Gene therapy for surfactant protein B deficiency using recombinant AAV

Gene therapy for surfactant protein B deficiency using recombinant AAV

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Meyer-Berg, H, Hyde, S, Gill, D
التنسيق:	Conference item
منشور في:	Elsevier 2019

مواد مشابهة

Gene therapy for surfactant protein B deficiency using recombinant AAV vectors
حسب: Meyer-Berg, H
منشور في: (2021)

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Identification of AAV serotypes for lung gene therapy in human embryonic stem cell-derived lung organoids
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Homologous recombination mediates functional recovery of dysferlin deficiency following AAV5 gene transfer.
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Single-Step Purification/Solubilization of Recombinant Proteins: Application to Surfactant Protein B
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Serotype-dependent recombinant adeno-associated vector (AAV) infection of Epstein–Barr virus-positive B-cells, towards recombinant AAV-based therapy of focal EBV + lymphoproliferative disorders
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Current Challenges and Future Directions in Recombinant AAV-Mediated Gene Therapy of Duchenne Muscular Dystrophy
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An AAV-Based NF-κB-Targeting Gene Therapy (rAAV-DMP-miR533) to Inflammatory Diseases
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Optimized riboswitch-regulated AAV vector for VEGF-B gene therapy
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Immunogenicity and toxicity of AAV gene therapy
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Allometric-like scaling of AAV gene therapy for systemic protein delivery
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Establishment of mouse model of inherited PIGO deficiency and therapeutic potential of AAV-based gene therapy
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Safety and efficacy of an engineered hepatotropic AAV gene therapy for ornithine transcarbamylase deficiency in cynomolgus monkeys
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Assessment of toxicity and biodistribution of recombinant AAV8 vector–mediated immunomodulatory gene therapy in mice with Pompe disease
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Probing recombinant AAV capsid integrity and genome release after thermal stress by mass photometry
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Variation in the surfactant protein B gene is associated with development of emphysema in alpha 1 anti-trypsin deficiency
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Gene Transfer in Rodent Nervous Tissue Following Hindlimb Intramuscular Delivery of Recombinant Adeno-Associated Virus Serotypes AAV2/6, AAV2/8, and AAV2/9
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Corrigendum: Optimized riboswitch-regulated AAV vector for VEGF-B gene therapy
حسب: Reetta A. E. Eriksson, وآخرون
منشور في: (2023-03-01)

Corrigendum to âAssessment of toxicity and biodistribution of recombinant AAV8 vectorâmediated immunomodulatory gene therapy in mice with Pompe diseaseâ
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Editorial: Immunogenicity and toxicity of AAV gene therapy
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Difficulties in the treatment of an infant survivor with inherited surfactant protein-B deficiency in Tunisia
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Inclusion of PF68 surfactant improves stability of rAAV titer when passed through a surgical device used in retinal gene therapy
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Robust AAV Genotyping Based on Genetic Distances in Rep Gene That Are Maintained by Ubiquitous Recombination
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Choroideremia: molecular mechanisms and development of AAV gene therapy
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