A. Alonzo-Rojo
Clinical features of Mexican patients with Mucopolysaccharidosis type I
Mucopolysaccharidosis type I (MPS-I) is an autosomal recessive lysosomal storage disorder caused by a deficiency or absence of α-l-iduronidase, which is involved in the catabolism of glycosaminoglycans (GAGs). This deficiency leads to the accumulation of GAGs in several organs. Given the wide spectrum of the disease, MPS-I has historically been classified into.. Read More»
Genet. Mol. Res. 16(3): gmr16032602
DOI: 10.4238/gmr16032602
Association of the tumor necrosis factor-alpha -308G>A polymorphism with breast cancer in Mexican women
The tumor necrosis factor-alpha (TNF-α) gene plays an important role in cell proliferation, differentiation, apoptosis, lipid metabolism, coagulation, insulin resistance, and endothelial function. Polymorphisms of TNF-α have been associated with cancer. We examined the role of the -308G>A polymorphism in this gene by comparing the genotypes of 294 healthy Mexican women with those.. Read More»
Genet. Mol. Res. 12(4): 2013.November.18.17
DOI: 10.4238/2013.November.18.17
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