Articoli con mandati relativi all'accesso pubblico - MARTA GARCIA DIEZUlteriori informazioni
Non disponibili pubblicamente: 5
Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies
M Bogliolo, R Pujol, M Aza-Carmona, N Muñoz-Subirana, ...
Journal of medical genetics 57 (4), 258-268, 2020
Mandati: Government of Spain
Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex
M García, JL Santiago, A Terrón, A Hernández‐Martín, A Vicente, ...
British Journal of Dermatology 165 (3), 683-692, 2011
Mandati: Government of Spain
Bioprinting for skin
C Quílez, G de Aranda Izuzquiza, M García, V López, A Montero, ...
3D Bioprinting: Principles and Protocols, 217-228, 2020
Mandati: Government of Spain
Recessive dystrophic epidermolysis bullosa: the origin of the c. 6527insC mutation in the Spanish population
C Sanchez‐Jimeno, N Cuadrado‐Corrales, E Aller, M García, ...
British Journal of Dermatology 168 (1), 226-229, 2013
Mandati: Government of Spain
Renal function in children assisted with extracorporeal membrane oxygenation
J López-Herce, E Casado, M Díez, A Sánchez, SN Fernández, JM Bellón, ...
The International Journal of Artificial Organs 43 (2), 119-126, 2020
Mandati: Government of Spain
Disponibili pubblicamente: 25
3D bioprinting of functional human skin: production and in vivo analysis
N Cubo, M Garcia, JF Del Cañizo, D Velasco, JL Jorcano
Biofabrication 9 (1), 015006, 2016
Mandati: Government of Spain
Clinically relevant correction of recessive dystrophic epidermolysis bullosa by dual sgRNA CRISPR/Cas9-mediated gene editing
J Bonafont, Á Mencía, M García, R Torres, S Rodríguez, M Carretero, ...
Molecular Therapy 27 (5), 986-998, 2019
Mandati: Government of Spain
Preclinical corrective gene transfer in xeroderma pigmentosum human skin stem cells
E Warrick, M Garcia, C Chagnoleau, O Chevallier, V Bergoglio, D Sartori, ...
Molecular Therapy 20 (4), 798-807, 2012
Mandati: Government of Spain
Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer‐prone genodermatoses
E Chacón‐Solano, C León, F Díaz, F García‐García, M García, ...
British journal of dermatology 181 (3), 512-522, 2019
Mandati: European Commission, Government of Spain
Mechanisms of natural gene therapy in dystrophic epidermolysis bullosa
D Kiritsi, M Garcia, R Brander, C Has, R Meijer, MJ Escámez, J Kohlhase, ...
Journal of Investigative Dermatology 134 (8), 2097-2104, 2014
Mandati: German Research Foundation, Government of Spain
Non-viral delivery of CRISPR–Cas9 complexes for targeted gene editing via a polymer delivery system
J O’Keeffe Ahern, I Lara-Sáez, D Zhou, R Murillas, J Bonafont, Á Mencía, ...
Gene therapy 29 (3), 157-170, 2022
Mandati: Science Foundation Ireland, Government of Spain
Development of skin-humanized mouse models of pachyonychia congenita
M García, F Larcher, RP Hickerson, E Baselga, SA Leachman, RL Kaspar, ...
Journal of investigative dermatology 131 (5), 1053-1060, 2011
Mandati: US National Institutes of Health
Correction of recessive dystrophic epidermolysis bullosa by homology-directed repair-mediated genome editing
J Bonafont, A Mencía, E Chacón-Solano, W Srifa, S Vaidyanathan, ...
Molecular Therapy 29 (6), 2008-2018, 2021
Mandati: Government of Spain
An RNA-targeted therapy for dystrophic epidermolysis bullosa
P Peking, U Koller, B Duarte, R Murillas, S Wolf, T Maetzig, M Rothe, ...
Nucleic Acids Research 45 (17), 10259-10269, 2017
Mandati: Austrian Science Fund, German Research Foundation, Government of Spain
Oxidative stress and mitochondrial dysfunction in Kindler syndrome
E Zapatero-Solana, JL García-Giménez, S Guerrero-Aspizua, M García, ...
Orphanet Journal of Rare Diseases 9, 1-10, 2014
Mandati: Government of Spain
Keratinocyte cell lines derived from severe generalized recessive Epidermolysis Bullosa patients carrying a highly recurrent COL7A1 homozygous mutation: models to assess cell and …
C Chamorro, D Almarza, B Duarte, SG Llames, R Murillas, M García, ...
Experimental Dermatology 22 (9), 601-603, 2013
Mandati: Government of Spain
Identification of two rare and novel large deletions in ITGB4 gene causing epidermolysis bullosa with pyloric atresia
Á Mencía, M García, E García, S Llames, A Charlesworth, R de Lucas, ...
Experimental Dermatology 25 (4), 269-274, 2016
Mandati: Government of Spain
Paired nicking-mediated COL17A1 reframing for junctional epidermolysis bullosa
J Bischof, OP March, B Liemberger, SA Haas, S Hainzl, I Petković, ...
Molecular Therapy 30 (8), 2680-2692, 2022
Mandati: Austrian Science Fund, Government of Spain
Preclinical model for phenotypic correction of dystrophic epidermolysis bullosa by in vivo CRISPR-Cas9 delivery using adenoviral vectors
M García, J Bonafont, J Martínez-Palacios, R Xu, G Turchiano, ...
Molecular Therapy-Methods & Clinical Development 27, 96-108, 2022
Mandati: National Institute for Health Research, UK, Wellcome Trust, Government of Spain
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative
J Luque, I Mendes, B Gomez, B Morte, M López de Heredia, E Herreras, ...
Clinical Genetics 101 (5-6), 481-493, 2022
Mandati: Government of Spain
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