1. Instituto Nacional de Pediatría

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Mostrando resultados 1 a 12 de 12
Fecha de publicaciónTítuloAutor(es)
2014A case of cervical cancer expressed three mRNA variant of Hyaluronan-mediated motility receptorVillegas Ruiz, Vanessa
2015A novel CD40LG deletion causes the hyper-IgM syndrome with normal CD40L expression in a 6-month-old childLopez Herrera, Gabriela
2012Análisis molecular del gen PAX8 en una muestra de pacientes mexicanos con hipotiroidismo congénito primario: identificación de la mutación p.Arg31His recurrenteAlcántara Ortigoza, Miguel Ángel
2013Clinical and genetic analysis of patients with X-linked hyper-IgM syndromeVargas Hernadez A
2011Cloning, sequencing and functional expression of cytosolic malate dehydrogenase from Taenia solium: Purification and characterization of the recombinant enzymeNava Gabriela
2012Consequences of two naturally occurring missense mutations in the structure and function of Bruton agammaglobulinemia tyrosine kinaseVargas Hernández A
2012CYP2W1, CYP4F11 and CYP8A1 polymorphisms and interaction of CYP2W1 genotypes with risk factors in mexican women with breast cancerCárdenas Rodríguez, Noemí
2009DD3 PCA3 gene expression in cancer and prostatic hyperplasiaFloriano Sánchez, Esaú
2012Expression of RUNX1 isoforms and its target gene BLK in childhood acute lymphoblastic leukemiaMontero Ruíz O
2015Functional characterization of two new STAT3 mutations associated with hyper-IgE syndrome in a Mexican cohortAlcántara Montiel JC
2013Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylationMoncada Vélez Marcela
2015Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis LaxaFischer Zirnsak B
Mostrando resultados 1 a 12 de 12