Found: 12
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Therapeutic expression of human clotting factors IX and X following adeno-associated viral vector-mediated intrauterine gene transfer in early-gestation fetal macaques.
- Published in:
- FASEB Journal, 2019, v. 33, n. 3, p. 3954, doi. 10.1096/fj.201801391R
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- Article
Feasibility of combined upper and lower gastrointestinal endoscopic biopsy in the common marmoset (Callithrix jacchus) to evaluate gastrointestinal diseases.
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- Journal of Medical Primatology, 2022, v. 51, n. 3, p. 172, doi. 10.1111/jmp.12580
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- Article
Performance of AAV8 vectors expressing human factor IX from a hepatic-selective promoter following intravenous injection into rats.
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- Genetic Vaccines & Therapy, 2008, v. 6, p. 1, doi. 10.1186/1479-0556-6-9
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- Article
Coating of adeno-associated virus with reactive polymers can ablate virus tropism, enable retargeting and provide resistance to neutralising antisera.
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- Journal of Gene Medicine, 2008, v. 10, n. 4, p. 400, doi. 10.1002/jgm.1161
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- Article
Stable Human FIX Expression After 0.9G Intrauterine Gene Transfer of Self-complementary Adeno-associated Viral Vector 5 and 8 in Macaques.
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- Molecular Therapy, 2011, v. 19, n. 11, p. 1950, doi. 10.1038/mt.2011.107
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- Article
Long-term Safety and Efficacy Following Systemic Administration of a Self-complementary AAV Vector Encoding Human FIX Pseudotyped With Serotype 5 and 8 Capsid Proteins.
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- Molecular Therapy, 2011, v. 19, n. 5, p. 876, doi. 10.1038/mt.2010.274
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- Article
490. Successful Readministration of AAV8 Following Administration of Nondepleting CD4 Antibody at the Time of Vector Administration.
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- Molecular Therapy, 2006, v. 13, p. S190, doi. 10.1016/j.ymthe.2006.08.560
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- Article
711. Treatment of Acute Myeloid Leukemia by rAAV 8 Vector Mediated Human Interferon-β Gene Transfer
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- 2005
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- Abstract
Potential limits of AAV‐based gene therapy with the use of new transgenes expressing factor IX fusion proteins.
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- Haemophilia, 2019, v. 25, n. 1, p. e11, doi. 10.1111/hae.13651
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- Article
Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors.
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- Human Molecular Genetics, 2010, v. 19, n. 4, p. 735, doi. 10.1093/hmg/ddp540
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- Article
Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 12, p. 2099, doi. 10.1093/hmg/ddp133
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- Publication type:
- Article
Adeno-associated virus gene therapy prevents progression of kidney disease in genetic models of nephrotic syndrome.
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- Science Translational Medicine, 2023, v. 15, n. 708, p. 1, doi. 10.1126/scitranslmed.abc8226
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- Article