5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference13 articles.
1. Spina bifida, 677T→C mutation, and role of folate
2. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
3. Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification
4. Relation Between Folate Status, a Common Mutation in Methylenetetrahydrofolate Reductase, and Plasma Homocysteine Concentrations
Cited by 172 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Non-syndromic Cleft Lip and Palate Patients of the North Indian Population and the Association of Methylenetetrahydrofolate Reductase Gene;Cureus;2024-07-18
2. Relationship between the methylenetetrahydrofolate reductase (MTHFR) rs1801133 SNP and serum homocysteine levels of Zhuang hypertensive patients in the central region of Guangxi;Clinical Hypertension;2023-10-01
3. Association of methylenetetrahydrofolate reductase ( MTHFR ) gene polymorphisms (C677T and A1298C) with thyroid dysfunction: A meta-analysis and trial sequential analysis;Archives of Endocrinology and Metabolism;2022-06-27
4. Genetic Susceptibility to Neural Tube Defect (NTD) and Hyperhomocysteinemia;Homocysteine Metabolism in Health and Disease;2022
5. Methylenetetrahydrofolate (MTHFR), the One-Carbon Cycle, and Cardiovascular Risks;Nutrients;2021-12-20
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3