BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (PubMed ID: 35011003)

  • 21. Deficient synthesis of MTHFD, a trifunctional folate-dependent enzyme, in the CHO Ade E mutant.
    Mascisch A; Rozen R
    Somat Cell Mol Genet; 1991 Jul; 17(4):391-8. PubMed ID: 1887335
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Relationship of the MTHFD1 (rs2236225), eNOS (rs1799983), CBS (rs2850144) and ACE (rs4343) gene polymorphisms in a population of Iranian pediatric patients with congenital heart defects.
    Khatami M; Ratki FM; Tajfar S; Akrami F
    Kaohsiung J Med Sci; 2017 Sep; 33(9):442-448. PubMed ID: 28865601
    [TBL] [Abstract][Full Text] [Related]  

  • 23. MTHFR deficiency or reduced intake of folate or choline in pregnant mice results in impaired short-term memory and increased apoptosis in the hippocampus of wild-type offspring.
    Jadavji NM; Deng L; Malysheva O; Caudill MA; Rozen R
    Neuroscience; 2015 Aug; 300():1-9. PubMed ID: 25956258
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Association of main folate metabolic pathway gene polymorphisms with neural tube defects in Han population of Northern China.
    Fang Y; Zhang R; Zhi X; Zhao L; Cao L; Wang Y; Cai C
    Childs Nerv Syst; 2018 Apr; 34(4):725-729. PubMed ID: 29392422
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic impairments in folate enzymes increase dependence on dietary choline for phosphatidylcholine production at the expense of betaine synthesis.
    Ganz AB; Shields K; Fomin VG; Lopez YS; Mohan S; Lovesky J; Chuang JC; Ganti A; Carrier B; Yan J; Taeswuan S; Cohen VV; Swersky CC; Stover JA; Vitiello GA; Malysheva OV; Mudrak E; Caudill MA
    FASEB J; 2016 Oct; 30(10):3321-3333. PubMed ID: 27342765
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Arsenic trioxide targets MTHFD1 and SUMO-dependent nuclear de novo thymidylate biosynthesis.
    Kamynina E; Lachenauer ER; DiRisio AC; Liebenthal RP; Field MS; Stover PJ
    Proc Natl Acad Sci U S A; 2017 Mar; 114(12):E2319-E2326. PubMed ID: 28265077
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Methylenetetrahydrofolate dehydrogenase - methenyltetrahydrofolate cyclohydrolase - formyltetrahydrofolate synthetase from porcine liver: evidence to support a common dehydrogenase-cyclohydrolase site.
    Drummond D; Smith S; MacKenzie RE
    Can J Biochem Cell Biol; 1983 Nov; 61(11):1166-71. PubMed ID: 6607769
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A pseudogene on the X chromosome for the human trifunctional enzyme MTHFD (methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase).
    Italiano C; John SW; Hum DW; MacKenzie RE; Rozen R
    Genomics; 1991 Aug; 10(4):1073-4. PubMed ID: 1916813
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Strain-dependent dysregulation of one-carbon metabolism in male mice is associated with choline- and folate-deficient diet-induced liver injury.
    Pogribny IP; Kutanzi K; Melnyk S; de Conti A; Tryndyak V; Montgomery B; Pogribna M; Muskhelishvili L; Latendresse JR; James SJ; Beland FA; Rusyn I
    FASEB J; 2013 Jun; 27(6):2233-43. PubMed ID: 23439872
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Transcriptional regulation of murine NADP(+)-dependent methylenetetrahydrofolate dehydrogenase-cyclohydrolase-synthetase.
    Peri KG; MacKenzie RE
    FEBS Lett; 1991 Dec; 294(1-2):113-5. PubMed ID: 1720740
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Formate Supplementation May Prevent Some Neural Tube Defects that Prove Resistant to Folic Acid: Supplementation with formate rescued normal neural tube closure in more than three quarters of the embryos of novel folic acid-resistant neural tube defect mouse models.
    Am J Med Genet A; 2018 Aug; 176(8):1697-1698. PubMed ID: 30136438
    [No Abstract]   [Full Text] [Related]  

  • 33. Genetic variation of folate-mediated one-carbon transfer pathway predicts susceptibility to choline deficiency in humans.
    Kohlmeier M; da Costa KA; Fischer LM; Zeisel SH
    Proc Natl Acad Sci U S A; 2005 Nov; 102(44):16025-30. PubMed ID: 16236726
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chromosomal localization of the gene for the human trifunctional enzyme, methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase.
    Rozen R; Barton D; Du J; Hum DW; MacKenzie RE; Francke U
    Am J Hum Genet; 1989 Jun; 44(6):781-6. PubMed ID: 2786332
    [TBL] [Abstract][Full Text] [Related]  

  • 35. MTHFD1 gene: role in disease susceptibility and pharmacogenetics.
    Krajinovic M
    Pharmacogenomics; 2008 Jul; 9(7):829-32. PubMed ID: 18597647
    [No Abstract]   [Full Text] [Related]  

  • 36. Metabotype analysis of Mthfd1l-null mouse embryos using desorption electrospray ionization mass spectrometry imaging.
    Vaughn A; DeHoog RJ; Eberlin LS; Appling DR
    Anal Bioanal Chem; 2021 May; 413(13):3573-3582. PubMed ID: 33829277
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Low dietary choline and low dietary riboflavin during pregnancy influence reproductive outcomes and heart development in mice.
    Chan J; Deng L; Mikael LG; Yan J; Pickell L; Wu Q; Caudill MA; Rozen R
    Am J Clin Nutr; 2010 Apr; 91(4):1035-43. PubMed ID: 20164309
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [G894T (NOS3) and G1958A (MTHFD1) gene polymorphisms and risk of ischemic heart disease in Yucatan, Mexico].
    García-González I; Solís-Cárdenas Ade J; Flores-Ocampo JA; Alejos-Mex R; Herrera-Sánchez LF; González-Herrera LJ
    Clin Investig Arterioscler; 2015; 27(2):64-73. PubMed ID: 25304051
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic variants in phosphatidylethanolamine N-methyltransferase and methylenetetrahydrofolate dehydrogenase influence biomarkers of choline metabolism when folate intake is restricted.
    Ivanov A; Nash-Barboza S; Hinkis S; Caudill MA
    J Am Diet Assoc; 2009 Feb; 109(2):313-8. PubMed ID: 19167960
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.