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Neurocase|February 19, 2019
TARDBP mutation associated with semantic variant primary progressive aphasia, case report and review of the literatureM González-Sánchez, V Puertas-Martín, J Esteban-Pérez, et al.
The Journal of Antimicrobial Chemotherapy|October 14, 2011
A non-infectious cell-based phenotypic assay for the assessment of HIV-1 susceptibility to protease inhibitorsMaria José Buzon, Itziar Erkizia, Christian Pou, et al.
Cancers|February 11, 2023
Current Landscape and Potential Challenges of Immune Checkpoint Inhibitors in Microsatellite Stable Metastatic Colorectal CarcinomaMaría San-Román-Gil, Javier Torres-Jiménez, Javier Pozas, et al.
Genes|August 26, 2022
A Novel Intragenic Duplication in the <i>HDAC8</i> Gene Underlying a Case of Cornelia de Lange SyndromeCristina Lucia-Campos, Irene Valenzuela, Ana Latorre-Pellicer, et al.
ACS Omega|June 16, 2025
Synthesis and Pharmacological Characterization of a Novel Cannabinoid Receptor 1 AntagonistIker Bengoetxea de Tena, Gorka Pereira-Castelo, Jonatan Martínez-Gardeazabal, et al.
Cancer Research|September 14, 2014
Modeling lung cancer evolution and preclinical response by orthotopic mouse allograftsChiara Ambrogio, Francisco J Carmona, August Vidal, et al.
Frontiers in Immunology|November 5, 2025
Immune checkpoint-based biomarkers for therapeutic response in patients with multiple sclerosisMariPaz López-Molina, Gabriel Torres Iglesias, Gonzalo Sáenz de Santa María-Diez, et al.
Autoimmunity Reviews|July 2, 2025
Epidemiological patterns and in-hospital mortality in ANCA-associated vasculitis: Insights from Spain's National Health Data (2016-2022)Francisco-Josué Cordero-Pérez, Pablo Martínez-Rodríguez, Luis Arribas-Pérez, et al.
Molecular Biology Reports|September 29, 2011
Characterization of splice variants of the genes encoding human mitochondrial HMG-CoA lyase and HMG-CoA synthase, the main enzymes of the ketogenesis pathwayBeatriz Puisac, Mónica Ramos, María Arnedo, et al.
International Journal of Molecular Sciences|February 9, 2020
Evaluating Face2Gene as a Tool to Identify Cornelia de Lange Syndrome by Facial PhenotypesAna Latorre-Pellicer, Ángela Ascaso, Laura Trujillano, et al.
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