Works matching DE "METHIONINE synthase reductase"
Results: 51
Individualized Supplementation of Folic Acid According to Polymorphisms of Methylenetetrahydrofolate Reductase (MTHFR), Methionine Synthase Reductase (MTRR) Reduced Pregnant Complications.
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- Gynecologic & Obstetric Investigation, 2015, v. 79, n. 2, p. 107, doi. 10.1159/000367656
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Association of polymorphisms in DNMT1, DNMT3A, DNMT3B, MTHFR and MTRR genes with global DNA methylation levels and prognosis of autoimmune thyroid disease.
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- Clinical & Experimental Immunology, 2012, v. 170, n. 2, p. 194, doi. 10.1111/j.1365-2249.2012.04646.x
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Methylcobalamin in Vitamin B<sub>12</sub> Deficiency: To Give or not to Give?
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- Journal of Pharmacology & Pharmacotherapeutics, 2017, v. 8, n. 1, p. 33, doi. 10.4103/jpp.JPP_173_16
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Are Genes Connected with Homocysteine Metabolism Associated with Bipolar Disorder?
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- Neuropsychobiology, 2014, v. 69, n. 2, p. 107, doi. 10.1159/000358091
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Joint associations of folate, homocysteine and MTHFR, MTR and MTRR gene polymorphisms with dyslipidemia in a Chinese hypertensive population: a cross-sectional study.
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- Lipids in Health & Disease, 2015, v. 14, n. 1, p. 1, doi. 10.1186/s12944-015-0099-x
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Association of methionine synthase rs1801394 and methionine synthase reductase rs1805087 polymorphisms with meningioma in adults: A meta-analysis.
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- Biomedical Reports, 2014, v. 2, n. 3, p. 432, doi. 10.3892/br.2014.248
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Identification and characterization of a bacterial core methionine synthase.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-58873-z
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Haplotype analysis of the folate-related genes MTHFR, MTRR, and MTR and migraine with aura.
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- Cephalalgia, 2013, v. 33, n. 7, p. 469, doi. 10.1177/0333102413477738
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Functional variant in methionine synthase reductase intron-1 is associated with pleiotropic congenital malformations.
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- Molecular & Cellular Biochemistry, 2015, v. 407, n. 1/2, p. 51, doi. 10.1007/s11010-015-2453-8
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- Article
Should we Still use Nitrous Oxide in our Clinical Practice? No!
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- Turkish Journal of Anesthesia & Reanimation, 2017, v. 45, n. 1, p. 3, doi. 10.5152/TJAR.2017.24011
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Nitrous Oxide is an Effective and Safe Anesthetic.
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- Turkish Journal of Anesthesia & Reanimation, 2017, v. 45, n. 1, p. 1, doi. 10.5152/TJAR.2017.23011
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- Article
Aberrant Expression of Folate Metabolism Enzymes and Its Diagnosis and Survival Prediction in Ovarian Carcinoma.
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- Analytical Cellular Pathology: Cellular Oncology, 2019, p. 1, doi. 10.1155/2019/1438628
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A study of MTRR 66A>G gene polymorphism in patients with autism from northern Iran.
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- Neurology Asia, 2017, v. 22, n. 1, p. 59
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Mouse model for deficiency of methionine synthase reductase exhibits short-term memory impairment and disturbances in brain choline metabolism.
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- Biochemical Journal, 2014, v. 461, n. 2, p. 205, doi. 10.1042/BJ20131568
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Role of polymorphisms of folate-cycle enzymes in diabetic retinopathy progression in patients with type 2 diabetic mellitus.
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- Journal of Ophthalmology (Ukraine) / Oftalʹmologičeskij Žurnal, 2022, n. 5, p. 3, doi. 10.31288/oftalmolzh20225311
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Methionine synthase A2756G polymorphism and lymphoma risk: a meta-analysis.
