Efficacy and long-term safety of alipogene tiparvovec (AAV1-LPLS447X) gene therapy for lipoprotein lipase deficiency: an open-label trial
Gaudet, D, Méthot, J, Déry, S, Brisson, D, Essiembre, C, Tremblay, G, Tremblay, K, de Wal, J +4 more·2013·Gene Therapy
Cited by (404)
Items 101–200 of 404
- Next-generation muscle-directed gene therapy by in silico vector designShilpita Sarcar, Warut Tulalamba, Melvin Y. Rincón, Jaitip Tipanee, H. Q. Pham, Hanneke Evens, Dimitri Boon, Ermira Samara-Kuko, Marleen Keyaerts, Mariana Loperfido et al. · 2019 · Nature Communications
- Mechanism of action of anti-hypercholesterolemia drugs and their resistanceVishvanath Tiwari, Manoj Khokhar · 2014 · European Journal of Pharmacology
- The Role of Recombinant AAV in Precise Genome EditingSwati Bijlani, Ka Ming Pang, Venkatesh Sivanandam, Amanpreet Singh, Saswati Chatterjee · 2022 · Frontiers in Genome Editing
- Nanobiomaterial vectors for improving gene editing and gene therapyShao Wei Hu, Tao Ding, Honghai Tang, Huiping Guo, Wenguo Cui, Yilai Shu · 2023 · Materials Today
- A versatile toolkit for overcoming AAV immunityLi, Xuefeng, Wei, Xiaoli, Lin, Jinduan, Ou, Li · 2022 · Frontiers in Immunology
- Precision medicine, genomics and drug discovery: Table 1.Lon R. Cardon, Tim Harris · 2016 · Human Molecular Genetics
- From Mutation Identification to Therapy: Discovery and Origins of the First Approved Gene Therapy in the Western WorldJohn J.P. Kastelein, Colin J. Ross, Michael R. Hayden · 2013 · Human Gene Therapy
- Vectored delivery of anti-SIV envelope targeting mAb via AAV8 protects rhesus macaques from repeated limiting dose intrarectal swarm SIVsmE660 challengeWelles, Hugh C., Jennewein, Madeleine F., Mason, Rosemarie D., Narpala, Sandeep, Wang, Lingshu, Cheng, Cheng, Zhang, Yi, Todd, John-Paul, Lifson, Jeffrey D., Balazs, Alejandro B. et al. · 2018 · PLOS Pathogens
- Humoral immune responses to <scp>AAV</scp> gene therapy in the ocular compartmentWhitehead, Michael, Osborne, Andrew, Yu‐Wai‐Man, Patrick, Martin, Keith · 2021 · Biological Reviews
- Controlled release strategies for rAAV-mediated gene deliveryAna Rey‐Rico, Magali Cucchiarini · 2015 · Acta Biomaterialia
- Disease correction by AAV-mediated gene therapy in a new mouse model of mucopolysaccharidosis type IIIDCarles Roca, Sandra Motas, Sara Marcó, Albert Ribera, Víctor Sánchez, Xavier Sánchez, Joan Bertolin, Xavier León, Jennifer Pérez, Miguel Garcia et al. · 2017 · Human Molecular Genetics
- Long-Term Efficacy and Safety of Insulin and Glucokinase Gene Therapy for Diabetes: 8-Year Follow-Up in DogsMaria Luisa Jaén, Laia Vilà, Ivet Elias, Verónica Jiménez, Jordi Rodó, Luca Maggioni, Rafael Ruiz de Gopegui i Fernández, Miguel Garcia, SERGIO A. MUÑOZ, David Callejas et al. · 2017 · Molecular Therapy — Methods & Clinical Development
- Recent Developments in Gene Therapy for Homozygous Familial HypercholesterolemiaEzim Ajufo, Marina Cuchel · 2016 · Current Atherosclerosis Reports
