Keywords: متیونین سنتاز ردوکتاز; Nitric oxide synthase; Cytochrome P450 reductase; Diflavin oxidoreductase; Fluorescence; Protein dynamics; NOS; nitric oxide synthase; CPR; cytochrome P450 reductase; CaM; calmodulin; MSR; methionine synthase reductase; P450 BM3; cytochrome P450 BM3; FAD;
مقالات ISI متیونین سنتاز ردوکتاز (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Analysis of occurrence of MTRR gene polymorphism in Down syndrome and other intellectually disabled children
Keywords: متیونین سنتاز ردوکتاز; Intellectual disability; Down syndrome; MTRR c.66Aâ¯>â¯G; PCR-RFLP analysis; Folate metabolism; Methionine synthase reductase; ID; Intellectual Disability; WHO; World Health Organization; IQ; Intelligence Quotient; DS; Down Syndrome; MTRR; 5-Methyltetra
Associations between genetic variation in one-carbon metabolism and leukocyte DNA methylation in valproate-treated patients with epilepsy
Keywords: متیونین سنتاز ردوکتاز; DNA methylation; Epilepsy; One-carbon metabolism; Single nucleotide polymorphism; Valproate; AED; antiepileptic drug; ANOVA; one-way analysis of variance; BHMT; betaine-homocysteine methyltransferas; FA; folate; Hcy; homocysteine; HWE; hardy-weinberg eq
A66G and C524T polymorphisms of methionine synthase reductase gene are linked to the development of acyanotic congenital heart diseases in Egyptian children
Keywords: متیونین سنتاز ردوکتاز; CHD; Congenital heart diseases; MTRR; Methionine synthase reductase; ASD; Atrial septal defect; VSD; Ventricular septal defect; PDA; Patent ductus arteriosus.; Acyanotic; CHD; MTRR; RFLP; A66G; C524T;
Methionine synthase and methionine synthase reductase interact with MMACHC and with MMADHC
Keywords: متیونین سنتاز ردوکتاز; Rare disease; Vitamin B12; Methionine synthase; Methionine synthase reductase; MMACHC; MMADHC;
Genetic animal models to decipher the pathogenic effects of vitamin B12 and folate deficiency
Keywords: متیونین سنتاز ردوکتاز; Vitamin B12; Folate; Methyl donor deficiency; Pathogenesis; Genetic animal models; B12; vitamin B12; SAM; S-adenosylmethionine; SAH; S-adenosylhomocysteine; HCY; homocysteine; KO; knock-out; ES cells; embryonic stem cells; OCM; one-carbon metabolism; NTD;
Proximal FAD histidine residue influences interflavin electron transfer in cytochrome P450 reductase and methionine synthase reductase
Keywords: متیونین سنتاز ردوکتاز; Methionine synthase reductase; Cytochrome P450 reductase; Electron transfer; Flavin; Stopped-flow spectroscopy;
Identification of one-electron reductases that activate both the hypoxia prodrug SN30000 and diagnostic probe EF5
Keywords: متیونین سنتاز ردوکتاز; Hypoxia; Hypoxia-activated prodrugs; SN30000; EF5; Methionine synthase reductase
Association between MTR A2756G and MTRR A66G polymorphisms and maternal risk for neural tube defects: A meta-analysis
Keywords: متیونین سنتاز ردوکتاز; CI; confidence interval; GCP II; glutamate carboxypeptidase II; HWE; Hardy-Weinberg equilibrium; MTR; methionine synthase; MTRR; methionine synthase reductase; MTHFR; methylenetetrahydrofolate reductase; NTD; neural tube defect; OR; odds ratio; MTR; MTRR;
NADPH-cytochrome P450 oxidoreductase: Prototypic member of the diflavin reductase family
Keywords: متیونین سنتاز ردوکتاز; CYPOR; NADPH-cytochrome P450 oxidoreductase; CYPOR/POR; CYPOR gene; P450; cytochrome P450; cyt c; cytochrome c; cyt b5; cytochrome b5; NOS; nitric oxide synthase; iNOS; inducible NOS; nNOS; neuronal NOS; eNOS; endotherial NOS; NOSred; the reductase doma
DNA methylation-based biomarkers in serum of patients with breast cancer
Keywords: متیونین سنتاز ردوکتاز; 5-Aza-CdR; 5-aza-2â²-deoxycytidine; 5-Aza-CR; 5-azacytidine; 5mC; 5-methylcytidine; AIMS; amplification of inter-methylated sites; APC; adenomatous polyposis coli; BiMP; bisulfite methylation profiling; BRCA1; breast cancer gene 1; BsPP; bisulfite padloc
Germline variation in the MTHFR and MTRR genes determines the nadir of bone density in pediatric acute lymphoblastic leukemia: A prospective study
Keywords: متیونین سنتاز ردوکتاز; Childhood cancer; Acute lymphoblastic leukemia; Bone density; Methylenetetrahydrofolate reductase; Methionine synthase reductase; Homocysteine
Polygenic association with total homocysteine in the post-folic acid fortification era: The CARDIA study
Keywords: متیونین سنتاز ردوکتاز; Cystathionine β-synthase; Folic acid; Homocysteine; Methylenetetrahydrofolate reductase; Methionine synthase; Methionine synthase reductase
Methylenetetrahydrofolate reductase (MTHFR) C677T and thymidylate synthase promoter (TSER) polymorphisms in Indonesian children with and without leukemia
Keywords: متیونین سنتاز ردوکتاز; ALL; acute lymphoblastic leukemia; CH2-THF; 5,10-methylenetetrahydrofolate; DDH; double distilled water; DHF; dihydrofolate; DHFR; dihydrofolate reductase; dTMP; deoxythymidine monophosphate; dTTP; deoxythymidine triphosphate; dUMP; deoxyuridine monophosp
Restricted role for methionine synthase reductase defined by subcellular localization
Keywords: متیونین سنتاز ردوکتاز; Methionine synthase reductase; Mitochondrial localization; Immunofluorescence; Cobalamin; Vitamin B12
His595Tyr Polymorphism in the Methionine Synthase Reductase (MTRR) Gene Is Associated With Pancreatic Cancer Risk
Keywords: متیونین سنتاز ردوکتاز; LD; linkage disequilibrium; MTRR; methionine synthase reductase; SNP; single nucleotide polymorphism;
Polymorphism C776G in the transcobalamin II gene and homocysteine, folate and vitamin B12 concentrations. Association with MTHFR C677T and A1298C and MTRR A66G polymorphisms in healthy children
Keywords: متیونین سنتاز ردوکتاز; TC II, transcobalamin II; HHcy, hyperhomocysteinemia; Hcy, homocysteine; MTHFR, methylenetetrahydrofolate reductase; MTRR, methionine synthase reductase; TC-R, transcobalamin-receptorHomocysteine; Transcobalamin II; Children; Methionine synthase reductase
Metabolic derangement of methionine and folate metabolism in mice deficient in methionine synthase reductase
Keywords: متیونین سنتاز ردوکتاز; Homocysteine; Hyperhomocyst(e)inemia; Folate metabolism; Gene trap; Methionine synthase reductase; Methionine metabolism; Hypomethioninemia; Methyl trap; S-Adenosylmethionine; S-Adenosylhomocysteine