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Carla Fuster García
Carla Fuster García
Institute for Transfusion Medicine and Gene Therapy (The University Medical Center Freiburg)
Dirección de correo verificada de uniklinik-freiburg.de
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Citado por
Citado por
Año
Targeted next generation sequencing for molecular diagnosis of Usher syndrome
MJ Aparisi, E Aller, C Fuster-García, G García-García, R Rodrigo, ...
Orphanet journal of rare diseases 9, 1-15, 2014
992014
USH2A gene editing using the CRISPR system
C Fuster-García, G García-García, E González-Romero, T Jaijo, ...
Molecular Therapy-Nucleic Acids 8, 529-541, 2017
672017
Usher syndrome: genetics of a human ciliopathy
C Fuster-García, B García-Bohórquez, A Rodríguez-Muñoz, E Aller, ...
International journal of molecular sciences 22 (13), 6723, 2021
472021
High-throughput sequencing for the molecular diagnosis of Usher syndrome reveals 42 novel mutations and consolidates CEP250 as Usher-like disease causative
C Fuster-García, G García-García, T Jaijo, N Fornés, C Ayuso, ...
Scientific Reports 8 (1), 17113, 2018
342018
Genotype–phenotype correlation in patients with Usher syndrome and pathogenic variants in MYO7A: implications for future clinical trials
L Galbis‐Martínez, F Blanco‐Kelly, G García‐García, A Ávila‐Fernández, ...
Acta Ophthalmologica 99 (8), 922-930, 2021
92021
Expanding the genetic landscape of usher-like phenotypes
C Fuster-Garcia, G Garcia-Garcia, T Jaijo, F Blanco-Kelly, L Tian, ...
Investigative Ophthalmology & Visual Science 60 (14), 4701-4710, 2019
92019
Application of CRISPR tools for variant interpretation and disease modeling in inherited retinal dystrophies
C Fuster-García, B García-Bohórquez, A Rodríguez-Muñoz, JM Millán, ...
Genes 11 (5), 473, 2020
72020
Genetic screening of the usher syndrome in Cuba
EE Santana, C Fuster-García, E Aller, T Jaijo, B García-Bohórquez, ...
Frontiers in genetics 10, 501, 2019
62019
Generation of the first human in vitro model for McArdle disease based on iPSC technology
MC Ortuño-Costela, V Cerrada, A Moreno-Izquierdo, I García-Consuegra, ...
International Journal of Molecular Sciences 23 (22), 13964, 2022
52022
Exome sequencing identifies PEX6 mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment
G García-García, I Sanchez-Navarro, E Aller, T Jaijo, C Fuster-Garcia, ...
Molecular Vision 26, 216, 2020
52020
Therapeutic approaches and development of genomic diagnostic tools for Usher syndrome
C Fuster García
Universitat Politècnica de València, 2020
22020
Integration of ζ-deficient CARs into the CD3-zeta gene conveys potent cytotoxicity in T and NK cells
J Kath, C Franke, V Drosdek, W Du, V Glaser, C Fuster-Garcia, M Stein, ...
Blood Journal, blood. 2023020973, 2024
2024
Gene editing of CD3 epsilon gene to redirect regulatory T cells for adoptive T cell transfer
W Du, F Noyan, O McCallion, V Drosdek, J Kath, V Glaser, ...
bioRxiv, 2024.03. 18.584896, 2024
2024
Repair of the prevalent c. 2299delG mutation in the USH2A gene using CRISPR/Cas9 nucleases
C Fuster-Garcia, G Garcia-Garcia, E Gonzalez-Romero, T Jaijo, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 26, 195-195, 2018
2018
USH2A gene editing by CRISPR/Cas9 system
C Fuster-Garcia, E Gonzalez-Romero, G Garcia-Garcia, T Jaijo, ...
HUMAN GENE THERAPY 27 (11), A142-A143, 2016
2016
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
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