|1.||Annichino-Bizzacchi, Joyce M: 3 articles (10/2008 - 07/2004)|
|2.||Barone, Concetta: 2 articles (09/2014 - 09/2003)|
|3.||Anello, Guido: 2 articles (09/2014 - 09/2003)|
|4.||Romano, Corrado: 2 articles (09/2014 - 09/2003)|
|5.||Coppedè, Fabio: 2 articles (09/2014 - 04/2010)|
|6.||Bosco, Paolo: 2 articles (09/2014 - 09/2003)|
|7.||Feng, Ling: 2 articles (02/2013 - 02/2008)|
|8.||Griffiths, Lyn R: 2 articles (10/2012 - 01/2012)|
|9.||Ouerhani, Slah: 2 articles (02/2011 - 11/2009)|
|10.||Chebil, Mohamed: 2 articles (02/2011 - 11/2009)|
|1.||Breast Neoplasms (Breast Cancer)
01/01/2014 - "Several studies have investigated the association between methionine synthase reductase (MTRR) A66G polymorphism and breast cancer risk, but controversial results were yielded. "
01/01/2014 - "Methionine synthase reductase A66G polymorphism is not associated with breast cancer susceptibility - a meta-analysis."
08/01/2012 - "A large number of studies investigated the role of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) polymorphisms in breast cancer with inconsistent results. "
12/01/2010 - "Methionine synthase reductase (MTRR) is one of the important enzymes involved in the folate metabolic pathway and its functional genetic polymorphisms may be associated with breast cancer risk. "
01/01/2008 - "Combined impact of polymorphism of folate metabolism genes; glutamate carboxypeptidase, methylene tetrahydrofolate reductase and methionine synthase reductase on breast cancer susceptibility in kashmiri women."
|2.||Down Syndrome (Down's Syndrome)
09/01/2014 - "We performed a large case-control study and a meta-analysis of the literature to address the role of the methionine synthase reductase (MTRR) c.66A>G polymorphism as a maternal risk factor for the birth of a child with Down Syndrome (DS) among Caucasian women. "
02/01/2013 - "Functional variant in methionine synthase reductase decreases the risk of Down syndrome in China."
04/01/2010 - "Reflections on the possible role of the methionine synthase reductase (MTRR) A66G polymorphism as a maternal risk factor for Down syndrome in Italy."
01/01/2006 - "A polymorphism in the gene for methionine synthase reductase (MTRR 66 A>G) has been shown to be associated with the risk of giving birth to a child with Down's syndrome, and the risk of having a foetus with neural tube defects. "
09/01/2003 - "Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome."
|3.||Spinal Dysraphism (Spina Bifida)
12/01/2006 - "The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida."
03/01/2003 - "The purpose of this study is to investigate whether gene polymorphisms of methionine synthase (MTR) and methionine synthase reductase (MTRR) are involved in the risk for NTDs, specifically spina bifida. "
01/01/2003 - "We analyzed the role of the C677T polymorphism of the 5,10-methylenetetrahydrofolate and the A66G polymorphism of the methionine synthase reductase genes as risk factors for occurrence of spina bifida. "
01/01/2003 - "Polymorphisms of the 5,10-methylenetetrahydrofolate and the methionine synthase reductase genes as independent risk factors for spina bifida."
08/01/1999 - "A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida."
10/01/2002 - "CblE type of homocystinuria due to methionine synthase reductase deficiency: clinical and molecular studies and prenatal diagnosis in two families."
11/01/2007 - "Methionine synthase reductase deficiency, cblE type of homocystinuria (OMIM 236270), is a rare autosomal recessive inherited disorder described only in 14 patients worldwide. "
01/01/2007 - "This scheme was used in evaluating the results obtained by testing urine of a woman suffering from impaired function of methionine synthase reductase (CblE type of homocystinuria). "
03/01/2005 - "cblE type of homocystinuria due to methionine synthase reductase deficiency: functional correction by minigene expression."
10/01/2007 - "Methionine synthase reductase (MTRR) is the locus of the cblE class of inborn errors of cobalamin metabolism that is characterized by megaloblastic anemia and homocystinuria. "
|5.||Hypertension (High Blood Pressure)
08/01/2015 - "To assess the association of plasma homocysteine (Hcy) level and 66A/G and 524C/T polymorphisms of methionine synthase reductase (MSR) gene with essential hypertension (EH) in ethnic Uygurs and Hans from Xinjiang. "
01/01/2012 - "We genotyped two polymorphisms in the methylenetetrahydrofolate reductase gene (MTHFR C677T and MTHFR A1298C), one polymorphism in the methionine synthase reductase gene (MTRR A66G), and one polymorphism in the methylenetetrahydrofolate dehydrogenase 1 gene (MTHFD1 G1958A) and assessed their association with hypertension using chi-square analysis. "
03/25/2012 - "[The role of homocysteine and methylenetetrahydrofolate reductase, methionine synthase, methionine synthase reductase polymorphisms in the development of cardiovascular diseases and hypertension]."
05/01/2015 - "The studies suggest that both polymorphisms and changes of expression in genes encoding enzymes involved in the methionine and homocysteine metabolism (MHM), such as methylenetetrahydrofolate, reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR) and cystathionine gamma-lyase (CSE), could play a role in the development of hypertension during pregnancy. "
|1.||Methylenetetrahydrofolate Reductase (NADPH2) (Methylenetetrahydrofolate Reductase)
|2.||5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase (Methyltetrahydrofolate Homocysteine Methyltransferase)
|5.||Folic Acid (Vitamin M)
|8.||Methylenetetrahydrofolate Dehydrogenase (NADP) (Dehydrogenase, Methylenetetrahydrofolate)
|10.||Reduced Folate Carrier Protein