Zobrazeno 1 - 10
of 50
pro vyhledávání: '"María Isabel Cadavid"'
Autor:
Jesús Martínez-Sotelo, Manuel Pinteño-Blanco, Rosario García-Ramos, María Isabel Cadavid-Torres
Publikováno v:
Atención Primaria, Vol 53, Iss 10, Pp 102124- (2021)
Resumen: Objetivos: Evaluar la efectividad de la revisión sistemática de medicación realizada por farmacéutico sobre medicaciones potencialmente inapropiadas (MPI), resultados en salud y costes. Diseño: Ensayo clínico prospectivo, abierto, cont
Externí odkaz:
https://doaj.org/article/ec13c2c98e5d449188c0e00fd88e1a1a
Autor:
Manuel Pinteño-Blanco, María Isabel Cadavid-Torres, Jesús Martínez-Sotelo, Rosario García-Ramos
Publikováno v:
Atención Primaria, Vol 53, Iss 10, Pp 102124-(2021)
Resumen: Objetivos: Evaluar la efectividad de la revisión sistemática de medicación realizada por farmacéutico sobre medicaciones potencialmente inapropiadas (MPI), resultados en salud y costes. Diseño: Ensayo clínico prospectivo, abierto, cont
Autor:
Jesús, Martínez-Sotelo, Manel, Pinteño-Blanco, Rosario, García-Ramos, Joan, Llobera-Cànaves, María Isabel, Cadavid-Torres
Publikováno v:
Farmacia hospitalaria : organo oficial de expresion cientifica de la Sociedad Espanola de Farmacia Hospitalaria. 45(4)
Polypharmacy and potentially inappropriate medications (that is, those associated with an unfavorable risk-benefit ratio) are common concerns in the context of elderly patients treated in primary care as they may increase the risk of morbidity and mo
Autor:
Ana M. García, José Brea, Alejandro González-García, Concepción Pérez, María Isabel Cadavid, María Isabel Loza, Ana Martinez, Carmen Gil
Publikováno v:
Molecules, Vol 22, Iss 9, p 1472 (2017)
Phosphodiesterase (PDE) enzymes regulate the levels of cyclic nucleotides, cAMP, and/or cGMP, being attractive therapeutic targets. In order to modulate PDE activity in a selective way, we focused our efforts on the search of allosteric modulators. B
Externí odkaz:
https://doaj.org/article/639d5c4f602e435fad3f53935fb52770
Autor:
Jesús, Martínez-Sotelo, Manuel, Pinteño-Blanco, Rosario, García-Ramos, María Isabel, Cadavid-Torres
Publikováno v:
Atencion Primaria
Objetivos Evaluar la efectividad de la revisión sistemática de medicación realizada por farmacéutico sobre medicaciones potencialmente inapropiadas (MPI), resultados en salud y costes. Diseño Ensayo clínico prospectivo, abierto, controlado y al
Autor:
Juan F. López-Giménez, María Isabel Cadavid, José Brea, María Isabel Loza, Marián Castro, Antón L. Martínez, L. Gómez-García, Marta Cimadevila, Alba Iglesias
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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The 5-HT receptor is a homodimeric G protein-coupled receptor implied in multiple diseases, including schizophrenia. Recently, its co-crystallisation with the antipsychotic drugs zotepine and risperidone has revealed the importance of its extracellul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a929469e3c7879c7e588b37e2699b20
http://hdl.handle.net/10261/216310
http://hdl.handle.net/10261/216310
Autor:
María Isabel Loza, María Isabel Cadavid, Jana Selent, Marta Cimadevila, Marián Castro, Maria Marti-Solano, José Brea, Rocio A. de la Fuente, Alba Iglesias
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
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The serotonin 2A (5-HT2A) receptor is a G-protein coupled receptor (GPCR) with a conserved disulfide bridge formed by Cys148 (transmembrane helix 3, TM3) and Cys227 (extracellular loop 2, ECL-2). We hypothesized that disulfide bridges may determine s
Autor:
Eddy Sotelo, Johan Åqvist, Vicente Yaziji, Hugo Gutiérrez-de-Terán, Ana Mallo, María Majellaro, María Isabel Cadavid, Willem Jespers, Olga Caamaño, María Isabel Loza, José Brea, Jhonny Azuaje
Publikováno v:
Journal of Medicinal Chemistry. 60:7502-7511
We report the first family of 2-acetamidopyridines as potent and selective A3 adenosine receptor (AR) antagonists. The computer-assisted design was focused on the bioisosteric replacement of the N1 atom by a CH group in a previous series of diarylpyr
Autor:
Christian F. Masaguer, Carlos Carbajales, María Isabel Cadavid, Xerardo García-Mera, Eddy Sotelo, Ana Oliveira, Hugo Gutiérrez-de-Terán, José Brea, María Isabel Loza, Jhonny Azuaje
Publikováno v:
Journal of Medicinal Chemistry. 60:3372-3382
A novel family of structurally simple, potent, and selective nonxanthine A2BAR ligands was identified, and its antagonistic behavior confirmed through functional experiments. The reported alkyl 2-cyanoimino-4-substituted-6-methyl-1,2,3,4-tetrahy-drop
Publikováno v:
European Journal of Pharmacology. 800:63-69
Different ligands differentially activate phospholipase A2 (PLA2) and phospholipase C (PLC) signalling pathways that are coupled to the serotonin 2A (5-HT2A) receptor, a class-A G-protein coupled receptor (GPCR). The serotonin 5-HT2A receptor has bee