109 related articles for article (PubMed ID: 24572589)
21. Lack of association between IL-1β, TNF-α, and IL-10 gene polymorphisms and sporadic Parkinson's disease in an Italian cohort.
Pascale E; Passarelli E; Purcaro C; Vestri AR; Fakeri A; Guglielmi R; Passarelli F; Meco G
Acta Neurol Scand; 2011 Sep; 124(3):176-81. PubMed ID: 20880267
[TBL] [Abstract][Full Text] [Related]
22. Novel and functional sequence variants within the TBX2 gene promoter in ventricular septal defects.
Pang S; Liu Y; Zhao Z; Huang W; Chen D; Yan B
Biochimie; 2013 Sep; 95(9):1807-9. PubMed ID: 23727221
[TBL] [Abstract][Full Text] [Related]
23. Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.
Grimes DA; Han F; Panisset M; Racacho L; Xiao F; Zou R; Westaff K; Bulman DE
Mov Disord; 2006 Jul; 21(7):906-9. PubMed ID: 16532445
[TBL] [Abstract][Full Text] [Related]
24. Genetic analysis of the promoter region of the GATA4 gene in patients with ventricular septal defects.
Wu G; Shan J; Pang S; Wei X; Zhang H; Yan B
Transl Res; 2012 May; 159(5):376-82. PubMed ID: 22500510
[TBL] [Abstract][Full Text] [Related]
25. Functional genetic variants within the SIRT2 gene promoter in type 2 diabetes mellitus.
Liu T; Yang W; Pang S; Yu S; Yan B
Diabetes Res Clin Pract; 2018 Mar; 137():200-207. PubMed ID: 29371109
[TBL] [Abstract][Full Text] [Related]
26. Polymorphism in the P-glycoprotein drug transporter MDR1 gene: a possible link between environmental and genetic factors in Parkinson's disease.
Droździk M; Białecka M; Myśliwiec K; Honczarenko K; Stankiewicz J; Sych Z
Pharmacogenetics; 2003 May; 13(5):259-63. PubMed ID: 12724617
[TBL] [Abstract][Full Text] [Related]
27. Novel and functional DNA sequence variants within the GATA5 gene promoter in ventricular septal defects.
Shan JP; Wang XL; Qiao YG; Wan Yan HX; Huang WH; Pang SC; Yan B
World J Pediatr; 2014 Nov; 10(4):348-53. PubMed ID: 25515806
[TBL] [Abstract][Full Text] [Related]
28. Identification of a risk haplotype of the alpha-synuclein gene in Japanese with sporadic Parkinson's disease.
Kobayashi H; Ujike H; Hasegawa J; Yamamoto M; Kanzaki A; Sora I
Mov Disord; 2006 Dec; 21(12):2157-64. PubMed ID: 17078049
[TBL] [Abstract][Full Text] [Related]
29. Uptake of cardiovascular drugs into the human heart: expression, regulation, and function of the carnitine transporter OCTN2 (SLC22A5).
Grube M; Meyer zu Schwabedissen HE; Präger D; Haney J; Möritz KU; Meissner K; Rosskopf D; Eckel L; Böhm M; Jedlitschky G; Kroemer HK
Circulation; 2006 Feb; 113(8):1114-22. PubMed ID: 16490820
[TBL] [Abstract][Full Text] [Related]
30. ABCB1: the role in Parkinson's disease and pharmacokinetics of antiparkinsonian drugs.
Vautier S; Fernandez C
Expert Opin Drug Metab Toxicol; 2009 Nov; 5(11):1349-58. PubMed ID: 19663741
[TBL] [Abstract][Full Text] [Related]
31. HSPA5 promoter polymorphisms and risk of Parkinson's disease in Taiwan.
Chen CM; Wu YR; Hu FJ; Chen YC; Chuang TJ; Cheng YF; Lee-Chen GJ
Neurosci Lett; 2008 Apr; 435(3):219-22. PubMed ID: 18343577
[TBL] [Abstract][Full Text] [Related]
32. 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. PubMed ID: 17174426
[TBL] [Abstract][Full Text] [Related]
33. Associations between the functional polymorphisms in the ABCB1 transporter gene and colorectal cancer risk: a case-control study in Turkish population.
Özhan G; Kara M; Sari FM; Yanar HT; Ercan G; Alpertunga B
Toxicol Mech Methods; 2013 May; 23(4):235-9. PubMed ID: 23193993
[TBL] [Abstract][Full Text] [Related]
34. A missense mutation in ABCB4 gene involved in progressive familial intrahepatic cholestasis type 3 leads to a folding defect that can be rescued by low temperature.
Delaunay JL; Durand-Schneider AM; Delautier D; Rada A; Gautherot J; Jacquemin E; Aït-Slimane T; Maurice M
Hepatology; 2009 Apr; 49(4):1218-27. PubMed ID: 19185004
[TBL] [Abstract][Full Text] [Related]
35. Genetic and Functional Sequence Variants of the SIRT3 Gene Promoter in Myocardial Infarction.
Yin X; Pang S; Huang J; Cui Y; Yan B
PLoS One; 2016; 11(4):e0153815. PubMed ID: 27078640
[TBL] [Abstract][Full Text] [Related]
36. Genetic and functional analysis of the TBX3 gene promoter in indirect inguinal hernia.
Zhao Z; Tian W; Wang L; Wang H; Qin X; Xing Q; Pang S; Yan B
Gene; 2015 Jan; 554(1):101-4. PubMed ID: 25455105
[TBL] [Abstract][Full Text] [Related]
37. Genetic analysis of NFE2L2 promoter variation in Taiwanese Parkinson's disease.
Chen YC; Wu YR; Wu YC; Lee-Chen GJ; Chen CM
Parkinsonism Relat Disord; 2013 Feb; 19(2):247-50. PubMed ID: 23176750
[TBL] [Abstract][Full Text] [Related]
38. The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications.
Bialecka M; Kurzawski M; Klodowska-Duda G; Opala G; Tan EK; Drozdzik M
Pharmacogenet Genomics; 2008 Sep; 18(9):815-21. PubMed ID: 18698234
[TBL] [Abstract][Full Text] [Related]
39. Correlation of tau gene polymorphism with age at onset of Parkinson's disease.
Kobayashi H; Ujike H; Hasegawa J; Yamamoto M; Kanzaki A; Sora I
Neurosci Lett; 2006 Sep; 405(3):202-6. PubMed ID: 16876320
[TBL] [Abstract][Full Text] [Related]
40. Interaction between ABCB1 and professional exposure to organochlorine insecticides in Parkinson disease.
Dutheil F; Beaune P; Tzourio C; Loriot MA; Elbaz A
Arch Neurol; 2010 Jun; 67(6):739-45. PubMed ID: 20558393
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
