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Common polymorphisms in MTHFR (show MTHFR ELISA Kits), methionine synthase (show MTR ELISA Kits) and cystathione beta lyase genes have no role in premature acute myocardial infarction in Pakistani population.
An association between the MTRR A66G polymorphism and LC ( p = 0.042) was found. In addition, this allele was observed more frequently in smokers compared to nonsmokers ( p = 0.030). In contrast, the distribution of the MTR (show MTR ELISA Kits) 2756A>G and the MTRR 524 C> T allele frequencies were similar in the subject cases and controls.
Meta-analysis suggests that MTRR 66A>G polymorphism may be associated with oligoasthenozoospermia risk.
Study in Egyptian children showed that MTRR A66G and C524T polymorphisms were associated with a higher congenital heart diseases risk in the homozygote comparison of wild and mutant genotypes and also in heterozygote and mutant comparison.
Our findings suggest that individuals with the MTHFR (show MTHFR ELISA Kits) 677TT or MTRR 66AG/GG genotypes are more susceptible to the detrimental effect of being overweight/obesity on Type 2 Diabetes Mellitus
The MTR (show MTR ELISA Kits) A2756G, MTRR A66G, MTHFR (show MTHFR ELISA Kits) C677T and MTHFR (show MTHFR ELISA Kits) A1298C polymorphisms were assessed. MTR (show MTR ELISA Kits) A2756G, MTRR A66G, and MTHFR (show MTHFR ELISA Kits) C677T gene polymorphisms were associated with the risk of NSCL (show NHLH1 ELISA Kits)/P (all p < 0.05). Logistic regression analysis revealed that MTR (show MTR ELISA Kits) A2756G, MTR (show MTR ELISA Kits) RA66G, and MTHFR (show MTHFR ELISA Kits) C667T might increase the risk of Nonsyndromic Cleft Lip/Palate
study widens the clinical, molecular, metabolic, and cytological knowledge of deficiency MTRR enzyme.
The present study suggests that the G allele of MTR (show MTR ELISA Kits) A2756G polymorphism is associated with an increased risk of autism.
MTHFR (show MTHFR ELISA Kits) C667T/A1298C and MTRR A66G genotypes are not associated with premature ovarian failure development, but they affect the patients' serum homocysteine concentrations.
MTRR genetic polymorphisms are risk factor for predicting cardiovascular manifestations in Marfan syndrome.
The Mtrr genotype of either maternal grandparent dictates the developmental potential of their wild-type grandprogeny. These effects are associated with altered DNA methylation (show HELLS ELISA Kits) patterns and two distinct phenotypes: intrauterine growth defects and congenital malformations that are separable through embryo transfer experiments.
Mtrr deficiency adversely impacts reproductive outcomes and cardiac development in mice.
Methionine is an essential amino acid required for protein synthesis and one-carbon metabolism. Its synthesis is catalyzed by the enzyme methionine synthase. Methionine synthase eventually becomes inactive due to the oxidation of its cob(I)alamin cofactor. The protein encoded by this gene regenerates a functional methionine synthase via reductive methylation. It is a member of the ferredoxin-NADP(+) reductase (FNR) family of electron transferases. Patients of the cbl-E complementation group of disorders of folate/cobalamin metabolism are defective in reductive activation of methionine synthase. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms.
, 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
, 5-methyltetrahydrofolate-homocysteine methyltransferase
, methionine synthase reductase
, 5-methyltetrahydrofolate--homocysteine methyltransferase
, [methionine synthase]-cobalamin methyltransferase (cob(II)alamin reducing)
, methionine synthase reductase, mitochondrial