144 related articles for article (PubMed ID: 23572340)
1. 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]
2. 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]
3. 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]
4. Genetic variations of ISL1 associated with human congenital heart disease in Chinese Han people.
Luo ZL; Sun H; Yang ZQ; Ma YH; Gu Y; He YQ; Wei D; Xia LB; Yang BH; Guo T
Genet Mol Res; 2014 Feb; 13(1):1329-38. PubMed ID: 24634231
[TBL] [Abstract][Full Text] [Related]
5. Genetic studies in the Pakistani population reveal novel associations with ventricular septal defects (VSDs).
Sarwar S; Shabana ; Sajjad K; Hasnain S
BMC Pediatr; 2023 Feb; 23(1):67. PubMed ID: 36759823
[TBL] [Abstract][Full Text] [Related]
6. ISL1 common variant rs1017 is not associated with susceptibility to congenital heart disease in a Chinese population.
Xue L; Wang X; Xu J; Xu X; Liu X; Hu Z; Shen H; Chen Y
Genet Test Mol Biomarkers; 2012 Jul; 16(7):679-83. PubMed ID: 22480195
[TBL] [Abstract][Full Text] [Related]
7. Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population.
Sarwar S; Shabana ; Tahir A; Liaqat Z; Naseer S; Seme RS; Mehmood S; Shahid SU; Hasnain S
Ital J Pediatr; 2022 Jul; 48(1):124. PubMed ID: 35870951
[TBL] [Abstract][Full Text] [Related]
8. Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population.
Cresci M; Vecoli C; Foffa I; Pulignani S; Ait-Ali L; Andreassi MG
Pediatr Cardiol; 2013 Apr; 34(4):938-41. PubMed ID: 23229290
[TBL] [Abstract][Full Text] [Related]
9. Rare Copy Number Variations Might Not be Involved in the Molecular Pathogenesis of PA-IVS in an Unselected Chinese Cohort.
He X; Zhang X; Jing H; Zhang X; Gao M; Chen H; Geng J; Zheng Z; Fu Q; Zhu Z; Zheng J
Pediatr Cardiol; 2019 Apr; 40(4):762-767. PubMed ID: 30868185
[TBL] [Abstract][Full Text] [Related]
10. Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD).
Radhakrishna U; Albayrak S; Zafra R; Baraa A; Vishweswaraiah S; Veerappa AM; Mahishi D; Saiyed N; Mishra NK; Guda C; Ali-Fehmi R; Bahado-Singh RO
PLoS One; 2019; 14(3):e0200229. PubMed ID: 30897084
[TBL] [Abstract][Full Text] [Related]
11. Genetic analysis of an enhancer of the NKX2-5 gene in ventricular septal defects.
Qin X; Xing Q; Ma L; Meng H; Liu Y; Pang S; Yan B
Gene; 2012 Oct; 508(1):106-9. PubMed ID: 22824467
[TBL] [Abstract][Full Text] [Related]
12. ISL1 loss-of-function mutation contributes to congenital heart defects.
Ma L; Wang J; Li L; Qiao Q; Di RM; Li XM; Xu YJ; Zhang M; Li RG; Qiu XB; Li X; Yang YQ
Heart Vessels; 2019 Apr; 34(4):658-668. PubMed ID: 30390123
[TBL] [Abstract][Full Text] [Related]
13. NOTCH1 Gene MicroRNA Target Variation and Ventricular Septal Defect Risk.
Ji L; Hou H; Zhu K; Liu X; Liu Y; Wang Q; Li J; Liu H; Zhang Q; Lv J; Alexander R; Wang W; Li D
OMICS; 2019 Jan; 23(1):28-35. PubMed ID: 30629480
[TBL] [Abstract][Full Text] [Related]
14. [Association between two SNPs of ISL1 gene and congenital heart disease in children].
Mu SY; Zhang HY
Zhongguo Dang Dai Er Ke Za Zhi; 2013 Oct; 15(10):822-6. PubMed ID: 24131831
[TBL] [Abstract][Full Text] [Related]
15. Two novel and functional DNA sequence variants within an upstream enhancer of the human NKX2-5 gene in ventricular septal defects.
Huang W; Meng H; Qiao Y; Pang S; Chen D; Yan B
Gene; 2013 Jul; 524(2):152-5. PubMed ID: 23644027
[TBL] [Abstract][Full Text] [Related]
16. Association of ISL1 polymorphisms and eosinophilic levels among otitis media patients.
Kondyarpu A; Ray CS; Panda KC; Biswal NC; Ramchander PV
J Clin Lab Anal; 2021 Mar; 35(3):e23702. PubMed ID: 33476445
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Presenilin-1 polymorphisms are not relevant in susceptibility to ventricular septal defect: a case-control study.
Chen Y; Li H; Zhou B; Peng Y; Zheng Q; Rao L
DNA Cell Biol; 2011 Aug; 30(8):565-8. PubMed ID: 21323574
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]