Uncovering and Dissecting the Genotoxicity of Self-inactivating Lentiviral Vectors In Vivo
Cesana, Daniela, Ranzani, Marco, Volpin, Monica, Bartholomae, Cynthia, Duros, Caroline, Artus, Alexandre, Merella, Stefania, Benedicenti, Fabrizio +11 more·2014·Molecular Therapy
Cited by (189)
Items 101–189 of 189
- Balancing efficacy and safety in lentiviral vector-mediated hematopoietic stem cell gene therapyEugenio Montini, Luigi Naldini, Claire Booth, Donald B. Kohn, Alessandro Aiuti · 2024 · Molecular Therapy
- Effective therapies for sickle cell disease: are we there yet?Merlin Crossley, Georgios E. Christakopoulos, Mitchell J. Weiss · 2022 · Trends in Genetics
- Optimization of Mucosal Responses after Intramuscular Immunization with Integrase Defective Lentiviral VectorAlessandra Rossi, Zuleika Michelini, Pasqualina Leone, Martina Borghi, Maria Blasi, Roberta Bona, Massimo Spada, Felicia Grasso, Alessio Gugliotta, Mary E. Klotman et al. · 2014 · PLoS ONE
- Safe and Effective Gene Therapy for Murine Wiskott-Aldrich Syndrome Using an Insulated Lentiviral VectorSingh, Swati, Khan, Iram, Khim, Socheath, Seymour, Brenda, Sommer, Karen, Wielgosz, Matthew, Norgaard, Zachary, Kiem, Hans-Peter, Adair, Jennifer, Liggitt, Denny et al. · 2017 · Molecular Therapy - Methods & Clinical Development
- Gene therapy's out-of-body experienceChristopher Thomas Scott, Laura DeFrancesco · 2016 · Nature Biotechnology
- Non-clinical safety assessment of novel drug modalities: Genome safety perspectives on viral-, nuclease- and nucleotide-based gene therapiesMyriam Lemmens, Lena Dorsheimer, Andreas Zeller, Yasmin Dietz · 2024 · Mutation Research/Genetic Toxicology and Environmental Mutagenesis
- The Current Landscape of Secondary Malignancies after CAR T-Cell Therapies: How Could Malignancies Be Prevented?Stella Bouziana, Dimitrios Bouzianas · 2024 · International Journal of Molecular Sciences
- Insulated Foamy Viral VectorsD. Browning, Casey Collins, Jonah D. Hocum, David J. Leap, Dustin T. Rae, G. Trobridge · 2016 · Human Gene Therapy
- Viral vectors as a promising nanotherapeutic approach against neurodegenerative disordersVaibhavi Srivastava, Ajit Singh, Gaurav Kumar Jain, Farhan Jalees Ahmad, Rahul Shukla, Prashant Kesharwani · 2021 · Process Biochemistry
- Evidence for the in vivo safety of insulated foamy viral vectorsDiana L. Browning, Elizabeth M. Everson, David J. Leap, Jonah D. Hocum, H Wang, George Stamatoyannopoulos, G D Trobridge · 2016 · Gene Therapy
- The IS2 Element Improves Transcription Efficiency of Integration-Deficient Lentiviral Vector EpisomesSabina Sánchez-Hernández, Alejandra Gutiérrez-Guerrero, Rocío Martín-Guerra, Marina Cortijo-Gutierréz, María Tristán‐Manzano, Sandra Rodríguez, Laura Sánchez, Jose Luis Garcia-Perez, Jesús Chato‐Astrain, Ricardo Fernández‐Valadés et al. · 2018 · Molecular Therapy — Nucleic Acids
- In vivo enrichment of genetically manipulated platelets for murine hemophilia B gene therapyYingyu Chen, Jocelyn A. Schroeder, Chunyan Gao, Jing Li, Jianda Hu, Qizhen Shi · 2020 · Journal of Cellular Physiology
- Barcoding of Macaque Hematopoietic Stem and Progenitor Cells: A Robust Platform to Assess Vector GenotoxicityIdalia M. Yabe, Lauren L. Truitt, Diego A. Espinoza, Chuanfeng Wu, Samson Koelle, Sandhya Ramanathan Panch, Marcus Alexandre Finzi Corat, Thomas Winkler, Kyung–Rok Yu, So Gun Hong et al. · 2018 · Molecular Therapy — Methods & Clinical Development
