These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 1887335)

  • 21. Site-directed mutagenesis of yeast C1-tetrahydrofolate synthase: analysis of an overlapping active site in a multifunctional enzyme.
    Barlowe CK; Williams ME; Rabinowitz JC; Appling DR
    Biochemistry; 1989 Mar; 28(5):2099-106. PubMed ID: 2541774
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mild Choline Deficiency and MTHFD1 Synthetase Deficiency Interact to Increase Incidence of Developmental Delays and Defects in Mice.
    Christensen KE; Malysheva OV; Carlin S; Matias F; MacFarlane AJ; Jacobs RL; Caudill MA; Rozen R
    Nutrients; 2021 Dec; 14(1):. PubMed ID: 35011003
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular genetic analysis of Saccharomyces cerevisiae C1-tetrahydrofolate synthase mutants reveals a noncatalytic function of the ADE3 gene product and an additional folate-dependent enzyme.
    Barlowe CK; Appling DR
    Mol Cell Biol; 1990 Nov; 10(11):5679-87. PubMed ID: 2233711
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase from porcine liver. Location of the activities in two domains of the multifunctional polypeptide.
    Tan LU; MacKenzie RE
    Can J Biochem; 1979 Jun; 57(6):806-12. PubMed ID: 476523
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Site-directed mutagenesis of a highly conserved aspartate in the putative 10-formyl-tetrahydrofolate binding site of yeast C1-tetrahydrofolate synthase.
    Kirksey TJ; Appling DR
    Arch Biochem Biophys; 1996 Sep; 333(1):251-9. PubMed ID: 8806778
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group.
    Brody LC; Conley M; Cox C; Kirke PN; McKeever MP; Mills JL; Molloy AM; O'Leary VB; Parle-McDermott A; Scott JM; Swanson DA
    Am J Hum Genet; 2002 Nov; 71(5):1207-15. PubMed ID: 12384833
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Methenyltetrahydrofolate cyclohydrolase is rate limiting for the enzymatic conversion of 10-formyltetrahydrofolate to 5,10-methylenetetrahydrofolate in bifunctional dehydrogenase-cyclohydrolase enzymes.
    Pawelek PD; MacKenzie RE
    Biochemistry; 1998 Jan; 37(4):1109-15. PubMed ID: 9454603
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mammalian fibroblasts lacking mitochondrial NAD+-dependent methylenetetrahydrofolate dehydrogenase-cyclohydrolase are glycine auxotrophs.
    Patel H; Pietro ED; MacKenzie RE
    J Biol Chem; 2003 May; 278(21):19436-41. PubMed ID: 12646567
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mutations in ADE3 reduce the efficiency of the omnipotent suppressor sup45-2.
    Song JM; Liebman SW
    Curr Genet; 1989 Dec; 16(5-6):315-21. PubMed ID: 2692849
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mthfd1 is a modifier of chemically induced intestinal carcinogenesis.
    MacFarlane AJ; Perry CA; McEntee MF; Lin DM; Stover PJ
    Carcinogenesis; 2011 Mar; 32(3):427-33. PubMed ID: 21156972
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Deletion of the neural tube defect-associated gene
    Bryant JD; Sweeney SR; Sentandreu E; Shin M; Ipas H; Xhemalce B; Momb J; Tiziani S; Appling DR
    J Biol Chem; 2018 Apr; 293(16):5821-5833. PubMed ID: 29483189
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A general method for generation and analysis of defined mutations in enzymes involved in a tetrahydrofolate-interconversion pathway.
    Barlowe CK; Appling DR
    Biofactors; 1989 Mar; 2(1):57-63. PubMed ID: 2679653
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mitochondrial methylenetetrahydrofolate dehydrogenase, methenyltetrahydrofolate cyclohydrolase, and formyltetrahydrofolate synthetases.
    Christensen KE; Mackenzie RE
    Vitam Horm; 2008; 79():393-410. PubMed ID: 18804703
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Methylenetetrahydrofolate dehydrogenase, methenyltetrahydrofolate cyclohydrolase and formyltetrahydrofolate synthetase from porcine liver. Isolation of a dehydrogenase-cyclohydrolase fragment from the multifunctional enzyme.
    Tan LU; Mackenzie RE
    Biochim Biophys Acta; 1977 Nov; 485(1):52-9. PubMed ID: 562190
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mitochondrial C1-tetrahydrofolate synthase (MTHFD1L) supports the flow of mitochondrial one-carbon units into the methyl cycle in embryos.
    Pike ST; Rajendra R; Artzt K; Appling DR
    J Biol Chem; 2010 Feb; 285(7):4612-20. PubMed ID: 19948730
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. The NADP-dependent methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase is not expressed in Spodoptera frugiperda cells.
    Tremblay GB; Mejia NR; MacKenzie RE
    J Biol Chem; 1992 Apr; 267(12):8281-5. PubMed ID: 1569082
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate-cyclohydrolase-formyltetrahy dro folate synthetase. Affinity labelling of the dehydrogenase-cyclohydrolase active site.
    Smith DD; MacKenzie RE
    Biochem Biophys Res Commun; 1985 Apr; 128(1):148-54. PubMed ID: 3872659
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A polymorphism in the MTHFD1 gene increases a mother's risk of having an unexplained second trimester pregnancy loss.
    Parle-McDermott A; Pangilinan F; Mills JL; Signore CC; Molloy AM; Cotter A; Conley M; Cox C; Kirke PN; Scott JM; Brody LC
    Mol Hum Reprod; 2005 Jul; 11(7):477-80. PubMed ID: 16123074
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Evidence that the folate-requiring enzymes of de novo purine biosynthesis are encoded by individual mRNAs.
    Wasserman GF; Mueller WT; Benkovic SJ; Liao WS; Taylor J
    Biochemistry; 1984 Dec; 23(26):6704-10. PubMed ID: 6335666
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.