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期刊名:Molecular therapy

缩写:MOL THER

ISSN:1525-0016

e-ISSN:1525-0024

IF/分区:11.4/Q1

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共收录本刊相关文章索引5917条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Gabriel Laghlali,Matthew J Wiest,Dilara Karadag et al. Gabriel Laghlali et al.
Current COVID-19 mRNA vaccines delivered intramuscularly (IM) induce effective systemic immunity, but with suboptimal immunity at mucosal sites, limiting their ability to impart sterilizing immunity. There is strong interest in rerouting im...
Yingying Bao,Jialing Liu,Zhishan Li et al. Yingying Bao et al.
IL-10+ regulatory B cells (Bregs) show great promise in treating graft-versus-host disease (GVHD), a life-threatening complication of post-hematopoietic stem cell transplantation. However, obtaining high-quality human IL-10+ Bregs in vitro ...
Veronica Jimenez,Victor Sacristan,Claudia Jambrina et al. Veronica Jimenez et al.
The highly prevalent metabolic dysfunction-associated steatohepatitis (MASH) is associated with liver steatosis, inflammation, and hepatocyte injury, which can lead to fibrosis and may progress to hepatocellular carcinoma and death. New tre...
Jiang-Hui Wang,Wei Zhan,Thomas L Gallagher et al. Jiang-Hui Wang et al.
Adeno-associated virus (AAV) has emerged as a leading platform for in vivo gene therapy, particularly in ocular diseases. AAV-based therapies are characterized by low pathogenicity and broad tissue tropism and have demonstrated clinical suc...
Fabio Dell&#x;Aquila,Roberto Di Cunto,Elena Marrocco et al. Fabio Dell&#x;Aquila et al.
Gyrate atrophy of the choroid and retina (GACR) is due to ornithine aminotransferase (OAT) deficiency, which causes hyperornithinemia, leading to retinal pigment epithelium, followed by choroidal and retinal degeneration. Adeno-associated v...
Patricia Lam,Deborah A Zygmunt,Anna Ashbrook et al. Patricia Lam et al.
Lysosomal acid lipase deficiency (LAL-D) is caused by mutations in the LIPA gene, which encodes the lysosomal enzyme that hydrolyzes triglycerides and cholesteryl esters to free fatty acids and free cholesterol. The objective of this study ...