- Risk and Benefit Assessment of Gene Therapy with Lentiviral Vectors and Hematopoietic Stem Cells: The Skysona CasePilar Puig-Serra, Ana Hinckley-Boned, María Tristán‐Manzano, Paula Rı́o, Raúl Torres-Ruiz, Sandra Rodríguez, Francisco Martı́n · 2025 · Human Gene Therapy
- Safety and efficiency modifications of SIV-based integrase-defective lentiviral vectors for immunizationRoberta Bona, Zuleika Michelini, Chiara Mazzei, Alessandra Gallinaro, Andrea Canitano, Martina Borghi, Maria Fenicia Vescio, Antonio Di Virgilio, Maria Franca Pirillo, Mary E. Klotman et al. · 2021 · Molecular Therapy — Methods & Clinical Development
- InsB9-23 Gene Transfer to Hepatocyte-Based Combined Therapy Abrogates Recurrence of Type 1 Diabetes After Islet TransplantationFabio Russo, Antonio Citro, Giorgia Squeri, Francesca Sanvito, Paolo Monti, Silvia Gregori, Maria Grazia Roncarolo, Andrea Annoni · 2020 · Diabetes
- Canstatin represses glioma growth by inhibiting formation of VM-like structuresYuqiang Ma, Tao Wu, Houjie Zhou, Guilu He, Yifei Li, Bocheng Wang, Qiang Guo, Baodong Chen, Weiping Li · 2021 · Translational Neuroscience
- Genome Editing of the Blood: Opportunities and ChallengesMatthew Hebden Porteus · 2015 · Current Stem Cell Reports
- Hepatotoxicity and Toxicology of In Vivo Lentiviral Vector Administration in Healthy and Liver-Injury Mouse ModelsRobert A. Kaiser, Clara T. Nicolas, Kari L. Allen, Jennifer A. Chilton, Zeji Du, Raymond Hickey, Joseph B. Lillegard · 2019 · Human Gene Therapy Clinical Development
- Lentiviral Vector Promoter is Decisive for Aberrant Transcript FormationSimone Scholz, Raffaele Fronza, Cynthia C. Bartholomae, Daniela Cesana, Eugenio Montini, Christof V. Kalle, Irene Gil-Fariña, Manfred Schmidt · 2017 · Human Gene Therapy
- Preclinical Development of Autologous Hematopoietic Stem Cell-Based Gene Therapy for Immune Deficiencies: A Journey from Mouse Cage to Bed SideLaura García-Pérez, Anita Ordas, Kirsten Canté-Barrett, Pauline Meij, Karin Pike‐Overzet, Arjan C. Lankester, Frank J. T. Staal · 2020 · Pharmaceutics
- Integrome signatures of lentiviral gene therapy for SCID-X1 patientsKoon‐Kiu Yan, Jose Condori, Zhijun Ma, Jean‐Yves Métais, Bensheng Ju, Liang Ding, Yogesh Dhungana, Lance E. Palmer, Deanna M. Langfitt, Francesca Ferrara et al. · 2023 · Science Advances
- Quantum pBac : An effective, high‐capacity piggyBac ‐ based gene integration vector system for unlocking gene therapy potentialWei‐Kai Hua, Jeff C. Hsu, Yi‐Chun Chen, Peter S. Chang, Kuo‐Lan Karen Wen, Po‐Nan Wang, Wei‐Cheng Yang, Chia‐Ning Shen, Yishan Yu, Ying‐Chun Chen et al. · 2023 · The FASEB Journal
- Safety and Efficacy of Retroviral and Lentiviral Vectors for Gene TherapyDaniela Cesana, Monica Volpin, Yasmin Natalia Serina Secanechia, Eugenio Montini · 2017 · Springer eBooks
- The steep uphill path leading to ex vivo gene therapy for genodermatosesMichele Palamenghi, Michele De Luca, Laura De Rosa · 2022 · American Journal of Physiology-Cell Physiology
- Determinants of Retroviral Integration and Implications for Gene Therapeutic MLV—Based Vectors and for a Cure for HIV-1 InfectionEline Pellaers, Anayat Bhat, Frauke Christ, Zeger Debyser · 2022 · Viruses
- Improving the Assessment of Risk Factors Relevant to Potential Carcinogenicity of Gene Therapies: A Consensus ArticleJan C Klapwijk, Alberto del Río Espínola, S. Libertini, P. Collin, Mick D. Fellows, Susan Jobling, Anthony M. Lynch, H. Martus, Catherine Vickers, Andreas Zeller et al. · 2024 · Human Gene Therapy
