BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 4080447)

  • 1. Comparison of folic acid coenzyme distribution patterns in patients with methylenetetrahydrofolate reductase and methionine synthetase deficiencies.
    Baumgartner ER; Stokstad EL; Wick SH; Watson JE; Kusano G
    Pediatr Res; 1985 Dec; 19(12):1288-92. PubMed ID: 4080447
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Methionine and serine formation in control and mutant human cultured fibroblasts: evidence for methyl trapping and characterization of remethylation defects.
    Fowler B; Whitehouse C; Wenzel F; Wraith JE
    Pediatr Res; 1997 Jan; 41(1):145-51. PubMed ID: 8979304
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic defects of folate and cobalamin metabolism.
    Fowler B
    Eur J Pediatr; 1998 Apr; 157 Suppl 2():S60-6. PubMed ID: 9587028
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Remethylation defects: guidelines for clinical diagnosis and treatment.
    Ogier de Baulny H; Gérard M; Saudubray JM; Zittoun J
    Eur J Pediatr; 1998 Apr; 157 Suppl 2():S77-83. PubMed ID: 9587031
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homocysteine, folate enzymes and neural tube defects.
    Molloy AM; Weir DG; Scott JM
    Haematologica; 1999 Jun; 84 Suppl EHA-4():53-6. PubMed ID: 10907468
    [No Abstract]   [Full Text] [Related]  

  • 6. [An adult case of homocystinuria probably due to methylenetetrahydrofolate-reductase deficiency--treatment with folic acid and the course of coagulation-fibrinolysis parameters].
    Hamano H; Nanba A; Nagayama M; Takizawa S; Shinohara Y
    Rinsho Shinkeigaku; 1996 Feb; 36(2):330-5. PubMed ID: 8752689
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The folate cycle and disease in humans.
    Fowler B
    Kidney Int Suppl; 2001 Feb; 78():S221-9. PubMed ID: 11169015
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Methylenetetrahydrofolate reductase deficiency: importance of early diagnosis.
    Fattal-Valevski A; Bassan H; Korman SH; Lerman-Sagie T; Gutman A; Harel S
    J Child Neurol; 2000 Aug; 15(8):539-43. PubMed ID: 10961793
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Inherited metabolic disorders of the transsulfuration pathway].
    Haraguchi H
    Nihon Rinsho; 1992 Jul; 50(7):1548-54. PubMed ID: 1404882
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c --> t methylenetetrahydrofolate reductase and 2756a --> g methionine synthase genotypes.
    Lucock M; Daskalakis I; Briggs D; Yates Z; Levene M
    Mol Genet Metab; 2000 May; 70(1):27-44. PubMed ID: 10833329
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Effect of nitrous oxide inactivation of vitamin B12 on the levels of folate coenzymes in rat bone marrow, kidney, brain, and liver.
    Wilson SD; Horne DW
    Arch Biochem Biophys; 1986 Jan; 244(1):248-53. PubMed ID: 3947060
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Disorders of homocysteine metabolism.
    Fowler B
    J Inherit Metab Dis; 1997 Jun; 20(2):270-85. PubMed ID: 9211199
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Effect of folic acid for treatment of homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency].
    Takenaka T; Shimomura T; Nakayasu H; Urakami K; Takahashi K
    Rinsho Shinkeigaku; 1993 Nov; 33(11):1140-5. PubMed ID: 8124871
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Methionine synthase deficiency without megaloblastic anaemia.
    Kvittingen EA; Spangen S; Lindemans J; Fowler B
    Eur J Pediatr; 1997 Dec; 156(12):925-30. PubMed ID: 9453374
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chronic carbamazepine treatment and folate-dependent one-carbon metabolism.
    Carl GF
    Res Commun Chem Pathol Pharmacol; 1990 Sep; 69(3):357-60. PubMed ID: 2236902
    [No Abstract]   [Full Text] [Related]  

  • 16. Homocysteine and ischaemic heart disease.
    Law MR; Wald NJ
    Haematologica; 1999 Jun; 84 Suppl EHA-4():57-60. PubMed ID: 10907469
    [No Abstract]   [Full Text] [Related]  

  • 17. Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism.
    Schuh S; Rosenblatt DS; Cooper BA; Schroeder ML; Bishop AJ; Seargeant LE; Haworth JC
    N Engl J Med; 1984 Mar; 310(11):686-90. PubMed ID: 6700644
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Methylenetetrahydrofolate reductase (MR) deficiency: thermolability of residual MR activity, methionine synthase activity, and methylcobalamin levels in cultured fibroblasts.
    Rosenblatt DS; Lue-Shing H; Arzoumanian A; Low-Nang L; Matiaszuk N
    Biochem Med Metab Biol; 1992 Jun; 47(3):221-5. PubMed ID: 1627352
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Age- and tumour-related changes in methionine biosynthesis in mice.
    Grzelakowska-Sztabert B; Manteuffel-Cymborowska M; Chmurzyńska W; Sikora E
    Cancer Lett; 1986 Aug; 32(2):207-17. PubMed ID: 3756847
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Single nucleotide polymorphism (SNP) genotyping in unprocessed whole blood and serum by real-time PCR: application to SNPs affecting homocysteine and folate metabolism.
    Ulvik A; Ueland PM
    Clin Chem; 2001 Nov; 47(11):2050-3. PubMed ID: 11673381
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.