Polymorphisms in Maternal Selected Folate Metabolism-Related Genes in Neural Tube Defect-Affected Pregnancy
暂无分享,去创建一个
A. Aklilu | S. Gebre | M. Gebremariam | A. Aklilu | D. Alemayehu | WinnerK Dewelle | D. Melka | M. Gebremariam | MarkosA Alemayehu | DawitH Alemayehu | TamrayehuS Woldemichael | D. S. Melka | Winner K. Dewelle | Markos A. Alemayehu | Tamrayehu S. Woldemichael
[1] Ji Li,et al. MTRR rs1532268 polymorphism and gastric cancer risk: evidence from a meta-analysis , 2022, The Journal of international medical research.
[2] D. Feng,et al. Association of MTHFR 677C > T gene polymorphism with neonatal defects: a meta-analysis of 81444 subjects , 2022, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.
[3] T. Matsha,et al. Methylenetetrahydrofolate (MTHFR), the One-Carbon Cycle, and Cardiovascular Risks , 2021, Nutrients.
[4] B. Wlodarczyk,et al. Gene Environment Interactions in the Etiology of Neural Tube Defects , 2021, Frontiers in Genetics.
[5] Everton Cruz dos Santos,et al. MTHFR C677T and A1298C Polymorphisms in Breast Cancer, Gliomas and Gastric Cancer: A Review , 2021, Genes.
[6] K. Nasri,et al. Association of MTHFR C677T, MTHFR A1298C, and MTRR A66G Polymorphisms with Neural Tube Defects in Tunisian Parents , 2019, Pathobiology.
[7] Wei Liu,et al. Association of neural tube defects with maternal alterations and genetic polymorphisms in one-carbon metabolic pathway , 2019, Italian Journal of Pediatrics.
[8] Yuying Wang,et al. Two Common MTHFR Gene Polymorphisms (C677T and A1298C) and Fetal Congenital Heart Disease Risk: An Updated Meta-Analysis with Trial Sequential Analysis , 2018, Cellular Physiology and Biochemistry.
[9] K. Kamali,et al. The study of association between reduced folate carrier 1 (RFC1) polymorphism and non-syndromic cleft lip/palate in Iranian population , 2017, BioImpacts : BI.
[10] A. Oussalah,et al. Association of TCN2 rs1801198 c.776G>C polymorphism with markers of one-carbon metabolism and related diseases: a systematic review and meta-analysis of genetic association studies. , 2017, The American journal of clinical nutrition.
[11] H. Ghazy,et al. MTHFR A1298C and C677T gene polymorphisms and susceptibility to chronic myeloid leukemia in Egypt. , 2014, International journal of clinical and experimental pathology.
[12] Yuan-yuan Li,et al. Association between MTR A2756G and MTRR A66G polymorphisms and maternal risk for neural tube defects: a meta-analysis. , 2013, Gene.
[13] Jian Zhang,et al. Reduced folate carrier A80G polymorphism and susceptibility to neural tube defects: a meta-analysis. , 2012, Gene.
[14] G. Chandak,et al. Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India. , 2011, Birth defects research. Part A, Clinical and molecular teratology.
[15] J. Yarnell,et al. The transcobalamin (TCN2) 776C>G polymorphism affects homocysteine concentrations among subjects with low vitamin B12 status , 2010, European Journal of Clinical Nutrition.
[16] E. Van Obberghen,et al. Nutritional and genetic determinants of vitamin B and homocysteine metabolisms in neural tube defects: A multicenter case–control study , 2008, American journal of medical genetics. Part A.
[17] A. Parle‐McDermott,et al. Reduced folate carrier polymorphisms and neural tube defect risk. , 2006, Molecular genetics and metabolism.
[18] M. Margaglione,et al. Homocysteine metabolism in families from southern Italy with neural tube defects: role of genetic and nutritional determinants , 2006, Prenatal diagnosis.
[19] M. Alikaşifoğlu,et al. Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population. , 2005, The Turkish journal of pediatrics.
[20] A. Parle‐McDermott,et al. Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association. , 2005, Molecular genetics and metabolism.
[21] M. Marazita,et al. Studies of reduced folate carrier 1 (RFC1) A80G and 5,10‐methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects , 2005, American journal of medical genetics. Part A.
[22] A. Parle‐McDermott,et al. Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population. , 2005, Birth defects research. Part A, Clinical and molecular teratology.
[23] G. Kauwell,et al. Methionine synthase reductase 66A->G polymorphism is associated with increased plasma homocysteine concentration when combined with the homozygous methylenetetrahydrofolate reductase 677C->T variant. , 2004, The Journal of nutrition.
[24] T. Félix,et al. Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil. , 2004, Birth defects research. Part A, Clinical and molecular teratology.
[25] M. Pearce,et al. Gene–gene interaction in folate-related genes and risk of neural tube defects in a UK population , 2004, Journal of Medical Genetics.
[26] P. Ueland,et al. High-level multiplex genotyping of polymorphisms involved in folate or homocysteine metabolism by matrix-assisted laser desorption/ionization mass spectrometry. , 2004, Clinical chemistry.
[27] A. Parle‐McDermott,et al. Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects , 2003, Journal of Human Genetics.
[28] H. Blom,et al. Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects , 2002, European Journal of Human Genetics.
[29] R. Finnell,et al. Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population , 2002, Journal of Human Genetics.
[30] A. Evans,et al. The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations. , 2001, Atherosclerosis.
[31] J H Eckfeldt,et al. The 1298A-->C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine. , 2001, Atherosclerosis.
[32] K. Volcik,et al. Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in Hispanics. , 2000, American journal of medical genetics.
[33] J. Kaufman,et al. A Common Polymorphism in Methionine Synthase Reductase Increases Risk of Premature Coronary Artery Disease , 2000, Journal of cardiovascular risk.
[34] R. Rozen,et al. A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida. , 1999, Molecular genetics and metabolism.
[35] D. Shields,et al. The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother. , 1999, American journal of human genetics.
[36] R. Rozen. Genetic Predisposition to Hyperhomocysteinemia: Deficiency of Methylenetetrahydrofolate Reductase (MTHFR) , 1997, Thrombosis and Haemostasis.
[37] L. Matherly,et al. Biology of the major facilitative folate transporters SLC19A1 and SLC46A1. , 2014, Current topics in membranes.
[38] Wan-I Li,et al. Correlation of polymorphism of MTHFRs and RFC-1 genes with neural tube defects in China. , 2008, Birth defects research. Part A, Clinical and molecular teratology.