- Investigating the Barrier Activity of Novel, Human Enhancer-Blocking Chromatin Insulators for Hematopoietic Stem Cell Gene TherapyPenelope Georgia Papayanni, Nikoletta Psatha, Panayota Christofi, Li X, Pâmela Melo, Monica Volpin, Eugenio Montini, Mingdong Liu, Georgios Kaltsounis, Minas Yiangou et al. · 2021 · Human Gene Therapy
- Dimethyloxaloylglycine increases bone repair capacity of adipose-derived stem cells in the treatment of osteonecrosis of the femoral headZhenhong Zhu, Wenqi Song, Changqing Zhang, Jimin Yin · 2016 · Experimental and Therapeutic Medicine
- Mutagenesis and Carcinogenesis Risk Evaluation for AAV and Lentiviral Gene TherapiesToufan Parman, Daniella M. Pizzurro, Jacquelynn Lucas, Zhechu Peng · 2025 · International Journal of Toxicology
- Adaptation of lentiviral vectors for viral gene therapy and their impact on host cell biologyCatherine W. Kaiser, Eric Christian Rouchka, Melissa L. Smith · 2026 · Journal of Translational Medicine
- Success Stories and Challenges Ahead in Hematopoietic Stem Cell Gene Therapy: Hemoglobinopathies as Disease ModelsEvangelia Yannaki, Nikoletta Psatha, Αναστασία Παπαδοπούλου, Takis Athanasopoulos, Achilleas Gravanis, Maria G. Roubelakis, Panagiotis D. Tsirigotis, Αchilles Anagnostopoulos, Nicholas P. Anagnou, George Vassilopoulos · 2021 · Human Gene Therapy
- Tightly regulated ‘all-in-one’ lentiviral vectors for protection of human hematopoietic cells from anticancer chemotherapyNico Lachmann, Sebastian Brennig, Roman Hillje, H Schermeier, Ruhi Phaltane, Julia Dahlmann, Ina Gruh, Niels Heinz, Bernhard Schiedlmeier, C Baum et al. · 2015 · Gene Therapy
- Multiple Genes Surrounding Bcl-x L , a Common Retroviral Insertion Site, Can Influence Hematopoiesis Individually or in ConcertTeng-Cheong Ha, Maike Stahlhut, Michael Rothe, Gabi Paul, Violetta Dziadek, Michael Alexander Morgan, Martijn H. Brugman, Boris Fehse, Olga S. Kustikova, Axel Schambach et al. · 2020 · Human Gene Therapy
- Microfluidic Platforms for Ex Vivo and In Vivo Gene TherapySungjun Kwak, Hyo‐Jeong Lee, Dongjun Yu, Tae‐Joon Jeon, Sun Min Kim, Hyunil Ryu · 2025 · Biosensors
- On the road to in vivo CAR-T success: Comparing promising viral and non-viral vectors.Sarah de la Mota, L. Suchet, M. van Wijk, D. Stibbs, Pedro Silva Couto, Qasim A. Rafiq · 2026 · Biotechnology Advances
- Non-Viral Episomal Vector Mediates Efficient Gene Transfer of the β-Globin Gene into K562 and Human Haematopoietic Progenitor CellsVasileios Lazaris, Emmanouil Simantirakis, Eleana F. Stavrou, Meletios Verras, Argyro Sgourou, Maria K. Keramida, George Vassilopoulos, Aglaia Athanassiadou · 2023 · Genes
- Regulatory issues for genetically modified animalsPerry B. Hackett · 2020 · Frontiers of Agricultural Science and Engineering
- Safety profiling of genetically engineered Pim-1 kinase overexpression for oncogenicity risk in human c-kit+ cardiac interstitial cellsKathleen M. Broughton, Kelli Korski, Oscar Echeagaray, Robert M. Adamson, Walter P. Dembitsky, Zhibing Lu, Erik M. SCHAEFER, Mark Alan Sussman · 2019 · Gene Therapy
- Editing T cell repertoire by thymic epithelial cell-directed gene transfer abrogates risk of type 1 diabetes developmentFabio Russo, Eliana Ruggiero, Rosalia Curto, Laura Passeri, Francesca Sanvito, Ileana Bortolomai, ANNA MARIA VILLA, Silvia Gregori, Andrea Annoni · 2022 · Molecular Therapy — Methods & Clinical Development
