The DOI matches its Crossref record; 263 of the 269 references it cites were found in a registry or an index.
Chapter 1 Folate‐Mediated One‐Carbon Metabolism
Abstract
Tetrahydrofolate (THF) polyglutamates are a family of cofactors that carry and chemically activate one-carbon units for biosynthesis. THF-mediated one-carbon metabolism is a metabolic network of interdependent biosynthetic pathways that is compartmentalized in the cytoplasm, mitochondria, and nucleus. One-carbon metabolism in the cytoplasm is required for the synthesis of purines and thymidylate and the remethylation of homocysteine to methionine. One-carbon metabolism in the mitochondria is required for the synthesis of formylated methionyl-tRNA; the catabolism of choline, purines, and histidine; and the interconversion of serine and glycine. Mitochondria are also the primary source of one-carbon units for cytoplasmic metabolism. Increasing evidence indicates that folate-dependent de novo thymidylate biosynthesis occurs in the nucleus of certain cell types. Disruption of folate-mediated one-carbon metabolism is associated with many pathologies and developmental anomalies, yet the biochemical mechanisms and causal metabolic pathways responsible for the initiation and/or progression of folate-associated pathologies have yet to be established. This chapter focuses on our current understanding of mammalian folate-mediated one-carbon metabolism, its cellular compartmentation, and knowledge gaps that limit our understanding of one-carbon metabolism and its regulation.
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“Folate is a crucial constituent of one‐carbon metabolism (OCM) and is important for biosynthesis of purines and thymidylate, and remethylation of homocysteine to methionine (Fox & Stover, 2008; Li, Vijayanathan, Gulinello, & Cole, 2010).”
From Brain structure, working memory and response inhibition in childhood leukemia survivors (2017) · cites this paper as Fox & Stover, 2008
In the citing paper
“Since MTX is delivered through all phases of ALL treatment, folate metabolism may be altered for an extended period, possibly resulting in build‐up of homocysteine (Fox & Stover, 2008; Krull et al., 2016; Li et al., 2010; Steinfeld et al., 2009), and/or secondary metabolic alterations (van der Plas et al., 2015; Steinfeld et al., 2009; Strain et al., 2013).”
From Brain structure, working memory and response inhibition in childhood leukemia survivors (2017) · cites this paper as Fox & Stover, 2008
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Metadata
- Authors
- Fox, J. T., & Stover, P. J.
- Affiliations
- Cornell University (US)
- Venue
- Vitamins & Hormones
- Publisher
- Elsevier
- Published
- 2008
- Volume
- 79
- Pages
- 1-44
- ISSN
- 0083-6729 (ISSN-L)
- OpenAlex
- W3975443
- Cited by
- 402
- References
- 269
- Citations by year
- 2026: 19 · 2025: 24 · 2024: 22 · 2023: 17 · 2022: 20 · 2021: 25 · 2020: 25 · 2019: 34 · 2018: 25 · 2017: 36 · 2016: 35 · 2015: 16 · 2014: 16 · 2013: 26 · 2012: 18
- FWCI
- 62.82
- Type
- book chapter
- Language
- en
- Open access
- closed
- Locations
- Vitamins and hormones (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (DK58144)
- Topics
- Health Sciences › Nursing › Nutrition and Dietetics › Folate and B Vitamins Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Molecular Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Keywords
- folic acid, one-carbon metabolism, thymidylate synthesis, purine biosynthesis, homocysteine remethylation, methionine biosynthesis, histidine catabolism, mitochondrial metabolism, folate deficiency, developmental anomalies
- MeSH terms
- Animals, Cell Nucleus, Cytoplasm, Folic Acid, Mammals, Mitochondria, One-Carbon Group Transferases
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