124 related articles for article (PubMed ID: 26233570)
1. Association between genetic polymorphisms and deep vein thrombosis in a Chinese population.
Jiang J; Jiao Y; Ding X; Zhang B
Thromb Res; 2015 Sep; 136(3):687-9. PubMed ID: 26233570
[No Abstract] [Full Text] [Related]
2. C9orf72 mutations may be rare in frontotemporal lobar degeneration patients in India.
Mukherjee O; Das G; Sen S; Dutt A; Alladi S; Ghosh A
Amyotroph Lateral Scler Frontotemporal Degener; 2015; 17(1-2):151-3. PubMed ID: 26465714
[No Abstract] [Full Text] [Related]
3. TUBA4A may not be a significant genetic factor in Chinese ALS patients.
Li J; He J; Tang L; Chen L; Xu L; Ma Y; Zhang N; Fan D
Amyotroph Lateral Scler Frontotemporal Degener; 2015; 17(1-2):148-50. PubMed ID: 26465396
[TBL] [Abstract][Full Text] [Related]
4. Association of polymorphisms in X-ray repair cross complementing 1 gene and risk of esophageal squamous cell carcinoma in a Chinese population.
Yun YX; Dai LP; Wang P; Wang KJ; Zhang JY; Xie W
Biomed Res Int; 2015; 2015():509215. PubMed ID: 25710005
[TBL] [Abstract][Full Text] [Related]
5. Association between NAD(P)H oxidase p22phox gene variants and acute myocardial infarction in a Han Chinese population.
Xu H; Ma S; Tang FY; Chen Y; Zhou H; Chen M; Wang B; Liu X; Xie X
Herz; 2016 Aug; 41(5):428-34. PubMed ID: 26660092
[TBL] [Abstract][Full Text] [Related]
6. The G534E-polymorphism of the gene encoding the factor VII-activating protease is a risk factor for venous thrombosis and recurrent events.
Ahmad-Nejad P; Dempfle CE; Weiss C; Bugert P; Borggrefe M; Neumaier M
Thromb Res; 2012 Sep; 130(3):441-4. PubMed ID: 22421107
[TBL] [Abstract][Full Text] [Related]
7. The rs3807989 G/A polymorphism in CAV1 is associated with the risk of atrial fibrillation in Chinese Han populations.
Liu Y; Ni B; Lin Y; Chen XG; Chen M; Hu Z; Zhang F
Pacing Clin Electrophysiol; 2015 Feb; 38(2):164-70. PubMed ID: 25196315
[TBL] [Abstract][Full Text] [Related]
8. Association of the hsa-mir-499 (rs3746444) polymorphisms with gastric cancer risk in the Chinese population.
Wu XJ; Mi YY; Yang H; Hu AK; Li C; Li XD; Zhang QG
Onkologie; 2013; 36(10):573-6. PubMed ID: 24107911
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Lack of Association between MDR1 G2677T/A Polymorphism and Leukemia Risk: An Updated Meta-Analysis.
Ma L; Yang H; Ruan L
Oncol Res Treat; 2015; 38(7-8):383-4. PubMed ID: 26278584
[No Abstract] [Full Text] [Related]
11. NR4A2 genetic variation and Parkinson's disease: Evidence from a systematic review and meta-analysis.
Liu H; Liu H; Li T; Cui J; Fu Y; Ren J; Sun X; Jiang P; Yu S; Li C
Neurosci Lett; 2017 May; 650():25-32. PubMed ID: 28385514
[TBL] [Abstract][Full Text] [Related]
12. Methylenetetrahydrofolate reductase polymorphisms and susceptibility to acute lymphoblastic leukemia in a Chinese population: a meta-analysis.
Xiao Y; Deng TR; Su CL; Shang Z
Oncol Res Treat; 2014; 37(10):576-82. PubMed ID: 25342508
[TBL] [Abstract][Full Text] [Related]
13. Biomarkers for arterial and venous thrombotic disorders.
Mannhalter C
Hamostaseologie; 2014; 34(2):115-20, 122-6, 128-30, passim. PubMed ID: 24819458
[TBL] [Abstract][Full Text] [Related]
14. Association between single nucleotide polymorphisms of asporin (ASPN) and BMP5 with the risk of knee osteoarthritis in a Chinese Han population.
Liang W; Gao B; Xu G; Weng D; Xie M; Qian Y
Cell Biochem Biophys; 2014 Dec; 70(3):1603-8. PubMed ID: 25030405
[TBL] [Abstract][Full Text] [Related]
15. Genetic variants in Cell Adhesion Molecule 1 (CADM1): a validation study of a novel endothelial cell venous thrombosis risk factor.
de Haan HG; Bezemer ID; Vossen CY; van Hylckama Vlieg A; Böehringer S; Hasstedt SJ; Levy S; Rosendaal FR; Bovill EG
Thromb Res; 2014 Dec; 134(6):1186-92. PubMed ID: 25306186
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Lack of association between PICALM rs3851179 polymorphism and Alzheimer's disease in Chinese population and APOEε4-negative subgroup.
Liu G; Zhang L; Feng R; Liao M; Jiang Y; Chen Z; Zhao B; Li K
Neurobiol Aging; 2013 Apr; 34(4):1310.e9-10. PubMed ID: 23040034
[TBL] [Abstract][Full Text] [Related]
18. Association of transforming growth factor-β1 T869C, G915C, and C509T gene polymorphisms with rheumatoid arthritis risk.
Zhou TB; Zhao HL; Fang SL; Drummen GP
J Recept Signal Transduct Res; 2014 Dec; 34(6):469-75. PubMed ID: 24840097
[TBL] [Abstract][Full Text] [Related]
19. Association of F11 polymorphism rs2289252 with deep vein thrombosis and related phenotypes in population of Latvia.
Rovite V; Maurins U; Megnis K; Vaivade I; Pečulis R; Rits J; Prave S; Klovins J
Thromb Res; 2014 Sep; 134(3):659-63. PubMed ID: 25091233
[TBL] [Abstract][Full Text] [Related]
20. Should the factor V Leiden mutation be screened among ethnic Malays with venous thrombosis?
Ng HJ; Koay ES; Abdul Ghafar A; Lim LC; Lee LH
Thromb Res; 2010 May; 125(5):471-2. PubMed ID: 19732941
[No Abstract] [Full Text] [Related]
[Next] [New Search]