BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 11896528)

  • 1. Neonatal sinovenous thrombosis associated with homozygous thermolabile methylenetetrahydrofolate reductase in both mother and infant.
    Grow JL; Fliman PJ; Pipe SW
    J Perinatol; 2002 Mar; 22(2):175-8. PubMed ID: 11896528
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Turkish patients with thrombosis.
    Balta G; Gürgey A
    Turk J Pediatr; 1999; 41(2):197-9. PubMed ID: 10770658
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Vascular diseases, spina bifida and schizophrenia in a single family associated with the heterozygote mutation of the heat-sensitive variant of methylenetetrahydrofolate reductase].
    Horváth A; Morava E; Tóth G; Czakó M; Melegh B; Kosztolányi G
    Orv Hetil; 2001 Jul; 142(27):1445-8. PubMed ID: 11481907
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects.
    Volcik KA; Shaw GM; Lammer EJ; Zhu H; Finnell RH
    Birth Defects Res A Clin Mol Teratol; 2003 Mar; 67(3):154-7. PubMed ID: 12797455
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The thermolabile variant 677C-->T can further reduce activity when expressed in cis with severe mutations for human methylenetetrahydrofolate reductase.
    Goyette P; Rozen R
    Hum Mutat; 2000; 16(2):132-8. PubMed ID: 10923034
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Methylenetetrahydrofolate reductase thermolabile variant and oral clefts.
    Mills JL; Kirke PN; Molloy AM; Burke H; Conley MR; Lee YJ; Mayne PD; Weir DG; Scott JM
    Am J Med Genet; 1999 Sep; 86(1):71-4. PubMed ID: 10440833
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Homozygous thermolabile methylenetetrahydrofolate reductase in schizophrenia-like psychosis.
    Regland B; Germgård T; Gottfries CG; Grenfeldt B; Koch-Schmidt AC
    J Neural Transm (Vienna); 1997; 104(8-9):931-41. PubMed ID: 9451725
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prospective evaluation of the risk conferred by factor V Leiden and thermolabile methylenetetrahydrofolate reductase polymorphisms in pregnancy.
    Murphy RP; Donoghue C; Nallen RJ; D'Mello M; Regan C; Whitehead AS; Fitzgerald DJ
    Arterioscler Thromb Vasc Biol; 2000 Jan; 20(1):266-70. PubMed ID: 10634828
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria.
    Sibani S; Christensen B; O'Ferrall E; Saadi I; Hiou-Tim F; Rosenblatt DS; Rozen R
    Hum Mutat; 2000; 15(3):280-7. PubMed ID: 10679944
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recurrent thrombosis in a patient with pseudohomozygous activated protein C resistance and homozygosity for MTHFR gene polymorphism C677T.
    Standen G; Morse C; Aslam S; Bowron A
    Thromb Haemost; 1999 Apr; 81(4):663-4. PubMed ID: 10235461
    [No Abstract]   [Full Text] [Related]  

  • 11. A common haplotype for the 677T thermolabile variant of the 5,10-methylenetetrahydrofolate reductase gene in thrombophilic patients and controls.
    Linnebank M; Homberger A; Nowak-Göttl U; Koch HG
    Hum Mutat; 2002 Dec; 20(6):478. PubMed ID: 12442281
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Heterozygous methylene tetrahydrofolate reductase mutation with mild hyperhomocysteinemia associated with deep vein thrombosis.
    Pathare A; al Kindi S; al Belushi T; Bayoumi R; Dennison D; Murlitharan S
    Haematologia (Budap); 2002; 32(4):551-6. PubMed ID: 12803132
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Homozygous methylenetetrahydrofolate reductase C677T mutation and male infertility.
    Bezold G; Lange M; Peter RU
    N Engl J Med; 2001 Apr; 344(15):1172-3. PubMed ID: 11302150
    [No Abstract]   [Full Text] [Related]  

  • 14. [The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans].
    Guo C; Guo Q; Gong Y; Chen B; Liu Q; Li J; Gao G; Zhou H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):295-7. PubMed ID: 12170465
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The methylentetrahydrofolate reductase C677T point mutation is a risk factor for vascular access thrombosis in hemodialysis patients.
    Fukasawa M; Matsushita K; Kamiyama M; Mikami Y; Araki I; Yamagata Z; Takeda M
    Am J Kidney Dis; 2003 Mar; 41(3):637-42. PubMed ID: 12612987
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Methylenetetrahydrofolate reductase deficiency in a patient with phenotypic findings of Angelman syndrome.
    Arn PH; Williams CA; Zori RT; Driscoll DJ; Rosenblatt DS
    Am J Med Genet; 1998 May; 77(3):198-200. PubMed ID: 9605586
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [C677T genetic polymorphism of methylenetetrahydrofolate reductase in premature coronary heart disease].
    Xu H; Chen Z; Tang J; Zhu D; Zhang C
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1999 Apr; 21(2):118-21. PubMed ID: 12569666
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation in the methylenetetrahydrofolate reductase gene might be a risk factor for cerebrovascular disease in peripartum and under oral contraceptive use.
    Korn-Lubetzki I; Gillis S; Steiner I
    Eur Neurol; 2001; 45(3):171-3. PubMed ID: 11306861
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hyperhomocysteinemia and the MTHFR C677T mutation in Budd-Chiari syndrome.
    Li XM; Wei YF; Hao HL; Hao YB; He LS; Li JD; Mei B; Wang SY; Wang C; Wang JX; Zhu JZ; Liang JQ
    Am J Hematol; 2002 Sep; 71(1):11-4. PubMed ID: 12221667
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos.
    Zetterberg H; Regland B; Palmér M; Ricksten A; Palmqvist L; Rymo L; Arvanitis DA; Spandidos DA; Blennow K
    Eur J Hum Genet; 2002 Feb; 10(2):113-8. PubMed ID: 11938441
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.