Manufacturing and characterizing AA V-based vectors for use in clinical studiesWRIGHT, J. F.Gene therapy (Basingstoke). 2008, Vol 15, Num 11, pp 840-848, issn 0969-7128, 9 p.Article

Site-Specific Integration by the Adeno-Associated Virus Rep Protein : Recombinase Technology for Gene TherapyRECCHIA, Alessandra; MAVILIO, Fulvio.Current gene therapy. 2011, Vol 11, Num 5, pp 399-405, issn 1566-5232, 7 p.Article

Adeno-associated viral vector-mediated neurotrophin gene transfer in the injured adult rat spinal cord improves hind-limb functionBLITS, B; OUDEGA, M; BOER, G. J et al.Neuroscience. 2003, Vol 118, Num 1, pp 271-281, issn 0306-4522, 11 p.Article

AAV-mediated expression of Bcl-X_L or XIAP fails to induce neuronal resistance against quinolinic acid-induced striatal lesioningKELLS, Adrian P; CONNOR, Bronwen.Neuroscience letters. 2008, Vol 436, Num 3, pp 326-330, issn 0304-3940, 5 p.Article

Capsid-expressing DNA in AAV vectors and its elimination by use of an oversize capsid gene for vector productionHALBERT, C. L; METZGER, M. J; LAM, S.-L et al.Gene therapy (Basingstoke). 2011, Vol 18, Num 4, pp 411-417, issn 0969-7128, 7 p.Article

Improved transduction of primary murine hepatocytes by recombinant adeno-associated virus 2 vectors in vivoZHONG, L; LI, W; YANG, Z et al.Gene therapy (Basingstoke). 2004, Vol 11, Num 14, pp 1165-1169, issn 0969-7128, 5 p.Article

Targeted gene repair : The ups and downs of a promising gene therapy approachDE SEMIR, David; ARAN, Josep M.Current gene therapy. 2006, Vol 6, Num 4, pp 481-504, issn 1566-5232, 24 p.Article

New recombinant serotypes of AAV vectorsGUANGPING GAO; VANDENBERGHE, Luk H; WILSON, James M et al.Current gene therapy. 2005, Vol 5, Num 3, pp 285-297, issn 1566-5232, 13 p.Article

Peptide affinity reagents for AAV capsid recognition and purificationPULICHERLA, N; ASOKAN, A.Gene therapy (Basingstoke). 2011, Vol 18, Num 10, pp 1020-1024, issn 0969-7128, 5 p.Article

Inducible adeno-associated virus vectors promote functional angiogenesis in adult organisms via regulated vascular endothelial growth factor expressionTAFURO, Sabrina; AYUSO, Eduard; ZACCHIGNA, Serena et al.Cardiovascular research. 2009, Vol 83, Num 4, pp 663-671, issn 0008-6363, 9 p.Article

Adeno-associated virus 2-mediated gene transfer : role of a cellular serine/threonine protein phosphatase in augmenting transduction efficiencyZHAO, W; WU, J; ZHONG, L et al.Gene therapy (Basingstoke). 2007, Vol 14, Num 6, pp 545-550, issn 0969-7128, 6 p.Article

Global gene transfer into the CNS across the BBB after neonatal systemic delivery of single-stranded AAV vectorsMIYAKE, Noriko; MIYAKE, Koichi; YAMAMOTO, Motoko et al.Brain research. 2011, Vol 1389, pp 19-26, issn 0006-8993, 8 p.Article

An Adeno-Associated Virus Vector Efficiently and Specifically Transduces Mouse Skeletal MuscleMURAKAMI, Isao; TAKEUCHI, Takamasa; MORI-UCHINO, Mayuyo et al.Molecular biotechnology. 2011, Vol 49, Num 1, pp 1-10, issn 1073-6085, 10 p.Article

Adeno-associated virus-mediated gene delivery into the scala media of the normal and deafened adult mouse earKILPATRICK, L. A; LI, Q; YANG, J et al.Gene therapy (Basingstoke). 2011, Vol 18, Num 6, pp 569-578, issn 0969-7128, 10 p.Article

Development of optimized AAV3 serotype vectors: mechanism of high-efficiency transduction of human liver cancer cellsCHENG, B; LING, C; SIEMANN, D et al.LING, C; Gene therapy (Basingstoke). 2012, Vol 19, Num 4, pp 375-384, issn 0969-7128, 10 p.Article

AAV-BDNF mediated attenuation of quinolinic acid-induced neuropathology and motor function impairmentKELLS, A. P; HENRY, R. A; CONNOR, B et al.Gene therapy (Basingstoke). 2008, Vol 15, Num 13, pp 966-977, issn 0969-7128, 12 p.Article

Oral administration of doxycycline allows tight control of transgene expression : a key step towards gene therapy of retinal diseasesSTIEGER, K; MENDES-MADEIRA, A; MEUR, G. L et al.Gene therapy (Basingstoke). 2007, Vol 14, Num 23, pp 1668-1673, issn 0969-7128, 6 p.Article

Efficient and long-term intracardiac gene transfer in δ-sarcoglycan-deficiency hamster by adeno-associated virus-2 vectorsLI, J; WANG, D; QIAN, S et al.Gene therapy (Basingstoke). 2003, Vol 10, Num 21, pp 1807-1813, issn 0969-7128, 7 p.Article

microRNA122-regulated transgene expression increases specificity of cardiac gene transfer upon intravenous del ivery of AAV9 vectorsGEISLER, A; JUNGMANN, A; KURRECK, J et al.Gene therapy (Basingstoke). 2011, Vol 18, Num 2, pp 199-209, issn 0969-7128, 11 p.Article

Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene productYUASA, K; SAKAMOTO, M; MIYAGOE-SUZUKI, Y et al.Gene therapy (Basingstoke). 2002, Vol 9, Num 23, pp 1576-1588, issn 0969-7128, 13 p.Article

AAV-based shRNA silencing of NF-κB ameliorates muscle pathologies in mdx miceYANG, Q; TANG, Y; IMBROGNO, K et al.Gene therapy (Basingstoke). 2012, Vol 19, Num 12, pp 1196-1204, issn 0969-7128, 9 p.Article

AAV vectors transduce hepatocytes in vivo as efficiently in cirrhotic as in healthy rat liversSOBREVALS, L; ENGUITA, M; RODRIGUEZ, C et al.Gene therapy (Basingstoke). 2012, Vol 19, Num 4, pp 411-417, issn 0969-7128, 7 p.Article

Gene transfer into human keloid tissue with Adeno-associated virus vectorHSU MA; RUIAN XU; CHENG, Henrich et al.The Journal of trauma, injury, infection, and critical care. 2003, Vol 54, Num 3, pp 569-573, issn 1079-6061, 5 p.Article

Systemic delivery of IL-10 by an AA V vector prevents vascular remodeling and end-organ damage in stroke-prone spontaneously hypertensive ratNOMOTO, T; OKADA, T; OOKAWARA, S et al.Gene therapy (Basingstoke). 2009, Vol 16, Num 3, pp 383-391, issn 0969-7128, 9 p.Article

Improvement of cardiac fibrosis in dystrophic mice by rAAV9-mediated microdystrophin transductionSHIN, J.-H; NITAHARA-KASAHARA, Y; HAYASHITA-KINOH, H et al.Gene therapy (Basingstoke). 2011, Vol 18, Num 9, pp 910-919, issn 0969-7128, 10 p.Article