Humans
Down-Klinefelter syndrome (48,XXY,+21) in a neonate associated with congenital heart disease.
“Down-Klinefelter syndrome (48,XXY,+21) in a neonate associated with congenital heart disease.”, Genet Mol Res, vol. 16, no. 3, 2017.
, Assessment of the rs4340 ACE gene polymorphism in acute coronary syndrome in a Western Mexican population.
“Assessment of the rs4340 ACE gene polymorphism in acute coronary syndrome in a Western Mexican population.”, Genet Mol Res, vol. 16, no. 3, 2017.
, Cytotoxic and genotoxic potential of geraniol in peripheral blood mononuclear cells and human hepatoma cell line (HepG2).
“Cytotoxic and genotoxic potential of geraniol in peripheral blood mononuclear cells and human hepatoma cell line (HepG2).”, Genet Mol Res, vol. 16, no. 3, 2017.
, Interleukin-18 (rs187238) and glucose transporter 4 (rs5435) polymorphisms in Euro-Brazilians with type 1 diabetes.
“Interleukin-18 (rs187238) and glucose transporter 4 (rs5435) polymorphisms in Euro-Brazilians with type 1 diabetes.”, Genet Mol Res, vol. 16, no. 3, 2017.
, Atherosclerosis: analysis of the eNOS (T786C) gene polymorphism.
“Atherosclerosis: analysis of the eNOS (T786C) gene polymorphism.”, Genet Mol Res, vol. 16, no. 3, 2017.
, Clinical features of Mexican patients with Mucopolysaccharidosis type I.
“Clinical features of Mexican patients with Mucopolysaccharidosis type I.”, Genet Mol Res, vol. 16, no. 3, 2017.
, Suppression of the biological activity of neuroglioma cells by down-regulation of miR-1.
“Suppression of the biological activity of neuroglioma cells by down-regulation of miR-1.”, Genet Mol Res, vol. 16, no. 3, 2017.
, Mutational screening in the LDLR gene among patients presenting familial hypercholesterolemia in the Southeast of Brazil.
“Mutational screening in the LDLR gene among patients presenting familial hypercholesterolemia in the Southeast of Brazil.”, Genet Mol Res, vol. 16, no. 3, 2017.
, Role of IL17A rs2275913 and rs3748067 polymorphisms in the risk cervical cancer.
“Role of IL17A rs2275913 and rs3748067 polymorphisms in the risk cervical cancer.”, Genet Mol Res, vol. 16, no. 3, 2017.
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