Lluisa Vilageliu
Affiliations: | Universitat de Barcelona, Barcelona, Cataluña, Spain |
Area:
lysosomal storage disorders, cellular and animal models, therapeutic approachesGoogle:
"Lluisa Vilageliu"Parents
Sign in to add mentor| Roser Gonzalez-Duarte | grad student | Universitat de Barcelona | |
| Chris Tyler-Smith | post-doc | Sanger Inst Cambridge |
Children
Sign in to add trainee| Isaac Canals | grad student | Universitat de Barcelona (Evolution Tree) | |
| Anna Diaz-Font | grad student | Universitat de Barcelona (Evolution Tree) | |
| Elena Garrido | grad student | Universitat de Barcelona (Evolution Tree) | |
| Marta Gomez-Grau | grad student | Universitat de Barcelona (Evolution Tree) | |
| Amàlia Martínez Mir | grad student | Universitat de Barcelona | |
| Magda Monfort | grad student | Universitat de Barcelona (Evolution Tree) | |
| Gessami Sanchez Olle | grad student | Universitat de Barcelona (Evolution Tree) | |
| Laura Rodriguez-Pascau | grad student | Universitat de Barcelona (Evolution Tree) | |
| Raül Santamaria | grad student | Universitat de Barcelona (Evolution Tree) | |
| Jenny Serra-Vinardell | grad student | Universitat de Barcelona (Evolution Tree) | |
| Bru Cormand | grad student | 1993-1997 | University of Barcelona, Spain (Evolution Tree) |
| Noelia Benetó | grad student | 2014-2020 | Universitat de Barcelona (Evolution Tree) |
Collaborators
Sign in to add collaborator| Daniel Grinberg | collaborator | 1990- | Universitat de Barcelona (Evolution Tree) |
BETA: Related publications
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Publications
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| Andrade I, Ribeiro R, Carneiro ZA, et al. (2022) Fifteen years of enzyme replacement therapy for mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): a case report. Journal of Medical Case Reports. 16: 46 |
| Griñán-Ferré C, Companys-Alemany J, Jarné-Ferrer J, et al. (2021) Inhibition of Soluble Epoxide Hydrolase Ameliorates Phenotype and Cognitive Abilities in a Murine Model of Niemann Pick Type C Disease. International Journal of Molecular Sciences. 22 |
| Benetó N, Grinberg D, Vilageliu L, et al. (2021) Genome Editing Using Cas9-gRNA Ribonucleoprotein in Human Pluripotent Stem Cells for Disease Modeling. Methods in Molecular Biology (Clifton, N.J.) |
| Benetó N, Vilageliu L, Grinberg D, et al. (2020) Sanfilippo Syndrome: Molecular Basis, Disease Models and Therapeutic Approaches. International Journal of Molecular Sciences. 21 |
| Dimitriou E, Moraitou M, Cozar M, et al. (2020) Gaucher disease: Biochemical and molecular findings in 141 patients diagnosed in Greece. Molecular Genetics and Metabolism Reports. 24: 100614 |
| Benetó N, Cozar M, Castilla-Vallmanya L, et al. (2020) Neuronal and Astrocytic Differentiation from Sanfilippo C Syndrome iPSCs for Disease Modeling and Drug Development. Journal of Clinical Medicine. 9 |
| Malekkou A, Sevastou I, Mavrikiou G, et al. (2020) A novel mutation deep within intron 7 of the GBA gene causes Gaucher disease. Molecular Genetics & Genomic Medicine. e1090 |
| Benetó N, Cozar M, Gort L, et al. (2019) Generation of two NAGLU-mutated homozygous cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo B syndrome. Stem Cell Research. 42: 101668 |
| Benetó N, Cozar M, García-Morant M, et al. (2019) Generation of two compound heterozygous HGSNAT-mutated lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo C syndrome. Stem Cell Research. 41: 101616 |
| Castellanos E, Rosas I, Negro A, et al. (2019) Mutational spectrum by phenotype: panel-based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café-au-lait macules. Clinical Genetics |