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31/03/2025 Role of Inflammatory and Proresolving Mediators in Endothelial Dysfunction
Briones, AM, Hernanz, R, García-Redondo, AB, Rodriguez, C, Blanco-Colio, LM, Val-Blasco, A, Alonso, MJ, Salaices, M. Role of Inflammatory and Proresolving Mediators in Endothelial Dysfunction. BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY. 2025; 136(5)DOI:10.1111/bcpt.70026. PMID:40159875. IF:3.300(Q2/4D).
12/02/2024 Upregulation of NOR-1 in calcified human vascular tissues: impact on osteogenic differentiation and calcification.
Ballester-Servera C, Cañes L, Alonso J, Puertas-Umbert L, Vázquez-Sufuentes P, Taurón M, Roselló-Díez E, Marín F, Rodríguez C, Martínez-González J. Upregulation of NOR-1 in calcified human vascular tissues: impact on osteogenic differentiation and calcification.. Translational Research. 2024; 264DOI:10.1016/j.trsl.2023.09.004. PMID:37690706. IF:5.900(Q1/1D).
01/01/2022 Interferon stimulated gene 15 pathway is a novel mediator of endothelial dysfunction and aneurysms development in angiotensin II infused mice through increased oxidative stress.
González-Amor M, García-Redondo AB, Jorge I, Zalba G, Becares M, Ruiz-Rodríguez MJ, Rodríguez C, Bermeo H, Rodrigues-Díez R, Rios FJ, Montezano AC, Martínez-González J, Vázquez J, Redondo JM, Touyz RM, Guerra S, Salaices M, Briones AM. Interferon stimulated gene 15 pathway is a novel mediator of endothelial dysfunction and aneurysms development in angiotensin II infused mice through increased oxidative stress.. CARDIOVASCULAR RESEARCH. 2022; 118(16)DOI:10.1093/cvr/cvab321. PMID:34672341. IF:10.800(Q1/1D).
01/01/2026 Pharmacogenetics in refractory psychiatric disorders: Clinical utility in two consanguineous patients
Panisello-Cardona, M, da Silva, IM, Riera, P, Bernal, S, Almenta, D, Lechuga, MG. Pharmacogenetics in refractory psychiatric disorders: Clinical utility in two consanguineous patients. EUROPEAN JOURNAL OF PSYCHIATRY. 2026; 40(1)DOI:10.1016/j.ejpsy.2025.100335. PMID:. IF:1.500(Q3/7D).
01/11/2025 Clinicopathological and molecular features of recurrence in ctDNA-negative resected colorectal cancer
Beltran, JS, Pérez, MARSM, Manrique, ACV, Cullell, BM, Munoz, MN, Mateo, FJP, Riera, P, Fuste, V, Fumagalli, C, Szafranska, J, Catasus, L, Gonzalez, A, Paez, D. Clinicopathological and molecular features of recurrence in ctDNA-negative resected colorectal cancer. ANNALS OF ONCOLOGY. 2025; 36DOI:10.1016/j.annonc.2025.08.1344. PMID:. IF:65.400(Q1/1D).
01/09/2025 A recurrent non-coding 3'UTR variant as a hidden second hit in 11 families with CAPN3-related limb girdle muscular dystrophy
Estévez-Arias, B, Segarra-Casas, A, Romo, L, Polavarapu, K, O'Heir, E, Singer-Berk, M, O'Leary, M, Nectoux, J, Spinazzi, M, Leturcq, F, Llanso, L, Domínguez, C, Topf, A, Lochmüller, H, Malfatti, E, Nascimento, A, Gallardo, E, González-Quereda, L, Natera-de Benito, D. A recurrent non-coding 3'UTR variant as a hidden second hit in 11 families with CAPN3-related limb girdle muscular dystrophy. NEUROMUSCULAR DISORDERS. 2025; 53DOI:10.1016/j.nmd.2025.105786. PMID:. IF:2.800(Q2/5D).
01/07/2025 Response to the Letter to the Editor regarding "Persistence, effectiveness, and tolerability of anti-calcitonin gene-related peptide monoclonal antibodies in patients with chronic migraine"
de Dios, A, Pagès-Puigdemont, N, Ojeda, S, Riera, P, Pelegrin, R, Morollon, N, Belvís, R, Real, J, Masip, M. Response to the Letter to the Editor regarding "Persistence, effectiveness, and tolerability of anti-calcitonin gene-related peptide monoclonal antibodies in patients with chronic migraine". HEADACHE. 2025; 65(7)DOI:10.1111/head.14983. PMID:40668957. IF:4.000(Q1/2D).
01/06/2025 Comprehensive Clinical and Genetic Characterization of a Spanish Cohort of 22 Patients With Bainbridge-Ropers Syndrome
Trujillano, L, Valenzuela, I, Costa-Roger, M, Cusco, I, Fernandez-Alvarez, P, Cueto-Gonzalez, A, Lasa-Aranzasti, A, Masotto, B, Abuli, A, Codina-Sola, M, del Campo, M, Moreno, JAR, Dominguez, CP, Milla, CP, de la Fuente, RP, Quesada-Espinosa, JF, Nunez-Enamorado, N, Gener, B, Ballesta-Martinez, MJ, Brea-Fernandez, AJ, Fernandez-Prieto, M, Trujillo-Quintero, JP, Ruiz, A, Santos-Simarro, F, Rosello, M, Orellana, C, Martinez, F, Martinez-Monseny, AF, Casas-Alba, D, Serrano, M, Palomares-Bralo, M, Rikeros-Orozco, E, Gomez-Cano, MA, Tirado-Requero, P, Juste, JP, Ramos, FJ, Garcia-Arumi, E, Tizzano, EF. Comprehensive Clinical and Genetic Characterization of a Spanish Cohort of 22 Patients With Bainbridge-Ropers Syndrome. CLINICAL GENETICS. 2025; 107(6)DOI:10.1111/cge.14701. PMID:39833101. IF:2.300(Q3/6D).