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 *

263 related articles for article (PubMed ID: 27743313)

  • 21. The MTHFR 677C>T polymorphism is associated with unmetabolized folic acid in breast milk in a cohort of Canadian women.
    Page R; Wong A; Arbuckle TE; MacFarlane AJ
    Am J Clin Nutr; 2019 Aug; 110(2):401-409. PubMed ID: 31005971
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Oxidative stress and platelet activation in subjects with moderate hyperhomocysteinaemia due to MTHFR 677 C→T polymorphism.
    Dragani A; Falco A; Santilli F; Basili S; Rolandi G; Cerasa L; Lattanzio S; Ciabattoni G; Patrono C; Davì G
    Thromb Haemost; 2012 Sep; 108(3):533-42. PubMed ID: 22782530
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Characterization of mutations in severe methylenetetrahydrofolate reductase deficiency reveals an FAD-responsive mutation.
    Sibani S; Leclerc D; Weisberg IS; O'Ferrall E; Watkins D; Artigas C; Rosenblatt DS; Rozen R
    Hum Mutat; 2003 May; 21(5):509-20. PubMed ID: 12673793
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A founder mutation causing a severe methylenetetrahydrofolate reductase (MTHFR) deficiency in Bukharian Jews.
    Ben-Shachar S; Zvi T; Rolfs A; Breda Klobus A; Yaron Y; Bar-Shira A; Orr-Urtreger A
    Mol Genet Metab; 2012 Nov; 107(3):608-10. PubMed ID: 22947400
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Early treatment using betaine and methionine for a neonate with MTHFR deficiency.
    Nishimoto E; Ito Y; Sakakibara T; Nishikubo T
    Pediatr Int; 2019 Dec; 61(12):1265-1266. PubMed ID: 31782227
    [No Abstract]   [Full Text] [Related]  

  • 26. High dietary folate in pregnant mice leads to pseudo-MTHFR deficiency and altered methyl metabolism, with embryonic growth delay and short-term memory impairment in offspring.
    Bahous RH; Jadavji NM; Deng L; Cosín-Tomás M; Lu J; Malysheva O; Leung KY; Ho MK; Pallàs M; Kaliman P; Greene NDE; Bedell BJ; Caudill MA; Rozen R
    Hum Mol Genet; 2017 Mar; 26(5):888-900. PubMed ID: 28069796
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Life-threatening methylenetetrahydrofolate reductase (MTHFR) deficiency with extremely early onset: characterization of two novel mutations in compound heterozygous patients.
    Forges T; Chery C; Audonnet S; Feillet F; Gueant JL
    Mol Genet Metab; 2010 Jun; 100(2):143-8. PubMed ID: 20356773
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegia.
    Lossos A; Teltsh O; Milman T; Meiner V; Rozen R; Leclerc D; Schwahn BC; Karp N; Rosenblatt DS; Watkins D; Shaag A; Korman SH; Heyman SN; Gal A; Newman JP; Steiner-Birmanns B; Abramsky O; Kohn Y
    JAMA Neurol; 2014 Jul; 71(7):901-4. PubMed ID: 24797679
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Severe methylenetetrahydrofolate reductase deficiency in mice results in behavioral anomalies with morphological and biochemical changes in hippocampus.
    Jadavji NM; Deng L; Leclerc D; Malysheva O; Bedell BJ; Caudill MA; Rozen R
    Mol Genet Metab; 2012 Jun; 106(2):149-59. PubMed ID: 22521626
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Methylenetetrahydrofolate Reductase deficiency and anesthesia: importance of a detailed preoperative evaluation].
    Santos CDSE; Grayson BE
    Braz J Anesthesiol; 2019; 69(6):637-638. PubMed ID: 31796301
    [No Abstract]   [Full Text] [Related]  

  • 31. Adult-onset severe methylenetetrahydrofolate reductase deficiency characterized by reversible spastic paraplegia with a novel mutation.
    Lin N; Jiang N; Dai Y; Gao J; Wang L
    Neurol Sci; 2016 Oct; 37(10):1735-7. PubMed ID: 27118298
    [No Abstract]   [Full Text] [Related]  

  • 32. Severe scoliosis in a patient with severe methylenetetrahydrofolate reductase deficiency.
    Munoz T; Patel J; Badilla-Porras R; Kronick J; Mercimek-Mahmutoglu S
    Brain Dev; 2015 Jan; 37(1):168-70. PubMed ID: 24726568
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prevalence of factor V leiden, MTHFR C677T and MTHFR A1298C polymorphisms in patients with deep vein thrombosis in Central Iran.
    Ehsani M; Imani A; Moravveji A
    Mol Biol Rep; 2018 Aug; 45(4):621-624. PubMed ID: 29855758
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Relations between molecular and biological abnormalities in 11 families from siblings affected with methylenetetrahydrofolate reductase deficiency.
    Tonetti C; Saudubray JM; Echenne B; Landrieu P; Giraudier S; Zittoun J
    Eur J Pediatr; 2003 Jul; 162(7-8):466-475. PubMed ID: 12733064
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mthfr deficiency induces endothelial progenitor cell senescence via uncoupling of eNOS and downregulation of SIRT1.
    Lemarié CA; Shbat L; Marchesi C; Angulo OJ; Deschênes ME; Blostein MD; Paradis P; Schiffrin EL
    Am J Physiol Heart Circ Physiol; 2011 Mar; 300(3):H745-53. PubMed ID: 21169404
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Homocysteinemia due to MTHFR deficiency in a young adult presenting with bilateral lens subluxations.
    Couser NL; McClure J; Evans MW; Haines NR; Burden SK; Muenzer J
    Ophthalmic Genet; 2017; 38(1):91-94. PubMed ID: 27046515
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR.
    Goyette P; Christensen B; Rosenblatt DS; Rozen R
    Am J Hum Genet; 1996 Dec; 59(6):1268-75. PubMed ID: 8940272
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Shifting landscapes of human MTHFR missense-variant effects.
    Weile J; Kishore N; Sun S; Maaieh R; Verby M; Li R; Fotiadou I; Kitaygorodsky J; Wu Y; Holenstein A; Bürer C; Blomgren L; Yang S; Nussbaum R; Rozen R; Watkins D; Gebbia M; Kozich V; Garton M; Froese DS; Roth FP
    Am J Hum Genet; 2021 Jul; 108(7):1283-1300. PubMed ID: 34214447
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic modulation of homocysteinemia.
    Rozen R
    Semin Thromb Hemost; 2000; 26(3):255-61. PubMed ID: 11011843
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sex-dependent behavioral effects of Mthfr deficiency and neonatal GABA potentiation in mice.
    Levav-Rabkin T; Blumkin E; Galron D; Golan HM
    Behav Brain Res; 2011 Jan; 216(2):505-13. PubMed ID: 20813139
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.