199 related articles for article (PubMed ID: 26853819)
21. Reduced MTHFD1 activity in male mice perturbs folate- and choline-dependent one-carbon metabolism as well as transsulfuration.
Field MS; Shields KS; Abarinov EV; Malysheva OV; Allen RH; Stabler SP; Ash JA; Strupp BJ; Stover PJ; Caudill MA
J Nutr; 2013 Jan; 143(1):41-5. PubMed ID: 23190757
[TBL] [Abstract][Full Text] [Related]
22. Cell cycle regulation of folate-mediated one-carbon metabolism.
Lan X; Field MS; Stover PJ
Wiley Interdiscip Rev Syst Biol Med; 2018 Nov; 10(6):e1426. PubMed ID: 29889360
[TBL] [Abstract][Full Text] [Related]
23. Association of dietary and supplemental folate intake and polymorphisms in three FOCM pathway genes with colorectal cancer in a population-based case-control study.
Ashmore JH; Lesko SM; Muscat JE; Gallagher CJ; Berg AS; Miller PE; Hartman TJ; Lazarus P
Genes Chromosomes Cancer; 2013 Oct; 52(10):945-53. PubMed ID: 23893618
[TBL] [Abstract][Full Text] [Related]
24. Molecular mechanisms of adaptation to folate deficiency.
Ifergan I; Assaraf YG
Vitam Horm; 2008; 79():99-143. PubMed ID: 18804693
[TBL] [Abstract][Full Text] [Related]
25. MTHFD1 formyltetrahydrofolate synthetase deficiency, a model for the MTHFD1 R653Q variant, leads to congenital heart defects in mice.
Christensen KE; Deng L; Bahous RH; Jerome-Majewska LA; Rozen R
Birth Defects Res A Clin Mol Teratol; 2015 Dec; 103(12):1031-8. PubMed ID: 26408344
[TBL] [Abstract][Full Text] [Related]
26. Polymorphisms in MTHFD1 Gene and Susceptibility to Neural Tube Defects: A Case-Control Study in a Chinese Han Population with Relatively Low Folate Levels.
Wu J; Bao Y; Lu X; Wu L; Zhang T; Guo J; Yang J
Med Sci Monit; 2015 Sep; 21():2630-7. PubMed ID: 26343515
[TBL] [Abstract][Full Text] [Related]
27. Association between MTHFD1 polymorphisms and neural tube defect susceptibility.
Meng J; Han L; Zhuang B
J Neurol Sci; 2015 Jan; 348(1-2):188-94. PubMed ID: 25524527
[TBL] [Abstract][Full Text] [Related]
28. Precision Molecular Diagnosis Defines Specific Therapy in Combined Immunodeficiency with Megaloblastic Anemia Secondary to MTHFD1 Deficiency.
Ramakrishnan KA; Pengelly RJ; Gao Y; Morgan M; Patel SV; Davies EG; Ennis S; Faust SN; Williams AP
J Allergy Clin Immunol Pract; 2016; 4(6):1160-1166.e10. PubMed ID: 27707659
[TBL] [Abstract][Full Text] [Related]
29. Independent and Interactive Influences of Environmental UVR, Vitamin D Levels, and Folate Variant
Jones P; Lucock M; Martin C; Thota R; Garg M; Yates Z; Scarlett CJ; Veysey M; Beckett E
Nutrients; 2020 May; 12(5):. PubMed ID: 32443475
[TBL] [Abstract][Full Text] [Related]
30. MTHFD1 interaction with BRD4 links folate metabolism to transcriptional regulation.
Sdelci S; Rendeiro AF; Rathert P; You W; Lin JG; Ringler A; Hofstätter G; Moll HP; Gürtl B; Farlik M; Schick S; Klepsch F; Oldach M; Buphamalai P; Schischlik F; Májek P; Parapatics K; Schmidl C; Schuster M; Penz T; Buckley DL; Hudecz O; Imre R; Wang SY; Maric HM; Kralovics R; Bennett KL; Müller AC; Mechtler K; Menche J; Bradner JE; Winter GE; Klavins K; Casanova E; Bock C; Zuber J; Kubicek S
Nat Genet; 2019 Jun; 51(6):990-998. PubMed ID: 31133746
[TBL] [Abstract][Full Text] [Related]
