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 *

105 related articles for article (PubMed ID: 33784681)

  • 1. Methylenetetrahydrofolate Reductase Dimer Configuration as a Risk Factor for Maternal Meiosis I-Derived Trisomy 21.
    Vraneković J; Babić Božović I; Bilić Čače I; Brajenović Milić B
    Hum Hered; 2020; 85(2):61-65. PubMed ID: 33784681
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Functional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia.
    Vraneković J; Babić Bozović I; Starcević Cizmarević N; Buretić-Tomljanović A; Ristić S; Petrović O; Kapović M; Brajenović-Milić B
    Dis Markers; 2010; 28(5):293-8. PubMed ID: 20592453
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome.
    James SJ; Pogribna M; Pogribny IP; Melnyk S; Hine RJ; Gibson JB; Yi P; Tafoya DL; Swenson DH; Wilson VL; Gaylor DW
    Am J Clin Nutr; 1999 Oct; 70(4):495-501. PubMed ID: 10500018
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Methylenetetrahydrofolate reductase gene polymorphisms in Egyptian Turner Syndrome patients.
    Ismail MF; Zarouk WA; Ruby MO; Mahmoud WM; Gad RS
    Acta Biochim Pol; 2015; 62(3):529-32. PubMed ID: 26217949
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Polymorphisms of the MTHFR gene in mothers of children with trisomy 21 (Down syndrome) in a Polish population.
    Czechowicz P; Małodobra-Mazur M; Lebioda A; Jonkisz A; Dobosz T; Śmigiel R
    Adv Clin Exp Med; 2020 Feb; 29(2):251-256. PubMed ID: 32073761
    [TBL] [Abstract][Full Text] [Related]  

  • 6. MTHFR C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome.
    Božović IB; Vraneković J; Cizmarević NS; Mahulja-Stamenković V; Prpić I; Brajenović-Milić B
    Pediatr Int; 2011 Aug; 53(4):546-50. PubMed ID: 21159028
    [TBL] [Abstract][Full Text] [Related]  

  • 7. MTHFR C677T and A1298C polymorphisms are risk factors for Down's syndrome in Indian mothers.
    Rai AK; Singh S; Mehta S; Kumar A; Pandey LK; Raman R
    J Hum Genet; 2006; 51(4):278-283. PubMed ID: 16489479
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Methylenetetrahydrofolate reductase polymorphisms C677T and A1298C as maternal risk factors for Down syndrome in Jordan.
    Sadiq MF; Al-Refai EA; Al-Nasser A; Khassawneh M; Al-Batayneh Q
    Genet Test Mol Biomarkers; 2011; 15(1-2):51-7. PubMed ID: 21198396
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome.
    Hobbs CA; Sherman SL; Yi P; Hopkins SE; Torfs CP; Hine RJ; Pogribna M; Rozen R; James SJ
    Am J Hum Genet; 2000 Sep; 67(3):623-30. PubMed ID: 10930360
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Maternal folate polymorphisms and the etiology of human nondisjunction.
    Hassold TJ; Burrage LC; Chan ER; Judis LM; Schwartz S; James SJ; Jacobs PA; Thomas NS
    Am J Hum Genet; 2001 Aug; 69(2):434-9. PubMed ID: 11443546
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
    Biselli JM; Machado FB; Zampieri BL; Alves da Silva AF; Goloni-Bertollo EM; Haddad R; Eberlin MN; Vannucchi H; Carvalho VM; Medina-Acosta E; Pavarino-Bertelli EC
    Genet Couns; 2009; 20(3):225-34. PubMed ID: 19852428
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MTHFR Gene variants C677T, A1298C and association with Down syndrome: A Case-control study from South India.
    Cyril C; Rai P; Chandra N; Gopinath PM; Satyamoorthy K
    Indian J Hum Genet; 2009 May; 15(2):60-4. PubMed ID: 20680153
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 5,10-Methylenetetrahydrofolate reductase single nucleotide polymorphisms and gene-environment interaction analysis in non-syndromic cleft lip/palate.
    Estandia-Ortega B; Velázquez-Aragón JA; Alcántara-Ortigoza MA; Reyna-Fabian ME; Villagómez-Martínez S; González-Del Angel A
    Eur J Oral Sci; 2014 Apr; 122(2):109-13. PubMed ID: 24460828
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gene polymorphism and folate metabolism: a maternal risk factor for Down syndrome.
    Sheth JJ; Sheth FJ
    Indian Pediatr; 2003 Feb; 40(2):115-23. PubMed ID: 12626825
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Altered LINE-1 Methylation in Mothers of Children with Down Syndrome.
    Božović IB; Stanković A; Živković M; Vraneković J; Kapović M; Brajenović-Milić B
    PLoS One; 2015; 10(5):e0127423. PubMed ID: 26017139
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synergistic effect of methyltetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphism as risk modifiers of pediatric acute lymphoblastic leukemia.
    Kamel AM; Moussa HS; Ebid GT; Bu RR; Bhatia KG
    J Egypt Natl Canc Inst; 2007 Jun; 19(2):96-105. PubMed ID: 19034339
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association between MTHFR C677T and A1298C gene polymorphisms and maternal risk for Down syndrome: A protocol for systematic review and/or meta-analysis.
    Ginani CTA; Luz JRDD; Silva SVE; Coppedè F; Almeida MDG
    Medicine (Baltimore); 2022 Jan; 101(3):e28293. PubMed ID: 35060496
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evaluation of C677T and A1298C polymorphisms of the MTHFR gene as maternal risk factors for Down syndrome and congenital heart defects.
    Brandalize AP; Bandinelli E; dos Santos PA; Roisenberg I; Schüler-Faccini L
    Am J Med Genet A; 2009 Oct; 149A(10):2080-7. PubMed ID: 19725133
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Polymorphisms of 5,10-methylenetetrahydrofolate reductase and thymidylate synthase, dietary folate intake, and the risk of leukemia in adults.
    Liu P; Zhang M; Xie X; Jin J; Holman CD
    Tumour Biol; 2016 Mar; 37(3):3265-75. PubMed ID: 26438060
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Methylenetetrahydrofolate reductase gene polymorphisms and their association with trisomy 21.
    Acácio GL; Barini R; Bertuzzo CS; Couto EC; Annichino-Bizzacchi JM; Júnior WP
    Prenat Diagn; 2005 Dec; 25(13):1196-9. PubMed ID: 16353284
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.