Engineering and Selection of Shuffled AAV Genomes: A New Strategy for Producing Targeted Biological Nanoparticles
Li, Wuping, Asokan, Aravind, Wu, Zhijian, Van Dyke, Terry, DiPrimio, Nina, Johnson, Jarrod S, Govindaswamy, Lakshmanan, Agbandje-McKenna, Mavis +6 more·2008·Molecular Therapy
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- Gene Therapy Today and TomorrowKenneth H. Lundstrom · 2019 · Diseases
- Ferret and Pig Models of Cystic Fibrosis: Prospects and Promise for Gene TherapyZiying Yan, Zoe A. Stewart, Patrick L. Sinn, John C. Olsen, Jim Hu, Paul B. McCray, John F. Engelhardt · 2014 · Human Gene Therapy Clinical Development
- Biologics-device combinations: Enabling prolonged therapies in the posterior segment ocular diseaseShuqian Zhu, Jianjun Zhang, Xuling Jiang, Cheng Peng, Huiqin Liu, Feng Qian · 2026 · Advanced Drug Delivery Reviews
- AAVolve: Concatenated long-read deep sequencing enables whole capsid tracking during shuffled AAV library selectionSuzanne Scott, Adrian Westhaus, Deborah Nazareth, Marti Cabanes‐Creus, Renina Gale Navarro, Deborah Chandra, Erhua Zhu, Aravind Venkateswaran, Ian E. Alexander, Denis C. Bauer et al. · 2024 · Molecular Therapy — Methods & Clinical Development
- Engineered virus-like particle-assembled Vegfa-targeting Cas9 ribonucleoprotein treatment alleviates neovascularization in wet age-related macular degenerationJun Wu, Hyewon Jang, Hyunjong Kwak, Minchae Son, Weiyan Jiang, Hye‐Yeon Hwang, Dong Hyun Jo, Daesik Kim, Seokjoong Kim, Jeong Hun Kim · 2025 · Genome biology
- Stem Cell Vaccination Against Cancer: Fighting Fire With Fire?Thomas P. Zwaka · 2010 · Molecular Therapy
- Viral Vectors for Gene DeliveryDavid J. Dismuke, Steven James Gray, Matthew Louis Hirsch, Richard Jude Samulski, Nicholas Muzyczka · 2010 · Royal Society of Chemistry eBooks
- Engineering Viruses For Gene TherapyJamie Bergen, David V. Schaffer · 2011 · Comprehensive Biomaterials
- hafoe: an interactive tool for the analysis of chimeric AAV libraries after random mutagenesisTatevik Jalatyan, Erik I. Aznauryan, Rokib Hasan, Valeri Vardanyan, Stepan A. Nersisyan, David B. Thompson, Noah Davidsohn, Sanya Thomas, Simon D. van Haren, Jenny M. Tam et al. · 2025 · Gene Therapy
- An Expanded Toolbox for Versatile Chemical Editing of Adeno‐Associated VirusQuan Thanh Pham, Jake Glicksman, Boyang Han, David Koo, Conor Loynd, Soumya Jyoti Singha Roy, Abhishek Chatterjee · 2026 · Angewandte Chemie International Edition
- Directed Evolution of AAV9 for Efficient Gene Expression in Cardiomyocytes In Vitro and In VivoLeonard Hüttermann, Lena C. Schröder, Prithviraj Manohar Vijaya Shetty, Timo Jonker, Susanne S. Hille, Anca Kliesow Remes, Andrea Matzen, Arnie Boender, Dirk Grimm, Derk Frank et al. · 2025 · Human Gene Therapy
- Identification of AAV variants with improved transduction of human vascular endothelial cells by screening AAV capsid libraries in non-human primatesMaria Stamataki, Julia Lüschow, Christina Schlumbohm, Malik Alawi, Lars Peter Lunding, Eberhard Fuchs, Martin Trepel, Markus Schwaninger, Jakob Körbelin · 2025 · Gene Therapy
- Endogenous migration modulators as parent compounds for the development of novel cardiovascular and anti‐inflammatory drugsWolfgang C. Poller, Madlen Rother, Carsten Skurk, Carmen Scheibenbogen · 2011 · British Journal of Pharmacology
- Progress and Challenges in AAV-Mediated Gene Therapy for Duchenne Muscular DystrophyShin’ichi Takeda, Takashi Ok · 2011 · InTech eBooks
