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Buscar por Autor Bonafont, J
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-2021 | Correction of recessive dystrophic epidermolysis bullosa by homology-directed repair-mediated genome editing | Bonafont, J; Mencía, A; Chacón-Solano, E; Srifa, W; Vaidyanathan, S; Romano, R; García, M; Hervás-Salcedo, R; Ugalde, L; Duarte, B; Porteus, MH; del Río, M; Larcher, F; Murillas, R |
| 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 |
| 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-2022 | Non-viral delivery of CRISPR-Cas9 complexes for targeted gene editing via a polymer delivery system | O'Keeffe Ahern, J; Lara-Saez, I; Zhou, D; Murillas, R; Bonafont, J; Mencía, A; García, M; Manzanares, D; Lynch, J; Foley, R; Qian, X; Sigen, A; Larcher, F; Wang, W |
| 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 |
Mostrando resultados 1 a 6 de 6
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