- Transgene Regulation Using the Tetracycline-Inducible TetR-KRAB System after AAV-Mediated Gene Transfer in Rodents and Nonhuman PrimatesCaroline Le Guiner, Knut Stieger, Alice Toromanoff, Mickaël Guilbaud, Alexandra Mendes-Madeira, Marie Devaux, Lydie Guigand, Yan Chérel, Philippe Moullier, Fabienne Rolling et al. · 2014 · PLoS ONE
- Future of rAAV Gene Therapy: Platform for RNAi, Gene Editing, and BeyondPaul N. Valdmanis, Mark A. Kay · 2017 · Human Gene Therapy
- Gene therapy and editing: Novel potential treatments for neuronal channelopathiesRobert C. Wykes, Gabriele Lignani · 2017 · Neuropharmacology
- Alipogene tiparvovec: gene therapy for lipoprotein lipase deficiencyAnthony S. Wierzbicki, Adie Viljoen · 2012 · Expert Opinion on Biological Therapy
- Evaluation of Cellular Immune Response to Adeno-Associated Virus-Based Gene TherapyBoris Gorovits, Mitra Azadeh, George Buchlis, Michele Fiscella, Travis Harrison, Mike Havert, Sylvia Janetzki, Vibha Jawa, Brian R. Long, Yolanda D. Mahnke et al. · 2023 · The AAPS Journal
- Engineering viral vectors for acoustically targeted gene deliveryHongyi Li, Manwal Harb, John E. Heath, James S. Trippett, Mikhail G. Shapiro, Jerzy O. Szablowski · 2024 · Nature Communications
- Pharmacological treatment options for severe hypertriglyceridemia and familial chylomicronemia syndromeRabia Chaudhry, Adie Viljoen, Anthony S. Wierzbicki · 2018 · Expert Review of Clinical Pharmacology
- Centronuclear myopathies under attack: A plethora of therapeutic targetsHichem Tasfaout, Belinda Simone Cowling, Jocelyn Laporte · 2018 · Journal of Neuromuscular Diseases
- Viral delivered gene therapy to treat catecholaminergic polymorphic ventricular tachycardia (CPVT2) in mouse modelsEfrat Kurtzwald-Josefson, Dor Yadin, Shiraz Haron‐Khun, Maayan Waldman, Dan J. Aravot, Asher Shainberg, Michael Eldar, Edith Hochhauser, Michael Arad · 2017 · Heart Rhythm
- Novel therapeutics in hypertriglyceridemiaGryn, Steven E., Hegele, Robert A. · 2015 · Current Opinion in Lipidology
- Current Diagnosis and Management of Primary ChylomicronemiaHiroaki Okazaki, Takanari Gotoda, Masatsune Ogura, Shun Ishibashi, Kyoko Inagaki, Hiroyuki Daida, Toshio Hayashi, Mika Hori, Daisaku Masuda, Kota Matsuki et al. · 2021 · Journal of Atherosclerosis and Thrombosis
- Improved adeno-associated virus (AAV) serotype 1 and 5 vectors for gene therapyDwaipayan Sen, Balaji Balakrishnan, Nishanth Gabriel, Prachi P. Agrawal, Vaani Roshini, Rekha Samuel, Alok Srivastava, Giridhara Rao Jayandharan · 2013 · Scientific Reports
- The Challenge of Gene Therapy for Neurological Diseases: Strategies and Tools to Achieve Efficient Delivery to the Central Nervous SystemFrançoise Piguet, Timothée De Saint-Denis, Emilie Audouard, Kévin Beccaria, Arthur André, Guillaume Wurtz, Raphael Schatz, Sandro Alves, Caroline Sevin, Michel Zérah et al. · 2020 · Human Gene Therapy
- Familial chylomicronemia syndrome and response to medium-chain triglyceride therapy in an infant with novel mutations in GPIHBP1Ahmad, Zahid, Wilson, Don P. · 2014 · Journal of clinical lipidology
- Treatment of Neurogenetic Developmental Conditions: From 2016 into the FutureClara van Karnebeek, Kristin Bowden, Elizabeth Berry‐Kravis · 2016 · Pediatric Neurology
