These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
181 related articles for article (PubMed ID: 32947497)
1. Genetic Variant of TBX1 Gene Is Functionally Associated With Adolescent Idiopathic Scoliosis in the Chinese Population. Li Y; Wu Z; Xu L; Feng Z; Wang Y; Dai Z; Liu Z; Sun X; Qiu Y; Zhu Z Spine (Phila Pa 1976); 2021 Jan; 46(1):17-21. PubMed ID: 32947497 [TBL] [Abstract][Full Text] [Related]
2. Genetic Variant of PAX1 Gene Is Functionally Associated With Adolescent Idiopathic Scoliosis in the Chinese Population. Xu L; Sheng F; Xia C; Qin X; Tang NL; Qiu Y; Cheng JC; Zhu Z Spine (Phila Pa 1976); 2018 Apr; 43(7):492-496. PubMed ID: 29095406 [TBL] [Abstract][Full Text] [Related]
3. Genetic Variants of ABO and SOX6 are Associated With Adolescent Idiopathic Scoliosis in Chinese Han Population. Wu Z; Wang Y; Dai Z; Qiu Y; Xu L; Zhu Z Spine (Phila Pa 1976); 2019 Sep; 44(18):E1063-E1067. PubMed ID: 30994600 [TBL] [Abstract][Full Text] [Related]
4. A Novel Coding Variant in SLC39A8 Is Associated With Adolescent Idiopathic Scoliosis in Chinese Han Population. Xu L; Wang Y; Wu Z; Dai Z; Liu Z; Qiu Y; Cheng JC; Zhu Z Spine (Phila Pa 1976); 2020 Feb; 45(4):226-233. PubMed ID: 31513097 [TBL] [Abstract][Full Text] [Related]
5. Genetic Variant of GPR126 Gene is Functionally Associated With Adolescent Idiopathic Scoliosis in Chinese Population. Qin X; Xu L; Xia C; Zhu W; Sun W; Liu Z; Qiu Y; Zhu Z Spine (Phila Pa 1976); 2017 Oct; 42(19):E1098-E1103. PubMed ID: 28198779 [TBL] [Abstract][Full Text] [Related]
6. Female-Specific Susceptibility Locus in BOC and SEC16B are Associated with Adolescent Idiopathic Scoliosis. Dai Z; Wang Y; Wu Z; Feng Z; Sun X; Qiu Y; Cheng JC; Xu L; Zhu Z Spine (Phila Pa 1976); 2021 Nov; 46(22):E1178-E1184. PubMed ID: 33958541 [TBL] [Abstract][Full Text] [Related]
7. Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population. Liu G; Liu S; Li X; Chen J; Chen W; Zuo Y; Liu J; Niu Y; Lin M; Zhao S; Long B; Zhao Y; Ye Y; Zhang J; Shen J; Qiu G; Wu Z; Wu N Gene; 2019 Mar; 688():215-220. PubMed ID: 30572100 [TBL] [Abstract][Full Text] [Related]
8. A single-nucleotide polymorphism rs708567 in the IL-17RC gene is associated with a susceptibility to and the curve severity of adolescent idiopathic scoliosis in a Chinese Han population: a case-control study. Zhou S; Qiu XS; Zhu ZZ; Wu WF; Liu Z; Qiu Y BMC Musculoskelet Disord; 2012 Sep; 13():181. PubMed ID: 22999050 [TBL] [Abstract][Full Text] [Related]
9. Genetic variant of BNC2 gene is functionally associated with adolescent idiopathic scoliosis in Chinese population. Xu L; Xia C; Qin X; Sun W; Tang NL; Qiu Y; Cheng JC; Zhu Z Mol Genet Genomics; 2017 Aug; 292(4):789-794. PubMed ID: 28342042 [TBL] [Abstract][Full Text] [Related]
10. A promoter polymorphism of neurotrophin 3 gene is associated with curve severity and bracing effectiveness in adolescent idiopathic scoliosis. Qiu Y; Mao SH; Qian BP; Jiang J; Qiu XS; Zhao Q; Liu Z Spine (Phila Pa 1976); 2012 Jan; 37(2):127-33. PubMed ID: 22158057 [TBL] [Abstract][Full Text] [Related]
