Pages that link to "Q78166277"
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The following pages link to A common mutation A1298C in human methylenetetrahydrofolate reductase gene: association with plasma total homocysteine and folate concentrations (Q78166277):
Displaying 50 items.
- Elevated plasma homocysteine is positively associated with age independent of C677T mutation of the methylenetetrahydrofolate reductase gene in selected Egyptian subjects (Q24791309) (← links)
- Potential Links between Impaired One-Carbon Metabolism Due to Polymorphisms, Inadequate B-Vitamin Status, and the Development of Alzheimer's Disease (Q28068353) (← links)
- Radical induction theory of ulcerative colitis (Q28245348) (← links)
- Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viability (Q28361131) (← links)
- Association of methylenetetrahydrofolate reductase (MTHFR 677C>T and 1298A>C) polymorphisms and haplotypes with silent brain infarction and homocysteine levels in a Korean population (Q33670582) (← links)
- MTHFR A1298C and C677T gene polymorphisms and susceptibility to chronic myeloid leukemia in Egypt (Q33802636) (← links)
- Methylenetetrahydrofolate reductase C677T polymorphism and type 2 diabetes mellitus in Chinese population: a meta-analysis of 29 case-control studies (Q33928280) (← links)
- Pharmacogenetics and pharmacogenomics in rheumatology. (Q34070615) (← links)
- Association of tagging SNPs in the MTHFR gene with risk of type 2 diabetes mellitus and serum homocysteine levels in a Chinese population (Q34073375) (← links)
- A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism (Q34115389) (← links)
- MTHFR polymorphisms in relation to ovarian cancer risk (Q34188679) (← links)
- Is the C677T polymorphism in methylenetetrahydrofolate reductase gene or plasma homocysteine a risk factor for diabetic peripheral neuropathy in Chinese individuals? (Q34720302) (← links)
- Methylenetetrahydrofolate reductase 677TT genotype may be associated with an increased lung cancer risk in North China: an updated meta-analysis (Q34852979) (← links)
- Methylenetetrahydrofolate reductase gene polymorphism and risk of type 2 diabetes mellitus (Q34984709) (← links)
- Methotrexate related adverse effects in patients with rheumatoid arthritis are associated with the A1298C polymorphism of the MTHFR gene (Q35553306) (← links)
- Colon Cancer and Genetic Variation in Folate Metabolism: The Clinical Bottom Line (Q35579927) (← links)
- Meta-analysis of the association of MTHFR polymorphisms with multiple myeloma risk (Q35663189) (← links)
- Joint associations of folate, homocysteine and MTHFR, MTR and MTRR gene polymorphisms with dyslipidemia in a Chinese hypertensive population: a cross-sectional study (Q36023213) (← links)
- The Genetic Diversity and Structure of Linkage Disequilibrium of the MTHFR Gene in Populations of Northern Eurasia (Q36025993) (← links)
- Benign intracranial hypertension: a diagnostic dilemma (Q36178045) (← links)
- MTHFR (Ala 222 Val) polymorphism and AMI in patients with type II diabetes mellitus (Q36263417) (← links)
- Leber hereditary optic neuropathy: do folate pathway gene alterations influence the expression of mitochondrial DNA mutation? (Q36348609) (← links)
- Genetic variations in MTHFR and gastric cardia adenocarcinoma susceptibility in the Chinese Han population (Q36412056) (← links)
- Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: an overview (Q36443604) (← links)
- Influence of combined methionine synthase (MTR 2756A > G) and methylenetetrahydrofolate reductase (MTHFR 677C > T) polymorphisms to plasma homocysteine levels in Korean patients with ischemic stroke (Q37065550) (← links)
- A Meta-Analysis of Association between Methylenetetrahydrofolate Reductase Gene (MTHFR) 677C/T Polymorphism and Diabetic Retinopathy (Q37202995) (← links)
- Syndromes, disorders and maternal risk factors associated with neural tube defects (IV). (Q37208056) (← links)
- Homocysteine, MTHFR gene polymorphisms, and cardio-cerebrovascular risk (Q37231486) (← links)
- Associations between single nucleotide polymorphisms in folate uptake and metabolizing genes with blood folate, homocysteine, and DNA uracil concentrations (Q37309187) (← links)
- Prevalence of genetic risk factors related with thrombophilia and hypofibrinolysis in patients with osteonecrosis of the femoral head in Poland (Q37357673) (← links)
- A systematic review of meta-analyses on gene polymorphisms and gastric cancer risk (Q37511742) (← links)
- Does the MTHFR A1298C Polymorphism Modulate the Cardiorespiratory Response to Training? (Q37535097) (← links)
- Mathematical modeling of folate metabolism: predicted effects of genetic polymorphisms on mechanisms and biomarkers relevant to carcinogenesis (Q37550780) (← links)
- A retrospective comparative exploratory study on two methylentetrahydrofolate reductase (MTHFR) polymorphisms in esophagogastric cancer: the A1298C MTHFR polymorphism is an independent prognostic factor only in neoadjuvantly treated gastric cancer p (Q37580616) (← links)
- Does the MTHFR C677T gene polymorphism indicate cardiovascular disease risk in type 2 diabetes mellitus patients? (Q37680631) (← links)
- Homocysteine and methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Tunisian patients with severe coronary artery disease (Q39022051) (← links)
- Polymorphisms in the MTHFR gene influence embryo viability and the incidence of aneuploidy (Q39858736) (← links)
- Associations of methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms with genetic susceptibility to rheumatoid arthritis: a meta-analysis (Q40648465) (← links)
- Methylenetetrahydrofolate reductase C677T gene mutation as risk factor for sudden sensorineural hearing loss: association with plasma homocysteine, folate and cholesterol concentrations (Q43056915) (← links)
- Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction (Q43672706) (← links)
- Prevalence of the methylenetetrahydrofolate reductase 677C > T mutation in the Mediterranean Spanish population. Association with cardiovascular risk factors (Q43779466) (← links)
- Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos (Q43951023) (← links)
- Comment on 'increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos'. (Q44161608) (← links)
- Reduced folate carrier polymorphism (80A-->G) and neural tube defects (Q44389085) (← links)
- An updated meta-analysis of methylenetetrahydrofolate reductase gene 677C/T polymorphism with diabetic nephropathy and diabetic retinopathy (Q44513343) (← links)
- Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage. (Q44562476) (← links)
- Prevalence of methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Taiwanese patients with Type 2 diabetic mellitus (Q44796417) (← links)
- Prevalence of MTHFR gene polymorphisms (C677T and A1298C) among Tamilians (Q45046893) (← links)
- Methylenetetrahydrofolate reductase, common polymorphisms, and relation to disease (Q46356448) (← links)
- Genetic determinants of methotrexate toxicity in rheumatoid arthritis patients: a study of polymorphisms affecting methotrexate transport and folate metabolism (Q46496885) (← links)