Niacinamide

5-methyltetrahydrofolate-homocysteine methyltransferase ; Homo sapiens







13 Article(s)
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1 25535791 Purification and interaction analyses of two human lysosomal vitamin B12 transporters: LMBD1 and ABCD4. 2014 Nov-Dec 1
2 23141461 Late onset of symptoms in an atypical patient with the cblJ inborn error of vitamin B12 metabolism: diagnosis and novel mutation revealed by exome sequencing. 2012 Dec 1
3 20808328 The transcobalamin (TCN2) 776C>G polymorphism affects homocysteine concentrations among subjects with low vitamin B(12) status. 2010 Nov 1
4 20876572 Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation. 2010 Dec 3 1
5 19298066 Spectroscopic and computational characterization of the base-off forms of cob(II)alamin. 2009 Apr 16 1
6 18606554 Transcobalamin in cultured fibroblasts from patients with inborn errors of vitamin B12 metabolism. 2008 Sep-Oct 1
7 18844488 Association between the 2756A> G variant in the gene encoding methionine synthase and myocardial infarction in Tunisian patients. 2008 3
8 17087642 MTRR 66A>G polymorphism in relation to congenital heart defects. 2006 1
9 15782407 Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population. 2005 Apr 1
10 14654360 Polymorphisms within the vitamin B12 dependent methylmalonyl-coA mutase are not risk factors for neural tube defects. 2003 Dec 1
11 11371572 Nitric oxide inhibits methionine synthase activity in vivo and disrupts carbon flow through the folate pathway. 2001 Jul 20 1
12 10444343 Methionine synthase: high-resolution mapping of the human gene and evaluation as a candidate locus for neural tube defects. 1999 Aug 1
13 10520212 Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations. 1999 Nov 1