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Human Molecular Genetics|September 15, 2018
Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analysesEncarnación Medina-Carmona, Isabel Betancor-Fernández, Jaime Santos, et al.Annals of Clinical and Translational Neurology|January 18, 2023
Common pathophysiology for ANXA11 disorders caused by aspartate 40 variantsDaniel Natera-de Benito, Jonathan Olival, Carla Garcia-Cabau, et al.Nature Structural & Molecular Biology|December 4, 2023
Rational optimization of a transcription factor activation domain inhibitorShaon Basu, Paula Martínez-Cristóbal, Marta Frigolé-Vivas, et al.Pageof 2