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  1. Urquiza, P., Laín, A., Sanz-Parra, A., et al. (2018). Repurposing ciclopirox as a pharmacological chaperone in a model of congenital erythropoietic porphyria. Science Translational Medicine, 10(459), eaat7467. https://doi.org/10.1126/scitranslmed.aat7467
  2. Pluta, P., Roversi, P., Bernardo-Seisdedos, G., et al. (2018). Structural basis of pyrrole polymerization in human porphobilinogen deaminase. Biochimica et Biophysica Acta (BBA) - General Subjects, 1862(9), 1948-1955. https://doi.org/10.1016/j.bbagen.2018.06.013
  3. Fasciani, I., Pluta, P., González-Nieto, D., et al. (2018). Directional coupling of oligodendrocyte connexin-47 and astrocyte connexin-43 gap junctions. Glia, 66(11), 2340-2352. https://doi.org/10.1002/glia.23471
  4. Ben Bdira, F., González, E., Pluta, P., et al. (2014). Tuning intracellular homeostasis of human uroporphyrinogen III synthase by enzyme engineering at a single hotspot of congenital erythropoietic porphyria. Human Molecular Genetics, 23(21), 5805-5813. https://doi.org/10.1093/hmg/ddu298
  5. Kantari, C., Millet, A., Gabillet, J., et al. (2011). Molecular analysis of the membrane insertion domain of proteinase 3, the Wegener's autoantigen, in RBL cells: Implication for its pathogenic activity. Journal of Leukocyte Biology, 90(5), 941-950. https://doi.org/10.1189/jlb.1210695

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