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Journal Abstract Search

312 related items for PubMed ID: 25105440

  • 41. Genetic variation in folate metabolism is associated with the risk of conotruncal heart defects in a Chinese population.
    Wang X, Wei H, Tian Y, Wu Y, Luo L.
    BMC Pediatr; 2018 Aug 30; 18(1):287. PubMed ID: 30165839
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  • 42. Analysis of MTR and MTRR Polymorphisms for Neural Tube Defects Risk Association.
    Wang Y, Liu Y, Ji W, Qin H, Wu H, Xu D, Tukebai T, Wang Z.
    Medicine (Baltimore); 2015 Sep 30; 94(35):e1367. PubMed ID: 26334892
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  • 43. Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and nonsyndromic orofacial clefts susceptibility in a southern Chinese population.
    Han Y, Pan Y, Du Y, Tong N, Wang M, Zhang Z, Wan L, Wang L.
    DNA Cell Biol; 2011 Dec 30; 30(12):1063-8. PubMed ID: 21612398
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  • 46. Relationship between methionine synthase, methionine synthase reductase genetic polymorphisms and deep vein thrombosis among South Indians.
    Naushad SM, Jain Jamal MN, Prasad CK, Rama Devi AR.
    Clin Chem Lab Med; 2008 Dec 30; 46(1):73-9. PubMed ID: 18034637
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  • 48. Association between genetic polymorphisms in folate-related enzyme genes and infertile men with non-obstructive azoospermia.
    Kim SY, Lim JW, Kim JW, Park SY, Seo JT.
    Syst Biol Reprod Med; 2015 Dec 30; 61(5):286-92. PubMed ID: 26196053
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  • 50. Genetic polymorphisms in MTHFR (C677T, A1298C), MTR (A2756G) and MTRR (A66G) genes associated with pathological characteristics of prostate cancer in the Ecuadorian population.
    López-Cortés A, Jaramillo-Koupermann G, Muñoz MJ, Cabrera A, Echeverría C, Rosales F, Vivar N, Paz-y-Miño C.
    Am J Med Sci; 2013 Dec 30; 346(6):447-54. PubMed ID: 23459165
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  • 51. Folate pathway gene polymorphisms and risk of childhood brain tumors: results from an Australian case-control study.
    Greenop KR, Scott RJ, Attia J, Bower C, de Klerk NH, Norris MD, Haber M, Jamieson SE, van Bockxmeer FM, Gottardo NG, Ashton LJ, Armstrong BK, Milne E.
    Cancer Epidemiol Biomarkers Prev; 2015 Jun 30; 24(6):931-7. PubMed ID: 25809864
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  • 53. Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.
    Wang B, Liu M, Yan W, Mao J, Jiang D, Li H, Chen Y.
    J Matern Fetal Neonatal Med; 2013 Dec 30; 26(18):1768-77. PubMed ID: 23701284
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  • 54. Transcobalamin-II variants, decreased vitamin B12 availability and increased risk of frailty.
    Matteini AM, Walston JD, Bandeen-Roche K, Arking DE, Allen RH, Fried LP, Chakravarti A, Stabler SP, Fallin MD.
    J Nutr Health Aging; 2010 Jan 30; 14(1):73-7. PubMed ID: 20082058
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  • 55. Genetic variants of the folate metabolic system and mild hyperhomocysteinemia may affect ADHD associated behavioral problems.
    Saha T, Chatterjee M, Verma D, Ray A, Sinha S, Rajamma U, Mukhopadhyay K.
    Prog Neuropsychopharmacol Biol Psychiatry; 2018 Jun 08; 84(Pt A):1-10. PubMed ID: 29407547
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  • 56. Non-syndromic cleft palate: Association analysis on three gene polymorphisms of the folate pathway in Asian and Italian populations.
    Carinci F, Palmieri A, Scapoli L, Cura F, Borelli F, Morselli PG, Nouri N, Abdali H, Gianni AB, Russillo A, Docimo R, Martinelli M.
    Int J Immunopathol Pharmacol; 2019 Jun 08; 33():2058738419858572. PubMed ID: 31663447
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  • 57. Association between NOGGIN and SPRY2 polymorphisms and nonsyndromic cleft lip with or without cleft palate.
    Song T, Shi J, Guo Q, Lv K, Jiao X, Hu T, Sun X, Fu S.
    Am J Med Genet A; 2015 Jan 08; 167A(1):137-41. PubMed ID: 25339627
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  • 60. Folate metabolism abnormalities in infertile patients with endometriosis.
    Guedes T, Santos AA, Vieira-Neto FH, Bianco B, Barbosa CP, Christofolini DM.
    Biomark Med; 2022 May 08; 16(7):549-557. PubMed ID: 35332781
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