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dc.rights.licenseopenen_US
dc.contributor.authorRAHMAN, Mujeeb Ur
dc.contributor.authorBILAL, Muhammad
dc.contributor.authorSHAH, Junaid Ali
dc.contributor.authorKAUSHIK, Ajeet
hal.structure.identifierUnité de Recherche Œnologie [Villenave d'Ornon] [OENO]
dc.contributor.authorTEISSEDRE, Pierre-Louis
dc.contributor.authorKUJAWSKA, Małgorzata
dc.date.accessioned2023-03-15T13:01:29Z
dc.date.available2023-03-15T13:01:29Z
dc.date.issued2022-06-13
dc.identifier.issn1999-4923en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/172322
dc.description.abstractEnParkinson’s disease (PD) and other chronic and debilitating neurodegenerative diseases (NDs) impose a substantial medical, emotional, and financial burden on individuals and society. The origin of PD is unknown due to a complex combination of hereditary and environmental risk factors. However, over the last several decades, a significant amount of available data from clinical and experimental studies has implicated neuroinflammation, oxidative stress, dysregulated protein degradation, and mitochondrial dysfunction as the primary causes of PD neurodegeneration. The new gene-editing techniques hold great promise for research and therapy of NDs, such as PD, for which there are currently no effective disease-modifying treatments. As a result, gene therapy may offer new treatment options, transforming our ability to treat this disease. We present a detailed overview of novel gene-editing delivery vehicles, which is essential for their successful implementation in both cutting-edge research and prospective therapeutics. Moreover, we review the most recent advancements in CRISPR-based applications and gene therapies for a better understanding of treating PD. We explore the benefits and drawbacks of using them for a range of gene-editing applications in the brain, emphasizing some fascinating possibilities.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enParkinson’s
dc.subject.enCRISPR-Cas9
dc.subject.engene therapy
dc.subject.endelivery
dc.subject.enapplications
dc.title.enCRISPR-Cas9-Based Technology and Its Relevance to Gene Editing in Parkinson’s Disease
dc.typeArticle de revueen_US
dc.identifier.doi10.3390/pharmaceutics14061252en_US
dc.subject.halSciences du Vivant [q-bio]/Biologie végétaleen_US
dc.identifier.pubmed35745824en_US
bordeaux.journalPharmaceuticsen_US
bordeaux.page1252en_US
bordeaux.volume14en_US
bordeaux.hal.laboratoriesOenologie - UMR 1366en_US
bordeaux.issue6en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.exportfalse
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Pharmaceutics&rft.date=2022-06-13&rft.volume=14&rft.issue=6&rft.spage=1252&rft.epage=1252&rft.eissn=1999-4923&rft.issn=1999-4923&rft.au=RAHMAN,%20Mujeeb%20Ur&BILAL,%20Muhammad&SHAH,%20Junaid%20Ali&KAUSHIK,%20Ajeet&TEISSEDRE,%20Pierre-Louis&rft.genre=article


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