31. Severe combined immunodeficiency resulting from mutations in MTHFD1.
Keller MD; Ganesh J; Heltzer M; Paessler M; Bergqvist AG; Baluarte HJ; Watkins D; Rosenblatt DS; Orange JS
Pediatrics; 2013 Feb; 131(2):e629-34. PubMed ID: 23296427
[TBL] [Abstract][Full Text] [Related]
32. B vitamin treatments modify the risk of myocardial infarction associated with a MTHFD1 polymorphism in patients with stable angina pectoris.
Ding YP; Pedersen EK; Johansson S; Gregory JF; Ueland PM; Svingen GF; Helgeland Ø; Meyer K; Fredriksen Å; Nygård OK
Nutr Metab Cardiovasc Dis; 2016 Jun; 26(6):495-501. PubMed ID: 26803590
[TBL] [Abstract][Full Text] [Related]
33. Small ubiquitin-like modifier-1 (SUMO-1) modification of thymidylate synthase and dihydrofolate reductase.
Anderson DD; Woeller CF; Stover PJ
Clin Chem Lab Med; 2007; 45(12):1760-3. PubMed ID: 18067453
[TBL] [Abstract][Full Text] [Related]
34. Formate overflow drives toxic folate trapping in MTHFD1 inhibited cancer cells.
Green AC; Marttila P; Kiweler N; Chalkiadaki C; Wiita E; Cookson V; Lesur A; Eiden K; Bernardin F; Vallin KSA; Borhade S; Long M; Ghahe EK; Jiménez-Alonso JJ; Jemth AS; Loseva O; Mortusewicz O; Meyers M; Viry E; Johansson AI; Hodek O; Homan E; Bonagas N; Ramos L; Sandberg L; Frödin M; Moussay E; Slipicevic A; Letellier E; Paggetti J; Sørensen CS; Helleday T; Henriksson M; Meiser J
Nat Metab; 2023 Apr; 5(4):642-659. PubMed ID: 37012496
[TBL] [Abstract][Full Text] [Related]
35. Mitochondrial one-carbon metabolism and neural tube defects.
Momb J; Appling DR
Birth Defects Res A Clin Mol Teratol; 2014 Aug; 100(8):576-83. PubMed ID: 24985542
[TBL] [Abstract][Full Text] [Related]
36. The MTHFD1 1958G>A variant is associated with elevated C-reactive protein and body mass index in Canadian women from a premature birth cohort.
Christensen KE; Dahhou M; Kramer MS; Rozen R
Mol Genet Metab; 2014 Mar; 111(3):390-392. PubMed ID: 24368157
[TBL] [Abstract][Full Text] [Related]
37. One-carbon metabolism-genome interactions in folate-associated pathologies.
Stover PJ
J Nutr; 2009 Dec; 139(12):2402-5. PubMed ID: 19812215
[TBL] [Abstract][Full Text] [Related]
38. Association study of MTHFD1 coding polymorphisms R134K and R653Q with migraine susceptibility.
Sutherland HG; Hermile H; Sanche R; Menon S; Lea RA; Haupt LM; Griffiths LR
Headache; 2014 Oct; 54(9):1506-14. PubMed ID: 25039261
[TBL] [Abstract][Full Text] [Related]
39. The negative effect of G1958A polymorphism on MTHFD1 protein stability and HCC growth.
Rao K; Zheng K; Zhao Q; He J; Zhou B; Hou G; Sha N; Wang W; Yan M; Zhou Y; Jin Y; Jiang Y; Xia Q
Cell Oncol (Dordr); 2023 Jun; 46(3):735-744. PubMed ID: 36913067
[TBL] [Abstract][Full Text] [Related]
40. Targeting nuclear thymidylate biosynthesis.
Chon J; Stover PJ; Field MS
Mol Aspects Med; 2017 Feb; 53():48-56. PubMed ID: 27876557
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
