BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 17965025)

  • 1. Genotypes of the C677T and A1298C polymorphisms of the MTHFR gene as a cause of human spontaneous embryo loss.
    Callejón G; Mayor-Olea A; Jiménez AJ; Gaitán MJ; Palomares AR; Martínez F; Ruiz M; Reyes-Engel A
    Hum Reprod; 2007 Dec; 22(12):3249-54. PubMed ID: 17965025
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Frequencies of C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene at the early stage of human individual development].
    Nazarenko MS; Puzyrev VP; Lebedev IN
    Genetika; 2006 May; 42(5):711-7. PubMed ID: 16808252
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [C677T and A1298C mutation of the methylenetetrahydrofolate reductase gene in unexplained recurrent spontaneous abortion].
    Wang XP; Lin QD; Ma ZW; Zhao AM
    Zhonghua Fu Chan Ke Za Zhi; 2004 Apr; 39(4):238-41. PubMed ID: 15130349
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prevalent genotypes of methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) in spontaneously aborted embryos.
    Bae J; Shin SJ; Cha SH; Choi DH; Lee S; Kim NK
    Fertil Steril; 2007 Feb; 87(2):351-5. PubMed ID: 17094971
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Polymorphism of methylenetetrahydrofolate reductase and sensitivity of stomach cancer to fluoropyrimidine-based chemotherapy].
    Gao CM; Lu JW; Toshiro T; Wu JZ; Cao HX; Chen HQ; Feng JF; Kazuo T
    Zhonghua Liu Xing Bing Xue Za Zhi; 2004 Dec; 25(12):1054-8. PubMed ID: 15769364
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genotype and allele frequencies of the polymorphic methylenetetrahydrofolate reductase gene in Turkey.
    Sazci A; Ergul E; Kaya G; Kara I
    Cell Biochem Funct; 2005; 23(1):51-4. PubMed ID: 15386535
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of the 5,10-methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) polymorphisms in Korean patients with adult acute lymphoblastic leukemia.
    Oh D; Kim NK; Jang MJ; Kim HC; Lee JH; Lee JA; Ahn MJ; Kim CS; Kim HS; Park S; Chio HS; Min YH;
    Anticancer Res; 2007; 27(5A):3419-24. PubMed ID: 17970089
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Association of the methylenetetrahydrofolate reductase polymorphism in Korean patients with childhood acute lymphoblastic leukemia.
    Kim NK; Chong SY; Jang MJ; Hong SH; Kim HS; Cho EK; Lee JA; Ahn MJ; Kim CS; Oh D
    Anticancer Res; 2006; 26(4B):2879-81. PubMed ID: 16886608
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 5,10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms and the risk of acute lymphoblastic leukemia (ALL) in Filipino children.
    Alcasabas P; Ravindranath Y; Goyette G; Haller A; Del Rosario L; Lesaca-Medina MY; Darga L; Ostrea EM; Taub JW; Everson RB
    Pediatr Blood Cancer; 2008 Aug; 51(2):178-82. PubMed ID: 18421714
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Methylenetetrahydrofolate reductase gene polymorphisms in patients with nonalcoholic steatohepatitis (NASH).
    Sazci A; Ergul E; Aygun C; Akpinar G; Senturk O; Hulagu S
    Cell Biochem Funct; 2008 Apr; 26(3):291-6. PubMed ID: 17563923
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Methylenetetrahydrofolate reductase gene, homocysteine and coronary artery disease: the A1298C polymorphism does matter. Inferences from a case study (Madeira, Portugal).
    Freitas AI; Mendonça I; Guerra G; Brión M; Reis RP; Carracedo A; Brehm A
    Thromb Res; 2008; 122(5):648-56. PubMed ID: 18384842
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Methylenetetrahydrofolate reductase genotype association with the risk of follicular lymphoma.
    Ismail SI; Ababneh NA; Khader Y; Abu-Khader AA; Awidi A
    Cancer Genet Cytogenet; 2009 Dec; 195(2):120-4. PubMed ID: 19963111
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A1298C polymorphism of the MTHFR gene and neural tube defects in the state of Yucatan, Mexico.
    Gonzalez-Herrera L; Castillo-Zapata I; Garcia-Escalante G; Pinto-Escalante D
    Birth Defects Res A Clin Mol Teratol; 2007 Aug; 79(8):622-6. PubMed ID: 17621650
    [TBL] [Abstract][Full Text] [Related]  

  • 15. MTHFR 677CC/1298CC genotypes are highly associated with chronic myelogenous leukemia: a case-control study in Korea.
    Moon HW; Kim TY; Oh BR; Min HC; Cho HI; Bang SM; Lee JH; Yoon SS; Lee DS
    Leuk Res; 2007 Sep; 31(9):1213-7. PubMed ID: 17156840
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Methylenetetrahydrofolate reductase gene C677T and A1298C polymorphisms in patients with small cell and non-small cell lung cancer.
    Siemianowicz K; Gminski J; Garczorz W; Slabiak N; Goss M; Machalski M; Magiera-Molendowska H
    Oncol Rep; 2003; 10(5):1341-4. PubMed ID: 12883704
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Relationship between three thrombophilic gene mutations and unexplained recurrent early spontaneous abortion].
    Xu L; Liu XM; Zhang HY; Zhao J; Qi QW; Chang YF
    Zhonghua Fu Chan Ke Za Zhi; 2007 Mar; 42(3):180-3. PubMed ID: 17537304
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Effect of the MTHFR C677T and A1298C polymorphisms on survival in patients with advanced CKD and ESRD: a prospective study.
    Jamison RL; Shih MC; Humphries DE; Guarino PD; Kaufman JS; Goldfarb DS; Warren SR; Gaziano JM; Lavori P;
    Am J Kidney Dis; 2009 May; 53(5):779-89. PubMed ID: 19272686
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Meta-analyses of the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and risk of head and neck and lung cancer.
    Boccia S; Boffetta P; Brennan P; Ricciardi G; Gianfagna F; Matsuo K; van Duijn CM; Hung RJ
    Cancer Lett; 2009 Jan; 273(1):55-61. PubMed ID: 18789576
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genotype frequencies and linkage disequilibrium in the CEPH human diversity panel for variants in folate pathway genes MTHFR, MTHFD, MTRR, RFC1, and GCP2.
    Shi M; Caprau D; Romitti P; Christensen K; Murray JC
    Birth Defects Res A Clin Mol Teratol; 2003 Aug; 67(8):545-9. PubMed ID: 14632302
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.