Centro de Investigación Biomédica en Red sobre Enfermedades Raras -ko ikertzaileekin lankidetzan egindako argitalpenak (4)

2018

  1. Impairment of photoreceptor ribbon synapses in a novel Pomt1 conditional knockout mouse model of dystroglycanopathy

    Scientific Reports, Vol. 8, Núm. 1

2013

  1. Triplication of dyrk1a causes retinal structural and functional alterations in down syndrome

    Human Molecular Genetics, Vol. 22, Núm. 14, pp. 2275-2284

2012

  1. Targeted knockdown of Cerkl, a retinal dystrophy gene, causes mild affectation of the retinal ganglion cell layer

    Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1822, Núm. 8, pp. 1258-1269

2008

  1. The Protein Kinase DYRK1A Regulates Caspase-9-Mediated Apoptosis during Retina Development

    Developmental Cell, Vol. 15, Núm. 6, pp. 841-853