179 related articles for article (PubMed ID: 7734111)
1. Homocysteinemia and schizophrenia as a case of methylation deficiency.
Regland B; Johansson BV; Gottfries CG
J Neural Transm Gen Sect; 1994; 98(2):143-52. PubMed ID: 7734111
[TBL] [Abstract][Full Text] [Related]
2. The C677T thermolabile variant of methylene tetrahydrofolate reductase on homocysteine, folate and vitamin B12 in a hemodialysis center.
Trimarchi H; Genoud V; Schiel A; Castañon M; Freixas E; Diaz ML; Schropp J; Martino D; Pereyra H; Kordich L
Medicina (B Aires); 2002; 62(2):149-53. PubMed ID: 12038037
[TBL] [Abstract][Full Text] [Related]
3. Homocysteinemia due to MTHFR deficiency in a young adult presenting with bilateral lens subluxations.
Couser NL; McClure J; Evans MW; Haines NR; Burden SK; Muenzer J
Ophthalmic Genet; 2017; 38(1):91-94. PubMed ID: 27046515
[TBL] [Abstract][Full Text] [Related]
4. Is the oral methionine loading test insensitive to the remethylation pathway of homocysteine?
Cattaneo M; Lombardi R; Lecchi A; Zighetti ML
Blood; 1999 Feb; 93(3):1118-20. PubMed ID: 10025987
[No Abstract] [Full Text] [Related]
5. Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase.
Kang SS; Zhou J; Wong PW; Kowalisyn J; Strokosch G
Am J Hum Genet; 1988 Oct; 43(4):414-21. PubMed ID: 3177384
[TBL] [Abstract][Full Text] [Related]
6. Atherogenic diet alters folate enzymes in mice: implications of folate deficient homocysteinemia.
Kulkarni MV; Kesavan V; Viswanathan G
Indian J Biochem Biophys; 1998 Oct; 35(5):303-7. PubMed ID: 10410464
[TBL] [Abstract][Full Text] [Related]
7. A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida.
Wilson A; Platt R; Wu Q; Leclerc D; Christensen B; Yang H; Gravel RA; Rozen R
Mol Genet Metab; 1999 Aug; 67(4):317-23. PubMed ID: 10444342
[TBL] [Abstract][Full Text] [Related]
8. Thermolability of residual methylene-tetrahydrofolate reductase (MR) activity, methionine synthase activity and methyl-cobalamin levels in cultured fibroblasts from patients with MR deficiency.
Rosenblatt DS; Lue-Shing H; Matiaszuk N; Low-Nang L; Arzoumanian A; Cooper BA
Adv Exp Med Biol; 1993; 338():703-6. PubMed ID: 8304210
[No Abstract] [Full Text] [Related]
9. 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]
10. 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]
11. Folate-responsive homocystinuria and "schizophrenia". A defect in methylation due to deficient 5,10-methylenetetrahydrofolate reductase activity.
Freeman JM; Finkelstein JD; Mudd SH
N Engl J Med; 1975 Mar; 292(10):491-6. PubMed ID: 1117892
[TBL] [Abstract][Full Text] [Related]
12. Homocysteinemia: association of a metabolic disorder with vascular disease and thrombosis.
Rees MM; Rodgers GM
Thromb Res; 1993 Sep; 71(5):337-59. PubMed ID: 8236162
[No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. [Hyperhomocysteinemia: an independent risk factor or a simple marker of vascular disease?. 1. Basic data].
Guilland JC; Favier A; Potier de Courcy G; Galan P; Hercberg S
Pathol Biol (Paris); 2003 Mar; 51(2):101-10. PubMed ID: 12801808
[TBL] [Abstract][Full Text] [Related]
16. A common mutation in the methylenetetrahydrofolate reductase gene and risk of coronary heart disease: results among U.S. men.
Verhoef P; Rimm EB; Hunter DJ; Chen J; Willett WC; Kelsey K; Stampfer MJ
J Am Coll Cardiol; 1998 Aug; 32(2):353-9. PubMed ID: 9708460
[TBL] [Abstract][Full Text] [Related]
17. Why are homocysteine levels increased in kidney failure? A metabolic approach.
Blom HJ; De Vriese AS
J Lab Clin Med; 2002 May; 139(5):262-8. PubMed ID: 12032486
[No Abstract] [Full Text] [Related]
18. The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events.
D'Angelo A; Coppola A; Madonna P; Fermo I; Pagano A; Mazzola G; Galli L; Cerbone AM
Thromb Haemost; 2000 Apr; 83(4):563-70. PubMed ID: 10780318
[TBL] [Abstract][Full Text] [Related]
19. Methylenetetrahydrofolate reductase and methionine synthase: biochemistry and molecular biology.
Matthews RG; Sheppard C; Goulding C
Eur J Pediatr; 1998 Apr; 157 Suppl 2():S54-9. PubMed ID: 9587027
[TBL] [Abstract][Full Text] [Related]
20. Nutritional regulation of homocysteine: effects of drugs.
Varela-Moreiras G
Biomed Pharmacother; 2001 Oct; 55(8):448-53. PubMed ID: 11686578
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
