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Título: | The Value of Mouse Models of Rare Diseases: A Spanish Experience |
Autor: | Murillo-Cuesta, Silvia CSIC ORCID; Artuch, Rafael; Asensio, Fernando; Villa, Pedro de la; Dierssen, Mara CSIC; Enríquez, José Antonio; Fillat, Cristina CSIC; Fourcade, Stéphane; Ibáñez, Borja; Montoliu, Lluís CSIC ORCID ; Oliver, Eduardo CSIC ORCID; Pujol, Aurora; Salido, Eduardo; Vallejo, Mario CSIC ORCID; Varela-Nieto, Isabel CSIC ORCID | Palabras clave: | Orphan diseases Animal models Preclinical research Novel therapies Ethics Transparency |
Fecha de publicación: | 14-oct-2020 | Editor: | Frontiers Media | Citación: | Frontiers in Genetics 11: 583932 (2020) | Resumen: | Animal models are invaluable for biomedical research, especially in the context of rare diseases, which have a very low prevalence and are often complex. Concretely mouse models provide key information on rare disease mechanisms and therapeutic strategies that cannot be obtained by using only alternative methods, and greatly contribute to accelerate the development of new therapeutic options for rare diseases. Despite this, the use of experimental animals remains controversial. The combination of respectful management, ethical laws and transparency regarding animal experimentation contributes to improve society’s opinion about biomedical research and positively impacts on research quality, which eventually also benefits patients. Here we present examples of current advances in preclinical research in rare diseases using mouse models, together with our perspective on future directions and challenges. | Descripción: | © 2020 Murillo-Cuesta, Artuch, Asensio, de la Villa, Dierssen, Enríquez, Fillat, Fourcade, Ibáñez, Montoliu, Oliver, Pujol, Salido, Vallejo and Varela-Nieto. | Versión del editor: | http://dx.doi.org/10.3389/fgene.2020.583932 | URI: | http://hdl.handle.net/10261/229991 | DOI: | 10.3389/fgene.2020.583932 | E-ISSN: | 1664-8021 |
Aparece en las colecciones: | (CNB) Artículos (IIBM) Artículos |
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