25101090 23809114 32165410 33828464 31330090 20578847 24461592 25342621 23852185 25503696 26865709 32258217 24949105 28789965 33895085 22734691 23686826 32799685 34509702 27027709 31642343 24468915 31115652 33399391 21345239 29451218 21776025 2330570 - Search Results

Year	Number of Results
2008	7
2009	16
2010	32
2011	44
2012	30
2013	46
2014	39
2015	29
2016	34
2017	30
2018	24
2019	29
2020	41
2021	37
2022	12

1

Cell-Mediated Immunity to AAV Vectors, Evolving Concepts and Potential Solutions.

Basner-Tschakarjan E, Mingozzi F. Basner-Tschakarjan E, et al. Front Immunol. 2014 Jul 23;5:350. doi: 10.3389/fimmu.2014.00350. eCollection 2014. Front Immunol. 2014. PMID: 25101090 Free PMC article. Review.

2

Gene therapy for hemophilia.

Chuah MK, Evens H, VandenDriessche T. Chuah MK, et al. J Thromb Haemost. 2013 Jun;11 Suppl 1:99-110. doi: 10.1111/jth.12215. J Thromb Haemost. 2013. PMID: 23809114 Free article. Review.

3

Targeted Krüppel-Like Factor 4 Gene Knock-Out in Retinal Ganglion Cells Improves Visual Function in Multiple Sclerosis Mouse Model.

Talla V, Koilkonda R. Talla V, et al. eNeuro. 2020 Apr 2;7(2):ENEURO.0320-19.2020. doi: 10.1523/ENEURO.0320-19.2020. Print 2020 Mar/Apr. eNeuro. 2020. PMID: 32165410 Free PMC article.

4

Dual-Viral Transduction Utilizing Highly Efficient Retrograde Lentivirus Improves Labeling of Long Propriospinal Neurons.

Brown BL, Zalla RM, Shepard CT, Howard RM, Kopechek JA, Magnuson DSK, Whittemore SR. Brown BL, et al. Front Neuroanat. 2021 Mar 22;15:635921. doi: 10.3389/fnana.2021.635921. eCollection 2021. Front Neuroanat. 2021. PMID: 33828464 Free PMC article.

5

Post-translational modifications in capsid proteins of recombinant adeno-associated virus (AAV) 1-rh10 serotypes.

Mary B, Maurya S, Arumugam S, Kumar V, Jayandharan GR. Mary B, et al. FEBS J. 2019 Dec;286(24):4964-4981. doi: 10.1111/febs.15013. Epub 2019 Aug 1. FEBS J. 2019. PMID: 31330090 Free PMC article.

6

Optimized transduction of human monocyte-derived dendritic cells by recombinant adeno-associated virus serotype 6.

Ussher JE, Taylor JA. Ussher JE, et al. Hum Gene Ther. 2010 Dec;21(12):1675-86. doi: 10.1089/hum.2010.087. Hum Gene Ther. 2010. PMID: 20578847

7

Pristimerin enhances recombinant adeno-associated virus vector-mediated transgene expression in human cell lines in vitro and murine hepatocytes in vivo.

Wang LN, Wang Y, Lu Y, Yin ZF, Zhang YH, Aslanidi GV, Srivastava A, Ling CQ, Ling C. Wang LN, et al. J Integr Med. 2014 Jan;12(1):20-34. doi: 10.1016/S2095-4964(14)60003-0. J Integr Med. 2014. PMID: 24461592

8

LHON gene therapy vector prevents visual loss and optic neuropathy induced by G11778A mutant mitochondrial DNA: biodistribution and toxicology profile.

Koilkonda R, Yu H, Talla V, Porciatti V, Feuer WJ, Hauswirth WW, Chiodo V, Erger KE, Boye SL, Lewin AS, Conlon TJ, Renner L, Neuringer M, Detrisac C, Guy J. Koilkonda R, et al. Invest Ophthalmol Vis Sci. 2014 Oct 23;55(12):7739-53. doi: 10.1167/iovs.14-15388. Invest Ophthalmol Vis Sci. 2014. PMID: 25342621 Free PMC article.

9

Gene therapy for hemophilia: advancing beyond the first clinical success.

Monahan PE, Gui T. Monahan PE, et al. Curr Opin Hematol. 2013 Sep;20(5):410-6. doi: 10.1097/MOH.0b013e328363c1a1. Curr Opin Hematol. 2013. PMID: 23852185 Review.

10

Antibody neutralization poses a barrier to intravitreal adeno-associated viral vector gene delivery to non-human primates.

Kotterman MA, Yin L, Strazzeri JM, Flannery JG, Merigan WH, Schaffer DV. Kotterman MA, et al. Gene Ther. 2015 Feb;22(2):116-26. doi: 10.1038/gt.2014.115. Epub 2014 Dec 11. Gene Ther. 2015. PMID: 25503696 Free PMC article.

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