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Frontiers in Physiology|April 12, 2019
In silico Characterization of Human Prion-Like Proteins: Beyond Neurological DiseasesValentin Iglesias, Lisanna Paladin, Teresa Juan-Blanco, et al.
Nature Communications|June 19, 2021
α-Helical peptidic scaffolds to target α-synuclein toxic species with nanomolar affinityJaime Santos, Pablo Gracia, Susanna Navarro, et al.
Frontiers in Microbiology|August 23, 2018
Discovering Putative Prion-Like Proteins in Plasmodium falciparum: A Computational and Experimental AnalysisIrantzu Pallarès, Natalia S de Groot, Valentín Iglesias, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 2, 2005
Structure of human carboxypeptidase A4 with its endogenous protein inhibitor, latexinIrantzu Pallarès, Roman Bonet, Raquel García-Castellanos, et al.
Database : the Journal of Biological Databases and Curation|November 27, 2023
aSynPEP-DB: a database of biogenic peptides for inhibiting α-synuclein aggregationCarlos Pintado-Grima, Oriol Bárcenas, Valentín Iglesias, et al.
Acta Crystallographica. Section D, Biological Crystallography|June 21, 2008
Direct interaction between a human digestive protease and the mucoadhesive poly(acrylic acid)Irantzu Pallarès, Daniel Fernández, Mireia Comellas-Bigler, et al.
Frontiers in Molecular Biosciences|July 28, 2022
CARs-DB: A Database of Cryptic Amyloidogenic Regions in Intrinsically Disordered ProteinsCarlos Pintado-Grima, Oriol Bárcenas, Zoe Manglano-Artuñedo, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 31, 2025
Mass spectrometry footprinting reveals how kinetic stabilizers counteract transthyretin dynamics altered by pathogenic mutationsFrancisca Pinheiro, Ravi Kant, Saketh Chemuru, et al.
ACS Medicinal Chemistry Letters|October 24, 2017
Discovery of Mechanism-Based Inactivators for Human Pancreatic Carboxypeptidase A from a Focused Synthetic LibrarySebastián A Testero, Carla Granados, Daniel Fernández, et al.
European Journal of Medicinal Chemistry|October 14, 2023
PITB: A high affinity transthyretin aggregation inhibitor with optimal pharmacokinetic propertiesFrancisca Pinheiro, Nathalia Varejão, Adrià Sánchez-Morales, et al.
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