- Cardiovascular Gene TherapyThomas J. LaRocca, Roger J. Hajjar · 2013 · Springer eBooks
- Viral vectors for gene deliveryKatharine J. Liang, Richard Jude Samulski · 2015
- Development of viral & non-viral episomal vectors for gene therapy applicationsHanna Kymäläinen · 2012 · OpenGrey (Institut de l'Information Scientifique et Technique)
- Metagenomic Reconstruction of Adeno-Associated Virus GenomesOlena Maiakovska, Lukas Link, Margarita Zayas, Yumi Sano, Teng Wei Koay, Kleopatra Rapti, Jixin Liu, Felix Bubeck, Man Xu, Conradin Baumgartl et al. · 2026 · Human Gene Therapy
- Role of nuclear import proteins in maintaining proteostasis and disease pathogenesisXiuling Zhao, Liping Pu, Xuhui Zeng, Junyu Nie · 2026 · Biochemical Pharmacology
- Gene- and Cell-Based Therapy for Cardiovascular DiseaseJosé Marı́n-Garcı́a · 2014 · Elsevier eBooks
- 4.33 Engineering Viruses For Gene TherapyJamie Bergen, David V. Schaffer · 2017 · Elsevier eBooks
- Nanoparticle: implication on genomeAmina Mohamed Zedan, Samar A. Omar, Nabil Ibrahim Elsheery · 2024 · Elsevier eBooks
- Engineered Bioactive MoleculesCharles A. Gersbach · 2011 · Comprehensive Biomaterials
- Advances in Overcoming Immune Responses following Hemophilia Gene TherapyH. Miao, Carol · 2012 · Journal of Genetic Syndromes & Gene Therapy
- Inhibition of Rift Valley Fever virus using RNA interference technologyTristan A. Scott · 2014 · University of the Witwatersrand, Johannesburg Institutional Repository on DSpace (University of the Witwatersrand, Johannesburg)
- The State of the Art and Future of Gene MedicinesFrank Jacobs, Stephanie C. Gordts, Bart De Geest · 2013 · Wiley eBooks
- Strategies for improving adeno-associated viral infection of airway epithelial cellsDavid D. Dickey · 2012
- Obstacles and Circumvention Strategies for Hematopoietic Stem Cell Transduction by Recombinant Adeno-associated Virus VectorsCaroline Njeri Maina · 2009 · IUScholarWorks (Indiana University)
- Rapidly evolving adeno-associated virus vectors: increasing possibility of gene therapy with custom-made vectorsHiroyuki Nakai · 2009 · Drug Delivery System
- Gene Therapy for Very Long Chain Acyl-coA Dehydrogenase Deficiency Using Adeno-Associated Virus Vectors: A DissertationAllison M. Keeler · 2012 · The Journal of the American Medical Association (JAMA) Network (American Medical Association)
- Gene therapy for arthritisFlorence Apparailly, Paul Peter Tak, Christian Jørgensen · 2010 · Springer eBooks
- Gene therapies for spinocerebellar ataxia type 1Megan Kathryn Keiser · 2013
- Genetic Modification of Adeno-Associated Virus Capsid for Enhanced Motor Neuron Delivery and Retrograde TransportAdam Davis · 2012 · OhioLink ETD Center (Ohio Library and Information Network)
- Engineering magnetic viral nanoheaters for targeted hyperthermia treatment of cancerK Horn · 2009 · Rice Research Repository (Rice University)
- Myokardialer Gentransfer mittels Adenoassoziierter Viraler VektorenGerhard Steinbeck · 2012
- Canadian Journal of Cardiology Symposium Review Targeted Gene Therapy for the Treatment of Heart FailureKleopatra Rapti, Antoine H. Chaanine, Roger J. Hajjar · 2011
- Modulation of adeno-associated virus transduction by the promyelocytic leukemia protein, arsenic trioxide, and proteasome inhibitorsAngela M. Mitchell · 2019 · Carolina Digital Repository (University of North Carolina at Chapel Hill)
