Genetic Association between the Risk of Dental Caries and MTR Gene Polymorphism in Chinese Children.

Autor: Weilian Du, Lingzhen Liu, Fang Li, Shusen Xu

Publikováno v: Tohoku Journal of Experimental Medicine; May2024, Vol. 263 Issue 1, p63-68, 6p

[Maternal MTR gene polymorphisms and their interactions with periconceptional folic acid supplementation in relation to offspring ventricular septal defects].

Autor: Ruan XR; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha 410013 China., Sun MT; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha 410013 China., Wei JH; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha 410013 China., Luo MJ; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha 410013 China., Liu HJ; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha 410013 China., Tang JP; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha 410013 China., Li LX; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha 410013 China., Qin JB; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha 410013 China.

Publikováno v: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics [Zhongguo Dang Dai Er Ke Za Zhi] 2024 Sept 15; Vol. 26 (9), pp. 899-906.

Association of maternal MTR gene polymorphism with offspring congenital heart disease: a case-control study

Autor: Yi-huan LI, Peng HUANG, Ting-ting WANG

Publikováno v: Zhongguo gonggong weisheng, Vol 38, Iss 2, Pp 161-166 (2022)

ObjectiveTo explore the association between maternal methionine synthase (MTR) gene polymorphism and the risk of congenital heart disease (CHD) in offsprings. MethodsA case-control study was conducted among 464 biological mothers of CHD children and

Externí odkaz: https://doaj.org/article/6d2c8a90a9d9483184df5ceb13cebdeb

'Association of MTHFR and MS/MTR gene polymorphisms with congenital heart defects in North Indian population (Jammu and Kashmir): a case–control study encompassing meta-analysis and trial sequential analysis'

Autor: Jyotdeep Kour Raina, Rakesh Kumar Panjaliya, Vikas Dogra, Sushil Sharma, Anupriya, Parvinder Kumar

Publikováno v: BMC Pediatrics, Vol 22, Iss 1, Pp 1-21 (2022)

Abstract Background The risk of Congenital Heart Defects (CHD) is greatly influenced by variants within the genes involved in folate-homocysteine metabolism. Polymorphism in MTHFR (C677T and G1793A) and MS/MTR (A2756G) genes increases the risk of dev

Externí odkaz: https://doaj.org/article/db9320a7f18e4d0ab6a624b5c7c25478

母亲MTR基因多态性及其与围孕期叶酸补充的 交互作用与子代室间隔缺损的关联研究. (Chinese)

Autor: 阮霄睿, 孙梦婷, 魏剑晖, 罗曼君, 刘涵君, 唐嘉鹏, 李柳萱, 秦家碧

Publikováno v: Chinese Journal of Contemporary Pediatrics; Sep2024, Vol. 26 Issue 9, p899-906, 8p