Publicacions
El coneixement generat a IrsiCaixa es comparteix amb la comunitat científica a través de la publicació d’articles a revistes científiques d’alt impacte.
Anti-HIV activity and resistance profile of the CXC chemokine receptor 4 antagonist POL3026.
Inter-population variability of DEFA3 gene absence: correlation with haplotype structure and population variability.
MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene.
Renal expression of parvalbumin is critical for NaCl handling and response to diuretics.
Coxsackie adenovirus receptor and alpha nu beta3/alpha nu beta5 integrins in adenovirus gene transfer of rat cochlea.
Characterization and evolution of the novel gene family FAM90A in primates originated by multiple duplication and rearrangement events.
Skewed expression and up-regulation of the IL-12 and IL-18 receptors in resting and activated CD4 T cells from HIV-1-infected patients.
Gitelman's syndrome: towards genotype-phenotype correlations?
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.
Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation.