Associated Papers
A66G and C524T polymorphisms of methionine synthase reductase gene are linked to the development of acyanotic congenital heart diseases in Egyptian children.
Hassan FM et al.
Gene, 2017
Analysis of MTR and MTRR Polymorphisms for Neural Tube Defects Risk Association.
Wang Y et al.
Medicine, 2015
Single nucleotide polymorphisms of one-carbon metabolism and cancers of the esophagus, stomach, and liver in a Chinese population.
Chang SC et al.
Plos One, 2014
A66G and C524T polymorphisms of the methionine synthase reductase gene are associated with congenital heart defects in the Chinese Han population.
Zeng W et al.
Genetics and Molecular Research : Gmr, 2011
Lack of association between genetic polymorphisms in enzymes associated with folate metabolism and unexplained reduced sperm counts.
Ravel C et al.
Plos One, 2009
Current perspectives on the genetic causes of neural tube defects.
De Marco P et al.
Neurogenetics, 2006
Methionine synthase reductase polymorphisms are associated with serum osteocalcin levels in postmenopausal women.
Kim DJ et al.
Experimental & Molecular Medicine, 2006
cblE type of homocystinuria due to methionine synthase reductase deficiency: functional correction by minigene expression.
Zavadáková P et al.
Human Mutation, 2005
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