- Delivery of RNA-based molecules to human hematopoietic stem and progenitor cells for modulation of gene expressionYvonne Diener, Andreas Bosio, Ute Bissels · 2016 · Experimental Hematology
- Hematopoietic stem cell gene therapy for the treatment of X-linked agammaglobulinemiaChristopher R. Luthers, Annika Mittelhauser, A. Colamartino, Wu Xiaomeng, Samuel Cirigliano, Joseph D. Long, Julie M. Sanchez, Zulema G. Romero, Donald B. Kohn · 2025 · Molecular Therapy — Methods & Clinical Development
- Promises and Challenges in Hematopoietic Stem Cell Gene TherapySaskia Kohlscheen, Halvard B. Bonig, Ute Modlich · 2017 · Human Gene Therapy
- WAS Promoter-Driven Lentiviral Vectors Mimic Closely the Lopsided WASP Expression during Megakaryocytic DifferentiationPilar Muñoz, María Tristán‐Manzano, Almudena Sánchez‐Gilabert, Giorgia Santilli, Anne H. M. Galy, Adrian James Thrasher, Francisco Martı́n · 2020 · Molecular Therapy — Methods & Clinical Development
- Characterization of an immune-evading doxycycline-inducible lentiviral vector for gene therapy in the spinal cordFred de Winter, Isaac Francos-Quijorna, Emily R. Burnside, Barbara Hobo, Ruben Eggers, Stefan A. Hoyng, H.P. Mulder, Rob C. Hoeben, Elizabeth M. Muir, Elizabeth J. Bradbury et al. · 2022 · Experimental Neurology
- Clonal reconstruction from co-occurrence of vector integration sites accurately quantifies expanding clones in vivoSebastian Wagner, Christoph Baldow, Andrea Calabria, Laura Rudilosso, Pierangela Gallina, Eugenio Montini, Daniela Cesana, Ingmar Glauche · 2022 · Nature Communications
- Tagmentation-based analysis reveals the clonal behavior of CAR-T cells in association with lentivector integration sitesJaeryuk Kim, Mi‐Young Park, Gyung Won Baek, Joo-Il Kim, Euna Kwon, Byeong‐Cheol Kang, Jong‐Il Kim, Hyoung Jin Kang · 2023 · Molecular Therapy — Oncolytics
- High level of fetal-globin reactivation by designed transcriptional activator-like effectorJun Zhan, Maria Johnson Irudayam, Yukio Nakamura, Ryo Kurita, Arthur W. Nienhuis · 2020 · Blood Advances
- Erosion of the pump mechanism of an inflatable penile prosthesis through the scrotum in a diabetic patient.Ihor S. Sawczuk, Michael E. Wechsler · 1985 · PubMed Central
- The long road traveled in hematopoietic stem cell gene therapyDavid A. Williams · 2022 · Molecular Therapy
- Clonal tracing of blood stem cells across mouse and human lifespansAlejo Rodriguez-Fraticelli · 2025 · Blood
- Gene therapy for Parkinson’s disease—Ample room for optimismIvette M. Sandoval, Michael F. Salvatore, Fredric P. Manfredsson · 2025 · Current Opinion in Neurobiology
- Harnessing lentiviral vectors for in vivo gene therapy of liver metastasesGiovanna Giacca, Luigi Naldini, Mario Leonardo Squadrito · 2024 · Clinical and Translational Medicine
- The cHS4 Chromatin Insulator Reduces the Rate of Retroviral Vector-Mediated Gene Dysregulation Associated with Aberrant Vector TranscriptionXianyao Zhou, Qiujun Liu, Da Wang, Xuemei Zhang, David W. Emery, Chang Long Li · 2017 · Cytogenetic and Genome Research
- Efficacy and safety of a clinically relevant foamy vector design in human hematopoietic repopulating cellsElizabeth M. Everson, Jonah D. Hocum, Grant D. Trobridge · 2018 · The Journal of Gene Medicine
- A Simple Nonviral Method to Generate Human Induced Pluripotent Stem Cells Using SMAR DNA VectorsAnna Hartley, Luisa Burger, Cornelia L. Wincek, Lieke Dons, Tracy M.W.Y. Li, Annabel Grewenig, Toros Taşgın, Manuela B. Urban, Alicia Roig‐Merino, Mehrnaz Ghazvini et al. · 2024 · Genes
