95 related articles for article (PubMed ID: 26278584)
21. Association between the 8473T>C polymorphism of PTGS2 and prostate cancer risk: a metaanalysis including 24,716 subjects.
Yang X; Li B; Si T; Liu Y; Guo Z
Onkologie; 2013; 36(4):182-6. PubMed ID: 23548966
[TBL] [Abstract][Full Text] [Related]
22. Association between the MDR1 gene variant C3435T and risk of leukaemia: a meta-analysis.
Zhang BB; Xuan C; Deng KF; Wu N; Lun LM
Eur J Cancer Care (Engl); 2013 Sep; 22(5):617-25. PubMed ID: 23731124
[TBL] [Abstract][Full Text] [Related]
23. FCGR2A rs1801274 polymorphism is associated with risk of childhood-onset idiopathic (immune) thrombocytopenic purpura: evidence from a meta-analysis.
Wang D; Hu SL; Cheng XL; Yang JY
Thromb Res; 2014 Dec; 134(6):1323-7. PubMed ID: 25457587
[TBL] [Abstract][Full Text] [Related]
24. Screening of VCP mutations in Chinese amyotrophic lateral sclerosis patients.
Zou ZY; Liu MS; Li XG; Cui LY
Neurobiol Aging; 2013 May; 34(5):1519.e3-4. PubMed ID: 23102936
[TBL] [Abstract][Full Text] [Related]
25. Association of P2X7 receptor gene polymorphisms with sporadic Parkinson's disease in a Han Chinese population.
Liu H; Han X; Li Y; Zou H; Xie A
Neurosci Lett; 2013 Jun; 546():42-5. PubMed ID: 23648388
[TBL] [Abstract][Full Text] [Related]
26. Role of toll-like receptors gene polymorphism in hepatocellular carcinoma.
Lin W; Chen J; Zhu B; Xu X; Dong Z
J Recept Signal Transduct Res; 2014 Oct; 34(5):345-7. PubMed ID: 24641696
[TBL] [Abstract][Full Text] [Related]
27. [Polymorphisms of complement factor genes and age-related macular degeneration in a German population].
Baatz H; Poupel L; Coudert M; Sennlaub F; Combadiere C
Klin Monbl Augenheilkd; 2009 Aug; 226(8):654-8. PubMed ID: 19399715
[TBL] [Abstract][Full Text] [Related]
28. Association study of SCARB2 rs6812193 polymorphism with Parkinson's disease in Han Chinese.
Chen S; Zhang Y; Chen W; Wang Y; Liu J; Rong TY; Ma JF; Wang G; Zhang J; Pan J; Xiao Q; Chen SD
Neurosci Lett; 2012 May; 516(1):21-3. PubMed ID: 22465138
[TBL] [Abstract][Full Text] [Related]
29. [Genodermatoses].
Happle R; Traupe H
Hautarzt; 2011 Feb; 62(2):80-1. PubMed ID: 21312019
[No Abstract] [Full Text] [Related]
30. CSTB null mutation associated with microcephaly, early developmental delay, and severe dyskinesia.
Mancini GM; Schot R; de Wit MC; de Coo RF; Oostenbrink R; Bindels-de Heus K; Berger LP; Lequin MH; de Vries FA; Wilke M; van Slegtenhorst MA
Neurology; 2016 Mar; 86(9):877-8. PubMed ID: 26843564
[No Abstract] [Full Text] [Related]
31. De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.
Zou ZY; Cui LY; Sun Q; Li XG; Liu MS; Xu Y; Zhou Y; Yang XZ
Neurobiol Aging; 2013 Apr; 34(4):1312.e1-8. PubMed ID: 23046859
[TBL] [Abstract][Full Text] [Related]
32. Lack of association between CCND1 G870A polymorphism and risk of esophageal squamous cell carcinoma.
Yu C; Lu W; Tan W; Xing D; Liang G; Miao X; Lin D
Cancer Epidemiol Biomarkers Prev; 2003 Feb; 12(2):176. PubMed ID: 12582032
[No Abstract] [Full Text] [Related]
33. A meta-analysis of association of vitamin D receptor BsmI gene polymorphism with the risk of type 1 diabetes mellitus.
Qin WH; Wang HX; Qiu JL; Huang XB; Huang Y; Wu NR; Liang HS
J Recept Signal Transduct Res; 2014 Oct; 34(5):372-7. PubMed ID: 24665917
[TBL] [Abstract][Full Text] [Related]
34. Association of MDR1 C3435T and C1236T single nucleotide polymorphisms with male factor infertility.
Aydos SE; Karadağ A; Özkan T; Altınok B; Bunsuz M; Heidargholizadeh S; Aydos K; Sunguroğlu A
Genet Mol Res; 2015 Jun; 14(2):6330-9. PubMed ID: 26125837
[TBL] [Abstract][Full Text] [Related]
35. Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans.
Brambilla P; Esposito F; Lindstrom E; Sorosina M; Giacalone G; Clarelli F; Rodegher M; Colombo B; Moiola L; Ghezzi A; Capra R; Collimedaglia L; Coniglio G; Celius EG; Galimberti D; Sørensen PS; Martinelli V; Oturai AB; Harbo HF; Hillert J; Comi G; Martinelli-Boneschi F
Neurosci Lett; 2012 Nov; 530(2):155-60. PubMed ID: 23069673
[TBL] [Abstract][Full Text] [Related]
36. Adolescent idiopathic scoliosis and the single-nucleotide polymorphism of the growth hormone receptor and IGF-1 genes.
Yang Y; Wu Z; Zhao T; Wang H; Zhao D; Zhang J; Wang Y; Ding Y; Qiu G
Orthopedics; 2009 Jun; 32(6):411. PubMed ID: 19634821
[TBL] [Abstract][Full Text] [Related]
37. Cytochrome P450 1A1 polymorphism and childhood leukemia: an analysis of matched pairs case-control genotype data.
Selvin S
Cancer Epidemiol Biomarkers Prev; 2004 Aug; 13(8):1371-4. PubMed ID: 15298960
[TBL] [Abstract][Full Text] [Related]
38. A family-based association study of dopamine receptor D4 and mental retardation in Qinba region of China.
Zhang K; Zhang M; He H; Zhang J; Chi W; Guo Y; Huang S; Zheng Z; Zhang F; Gao X
Neurosci Lett; 2012 May; 516(1):1-4. PubMed ID: 22366260
[TBL] [Abstract][Full Text] [Related]
39. [Genetics of atopic eczema. An update].
Rodríguez E; Weidinger S
Hautarzt; 2015 Feb; 66(2):84-9. PubMed ID: 25648547
[TBL] [Abstract][Full Text] [Related]
40. Glutathione S-transferase T1 and M1 polymorphisms are associated with lung cancer risk in a gender-specific manner.
Pan C; Zhu G; Yan Z; Zhou Y; Liu Z
Oncol Res Treat; 2014; 37(4):164-9. PubMed ID: 24732639
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
