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Buscar por Autor Escámez, MJ
Mostrando resultados 1 a 6 de 6
| Fecha de publicación | Título | Autor(es) | | may-2019 | Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing | Bonafont, J; Mencía, A; García, M; Torres, R; Rodríguez, S; Carretero, M; Chacón-Solano, E; Modamio-Høybjør, S; Marinas, L; León, C; Escámez, MJ; Hausser, I; del Río, M; Murillas, R; Larcher, F |
| jun-2018 | Deletion of a Pathogenic Mutation-Containing Exon of COL7A1 Allows Clonal Gene Editing Correction of RDEB Patient Epidermal Stem Cells | Mencía, A; Chamorro, C; Bonafont, J; Duarte, B; Holguin, A; Illera, N; Llames, SG; Escámez, MJ; Hausser, I; del Río, M; Larcher, F; Murillas, R |
| sep-2019 | Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses | Chacón-Solano, E; León, C; Díaz, F; García-García, F; García, M; Escámez, MJ; Guerrero-Aspizua, S; Conti, CJ; Mencía, A; Martínez-Santamaría, L; Llames, S; Pévida, M; Carbonell-Caballero, J; Puig-Butillé, JA; Maseda, R; Puig, S; de Lucas, R; Baselga, E; Larcher, J; Dopazo, J; del Río, M |
| ago-2024 | Identification of novel small molecule-based strategies of COL7A1 upregulation and readthrough activity for the treatment of recessive dystrophic epidermolysis bullosa | Jover, I; Ramos, MC; Escámez, MJ; Lozoya, E; Tormo, JR; de Prado-Verdún, D; Mencía, A; Pont, M; Puig, C; Larraufie, MH; Gutiérrez-Caballero, C; Reyes, F; Trincado, JL; García-Gonzalez, V; Cerrato, R; Andrés, M; Crespo, M; Vicente, F; Godessart, N; Genilloud, O; Larcher, F; Nueda, A |
| sep-2013 | Keratinocyte cell lines derived from severe generalized recessive epidermolysis bullosa patients carrying a highly recurrent COL7A1 homozygous mutation: models to assess cell and gene therapies in vitro and in vivo | Chamorro, C; Almarza, D; Duarte, B; Llames, SG; Murillas, R; García, M; Cigudosa, JC; Espinosa-Hevia, L; Escámez, MJ; Mencía, A; Meana, A; García-Escudero, R; Moro, R; Conti, CJ; del Río, M; Larcher, F |
| sep-2025 | Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutation | Warshauer, EM; Maier, PA; Runfeldt, G; Fuentes, I; Escámez, MJ; Valinotto, L; Natale, M; Manzur, G; Illera, N; García, M; del Río, M; Mencía, A; Holguín, A; Larcher, F; Hellenthal, G; Brown, AR; Consuegra, L; Rivera, C; Nogueiro, I; Tang, J; Oro, A; Marinkovich, P; Palisson, F; Titeux, M; Hovnanian, A; Sprecher, E; Skorecki, K; Norris, D; Bruckner, A; Kogut, I; Bilousova, G; Roop, D |
Mostrando resultados 1 a 6 de 6
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