- Lipid Metabolism and Emerging Targets for Lipid-Lowering TherapyDaniel Gaudet, Jean‐Philippe Drouin‐Chartier, Patrick Couture · 2017 · Canadian Journal of Cardiology
- Regulatory and Exhausted T Cell Responses to AAV CapsidGwladys Gernoux, James M. Wilson, Christian Mueller · 2017 · Human Gene Therapy
- Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemiaPiero Pingitore, Saverio Massimo Lepore, Carlo Pirazzi, Rosellina Margherita Mancina, Benedetta Maria Motta, Luca V. C. Valenti, Knut Erik Berge, Kjetil Retterstøl, Trond P. Leren, Olov Wiklund et al. · 2016 · Journal of clinical lipidology
- 2016 ESC/EAS Guidelines for the Management of DyslipidaemiasAlberico Luigi Catapano, Ian M Graham, Guy De Backer, Olov Wiklund, M. John Chapman, Heinz Drexel, Arno Wilhelmus Hoes, Catriona Sian Jennings, Ulf Landmesser, Terje Rolf Pedersen et al. · 2016 · Kardiologia Polska
- Targeting Visceral Fat by Intraperitoneal Delivery of Novel AAV Serotype Vector Restricting Off-Target Transduction in LiverWei Huang, Xianglan Liu, Nicholas J. Queen, Lei Cao · 2017 · Molecular Therapy — Methods & Clinical Development
- The role of antisense oligonucleotide therapy against apolipoprotein-CIII in hypertriglyceridemiaIoanna Gouni‐Berthold · 2017 · Atherosclerosis Supplements
- Gene and Cell-Based Therapies for Parkinson's Disease: Where Are We?Philip C. Buttery, Roger A. Barker · 2020 · Neurotherapeutics
- Advanced Therapies and Regulatory Framework in Different Areas of the Globe: Past, Present, and FutureCleila Guimarães Pimenta Bosio, Vitória Loureiro Bettiol, Thuany Alencar‐Silva, Octávio Luiz Franco, Robert Edward Pogue, Juliana Lott Carvalho, Maria Sueli Soares Felipe · 2021 · Clinical Therapeutics
- The menace of severe adverse events and deaths associated with viral gene therapy and its potential solutionArtyom Kachanov, Anastasiya Kostyusheva, Sergey Brezgin, Ivan Karandashov, N. I. Ponomareva, Andrey Tikhonov, Alexander N. Lukashev, Vadim S. Pokrovsky, Andrey A. Zamyatnin, Alessandro Parodi et al. · 2024 · Medicinal Research Reviews
- Safety and efficacy of therapies for chylomicronemiaIsabel Shamsudeen, Robert Alexander Hegele · 2022 · Expert Review of Clinical Pharmacology
- A potassium leak channel silences hyperactive neurons and ameliorates status epilepticusDeblina Dey, Veit‐Simon Eckle, Iuliia Vitko, Kyle A. Sullivan, Zofia Maria Lasiecka, Bettina Winckler, Ruth L. Stornetta, John M. Williamson, Jaideep Kapur, Edward Perez‐Reyes · 2013 · Epilepsia
- rAAV-Mediated Tumorigenesis: Still Unresolved After an AAV AssaultPaul N. Valdmanis, Leszek Lisowski, Mark A. Kay · 2012 · Molecular Therapy
- The 2.8 Å Electron Microscopy Structure of Adeno-Associated Virus-DJ Bound by a Heparinoid PentasaccharideQing Xie, John M. Spear, Alex J. Noble, Duncan R. Sousa, Nancy Meyer, Omar Davulcu, Fuming Zhang, Robert J. Linhardt, Scott M. Stagg, Michael Stewart Chapman · 2017 · Molecular Therapy — Methods & Clinical Development
- The ice age – A review on formulation of Adeno-associated virus therapeuticsPhilip Grossen, Irini Skaripa-Koukelli, Joost van Haasteren, Alexandra H.E. Machado, Christoph Dürr · 2023 · European Journal of Pharmaceutics and Biopharmaceutics
