Lluisa Vilageliu

Affiliations: 
Universitat de Barcelona, Barcelona, Cataluña, Spain 
Area:
lysosomal storage disorders, cellular and animal models, therapeutic approaches
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"Lluisa Vilageliu"

Children

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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

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Daniel Grinberg collaborator 1990- Universitat de Barcelona (Evolution Tree)
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Publications

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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
Serra-Vinardell J, Roca-Ayats N, De-Ugarte L, et al. (2019) Bone development and remodeling in metabolic disorders. Journal of Inherited Metabolic Disease
Urreizti R, Damanti S, Esteve C, et al. (2018) A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome. Scientific Reports. 8: 694
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