Polymorphisms in maternal folate pathway genes interact with arsenic in drinking water to influence risk of myelomeningocele-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Polymorphisms in maternal folate pathway genes interact with arsenic in drinking water to influence risk of myelomeningocele

Published:2015-08-06 Issue:9 Volume:103 Page:754-762
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research Part A: Clinical and Molecular Teratology

Author:

Mazumdar Maitreyi¹²,Valeri Linda³,Rodrigues Ema G.¹²,Ibne Hasan Md Omar Sharif⁴,Hamid Rezina⁵,Paul Ligi⁶,Selhub Jacob⁶,Silva Fareesa¹,Mostofa Md Golam⁴,Quamruzzaman Quazi⁴,Rahman Mahmuder⁴,Christiani David C.²

Affiliation:

1. Department of Neurology; Boston Children's Hospital; Boston Massachusetts

2. Department of Environmental Health; Harvard T.H. Chan School of Public Health; Boston Massachusetts

3. Department of Biostatistics; Harvard T.H. Chan School of Public Health; Boston Massachusetts

4. Dhaka Community Hospital Trust; Dhaka Bangladesh

5. Bangladesh Medical College; Dhaka Bangladesh

6. Jean Mayer USDA Human Nutrition Research Center on Aging; Tufts University; Boston Massachusetts

Funder

Child Neurology Foundation

Harvard T.H. Chan School of Public Health NIEHS Center

Mentored Career Development Award from the NIEHS

National Institutes of Health

NIEHS

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference55 articles.

1. Molecular genetic analysis of Saccharomyces cerevisiae C1-tetrahydrofolate synthase mutants reveals a noncatalytic function of the ADE3 gene product and an additional folate-dependent enzyme;Barlowe;Mol Cell Biol,1990

2. Teratogenicity of sodium arsenate in rats;Beaudoin;Teratology,1974

3. Maternal exposure to arsenic, cadmium, lead, and mercury and neural tube defects in offspring;Brender;Environ Res,2006

4. A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group;Brody;Am J Hum Genet,2002

Cited by 25 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. Maternal arsenic exposure modifies associations between arsenic, folate and arsenic metabolism gene variants, and spina bifida risk: A case‒control study in Bangladesh;Environmental Research;2024-11

2. The Importance of Neurosurgical Intervention and Surgical Timing for Management of Pediatric Patients with Myelomeningoceles in Bangladesh;World Neurosurgery;2024-07

3. Genome‐wide analysis of spina bifida risk variants in a case–control study from Bangladesh;Birth Defects Research;2024-03

4. Mutational analysis of FOLR1 and FOLR2 genes in children with Myelomeningocele;Acta Biochimica Polonica;2023-10-26

5. Gene–environment interactions underlying the etiology of neural tube defects;Current Topics in Developmental Biology;2023

同舟云学术

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