- Sustained and Efficient Delivery of Antivascular Endothelial Growth Factor by the Adeno‐associated Virus for the Treatment of Corneal Neovascularization: An Outlook for Its Clinical TranslationMengzhen Xie, Lixiang Wang, Yingping Deng, Ke Ma, Hongbo Yin, Xiaolan Zhang, Xingye Xiang, Jin Tang · 2024 · Journal of Ophthalmology
- hInGeTox: a human-based in vitro platform to evaluate lentivirus/host interactions that contribute to genotoxicitySaqlain Suleman, Sharmin Alhaque, Andrew Y. Guo, Huairen Zhang, Annette M. Payne, Marco Zahn, Serena Fawaz, Mohammad S. Khalifa, Susan Jobling, David C. Hay et al. · 2025 · Gene Therapy
- Gene Therapy for Sickle Cell Anemia in India - Current Status and ChallengesArushi Goel, Varsha Dalal, Rishi Dhawan, Souvik Maiti, Debojyoti Chakraborty · 2025 · Indian Journal of Hematology and Blood Transfusion
- Liver-directed lentiviral gene therapy confers durable hepatic and systemic amelioration of methylmalonic acidemia in miceElena Barbon, Chiara Simoni, Amy Argabright, Molly Boettiger, Camilla Negri, Elisabetta Manta, Andrea Raimondi, Elena Vezzoli, Cesare Canepari, Mauro Biffi et al. · 2026 · Journal of Hepatology
- From huntingtin gene to Huntington’s disease-altering strategiesNicole Déglon · 2017 · Elsevier eBooks
- Viral Vector Gene Delivery to the Brain for Treating Neurogenetic DiseasesLinnet Ramos, Jacqueline E. Hunter, John H N Wolfe · 2017 · Springer eBooks
- Optimizing Treatment for Cerebral Adrenoleukodystrophy in the Era of Gene TherapyMarc Engelen · 2017 · New England Journal of Medicine
- Gene Therapy for Spinal Cord InjuryJoost Verhaagen, Jared D. Sydney-Smith, Skip Middelhoff, Lieve C. Butter, Fred de Winter, Elizabeth J. Bradbury · 2025 · Springer eBooks
- Toward precision immunotherapy: In vivo gene editing of T, NK, and myeloid cellsKhanh Ha Nguyen, Soumyajit Das, Sandro Matosevic · 2026 · Med
- Rewriting hepatic fate: emerging gene therapy strategies for liver diseaseRalf Weiskirchen · 2026 · Journal of Translational Genetics and Genomics
- Safety and efficacy analysis of in vivo lentiviral gene therapy in pre-clinical ARC syndrome modelsAndrei Claudiu Cozmescu, Mina Nazari, Loukia Touramanidou, Sonam Gurung, Dany P.B. Perocheau, Neil James Sebire, Yiting Hu, Sian Goldsworthy, Jemima J. Burden, Youssef Khalil et al. · 2026 · Nature Communications
- InCliniGene enables high-throughput and comprehensive in vivo clonal tracking toward clinical genomics data integrationIvan Merelli, Stefano Beretta, Daniela Cesana, Alessandro Gennari, Fabrizio Benedicenti, Giulio Spinozzi, Daniele Cesini, Eugenio Montini, Daniele D’Agostino, Andrea Calabria · 2023 · Database
- Preclinical efficacy of a modified gamma-globin lentivirus gene therapy in Berkeley sickle cell anemia mice and human xenograft modelsArchana Shrestha, Devin M. Pillis, Sydney Felker, Mengna Chi, Kimberly Wagner, Oluwabukola T. Gbotosho, Joseph Sieling, Mohammad Shadid, Punam Malik · 2025 · Molecular Therapy — Methods & Clinical Development
- Lentiviral Hematopoietic Stem Cell Gene Therapy in Inherited Immune and Lysoso- mal Enzyme DeficienciesGerard Wagemaker · 2016 · Cellular Therapy and Transplantation
- Anemi tedavisinde gen düzenleme çalışmalarıGulcin Delal Nozhatzadeh Fatih Kocabas- Batuhan Mert Kalkan · 2020 · Gene Editing
