dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
dc.contributor.author | Koehorst, Emma |
dc.contributor.author | Núñez-Manchón, Judit |
dc.contributor.author | Ballester-López, Alfonsina |
dc.contributor.author | Almendrote, Miriam |
dc.contributor.author | Lucente, Giuseppe |
dc.contributor.author | Arbex, Andrea |
dc.contributor.author | Pintos Morell, Guillem |
dc.date.accessioned | 2022-05-18T08:12:03Z |
dc.date.available | 2022-05-18T08:12:03Z |
dc.date.issued | 2021-12 |
dc.identifier.citation | Koehorst E, Núñez-Manchón J, Ballester-López A, Almendrote M, Lucente G, Arbex A, et al. Characterization of RAN Translation and Antisense Transcription in Primary Cell Cultures of Patients with Myotonic Dystrophy Type 1. J Clin Med. 2021 Dec;10(23):5520. |
dc.identifier.issn | 2077-0383 |
dc.identifier.uri | https://hdl.handle.net/11351/7544 |
dc.description | Traducción RAN; Transcripción antisentido; Moduladores fenotípicos |
dc.language.iso | eng |
dc.publisher | MDPI |
dc.relation.ispartofseries | Journal of Clinical Medicine;10(23) |
dc.rights | Attribution 4.0 International |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
dc.source | Scientia |
dc.subject | Miotonia atròfica - Aspectes genètics |
dc.subject | Cultiu cel·lular |
dc.subject | Empalmament (Genètica) |
dc.subject.mesh | Myotonic Dystrophy |
dc.subject.mesh | /genetics |
dc.subject.mesh | Cells, Cultured |
dc.subject.mesh | RNA, Messenger |
dc.title | Characterization of RAN Translation and Antisense Transcription in Primary Cell Cultures of Patients with Myotonic Dystrophy Type 1 |
dc.type | info:eu-repo/semantics/article |
dc.identifier.doi | 10.3390/jcm10235520 |
dc.subject.decs | distrofia miotónica |
dc.subject.decs | /genética |
dc.subject.decs | células cultivadas |
dc.subject.decs | ARN mensajero |
dc.relation.publishversion | https://doi.org/10.3390/jcm10235520 |
dc.type.version | info:eu-repo/semantics/publishedVersion |
dc.audience | Professionals |
dc.contributor.organismes | Institut Català de la Salut |
dc.contributor.authoraffiliation | [Koehorst E, Núñez-Manchón J] Neuromuscular and Neuropediatric Research Group, Institut d’Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP), Campus Can Ruti, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Ballester-López A] Neuromuscular and Neuropediatric Research Group, Institut d’Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP), Campus Can Ruti, Universitat Autònoma de Barcelona, Bellaterra, Spain. Centre for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, 28029 Madrid, Spain. [Almendrote M, Lucente G, Arbex A] Neuromuscular and Neuropediatric Research Group, Institut d’Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP), Campus Can Ruti, Universitat Autònoma de Barcelona, Bellaterra, Spain. Neuromuscular Pathology Unit, Neurology Service, Neuroscience Department, Hospital Universitari Germans Trias i Pujol, 08916 Badalona, Spain. [Pintos-Morell G] Neuromuscular and Neuropediatric Research Group, Institut d’Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP), Campus Can Ruti, Universitat Autònoma de Barcelona, Bellaterra, Spain. Unitat de Trastorns Metabòlics Hereditaris (MetabERN), Vall d’Hebron Hospital Universitari, Barcelona, Spain |
dc.identifier.pmid | 34884222 |
dc.identifier.wos | 000735006100001 |
dc.rights.accessrights | info:eu-repo/semantics/openAccess |