Adenovirus: The First Effective In Vivo Gene Delivery Vector
2014; Mary Ann Liebert, Inc.; Volume: 25; Issue: 1 Linguagem: Inglês
10.1089/hum.2013.2527
ISSN1557-7422
Autores Tópico(s)CRISPR and Genetic Engineering
ResumoHuman Gene TherapyVol. 25, No. 1 Pioneer PerspectiveAdenovirus: The First Effective In Vivo Gene Delivery VectorRonald G. CrystalRonald G. CrystalPublished Online:20 Jan 2014https://doi.org/10.1089/hum.2013.2527AboutSectionsView articleView Full TextSupplemental MaterialPDF/EPUBView Supplemental Data ToolsPermissionsDownload CitationsTrack CitationsAdd to favorites Back To Publication ShareShare onFacebookTwitterLinked InRedditEmail View articleFiguresReferencesRelatedDetailsCited ByAdenoviral delivery of soluble ovine OX40L or CD70 costimulatory molecules improves adaptive immune responses to a model antigen in sheep23 September 2022 | Frontiers in Cellular and Infection Microbiology, Vol. 12Preclinical model for phenotypic correction of Recessive Dystrophic Epidermolysis Bullosa by in vivo CRISPR / Cas9 delivery using adenoviral vectors.Molecular Therapy - Methods & Clinical DevelopmentCurrent clinical landscape of oncolytic viruses as novel cancer immunotherapeutic and recent preclinical advancements25 August 2022 | Frontiers in Immunology, Vol. 13BMP Gene‐Immobilization to Dental Implants Enhances Bone Regeneration25 June 2022 | Advanced Materials Interfaces, Vol. 9, No. 22Gene Therapy for Cardiac Transplantation13 July 2022Gene Therapy: Will the Promise of Optimizing Lung Allografts Become Reality?1 July 2022 | Frontiers in Immunology, Vol. 13No Genus-Specific Gene Is Essential for the Replication of Fowl Adenovirus 4 in Chicken LMH CellsMicrobiology Spectrum, Vol. 10, No. 3Role of Adenoviruses in Cancer Therapy9 June 2022 | Frontiers in Oncology, Vol. 12Hematopoietic Stem Cell Gene-Addition/Editing Therapy in Sickle Cell Disease4 June 2022 | Cells, Vol. 11, No. 11Nestin promotes pulmonary fibrosis via facilitating recycling of TGF-β receptor I8 October 2021 | European Respiratory Journal, Vol. 59, No. 5Recent Advances in the Therapeutic Strategies of Glioblastoma MultiformeNeuroscience, Vol. 491Gene therapy in neuromuscular disorders1 May 2022 | Arquivos de Neuro-Psiquiatria, Vol. 80, No. 5 suppl 1Gene therapy: Comprehensive overview and therapeutic applicationsLife Sciences, Vol. 294Restriction-Assembly: A Solution to Construct Novel Adenovirus Vector6 March 2022 | Viruses, Vol. 14, No. 3Avances en terapia génica en humanos: algunos conceptos básicos y un recorrido históricoRevista Médica Clínica Las Condes, Vol. 33, No. 2Adenoviral Transduction of Dickkopf-1 Alleviates Silica-Induced Silicosis Development in Lungs of Mice Qian Cai, Jia Ma, Jing Wang, Juying Wang, Jieda Cui, Shuang Wu, Zhaojun Wang, Na Wang, Jiaqi Wang, Dandan Yang, Jiali Yang, Jing Xue, Feng Li, Juan Chen, and Xiaoming Liu14 February 2022 | Human Gene Therapy, Vol. 33, No. 3-4Delivery of CRISPR-Cas tools for in vivo genome editing therapy: Trends and challengesJournal of Controlled Release, Vol. 342COVID-19 Vaccines: Adenoviral VectorsAnnual Review of Medicine, Vol. 73, No. 1Gene Therapy for Acute Respiratory Distress Syndrome17 January 2022 | Frontiers in Physiology, Vol. 12Recombinant Adenoviruses for Delivery of Therapeutics Following Spinal Cord Injury10 January 2022 | Frontiers in Pharmacology, Vol. 12Study of the Therapeutic Efficiency of Transduced Olfactory Ensheathing Cells in Spinal Cord Cysts Olga V. 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Baker22 April 2014 | Human Gene Therapy, Vol. 25, No. 4 Volume 25Issue 1Jan 2014 InformationCopyright 2014, Mary Ann Liebert, Inc.To cite this article:Ronald G. Crystal.Adenovirus: The First Effective In Vivo Gene Delivery Vector.Human Gene Therapy.Jan 2014.3-11.http://doi.org/10.1089/hum.2013.2527Published in Volume: 25 Issue 1: January 20, 2014PDF download
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