81 related articles for article (PubMed ID: 21323574)
21. [Association study of the polymorphisms of monoamine oxidase A genes with schizophrenia].
Shi YZ; Wang CH; Lv LX; Wang YH; Zhang HX; Lou BY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):457-9. PubMed ID: 17680543
[TBL] [Abstract][Full Text] [Related]
22. Genetic susceptibility to keloid disease: transforming growth factor beta receptor gene polymorphisms are not associated with keloid disease.
Bayat A; Bock O; Mrowietz U; Ollier WE; Ferguson MW
Exp Dermatol; 2004 Feb; 13(2):120-4. PubMed ID: 15009106
[TBL] [Abstract][Full Text] [Related]
23. Polymorphisms of IL23R and Vogt-Koyanagi-Harada syndrome in a Chinese Han population.
Jiang Z; Yang P; Hou S; Li F; Zhou H
Hum Immunol; 2010 Apr; 71(4):414-7. PubMed ID: 20116410
[TBL] [Abstract][Full Text] [Related]
24. Association of CDH1 promoter polymorphism and the risk of non-syndromic orofacial clefts in a Chinese Han population.
Song Y; Zhang S
Arch Oral Biol; 2011 Jan; 56(1):68-72. PubMed ID: 20880515
[TBL] [Abstract][Full Text] [Related]
25. Association study and meta-analysis of Alzheimer's disease risk and presenilin-1 intronic polymorphism.
Rodríguez-Manotas M; Amorín-Díaz M; Cañizares-Hernández F; Ruíz-Espejo F; Martínez-Vidal S; González-Sarmiento R; Martínez-Hernández P; Cabezas-Herrera J
Brain Res; 2007 Sep; 1170():119-28. PubMed ID: 17719017
[TBL] [Abstract][Full Text] [Related]
26. [Association analysis between attention-deficit hyperactivity disorder and Val158Met polymorphism of catechol-O-methyltransferase gene].
Zhang XN; Ruan LM; Le YP; Zhang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):322-4. PubMed ID: 12903043
[TBL] [Abstract][Full Text] [Related]
27. MDR1 C3435T polymorphism in patients with breast cancer.
Turgut S; Yaren A; Kursunluoglu R; Turgut G
Arch Med Res; 2007 Jul; 38(5):539-44. PubMed ID: 17560460
[TBL] [Abstract][Full Text] [Related]
28. Association of DARS gene polymorphisms with the risk of isolated ventricular septal defects in the Chinese Han population.
Feng Y; Chen R; Mo X
Ital J Pediatr; 2016 Nov; 42(1):102. PubMed ID: 27871331
[TBL] [Abstract][Full Text] [Related]
29. Analysis of RTN4 3'UTR insertion/deletion polymorphisms in ventricular septal defect in a Chinese Han population.
Chen Y; Zhou B; Li H; Peng Y; Wang Y; Rao L
DNA Cell Biol; 2011 May; 30(5):323-7. PubMed ID: 21166502
[TBL] [Abstract][Full Text] [Related]
30. TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese Population.
Yang L; Gao X; Luo H; Huang Q; Su D; Tan X; Lu C
Genet Test Mol Biomarkers; 2017 May; 21(5):312-315. PubMed ID: 28346832
[TBL] [Abstract][Full Text] [Related]
31. Genetic analysis of the TBX3 gene promoter in ventricular septal defects.
Chen D; Qiao Y; Meng H; Pang S; Huang W; Zhang H; Yan B
Gene; 2013 Jan; 512(2):185-8. PubMed ID: 23116943
[TBL] [Abstract][Full Text] [Related]
32. First report of polymorphisms in MTRR, GATA4, VEGF, and ISL1 genes in Pakistani children with isolated ventricular septal defects (VSD).
Sarwar S; Ehsan F; Shabana ; Tahir A; Jamil M; Shahid SU; Khan A; Hasnain S
Ital J Pediatr; 2021 Mar; 47(1):70. PubMed ID: 33757570
[TBL] [Abstract][Full Text] [Related]
33. Association of TGFBR2 rs6785358 Polymorphism with Increased Risk of Congenital Ventricular Septal Defect in a Chinese Population.
Li XT; Shen CQ; Zhang R; Shi JK; Li ZH; Liu HY; Sun B; Wang K; Yan LR
Pediatr Cardiol; 2015 Oct; 36(7):1476-82. PubMed ID: 26022443
[TBL] [Abstract][Full Text] [Related]
34. Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis.
Scott AP; Laing NG; Mastaglia F; Dalakas M; Needham M; Allcock RJ
J Neuroimmunol; 2012 Sep; 250(1-2):66-70. PubMed ID: 22732452
[TBL] [Abstract][Full Text] [Related]
35. Genetic analysis of the TBX20 gene promoter region in patients with ventricular septal defects.
Qiao Y; Wanyan H; Xing Q; Xie W; Pang S; Shan J; Yan B
Gene; 2012 May; 500(1):28-31. PubMed ID: 22465533
[TBL] [Abstract][Full Text] [Related]
36. Association between ISL1 variants and susceptibility to ventricular septal defect in a Chinese cohort.
Lang J; Tian W; Sun X
Mol Diagn Ther; 2013 Apr; 17(2):101-6. PubMed ID: 23572340
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Association between polymorphisms in IL27 and risk for CHD in a Chinese population.
Zhang D; Ma M; Yang Y; Wan L; Yang Z; Lv J; Li X; Yang H; Huang P; Li L
Cardiol Young; 2016 Feb; 26(2):237-43. PubMed ID: 25662568
[TBL] [Abstract][Full Text] [Related]
39. Genetic analysis of the CITED2 gene promoter in isolated and sporadic congenital ventricular septal defects.
Zheng SQ; Chen HX; Liu XC; Yang Q; He GW
J Cell Mol Med; 2021 Feb; 25(4):2254-2261. PubMed ID: 33439552
[TBL] [Abstract][Full Text] [Related]
40. Identification of variants of
Zheng SQ; Chen HX; Liu XC; Yang Q; He GW
Am J Physiol Cell Physiol; 2021 Sep; 321(3):C443-C452. PubMed ID: 34260301
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]