gene antisense to ATXN2, is associated with spinocerebellar ataxia type 2 and amyotrophic lateral sclerosis.
Li PP; Sun X; Xia G; Arbez N; Paul S; Zhu S; Peng HB; Ross CA; Koeppen AH; Margolis RL; Pulst SM; Ashizawa T; Rudnicki DD
Ann Neurol; 2016 Oct; 80(4):600-15. PubMed ID: 27531668
[TBL] [Abstract][Full Text] [Related]
18. Progression of early features of spinocerebellar ataxia type 2 in individuals at risk: a longitudinal study.
Velázquez-Pérez L; Rodríguez-Labrada R; Canales-Ochoa N; Montero JM; Sánchez-Cruz G; Aguilera-Rodríguez R; Almaguer-Mederos LE; Laffita-Mesa JM
Lancet Neurol; 2014 May; 13(5):482-9. PubMed ID: 24657153
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial complex I gene variant associated with early age at onset in spinocerebellar ataxia type 2.
Simon DK; Zheng K; Velázquez L; Santos N; Almaguer L; Figueroa KP; Pulst SM
Arch Neurol; 2007 Jul; 64(7):1042-4. PubMed ID: 17620498
[TBL] [Abstract][Full Text] [Related]
20. Factors associated with ATXN2 CAG/CAA repeat intergenerational instability in Spinocerebellar ataxia type 2.
Almaguer-Mederos LE; Mesa JML; González-Zaldívar Y; Almaguer-Gotay D; Cuello-Almarales D; Aguilera-Rodríguez R; Falcón NS; Gispert S; Auburger G; Velázquez-Pérez L
Clin Genet; 2018 Oct; 94(3-4):346-350. PubMed ID: 29756284
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
