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Polymorphisms of methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), and thymidylate synthase (TYMS) in multiple myeloma risk
(Pergamon-elsevier Science LtdOxfordInglaterra, 2008)
Molecular analysis of homocystinuria in Brazilian patients
(Elsevier B.V., 2005-12-01)
Background: Cystathionine beta-synthase (CBS) deficiency is the most common cause of homocystinuria. However, no data are available concerning the molecular basis of this disease in Brazilian populations.Methods: We studied ...
Polymorphism C776G in the transcobalamin II gene and homocysteine, folate and vitamin B-12 concentrations. Association with MTHFR C677T and A1298C and MTRR A66G polymorphisms in healthy children
(Pergamon-elsevier Science LtdOxfordInglaterra, 2007)
Gene polymorphisms involved in folate and methionine metabolism and increased risk of sporadic colorectal adenocarcinoma
(SpringerDordrechtHolanda, 2011)
Enzymes of lysine metabolism from Coix lacryma-jobi seeds
(Gauthier-villars/editions ElsevierParisFrança, 2002)
Polimorfismo A66G del gen MTRR en niños con trastorno del espectro autista
(Sociedad Venezolana de Puericultura y Pediatría, 2022)