- Why commercialization of gene therapy stalled; examining the life cycles of gene therapy technologiesFred David Ledley, Laura M. McNamee, V Uzdil, Irwin Morgan · 2013 · Gene Therapy
- Liver‐targeted gene therapy: Approaches and challengesRajagopal N. Aravalli, John D. Belcher, Clifford J. Steer · 2015 · Liver Transplantation
- Simple downstream process based on detergent treatment improves yield and in vivo transduction efficacy of adeno-associated virus vectorsGabriella Dias Florencio Leite, Guillaume Précigout, Cyriaque Beley, Pierre-Olivier Buclez, Luis Garcı́a, Rachid Benchaouir · 2015 · Molecular Therapy — Methods & Clinical Development
- Efficient Production of Dual Recombinant Adeno-Associated Viral Vectors for Factor VIII DeliveryWang Qizhao, Biao Dong, Jenni Firrman, Sean Roberts, Andrea Rossi Moore, Wenjing Cao, Yong Diao, Philipp Kapranov, Ruian Xu, Weidong Xiao · 2014 · Human Gene Therapy Methods
- Gene therapy for hemophiliaSteven W. Pipe · 2017 · Pediatric Blood & Cancer
- Gene Therapy in Lipoprotein Lipase Deficiency: Case Report on the First Patient Treated with Alipogene Tiparvovec Under Daily Practice ConditionsUrsula Kassner, Tim Hollstein, Thomas Grenkowitz, Marion Wühle-Demuth, Bastian Salewsky, Ilja Demuth, Michaela Dippel, Elisabeth Steinhagen‐Thiessen · 2018 · Human Gene Therapy
- Causes, clinical findings and therapeutic options in chylomicronemia syndrome, a special form of hypertriglyceridemiaGyörgy Paragh, Ákos Németh, Mariann Harangi, Maciej Banach, Péter Fülöp · 2022 · Lipids in Health and Disease
- Current status of gene therapy for α-1 antitrypsin deficiencyHeather S. Loring, Terence R. Flotte · 2014 · Expert Opinion on Biological Therapy
- Obstacles and future of gene therapy for hemophiliaArruda, Valder R, Samelson-Jones, Ben J · 2015 · Expert Opinion on Orphan Drugs
- New Insights Into the Treatment of Hyperlipidemia: Pharmacological Updates and Emerging TreatmentsSeema Abbasi, Adnan Ahmed Khan, Muhammad W. Choudhry · 2024 · Cureus
- Regulatory Considerations for Gene Therapy Products in the US, EU, and Japan.Celine-Lea Halioua-Haubold, James G. Peyer, James Smith, Zeeshaan Arshad, Matthew Scholz, David A. Brindley, Robert Edward MacLaren · 2017 · PubMed Central
- The Unusual Properties of the AAV Inverted Terminal RepeatKenneth I. Berns · 2020 · Human Gene Therapy
- Synthetic Biology—Toward Therapeutic SolutionsViktor Haellman, Martin Fussenegger · 2015 · Journal of Molecular Biology
- Emerging therapies and therapeutic concepts for lysosomal storage diseasesThomas Kirkegaard · 2013 · Expert Opinion on Orphan Drugs
- A missense variant in CST3 exerts a recessive effect on susceptibility to age-related macular degeneration resembling its association with Alzheimer’s diseaseJoe M. Butler, Umar Sharif, Manir Ali, Martin McKibbin, Joseph P. Thompson, Richard Peter Gale, Yit Chiun Yang, Chris F. Inglehearn, Luminita Paraoan · 2015 · Human Genetics
- Viral Vector-Mediated Antisense Therapy for Genetic DiseasesMarine Imbert, Gabriella Dias-Florencio, Aurélie Goyenvalle · 2017 · Genes
