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Buscar por Materia genodermatoses
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| Fecha de publicación | Título | Autor(es) | | jun-2020 | Efficient CRISPR-Cas9-Mediated Gene Ablation in Human Keratinocytes to Recapitulate Genodermatoses: Modeling of Netherton Syndrome | Gálvez, V; Chacón-Solano, E; Bonafont, J; Mencía, A; Wei-Li, D; Murillas, R; Llames, S; Vicente, A; del Río, M; Carretero, M; Larcher, F |
| abr-2016 | Identification of two rare and novel large deletions in ITGB4 gene causing epidermolysis bullosa with pyloric atresia | Mencía, A; García, M; García, E; Llames, S; Charlesworth, A; de Lucas, R; Vicente, A; Trujillo-Tiebas, MJ; Coto, P; Costa, M; Vera, A; López-Pestaña, A; Murillas, R; Meneguzzi, G; Jorcano, JL; Conti, CJ; Escámez-Toledano, MJ; del Río, M |
| 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-2022 | Preclinical model for phenotypic correction of dystrophic epidermolysis bullosa by in vivo CRISPR-Cas9 delivery using adenoviral vectors | García, M; Bonafont, J; Martínez-Palacios, J; Xu, R; Turchiano, G; Svenson, S; Thrasher, AJ; Larcher, F; del Río, M; Hernández-Alcoceba, R; Garín, MI; Mencía, A; Murillas, R |
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