- Safety of Retroviral Vectors in Clinical Applications: Lessons from Retroviral Biology and PathogenesisJames C. Neil · 2017 · Encyclopedia of Life Sciences
- [Use of a new peroral anticoryza drug. Experience in the industrial medical practice].G Schäfer · 1971 · PubMed
- Assessing the Therapeutic Potential of CRISPR/Cas9-Mediated Gene Modulation in Merosin-Deficient Congenital Muscular Dystrophy Type 1APrabhpreet S. Bassi · 2017 · TSpace (University of Toronto)
- North Slope pipeline work strong; gas pipeline project deferredD. Hale · 1982 · Pipeline Gas J.; (United States)
- Therapeutic approaches to imprinting diseasesHela Sassi, Léa Guerrini‐Rousseau, Jacques Grill, Étienne Rouleau · 2023 · Elsevier eBooks
- Identification of c.146G > A mutation in a Fabry patient and its correction by customized Cas9 base editors in vitroZhi Yang, Hao Li, Mei Luo, Haonan Yi, Xinyu Han, Enze Liu, Shaohua Yao, Zhangxue Hu · 2024 · International Journal of Biological Macromolecules
- Response to: Safety and efficacy considerations of HSC-based gene therapy for RAG1-deficient SCIDEugenio Montini, Luigi Naldini, Claire Booth, Donald B. Kohn, Alessandro Aiuti · 2025 · Molecular Therapy
- Tweaking lentiviral vector design balances efficacy and safety in liver-directed gene therapy for familial hypercholesterolemiaCesare Canepari, Michela Milani, Sara Degl’Innocenti, Marco Monti, Monica Volpin, Francesco Starinieri, Maurizio Cavallo, Anna Fabiano, Mauro Biffi, Marialucia Longo et al. · 2025 · Molecular Therapy
- Enhanced transcriptional insulation of lentiviral vectors using “sequence-upgraded polyA long terminal repeats” or “supA-LTRs”Jordan Wright, Ben M. Alberts, María Lorena Martínez Quiles, Alessandra Guarino, Daniel Chipchase, Nicholas G. Clarkson, Kyriacos A. Mitrophanous, Daniel C. Farley · 2025 · Molecular Therapy Advances
- SAGA-Q: Gene Expression Differences Enable Detection of Retroviral Vectors with Mutagenic PotentialFriederike Mansel, Antonella Lucía Bastone, Philipp John-Neek, Jenni Fleischauer, Violetta Dziadek, Maike Hagedorn, Axel Schambach, Michael Rothe · 2026 · Human Gene Therapy
- Génotoxicité des systèmes CRISPR-Cas9.Grégoire Cullot · 2019 · theses.fr (ABES)
- Measurement and analysis of the protective effects of anti-sickling hemoglobins in sickle cell disease : application to gene therapy strategiesNicolas Hebert · 2020 · theses.fr (ABES)
- CRISPR-Cas9-based strategies for enhanced targeted integrationLaurie Lacombe · 2024
- Sickle Cell Disease: Historical Overview and Current TherapiesOluwaseun O. Babatunde, Madeleine G. Bibby, Anthony Atala, Graça D. Almeida-Porada, Christopher D. Porada · 2026 · Prenatal Diagnosis
- Characterization of Lentiviral Vector Products Using Orthogonal MeasurementsJerilyn R. Izac, Zhiyong He, Linhua Tian, Edward J. Kwee, Sahana Audithan, Lili Wang · 2026 · Cytotherapy
- From oncogenesis to approval: the lentiviral gene therapy revolution in Wiskott–Aldrich syndromeZahra Karimizadeh, Amirali Kalantari, Maryam Behfar, Dorna Karimizadeh, Leila Jafari, Amir Ali Hamidieh · 2026 · Regenerative Medicine
- Evaluation of Anti-HIV-1 HSPC-Based Gene Therapy with Negative Selection Marker in Pigtail MacaquesJian Zhang, Jason Murray, Wenli Mu, Surya Venugopal, Ella Yim, Teresa Einhaus, Stefan Radtke, Christopher W. Peterson, Hans–Peter Kiem, Dong Sung An · 2026 · Viruses
- Bioengineering strategies for prenatal therapyElizabeth Reynolds, Diana Lee Farmer, Aijun Wang · 2026 · Nature Reviews Bioengineering