- Disorders of Lipid MetabolismClay F. Semenkovich, Anne Carol Goldberg, Ira J. Goldberg · 2011 · Elsevier eBooks
- Current guidelines for high-density lipoprotein cholesterol in therapy and future directionsErin D. Michos, Bishnu Hari Subedi, Parag H. Joshi, Steven Richard Jones, Seth Shay Martin, Michael Joseph Blaha · 2014 · Vascular Health and Risk Management
- AAV3-miRNA vectors for growth suppression of human hepatocellular carcinoma cells in vitro and human liver tumors in a murine xenograft model in vivoLing Yin, Geoffrey D. Keeler, Yuanhui Zhang, Brad E. Hoffman, Chen Ling, Keyun Qing, Arun Srivastava · 2020 · Gene Therapy
- The burden of familial chylomicronemia syndrome in Canadian patientsDaniel Gaudet, Michael T. Stevenson, Nelly Komari, Grace A. Trentin, Caroline Crowson, Nandini Hadker, Sophie Bernard · 2020 · Lipids in Health and Disease
- Opportunities and challenges for applying model‐informed drug development approaches to gene therapiesArtur A. Belov, Kimberly L. W. Schultz, Richard A. Forshee, Million A. Tegenge · 2021 · CPT Pharmacometrics & Systems Pharmacology
- Cell-penetrating peptides enhance the transduction of adeno-associated virus serotype 9 in the central nervous systemYuan Meng, Dong Sun, Yiyan Qin, Xiaoyi Dong, Guangzuo Luo, Ying Liu · 2021 · Molecular Therapy — Methods & Clinical Development
- Development of a Novel Recombinant Adeno-Associated Virus Production System Using Human Bocavirus 1 Helper GenesZekun Wang, Fang Cheng, John F. Engelhardt, Ziying Yan, Jianming Qiu · 2018 · Molecular Therapy — Methods & Clinical Development
- Genetic burden linked to founder effects in Saguenay–Lac-Saint-Jean illustrates the importance of genetic screening test availabilityMbarka Bchetnia, Luigi Bouchard, Jean Mathieu, Philippe M. Campeau, Charles Morin, Diane Brisson, Anne‐Marie Laberge, Hélène Vézina, Daniel Gaudet, Catherine Laprise · 2021 · Journal of Medical Genetics
- Lipoprotein abnormalities in compound heterozygous lipoprotein lipase deficiency after treatment with a low-fat diet and orlistatPiers R. Blackett, Jeanie B. Tryggestad, Sowmya Krishnan, Shibo Li, Weihong Xu, Petar Alaupovic, Carmen Quiroga, Kenneth C. Copeland · 2012 · Journal of clinical lipidology
- Generation and in vivo evaluation of IL10-treated dendritic cells in a nonhuman primate model of AAV-based gene transferAurélie Moreau, Céline Vandamme, Mercedes Segovia, Marie Devaux, Mickaël Guilbaud, Gaëlle Tilly, Nicolas Jaulin, Johanne Le Duff, Yan Chérel, Jack‐Yves Deschamps et al. · 2014 · Molecular Therapy — Methods & Clinical Development
- How Will Genetics Inform the Clinical Care of Atrial Fibrillation?Shoemaker, M. Benjamin, Shah, Rajan L., Roden, Dan M., Perez, Marco V. · 2020 · Circulation Research
- Increasing the Clinical Potential and Applications of Anti-HIV AntibodiesCasey K. Hua, Margaret E. Ackerman · 2017 · Frontiers in Immunology
- Gene Therapy for Progressive Familial Intrahepatic Cholestasis: Current Progress and Future ProspectsPiter J. Bosma, Marius Wits, Ronald P.J. Oude Elferink · 2020 · International Journal of Molecular Sciences