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- European Review for Medical & Pharmacological Sciences, 2017, v. 21, n. 13, p. 3075
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Geographical and Ethnic Distributions of the MTHFR C677T, A1298C and MTRR A66G Gene Polymorphisms in Chinese Populations: A Meta-Analysis.
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- PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0152414
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Identification of metE as a Second Target of the sRNA scr5239 in Streptomyces coelicolor.
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- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0120147
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Polymorphisms in Folate-Related Enzyme Genes in Idiopathic Infertile Brazilian Men.
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- Reproductive Sciences, 2011, v. 18, n. 12, p. 1267, doi. 10.1177/1933719111411729
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The polymorphisms of methionine synthase (MTR) and methionine synthase reductase (MTRR) genes in pathogenesis of preeclampsia.
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- 2017
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- journal article
Meta-analyses on the association of MTR A2756G and MTRR A66G polymorphisms with neural tube defect risks in Caucasian children.
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- Journal of Maternal-Fetal & Neonatal Medicine, 2013, v. 26, n. 12, p. 1166, doi. 10.3109/14767058.2013.777699
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- Article
Reductive elimination pathway for homocysteine to methionine conversion in cobalamin-dependent methionine synthase.
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- Journal of Biological Inorganic Chemistry (JBIC), 2012, v. 17, n. 4, p. 611, doi. 10.1007/s00775-012-0881-4
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Differentially expressed proteins in fluconazole-susceptible and fluconazole-resistant isolates of Candida glabrata.
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- Drug Discoveries & Therapeutics, 2015, v. 9, n. 3, p. 191, doi. 10.5582/ddt.2015.01010
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- Article
Risk of congenital heart defects is influenced by genetic variation in folate metabolism.
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- Cardiology in the Young, 2013, v. 23, n. 1, p. 89, doi. 10.1017/S1047951112000431
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Gating mechanisms for biological electron transfer: Integrating structure with biophysics reveals the nature of redox control in cytochrome P450 reductase and copper-dependent nitrite reductase
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- FEBS Letters, 2012, v. 586, n. 5, p. 578, doi. 10.1016/j.febslet.2011.07.003
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5,10-Methylenetetrahydrofolate reductase ( MTHFR), methionine synthase ( MTRR), and methionine synthase reductase ( MTR) gene polymorphisms and adult meningioma risk.
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- Journal of Neuro-Oncology, 2013, v. 115, n. 2, p. 233, doi. 10.1007/s11060-013-1218-z
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A Polymorphism in the MTRR Gene Is Associated with Early Childhood Caries and Underweight.
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- Caries Research, 2017, v. 51, n. 2, p. 102, doi. 10.1159/000451037
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A Polymorphism in the MTRR Gene Is Associated with Early Childhood Caries and Underweight.
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- 2017
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- journal article
Are MTHFR C677T and MTRR A66G Polymorphisms Associated with Overweight/Obesity Risk? From a Case-Control to a Meta-Analysis of 30,327 Subjects.
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- International Journal of Molecular Sciences, 2015, v. 16, n. 6, p. 11849, doi. 10.3390/ijms160611849
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Associations of MTHFR C677T and MTRR A66G Gene Polymorphisms with Metabolic Syndrome: A Case-Control Study in Northern China.
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- International Journal of Molecular Sciences, 2014, v. 15, n. 12, p. 21687, doi. 10.3390/ijms151221687
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NaCl stress induces CsSAMs gene expression in Cucumis sativus by mediating the binding of CsGT-3b to the GT-1 element within the CsSAMs promoter.
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- Planta: An International Journal of Plant Biology, 2017, v. 245, n. 5, p. 889, doi. 10.1007/s00425-017-2650-7
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Biochemical profile of children with autism spectrum disorders associated with genetic deficiency of the folate cycle.
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- Biochimica Clinica, 2023, v. 47, n. 2, p. 132, doi. 10.19186/BC_2022.082
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Methionine synthase reductase A66G polymorphism and leukemia risk: evidence from published studies.
