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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorMachuca, Candela
dc.contributor.authorCorrea Vela, Marta
dc.contributor.authorGarcía-Navas, Deyanira
dc.contributor.authorDarling, Alejandra
dc.contributor.authorVillalón-García, Irene
dc.contributor.authorSánchez-Alcázar, José Antonio
dc.contributor.authorPerez Dueñas, Belen
dc.date.accessioned2022-01-12T11:32:36Z
dc.date.available2022-01-12T11:32:36Z
dc.date.issued2021-05
dc.identifier.citationMachuca C, Correa-Vela M, García-Navas D, Darling A, Villalón-García I, Sánchez-Alcázar JA, et al. Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients. Stem Cell Res. 2021 May;53:102338.
dc.identifier.issn1873-5061
dc.identifier.urihttps://hdl.handle.net/11351/6763
dc.descriptionNeurodegeneració; Mutació
dc.description.sponsorshipThis work was supported by the Instituto de Salud Carlos III (ISCIII) - Subdirección General de Evaluación y Fomento de la Investigación [PI18/00147to CE and PI18/01319 to BPD], and by the Generalitat Valenciana [PROMETEO/2018/135], within the framework of the National R + D + I Plan co-funded with ERDF funds. CM has a CIPF-PhD fellowship [P.I.06/2017]. Part of the equipment employed in this work has been funded by Generalitat Valenciana and co-financed with ERDF funds (OP ERDF of Comunitat Valenciana 2014–2020).
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesStem Cell Research;53
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectSistema nerviós - Degeneració
dc.subjectMalalties rares
dc.subjectGenètica
dc.subject.meshNeurodegenerative Diseases
dc.subject.meshInduced Pluripotent Stem Cells
dc.titleGeneration of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.scr.2021.102338
dc.subject.decsenfermedades neurodegenerativas
dc.subject.decscélulas madre pluripotentes inducidas
dc.relation.publishversionhttps://doi.org/10.1016/j.scr.2021.102338
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Machuca C] Unit of Rare Neurodegenerative Diseases, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain. Rare Diseases Joint Units, CIPF-IIS La Fe & INCLIVA, Valencia, Spain. Stem Cells Therapies in Neurodegenerative Diseases Lab, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain. [Correa-Vela M] Servei de Neurologia Pediàtrica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [García-Navas D] Department of Pediatric Neurology. Hospital Universitario San Pedro de Alcántara, Cáceres, Spain. [Darling A] Unit of Pediatric Movement Disorders, Hospital Sant Joan de Déu, Barcelona, Spain. [Villalón-García I, Sánchez-Alcázar JA] Centro Andaluz de Biología del Desarrollo (CABD-CSIC), Universidad Pablo de Olavide, Seville, Spain. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain. [Pérez-Dueñas B] Servei de Neurologia Pediàtrica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.pmid34087982
dc.identifier.wos000663439300012
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2013-2016/PI18%2F01319
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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