- The Role of Assembly-Activating Protein in the Capsid Assembly of Different Adeno-Associated Virus SerotypesLauriel F. Earley · 2016
- Chemical Modulation of AAV TraffickingGarrett E. Berry · 2019 · Carolina Digital Repository (University of North Carolina at Chapel Hill)
- [Use of a new peroral anticoryza drug. Experience in the industrial medical practice].G Schäfer · 1971 · PubMed
- UNCOVERING STRUCTURAL COMPONENTS OF THE ADENO-ASSOCIATED VIRAL CAPSID THAT CAN BE MODIFIED TO IMPROVE CLINICAL GENE THERAPY OUTCOMESJayme K. Warischalk · 2019 · Carolina Digital Repository (University of North Carolina at Chapel Hill)
- RNA interference therapy for the Spinocerebellar ataxiasPavitra S. Ramachandran · 2014
- Pharmacological and Biophysical Dissections of the Trafficking and Infection of Adeno-Associated Virus (AAV) In Vitro and In VivoPing‐Jie Xiao · 2019 · Carolina Digital Repository (University of North Carolina at Chapel Hill)
- Understanding mechanisms of Adeno-associated virus vector transduction through pharmacological and biological approachesSarah C. Nicolson · 2019 · Carolina Digital Repository (University of North Carolina at Chapel Hill)
- AAV-Nrf2 Mediated Rescue of Oxidative Stress in Mouse ModelsKatharine J. Liang · 2019 · Carolina Digital Repository (University of North Carolina at Chapel Hill)
- AAV Jude: An Interview with R. Jude SamulskiKevin Davies · 2021 · Human Gene Therapy
- Advances in Overcoming Immune Responses following Hemophilia GeneTherapyH . Miao · 2011
- Gene Therapy for the HeartEleni Papanikolaou, Nicholas P. Anagnou · 2014 · Springer eBooks
- AAV Jude: A Conversation with AskBio's Jude SamulskiKevin Davies · 2021 · GEN Edge
- Faculty Opinions recommendation of A myocardium tropic adeno-associated virus (AAV) evolved by DNA shuffling and in vivo selection.David Evans · 2009 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Cryo-EM reveals how adeno-associated virus engages its receptor AAVR and an investigation of the GPR108 ectodomainMark Silveria · 2022
- Selection and characterization of targeted vector capsids from random adeno-associated virus type 2 (AAV-2) display peptide librariesStefan Michelfelder · 2008
- An Expanded Toolbox for Versatile Chemical Editing of Adeno‐Associated VirusQuan Thanh Pham, Jake Glicksman, Boyang Han, David Koo, Conor Loynd, Soumya Jyoti Singha Roy, Abhishek Chatterjee · 2026 · Angewandte Chemie
- Adeno-associated virus (AAV) mediated advanced therapeutic interventions for inherited and non-inherited cardiac disordersIndu Singh, Anil Kumar, Awdhesh Kumar Chaudhary, Jasbir Singh Dalal, Anusha Sharma, Juhi Sharma, Arun Ratn, Megh Singh Dhakad, Divakar Sharma · 2026 · Journal of the Renin-Angiotensin-Aldosterone System
- Dynamique et mécanique de complexes dystrophine-actine-lipides membranairesDominique Mias‐Lucquin · 2018 · theses.fr (ABES)
- Développement d'un traitement de thérapie génique pour la glycogénose de type IIIPatrice Vidal · 2018
- Distinct YY dinucleotide periodicity in adeno-associated virus DNAConradin Baumgartl, Jonas Becker, Lena Naber, Man Xu, Emma Gerstmann, Julie Garcia Gonzalez-Calero, Joyce Suppacher, S. Hess, Felix Bubeck, Dirk Grimm · 2026 · Molecular Therapy
- Development of AAV vectors for the therapy of autoimmune and inflammatory diseasesChengwen Li, Matthew Louis Hirsch, Richard Jude Samulski · 2010 · Springer eBooks
- TREATMENTS (NON-ANTIEPILEPTIC DRUGS) | Viral Vector Approaches for Antiepileptic Gene TherapyThomas J. McCown · 2009 · Elsevier eBooks