- Rapid, scalable, and low-cost purification of recombinant adeno-associated virus produced by baculovirus expression vector systemPierre-Olivier Buclez, Gabriella Dias Florencio Leite, Karima Relizani, Cyriaque Beley, Luis Garcı́a, Rachid Benchaouir · 2016 · Molecular Therapy — Methods & Clinical Development
- Chylomicronemia SyndromeAnthony S. Wierzbicki · 2018 · Wiley eBooks
- Intrinsic Transgene Immunogenicity Gears CD8+ T-cell Priming After rAAV-Mediated Muscle Gene TransferMaxime Carpentier, Stéphanie Lorain, Pascal Chappert, Mélanie Lalfer, Romain Hardet, Dominique Urbain, Cécile Peccate, Sahil Adriouch, Luis Garcı́a, Jean M. Davoust et al. · 2014 · Molecular Therapy
- AAV Production Using Baculovirus Expression Vector SystemSandro, Quentin, Relizani, Karima, Benchaouir, Rachid · 2019 · Methods in Molecular Biology
- Gene Therapy-Associated Uveitis (GTAU): Understanding and mitigating the adverse immune response in retinal gene therapyPurdy, Ryan, John, Molly, Bray, Alissa, Clare, Alison J., Copland, David A., Chan, Ying Kai, Henderson, Robert H., Nerinckx, Fanny, Leroy, Bart P., Yang, Paul et al. · 2025 · Progress in Retinal and Eye Research
- Inhibition of ApoCIIISophie J. Bernelot Moens, Julian C. van Capelleveen, Erik S.G. Stroes · 2014 · Current Opinion in Lipidology
- Gene therapy for the neurological manifestations in lysosomal storage disordersSeng H. Cheng · 2014 · Journal of Lipid Research
- Delivery methods for site-specific nucleases: Achieving the full potential of therapeutic gene editingJia Liu, Sailan Shui · 2016 · Journal of Controlled Release
- Current AAV-mediated gene therapy in sensorineural hearing lossJieyu Qi, Xiaolong Fu, Liyan Zhang, Fangzhi Tan, Nianci Li, Qiuhan Sun, Xiaojie Hu, Zuhong He, Ming Xia, Renjie Chai · 2022 · Fundamental Research
- Origin and therapy for hypertriglyceridaemia in type 2 diabetesJing Pang, Dick C. Chan, Gerald Francis Watts · 2014 · World Journal of Diabetes
- Treatment of primary hypertriglyceridemia states – General approach and the role of extracorporeal methodsClaudia Stefanutti, Ulrich Julius · 2015 · Atherosclerosis Supplements
- Orlistat Therapy for Children With Type 1 Hyperlipoproteinemia: A Randomized Clinical TrialNivedita Patni, Claudia Quittner, Abhimanyu Garg · 2018 · The Journal of Clinical Endocrinology & Metabolism
- Assessment of Pre-Clinical Liver Models Based on Their Ability to Predict the Liver-Tropism of Adeno-Associated Virus VectorsAdrian Westhaus, Marti Cabanes‐Creus, Kimberley L. Dilworth, Erhua Zhu, David Salas Gómez, Renina Gale Navarro, Anais K. Amaya, Suzanne Scott, Magdalena Kwiatek, Alexandra L. McCorkindale et al. · 2023 · Human Gene Therapy
- The role of registries in rare genetic lipid disorders: Review and introduction of the first global registry in lipoprotein lipase deficiencyElisabeth Steinhagen‐Thiessen, Erik S.G. Stroes, Handrean Soran, Colin Johnson, Philippe Moulin, Giorgio Iotti, Marco Zibellini, Bas Ossenkoppele, Michaela Dippel, Maurizio Rocco Averna · 2016 · Atherosclerosis
