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Transplantation 104 , 10191025 (2020)

[DOI] [PubMed] [Google Scholar] 66.Davizon-Castillo P, McMahon B, Aguila S, Bark D, Ashworth K, Allawzi A, Campbell RA, Montenont E, Nemkov T, D'Alessandro A, Clendenen N, Shih L, Sanders NA, Higa K, Cox A, Padilla-Romo Z, Hernandez G, Wartchow E, Trahan GD, Nozik-Grayck E, et al

There is a great deal of evidence suggesting that DNA methylation defects are associated with ASDs, and the role of the methylenetetrahydrofolate reductase (MTHFR) gene in folate metabolism may contribute to epigenetic mechanisms that modify complex gene expression, thus causing autism

There is a C-to-T single-nucleotide polymorphism at the 718 position (rs713041) located in the 3-untranslated region of the GPX4 gene close to the predicted selenocysteine insertion sequence structure (SECIS, a region of the mRNA required for incorporation of the amino acid Sec into GPX4)

More recent investigations in animal models have focused on the survival and differentiation of implanted cells

GCH1, Guanosine triphosphate cyclohydrolase-1