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- Leukemia & Lymphoma, 2014, v. 55, n. 8, p. 1910, doi. 10.3109/10428194.2013.867492
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MTRR gene variants may predispose to the risk of Congenital Heart Disease in Down syndrome patients of Indian origin.
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- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 61, doi. 10.1016/j.ejmhg.2016.02.006
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Methionine synthase A2756G and reduced folate carrier1 A80G gene polymorphisms as maternal risk factors for Down syndrome in Egypt.
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- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 217, doi. 10.1016/j.ejmhg.2015.09.003
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Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease.
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- Free Radical Research, 2013, v. 47, n. 6/7, p. 498, doi. 10.3109/10715762.2013.793319
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- Article
Massive hyperhomocysteinaemia as a complication of nitrous oxide inhalation.
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- British Journal of Clinical Pharmacology, 2016, v. 81, n. 2, p. 391, doi. 10.1111/bcp.12813
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Folate metabolism-related gene polymorphisms and susceptibility to primary liver cancer in North China.
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- Medical Oncology, 2012, v. 29, n. 3, p. 1837, doi. 10.1007/s12032-011-0066-y
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- Article
Association between genetic polymorphisms in folate-related enzyme genes and infertile men with non-obstructive azoospermia.
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- Systems Biology in Reproductive Medicine, 2015, v. 61, n. 5, p. 286, doi. 10.3109/19396368.2015.1049752
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- Article
Gender-specific interactions of MTHFR C677T and MTRR A66G polymorphisms with overweight/obesity on serum lipid levels in a Chinese Han population.
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- Lipids in Health & Disease, 2016, v. 15, p. 1, doi. 10.1186/s12944-016-0354-9
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- Article
Association Between Methionine Synthase Reductase A66G Polymorphism and the Risk of Congenital Heart Defects: Evidence From Eight Case-Control Studies.
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- Pediatric Cardiology, 2014, v. 35, n. 7, p. 1091, doi. 10.1007/s00246-014-0948-9
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Effects of increased temperature on dimethylsulfoniopropionate (DMSP) concentration and methionine synthase activity in Symbiodinium microadriaticum.
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- Biogeochemistry, 2012, v. 110, n. 1-3, p. 17, doi. 10.1007/s10533-012-9733-0
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Update analysis on the association between Methionine synthase rs1805087 A/G variant and risk of prostate cancer.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-70223-7
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Methionine synthase 2756AA polymorphism is associated with the risk of cognitive impairment in patients with late-life depression.
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- Asia-Pacific Psychiatry, 2017, v. 9, n. 1, p. n/a, doi. 10.1111/appy.12242
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The MTRR 66A>G polymorphism and maternal risk of birth of a child with Down syndrome in Caucasian women: a case-control study and a meta-analysis.
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- Molecular Biology Reports, 2014, v. 41, n. 9, p. 5571, doi. 10.1007/s11033-014-3462-5
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Maternal gene polymorphisms involved in folate metabolism and the risk of having a Down syndrome offspring: a meta-analysis.
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- Mutagenesis, 2013, v. 28, n. 6, p. 661, doi. 10.1093/mutage/get045
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Genetic Variant in <i>MTRR</i>, but Not <i>MTR</i>, Is Associated with Risk of Congenital Heart Disease: An Integrated Meta-Analysis.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0089609
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Methionine Synthase A2756G Polymorphism and Risk of Colorectal Adenoma and Cancer: Evidence Based on 27 Studies.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0060508
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Age-Dependent Decrease and Alternative Splicing of Methionine Synthase mRNA in Human Cerebral Cortex and an Accelerated Decrease in Autism.
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- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0056927
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- Article
Unraveling Vitamin B<sub>12</sub>-Responsive Gene Regulation in Algae.
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- Plant Physiology, 2014, v. 165, n. 1, p. 388, doi. 10.1104/pp.113.234369
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- Article