- Development of a Chemiluminescent ELISA Method for the Detection of Total Anti-Adeno Associated Virus Serotype 9 (AAV9) AntibodiesUma Kavita, Yan‐Shan Dai, Lisa Salvador, Wendy Miller, Leonard P. Adam, Paul Lévesque, Yan J Zhang, Qin Ji, Renuka C. Pillutla · 2018 · Human Gene Therapy Methods
- Next Generation of Adeno-Associated Virus Vectors for Gene Therapy for Human Liver DiseasesKenneth I. Berns, Arun Srivastava · 2019 · Gastroenterology Clinics of North America
- PCR-based detection of gene transfer vectors: application to gene doping surveillanceIrene C. Perez, Caroline Le Guiner, Weiyi Ni, Jennifer K Lyles, Philippe Moullier, Richard O. Snyder · 2013 · Analytical and Bioanalytical Chemistry
- Changing channels in pain and epilepsy: Exploiting ion channel gene therapy for disorders of neuronal hyperexcitabilityAlbert Snowball, Stéphanie Schorge · 2015 · FEBS Letters
- Gene editing technology as an approach to the treatment of liver diseasesRajagopal N. Aravalli, Clifford J. Steer · 2016 · Expert Opinion on Biological Therapy
- Identification of candidate protective variants for common diseases and evaluation of their protective potentialJoe M. Butler, Neil Hall, Niro Narendran, Yit Chiun Yang, Luminita Paraoan · 2017 · BMC Genomics
- Preclinical Toxicity Evaluation of AAV for Pain: Evidence from Human AAV Studies and from the Pharmacology of Analgesic DrugsPleticha, Josef, Heilmann, Lukas F, Evans, Christopher H, Asokan, Aravind, Samulski, Richard Jude, Beutler, Andreas S · 2014 · Molecular Pain
- Hypertriglyceridemia and acute pancreatitis: clinical and basic research—a narrative reviewLin Gao, Weiqin Li · 2023 · Journal of Pancreatology
- New trends in articular cartilage repairMagali Cucchiarini, Christel Henrionnet, Didier Mainard, Astrid Pinzano, Henning Madry · 2015 · Journal of Experimental Orthopaedics
- Development of Optimized AAV Serotype Vectors for High-Efficiency Transduction at Further Reduced DosesChen Ling, Baozheng Li, Wenqin Ma, Arun Srivastava · 2016 · Human Gene Therapy Methods
- Of rAAV and Men: From Genetic Neuromuscular Disorder Efficacy and Toxicity Preclinical Studies to Clinical Trials and BackLaurine Buscara, David‐Alexandre Gross, Nathalie Danièle · 2020 · Journal of Personalized Medicine
- Recombinant AAV Vectors for Enhanced Expression of Authentic IgGSebastian P. Fuchs, José M. Martinez-Navío, Guangping Gao, Ronald C. Desrosiers · 2016 · PLoS ONE
- Allometric-like scaling of AAV gene therapy for systemic protein deliveryAlexandra Burr, Patrick Erickson, Raphaela Bento, Kariman A. Shama, Charles M. Roth, Biju Parekkadan · 2022 · Molecular Therapy — Methods & Clinical Development
- Oral-tolerization Prevents Immune Responses and Improves Transgene Persistence Following Gene Transfer Mediated by Adeno-associated Viral VectorRomain Hardet, Benjamin Chevalier, Léa Dupaty, Yassine Naïmi, Gaëtan Riou, Laurent Drouot, Laetitia Jean, Anna Salvetti, Olivier Boyer, Sahil Adriouch · 2015 · Molecular Therapy
- Overcoming the Undesirable CRISPR-Cas9 Expression in Gene CorrectionEmily Xia, Rongqi Cathleen Duan, Fushan Shi, Kyle E. Seigel, Hartmut Grasemann, Jim Hu · 2018 · Molecular Therapy — Nucleic Acids