24319629 24460861 27019999 34135899 28284982 28888664 28828393 25363772 - Search Results

Year	Number of Results
2013	1
2014	2
2015	1
2016	1
2017	3
2019	1
2021	1
2022	0

1

Improved Adeno-associated Viral Gene Transfer to Murine Glioma.

Zolotukhin I, Luo D, Gorbatyuk O, Hoffman B, Warrington K Jr, Herzog R, Harrison J, Cao O. Zolotukhin I, et al. J Genet Syndr Gene Ther. 2013 Apr 29;4(133):12815. doi: 10.4172/2157-7412.1000133. J Genet Syndr Gene Ther. 2013. PMID: 24319629 Free PMC article.

2

Role of the vector genome and underlying factor IX mutation in immune responses to AAV gene therapy for hemophilia B.

Rogers GL, Martino AT, Zolotukhin I, Ertl HC, Herzog RW. Rogers GL, et al. J Transl Med. 2014 Jan 25;12:25. doi: 10.1186/1479-5876-12-25. J Transl Med. 2014. PMID: 24460861 Free PMC article.

3

Superior In vivo Transduction of Human Hepatocytes Using Engineered AAV3 Capsid.

Vercauteren K, Hoffman BE, Zolotukhin I, Keeler GD, Xiao JW, Basner-Tschakarjan E, High KA, Ertl HC, Rice CM, Srivastava A, de Jong YP, Herzog RW. Vercauteren K, et al. Mol Ther. 2016 Jun;24(6):1042-1049. doi: 10.1038/mt.2016.61. Epub 2016 Mar 29. Mol Ther. 2016. PMID: 27019999 Free PMC article.

4

Effect of CpG Depletion of Vector Genome on CD8⁺ T Cell Responses in AAV Gene Therapy.

Bertolini TB, Shirley JL, Zolotukhin I, Li X, Kaisho T, Xiao W, Kumar SRP, Herzog RW. Bertolini TB, et al. Front Immunol. 2021 May 31;12:672449. doi: 10.3389/fimmu.2021.672449. eCollection 2021. Front Immunol. 2021. PMID: 34135899 Free PMC article.

5

The Balance between CD8⁺ T Cell-Mediated Clearance of AAV-Encoded Antigen in the Liver and Tolerance Is Dependent on the Vector Dose.

Kumar SRP, Hoffman BE, Terhorst C, de Jong YP, Herzog RW. Kumar SRP, et al. Mol Ther. 2017 Apr 5;25(4):880-891. doi: 10.1016/j.ymthe.2017.02.014. Epub 2017 Mar 9. Mol Ther. 2017. PMID: 28284982 Free PMC article.

6

Regulatory T cells and TLR9 activation shape antibody formation to a secreted transgene product in AAV muscle gene transfer.

Herzog RW, Cooper M, Perrin GQ, Biswas M, Martino AT, Morel L, Terhorst C, Hoffman BE. Herzog RW, et al. Cell Immunol. 2019 Aug;342:103682. doi: 10.1016/j.cellimm.2017.07.012. Epub 2017 Aug 1. Cell Immunol. 2019. PMID: 28888664 Free PMC article.

7

Neonatal Gene Therapy for Hemophilia B by a Novel Adenovirus Vector Showing Reduced Leaky Expression of Viral Genes.

Iizuka S, Sakurai F, Tachibana M, Ohashi K, Mizuguchi H. Iizuka S, et al. Mol Ther Methods Clin Dev. 2017 Jul 8;6:183-193. doi: 10.1016/j.omtm.2017.07.001. eCollection 2017 Sep 15. Mol Ther Methods Clin Dev. 2017. PMID: 28828393 Free PMC article.

8

Promoterless gene targeting without nucleases ameliorates haemophilia B in mice.

Barzel A, Paulk NK, Shi Y, Huang Y, Chu K, Zhang F, Valdmanis PN, Spector LP, Porteus MH, Gaensler KM, Kay MA. Barzel A, et al. Nature. 2015 Jan 15;517(7534):360-4. doi: 10.1038/nature13864. Epub 2014 Oct 29. Nature. 2015. PMID: 25363772 Free PMC article.

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