555 related articles for article (PubMed ID: 11177545)
21. AAV-Mediated Gene Transfer to Dorsal Root Ganglion.
Yu H; Fischer G; Hogan QH
Methods Mol Biol; 2016; 1382():251-61. PubMed ID: 26611592
[TBL] [Abstract][Full Text] [Related]
22. Partial correction of sensitivity to oxidant stress in Friedreich ataxia patient fibroblasts by frataxin-encoding adeno-associated virus and lentivirus vectors.
Fleming J; Spinoulas A; Zheng M; Cunningham SC; Ginn SL; McQuilty RC; Rowe PB; Alexander IE
Hum Gene Ther; 2005 Aug; 16(8):947-56. PubMed ID: 16076253
[TBL] [Abstract][Full Text] [Related]
23. Peripheral AAV Injection for Retrograde Transduction of Dorsal Root and Trigeminal Ganglia.
Bloom DC; Watson ZL; Neumann DM
Methods Mol Biol; 2019; 1950():237-247. PubMed ID: 30783977
[TBL] [Abstract][Full Text] [Related]
24. Comparative analysis of the transduction efficiency of five adeno associated virus serotypes and VSV-G pseudotype lentiviral vector in lung cancer cells.
Chen C; Akerstrom V; Baus J; Lan MS; Breslin MB
Virol J; 2013 Mar; 10():86. PubMed ID: 23497017
[TBL] [Abstract][Full Text] [Related]
25. Recombinant adeno-associated virus serotype 6 (rAAV2/6)-mediated gene transfer to nociceptive neurons through different routes of delivery.
Towne C; Pertin M; Beggah AT; Aebischer P; Decosterd I
Mol Pain; 2009 Sep; 5():52. PubMed ID: 19737386
[TBL] [Abstract][Full Text] [Related]
26. Neuron-specific gene transfer through retrograde transport of lentiviral vector pseudotyped with a novel type of fusion envelope glycoprotein.
Kato S; Kuramochi M; Takasumi K; Kobayashi K; Inoue K; Takahara D; Hitoshi S; Ikenaka K; Shimada T; Takada M; Kobayashi K
Hum Gene Ther; 2011 Dec; 22(12):1511-23. PubMed ID: 21806473
[TBL] [Abstract][Full Text] [Related]
27. Efficient human immunodeficiency virus-based vector transduction of unstimulated human mobilized peripheral blood CD34+ cells in the SCID-hu Thy/Liv model of human T cell lymphopoiesis.
Douglas JL; Lin WY; Panis ML; Veres G
Hum Gene Ther; 2001 Mar; 12(4):401-13. PubMed ID: 11242532
[TBL] [Abstract][Full Text] [Related]
28. Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors.
Kafri T; Blömer U; Peterson DA; Gage FH; Verma IM
Nat Genet; 1997 Nov; 17(3):314-7. PubMed ID: 9354796
[TBL] [Abstract][Full Text] [Related]
29. Gene delivery to airway epithelial cells in vivo: a direct comparison of apical and basolateral transduction strategies using pseudotyped lentivirus vectors.
Kremer KL; Dunning KR; Parsons DW; Anson DS
J Gene Med; 2007 May; 9(5):362-8. PubMed ID: 17380490
[TBL] [Abstract][Full Text] [Related]
30. Transduction of bone-marrow-derived mesenchymal stem cells by using lentivirus vectors pseudotyped with modified RD114 envelope glycoproteins.
Zhang XY; La Russa VF; Reiser J
J Virol; 2004 Feb; 78(3):1219-29. PubMed ID: 14722277
[TBL] [Abstract][Full Text] [Related]
31. High levels of transgene expression following transduction of long-term NOD/SCID-repopulating human cells with a modified lentiviral vector.
Gao Z; Golob J; Tanavde VM; Civin CI; Hawley RG; Cheng L
Stem Cells; 2001; 19(3):247-59. PubMed ID: 11359950
[TBL] [Abstract][Full Text] [Related]
32. Efficiencies of transgene expression in nociceptive neurons through different routes of delivery of adeno-associated viral vectors.
Xu Y; Gu Y; Wu P; Li GW; Huang LY
Hum Gene Ther; 2003 Jun; 14(9):897-906. PubMed ID: 12828860
[TBL] [Abstract][Full Text] [Related]
33. Targeting functional subtypes of spinal motoneurons and skeletal muscle fibers in vivo by intramuscular injection of adenoviral and adeno-associated viral vectors.
Martinov VN; Sefland I; Walaas SI; Lømo T; Njå A; Hoover F
Anat Embryol (Berl); 2002 Jun; 205(3):215-21. PubMed ID: 12107491
[TBL] [Abstract][Full Text] [Related]
34. Efficient delivery of Cre-recombinase to neurons in vivo and stable transduction of neurons using adeno-associated and lentiviral vectors.
Ahmed BY; Chakravarthy S; Eggers R; Hermens WT; Zhang JY; Niclou SP; Levelt C; Sablitzky F; Anderson PN; Lieberman AR; Verhaagen J
BMC Neurosci; 2004 Jan; 5():4. PubMed ID: 15005815
[TBL] [Abstract][Full Text] [Related]
35. Pseudotyped adeno-associated viral vectors for gene transfer in dermal fibroblasts: implications for wound-healing applications.
Balaji S; King A; Dhamija Y; Le LD; Shaaban AF; Crombleholme TM; Keswani SG
J Surg Res; 2013 Sep; 184(1):691-8. PubMed ID: 23590866
[TBL] [Abstract][Full Text] [Related]
36. Systematic improvement of lentivirus transduction protocols by antibody fragments fused to VSV-G as envelope glycoprotein.
Höfig I; Barth S; Salomon M; Jagusch V; Atkinson MJ; Anastasov N; Thirion C
Biomaterials; 2014 Apr; 35(13):4204-12. PubMed ID: 24529898
[TBL] [Abstract][Full Text] [Related]
37. Glial fibrillary acidic protein promoter determines transgene expression in satellite glial cells following intraganglionic adeno-associated virus delivery in adult rats.
Xiang H; Xu H; Fan F; Shin SM; Hogan QH; Yu H
J Neurosci Res; 2018 Mar; 96(3):436-448. PubMed ID: 28941260
[TBL] [Abstract][Full Text] [Related]
38. Stable transgene expression in tumors and metastases after transduction with lentiviral vectors based on human immunodeficiency virus type 1.
Bao L; Jaligam V; Zhang XY; Kutner RH; Kantrow SP; Reiser J
Hum Gene Ther; 2004 May; 15(5):445-56. PubMed ID: 15144575
[TBL] [Abstract][Full Text] [Related]
39. Simian immunodeficiency virus vector pseudotypes differ in transduction efficiency and target cell specificity in brain.
Liehl B; Hlavaty J; Moldzio R; Tonar Z; Unger H; Salmons B; Günzburg WH; Renner M
Gene Ther; 2007 Sep; 14(18):1330-43. PubMed ID: 17611586
[TBL] [Abstract][Full Text] [Related]
40. AAV-mediated delivery of ciliary neurotrophic factor prolongs photoreceptor survival in the rhodopsin knockout mouse.
Liang FQ; Dejneka NS; Cohen DR; Krasnoperova NV; Lem J; Maguire AM; Dudus L; Fisher KJ; Bennett J
Mol Ther; 2001 Feb; 3(2):241-8. PubMed ID: 11237681
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
