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Frontiers in Genetics|May 27, 2021
Gene Environment Interactions in the Etiology of Neural Tube DefectsRichard H Finnell, Carlo Donato Caiaffa, Sung-Eun Kim, et al.Reproductive Toxicology (Elmsford, N.Y.)|August 14, 2018
Combining mouse embryonic stem cells and zebrafish embryos to evaluate developmental toxicity of chemical exposureJavier Conde-Vancells, Mercedes Vazquez-Chantada, Catherine W McCollum, et al.Epigenetics|January 25, 2021
Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defectsTian Tian, Xinyuan Lai, Kuanhui Xiang, et al.Journal of Pediatric Surgery|July 15, 2019
Heritable spina bifida in sheep: A potential model for fetal repair of myelomeningoceleJohn W Steele, Sharon Bayliss, John Bayliss, et al.Blood|February 25, 2011
A mouse model of hereditary folate malabsorption: deletion of the PCFT gene leads to systemic folate deficiencyKonstantin V Salojin, Robert M Cabrera, Weimei Sun, et al.Pediatric Research|December 3, 2009
Autoantibodies to folate receptor alpha during early pregnancy and risk of oral clefts in DenmarkCamilla Bille, Dorthe Almind Pedersen, Anne-Marie Nybo Andersen, et al.Journal of Medical Genetics|August 22, 2020
<i>CIC de novo</i> loss of function variants contribute to cerebral folate deficiency by downregulating <i>FOLR1</i> expressionXuanye Cao, Annika Wolf, Sung-Eun Kim, et al.Frontiers in Molecular Neuroscience|June 3, 2024
Dolutegravir induces FOLR1 expression during brain organoid developmentCarlo Donato Caiaffa, Gabriel Tukeman, Christian Zevallos Delgado, et al.Human Mutation|September 2, 2022
CIC missense variants contribute to susceptibility for spina bifidaXiao Han, Xuanye Cao, Vanessa Aguiar-Pulido, et al.Proceedings of the National Academy of Sciences of the United States of America|April 19, 2018
Formate rescues neural tube defects caused by mutations in <i>Slc25a32</i>Jimi Kim, Yunping Lei, Jin Guo, et al.Pageof 5