These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

738 related articles for article (PubMed ID: 31238314)

  • 21. Associations of variants in MTHFR and MTRR genes with male infertility in the Jordanian population.
    Mfady DS; Sadiq MF; Khabour OF; Fararjeh AS; Abu-Awad A; Khader Y
    Gene; 2014 Feb; 536(1):40-4. PubMed ID: 24334125
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 5,10-Methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTRR), and methionine synthase reductase (MTR) gene polymorphisms and adult meningioma risk.
    Zhang J; Zhou YW; Shi HP; Wang YZ; Li GL; Yu HT; Xie XY
    J Neurooncol; 2013 Nov; 115(2):233-9. PubMed ID: 23959833
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Association of MTHFR, MTR, MTRR, RFC1, and DHFR gene polymorphisms with susceptibility to sporadic colon cancer.
    Jokić M; Brčić-Kostić K; Stefulj J; Catela Ivković T; Božo L; Gamulin M; Kapitanović S
    DNA Cell Biol; 2011 Oct; 30(10):771-6. PubMed ID: 21438757
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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; 18(1):287. PubMed ID: 30165839
    [TBL] [Abstract][Full Text] [Related]  

  • 25. MTRR and MTHFR polymorphism: link to Down syndrome?
    O'Leary VB; Parle-McDermott A; Molloy AM; Kirke PN; Johnson Z; Conley M; Scott JM; Mills JL
    Am J Med Genet; 2002 Jan; 107(2):151-5. PubMed ID: 11807890
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association of neural tube defects with maternal alterations and genetic polymorphisms in one-carbon metabolic pathway.
    Cai CQ; Fang YL; Shu JB; Zhao LS; Zhang RP; Cao LR; Wang YZ; Zhi XF; Cui HL; Shi OY; Liu W
    Ital J Pediatr; 2019 Mar; 45(1):37. PubMed ID: 30867013
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Individualized supplementation of folic acid according to polymorphisms of methylenetetrahydrofolate reductase (MTHFR), methionine synthase reductase (MTRR) reduced pregnant complications.
    Li X; Jiang J; Xu M; Xu M; Yang Y; Lu W; Yu X; Ma J; Pan J
    Gynecol Obstet Invest; 2015; 79(2):107-12. PubMed ID: 25634728
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Polymorphisms in folate-related enzyme genes in idiopathic infertile Brazilian men.
    Gava MM; Kayaki EA; Bianco B; Teles JS; Christofolini DM; Pompeo AC; Glina S; Barbosa CP
    Reprod Sci; 2011 Dec; 18(12):1267-72. PubMed ID: 21775772
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic variants in the folate pathway and the risk of neural tube defects: a meta-analysis of the published literature.
    Zhang T; Lou J; Zhong R; Wu J; Zou L; Sun Y; Lu X; Liu L; Miao X; Xiong G
    PLoS One; 2013; 8(4):e59570. PubMed ID: 23593147
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Gender-specific interactions of MTHFR C677T and MTRR A66G polymorphisms with overweight/obesity on serum lipid levels in a Chinese Han population.
    Zhi X; Yang B; Fan S; Wang Y; Wei J; Zheng Q; Sun G
    Lipids Health Dis; 2016 Oct; 15(1):185. PubMed ID: 27793164
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India.
    Naushad SM; Devi AR
    J Perinat Med; 2010; 38(1):63-9. PubMed ID: 20047525
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Folate, vitamin B12, homocysteine and polymorphisms in folate metabolizing genes in children with congenital heart disease and their mothers.
    Elizabeth KE; Praveen SL; Preethi NR; Jissa VT; Pillai MR
    Eur J Clin Nutr; 2017 Dec; 71(12):1437-1441. PubMed ID: 28876333
    [TBL] [Abstract][Full Text] [Related]  

  • 34. MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases.
    Zidan HE; Rezk NA; Mohammed D
    Gene; 2013 Oct; 529(1):119-24. PubMed ID: 23933414
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Gene polymorphisms involved in folate and methionine metabolism and increased risk of sporadic colorectal adenocarcinoma.
    Guimarães JL; Ayrizono Mde L; Coy CS; Lima CS
    Tumour Biol; 2011 Oct; 32(5):853-61. PubMed ID: 21603981
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects.
    Cunha AL; Hirata MH; Kim CA; Guerra-Shinohara EM; Nonoyama K; Hirata RD
    Clin Chim Acta; 2002 Apr; 318(1-2):139-43. PubMed ID: 11880124
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Polymorphisms in the methylenetetrahydrofolate reductase and methionine synthase reductase genes and homocysteine levels in Brazilian children.
    Aléssio AC; Annichino-Bizzacchi JM; Bydlowski SP; Eberlin MN; Vellasco AP; Höehr NF
    Am J Med Genet A; 2004 Jul; 128A(3):256-60. PubMed ID: 15216546
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Geographical and Ethnic Distributions of the MTHFR C677T, A1298C and MTRR A66G Gene Polymorphisms in Chinese Populations: A Meta-Analysis.
    Wang X; Fu J; Li Q; Zeng D
    PLoS One; 2016; 11(4):e0152414. PubMed ID: 27089387
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Design and Evaluation of a Method for Testing Polymorphisms of Folate-Related Genes Using the Luminex Liquichip System.
    Jiang X; Huang T; Lin W; Li X
    Genet Test Mol Biomarkers; 2020 Mar; 24(3):150-155. PubMed ID: 32119787
    [No Abstract]   [Full Text] [Related]  

  • 40. Association between MTHFR C677T polymorphism and neural tube defect risks: A comprehensive evaluation in three groups of NTD patients, mothers, and fathers.
    Yang Y; Chen J; Wang B; Ding C; Liu H
    Birth Defects Res A Clin Mol Teratol; 2015 Jun; 103(6):488-500. PubMed ID: 25808073
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 37.