Ge YL - Search Results

1

[DUOX2 mutations in children with congenital hypothyroidism].

Chai J, Yang XL, Guo MZ, Liu L, Liu SG, Yan SL, Ge YL. Chai J, et al. Among authors: ge yl. Zhongguo Dang Dai Er Ke Za Zhi. 2015 Jan;17(1):40-4. Zhongguo Dang Dai Er Ke Za Zhi. 2015. PMID: 25616291 Free article. Chinese.

2

Family-based association study between monoamine oxidase A (MAOA) gene promoter VNTR polymorphism and Tourette's syndrome in Chinese Han population.

Liu S, Wang X, Xu L, Zheng L, Ge Y, Ma X. Liu S, et al. Neurocase. 2015 Feb;21(1):106-8. doi: 10.1080/13554794.2013.873061. Epub 2014 Jan 14. Neurocase. 2015. PMID: 24422758

3

Support of positive association in family-based genetic analysis between COL27A1 and Tourette syndrome.

Liu S, Yu X, Xu Q, Cui J, Yi M, Zhang X, Ge Y, Ma X. Liu S, et al. Sci Rep. 2015 Aug 3;5:12687. doi: 10.1038/srep12687. Sci Rep. 2015. PMID: 26235311 Free PMC article.

4

Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis.

Liu S, Chai J, Zheng G, Li H, Lu D, Ge Y. Liu S, et al. J Clin Res Pediatr Endocrinol. 2016 Mar 5;8(1):21-5. doi: 10.4274/jcrpe.2456. Epub 2015 Dec 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 26757609 Free PMC article.

5

Identification and characterization of novel PAX8 mutations in Congenital Hypothyroidism(CH) in a Chinese population.

Liu S, Wang X, Zou H, Ge Y, Wang F, Wang Y, Yan S, Xia H, Xing M. Liu S, et al. Oncotarget. 2017 Jan 31;8(5):8707-8716. doi: 10.18632/oncotarget.14419. Oncotarget. 2017. PMID: 28060725 Free PMC article.

6

Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H₂O₂ Generation.

Liu S, Han W, Zang Y, Zang H, Wang F, Jiang P, Wei H, Liu X, Wang Y, Ma X, Ge Y. Liu S, et al. Front Endocrinol (Lausanne). 2019 Aug 2;10:526. doi: 10.3389/fendo.2019.00526. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31428054 Free PMC article.

7

Mutations in ASH1L confer susceptibility to Tourette syndrome.

Liu S, Tian M, He F, Li J, Xie H, Liu W, Zhang Y, Zhang R, Yi M, Che F, Ma X, Zheng Y, Deng H, Wang G, Chen L, Sun X, Xu Y, Wang J, Zang Y, Han M, Wang X, Guan H, Ge Y, Wu C, Wang H, Liang H, Li H, Ran N, Yang Z, Huang H, Wei Y, Zheng X, Sun X, Feng X, Zheng L, Zhu T, Luo W, Chen Q, Yan Y, Huang Z, Jing Z, Guo Y, Zhang X, Schaaf CP, Xing J, Wang C, Yu F, Guan JS. Liu S, et al. Mol Psychiatry. 2020 Feb;25(2):476-490. doi: 10.1038/s41380-019-0560-8. Epub 2019 Oct 31. Mol Psychiatry. 2020. PMID: 31673123

8

Decreased expression of the DBC2 gene and its clinicopathological significance in breast cancer: correlation with aberrant DNA methylation.

Han L, Hou L, Song J, Lin D, Wu L, Ge Y, Ma Z. Han L, et al. Biotechnol Lett. 2013 Aug;35(8):1175-81. doi: 10.1007/s10529-013-1190-x. Epub 2013 Apr 2. Biotechnol Lett. 2013. PMID: 23546941

9

[Effect of siRNA transfection targeting VEGF gene on proliferation and apoptosis of human breast cancer cells].

Zhang X, Xu WH, Ge YL, Hou L, Li Q. Zhang X, et al. Among authors: ge yl. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2007 Jan;23(1):14-7. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2007. PMID: 17210097 Chinese.

10

PUFA diets alter the microRNA expression profiles in an inflammation rat model.

Zheng Z, Ge Y, Zhang J, Xue M, Li Q, Lin D, Ma W. Zheng Z, et al. Mol Med Rep. 2015 Jun;11(6):4149-57. doi: 10.3892/mmr.2015.3318. Epub 2015 Feb 9. Mol Med Rep. 2015. PMID: 25672643 Free PMC article.

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