Found: 16
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Synergistic inhibition of PARP-1 and NF-κB signaling downregulates immune response against recombinant AAV2 vectors during hepatic gene therapy.
- Published in:
- European Journal of Immunology, 2016, v. 46, n. 1, p. 154, doi. 10.1002/eji.201545867
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- Article
Adeno-associated virus (AAV) vectors in gene therapy: immune challenges and strategies to circumvent them.
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- Reviews in Medical Virology, 2013, v. 23, n. 6, p. 399, doi. 10.1002/rmv.1762
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- Article
MicroRNA-15b Modulates Molecular Mediators of Blood Induced Arthropathy in Hemophilia Mice.
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- International Journal of Molecular Sciences, 2016, v. 17, n. 4, p. 492, doi. 10.3390/ijms17040492
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- Article
High-Efficiency Transduction of Primary Human Hematopoietic Stem Cells and Erythroid Lineage-Restricted Expression by Optimized AAV6 Serotype Vectors <i>In Vitro</i> and in a Murine Xenograft Model <i>In Vivo</i>.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058757
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- Article
Activation of the Cellular Unfolded Protein Response by Recombinant Adeno-Associated Virus Vectors.
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- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0053845
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- Article
Post‐translational modifications in capsid proteins of recombinant adeno‐associated virus (AAV) 1‐rh10 serotypes.
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- FEBS Journal, 2019, v. 286, n. 24, p. 4964, doi. 10.1111/febs.15013
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- Article
MicroRNA‐based recombinant AAV vector assembly improves efficiency of suicide gene transfer in a murine model of lymphoma.
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- Cancer Medicine, 2020, v. 9, n. 9, p. 3188, doi. 10.1002/cam4.2935
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- Article
Infectivity of adeno-associated virus serotypes in mouse testis.
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- BMC Biotechnology, 2018, v. 18, n. 1, p. N.PAG, doi. 10.1186/s12896-018-0479-1
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- Article
AAV mediated repression of Neat1 lncRNA combined with F8 gene augmentation mitigates pathological mediators of joint disease in haemophilia.
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- Journal of Cellular & Molecular Medicine, 2024, v. 28, n. 11, p. 1, doi. 10.1111/jcmm.18460
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- Article
Potential role of long non‐coding RNA H19 and Neat1 in haemophilic arthropathy.
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- Journal of Cellular & Molecular Medicine, 2023, v. 27, n. 12, p. 1745, doi. 10.1111/jcmm.17770
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- Article
Novel Properties of Tyrosine-mutant AAV2 Vectors in the Mouse Retina.
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- Molecular Therapy, 2011, v. 19, n. 2, p. 293, doi. 10.1038/mt.2010.234
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- Article
High-efficiency Transduction and Correction of Murine Hemophilia B Using AAV2 Vectors Devoid of Multiple Surface-exposed Tyrosines.
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- Molecular Therapy, 2010, v. 18, n. 12, p. 2048, doi. 10.1038/mt.2010.172
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- Article
Ezh2 mediated H3K27me3 activity facilitates somatic transition during human pluripotent reprogramming.
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- Scientific Reports, 2015, p. 8229, doi. 10.1038/srep08229
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- Article
Optimized AAV rh.10 Vectors That Partially Evade Neutralizing Antibodies during Hepatic Gene Transfer.
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- Frontiers in Pharmacology, 2017, p. 1, doi. 10.3389/fphar.2017.00441
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- Article
Targeted delivery of AAV-transduced mesenchymal stromal cells to hepatic tissue for ex vivo gene therapy.
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- Journal of Tissue Engineering & Regenerative Medicine, 2017, v. 11, n. 5, p. 1354, doi. 10.1002/term.2034
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- Article
Cellular unfolded protein response against viruses used in gene therapy.
- Published in:
- Frontiers in Microbiology, 2014, v. 5, p. 1, doi. 10.3389/fmicb.2014.00250
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- Article