Hybrid non-viral and viral delivery strategy achieves potent gene editing in growing livers with reduced viral dosage-Reference-Cited by-同舟云学术

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Hybrid non-viral and viral delivery strategy achieves potent gene editing in growing livers with reduced viral dosage

Published:2024-09 Issue: Volume: Page:
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Gong Fanglin,Li Bowen^ORCID

Publisher

Elsevier BV

Reference7 articles.

1. Adeno-associated virus as a delivery vector for gene therapy of human diseases;Wang;Signal. Transduct. Target. Ther.,2024

2. Engineering adeno-associated virus vectors for gene therapy;Li;Nat. Rev. Genet.,2020

3. Sleeping Beauty mRNA-LNP enables stable rAAV transgene expression in mouse and NHP hepatocytes and improves vector potency;Zakas;Mol. Ther.,2024

4. Modeling correction of severe urea cycle defects in the growing murine liver using a hybrid recombinant adeno-associated virus/piggyBac transposase gene delivery system;Cunningham;Hepatology,2015

5. Hepatocyte Deletion of Triglyceride-Synthesis Enzyme Acyl CoA: Diacylglycerol Acyltransferase 2 Reduces Steatosis Without Increasing Inflammation or Fibrosis in Mice;Gluchowski;Hepatology,2019

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