11. Lack of association between AKAP2 and the susceptibility of adolescent idiopathic scoliosis in the Chinese population. Xu L; Xia C; Zhu W; Feng Z; Qin X; Sun W; Qiu Y; Zhu Z BMC Musculoskelet Disord; 2017 Aug; 18(1):368. PubMed ID: 28838314 [TBL] [Abstract][Full Text] [Related]
12. A Genetic Variant of the ROBO3 Gene is Associated With Adolescent Idiopathic Scoliosis in the Chinese Population. Zhang Z; Zhang Z; Shu L; Meng Y; Ma J; Gao R; Zhou X Spine (Phila Pa 1976); 2023 Jan; 48(2):E20-E24. PubMed ID: 36149840 [TBL] [Abstract][Full Text] [Related]
13. The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population. Fei Q; Wu Z; Wang H; Zhou X; Wang N; Ding Y; Wang Y; Qiu G Spine (Phila Pa 1976); 2010 Apr; 35(9):983-8. PubMed ID: 20228709 [TBL] [Abstract][Full Text] [Related]
14. Novel Mutations in UTS2R are Associated with Adolescent Idiopathic Scoliosis in the Chinese Population. Dai Z; Wang Y; Wu Z; Feng Z; Liu Z; Qiu Y; Cheng JC; Xu L; Zhu Z Spine (Phila Pa 1976); 2021 Mar; 46(5):E288-E293. PubMed ID: 33156271 [TBL] [Abstract][Full Text] [Related]
15. Investigation of the 53 Markers in a DNA-Based Prognostic Test Revealing New Predisposition Genes for Adolescent Idiopathic Scoliosis. Xu L; Huang S; Qin X; Mao S; Qiao J; Qian BP; Qiu Y; Zhu Z Spine (Phila Pa 1976); 2015 Jul; 40(14):1086-91. PubMed ID: 25811265 [TBL] [Abstract][Full Text] [Related]
16. New Evidence Supporting the Role of FBN1 in the Development of Adolescent Idiopathic Scoliosis. Sheng F; Xia C; Xu L; Qin X; Tang NL; Qiu Y; Cheng JC; Zhu Z Spine (Phila Pa 1976); 2019 Feb; 44(4):E225-E232. PubMed ID: 30044367 [TBL] [Abstract][Full Text] [Related]
17. Lack of association between DSCAM gene polymorphisms and adolescent idiopathic scoliosis susceptibility in a Chinese Han population. Wu W; Zhu Z; Mao S; Qiu X; Qian B; Liu Z; Qiu Y J Back Musculoskelet Rehabil; 2015; 28(4):681-7. PubMed ID: 25408124 [TBL] [Abstract][Full Text] [Related]
18. A Genetic Variant of FAM46A is Associated With the Development of Adolescent Idiopathic Scoliosis in the Chinese Population. Min K; Li Y; Wu Z; Dai Z; Feng Z; Qian Z; Sun X; Qiu Y; Xu L; Zhu Z Spine (Phila Pa 1976); 2023 Sep; 48(17):1253-1258. PubMed ID: 37141460 [TBL] [Abstract][Full Text] [Related]
19. Investigating Role of IRX Family in Development of Female Adolescent Idiopathic Scoliosis: Which One Is Real Cause? Xia C; Xue B; Wang Y; Qin X; Qiu Y; Zhu Z; Xu L World Neurosurg; 2019 Jul; 127():e132-e136. PubMed ID: 30862593 [TBL] [Abstract][Full Text] [Related]
20. Genetic variant of MIR4300HG is associated with progression of adolescent idiopathic scoliosis in a Chinese population. Wang Y; Dai Z; Wu Z; Feng Z; Liu Z; Sun X; Xu L; Qiu Y; Zhu Z J Orthop Surg Res; 2021 May; 16(1):311. PubMed ID: 33985553 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]