Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Neural Tube Defects and DHFR[original query] |
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| The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population. American journal of medical genetics. Part A 2007 Jun 143A (11): 1174-80. Parle-McDermott Anne, Pangilinan Faith, Mills James L, Kirke Peadar N, Gibney Eileen R, Troendle James, O'Leary Valerie B, Molloy Anne M, Conley Mary, Scott John M, Brody Lawrence |
| An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women. Human genetics 2008 Apr 123 (3): 289-95. Stanis?awska-Sachadyn Anna, Brown Karen S, Mitchell Laura E, Woodside Jayne V, Young Ian S, Scott John M, Murray Liam, Boreham Colin A, McNulty Helene, Strain J J, Whitehead Alexander |
| A 19-base pair deletion polymorphism in dihydrofolate reductase is associated with increased unmetabolized folic acid in plasma and decreased red blood cell folate. The Journal of nutrition 2008 Dec 138 (12): 2323-7. Kalmbach Renee D, Choumenkovitch Silvina F, Troen Aron P, Jacques Paul F, D'Agostino Ralph, Selhub Jac |
| Association of FOLH1, DHFR, and MTHFR gene polymorphisms with susceptibility of Neural Tube Defects: A case control study from Eastern India. Birth defects research 2018 Aug . Paul Silpita, Sadhukhan Susanta, Munian Dinesh, Bankura Biswabandhu, Das Madhusud |
| Maternal association and influence of DHFR 19?bp deletion variant predisposes foetus to anencephaly susceptibility: a family-based triad study. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2018 Apr 1-19. Prasoona K R, Sunitha T, Srinadh B, Muni Kumari T, Jyothy |
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