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Items: 1 to 20 of 38


"Marker of Self" CD47 on lentiviral vectors decreases macrophage-mediated clearance and increases delivery to SIRPA-expressing lung carcinoma tumors.

Sosale NG, Ivanovska II, Tsai RK, Swift J, Hsu JW, Alvey CM, Zoltick PW, Discher DE.

Mol Ther Methods Clin Dev. 2016 Dec 7;3:16080. doi: 10.1038/mtm.2016.80. eCollection 2016.


Hemophilia A gene therapy via intraosseous delivery of factor VIII-lentiviral vectors.

Miao CH.

Thromb J. 2016 Oct 4;14(Suppl 1):41. eCollection 2016. Review.


Intraosseous delivery of lentiviral vectors targeting factor VIII expression in platelets corrects murine hemophilia A.

Wang X, Shin SC, Chiang AF, Khan I, Pan D, Rawlings DJ, Miao CH.

Mol Ther. 2015 Apr;23(4):617-26. doi: 10.1038/mt.2015.20. Epub 2015 Feb 6.


Effects of vector backbone and pseudotype on lentiviral vector-mediated gene transfer: studies in infant ADA-deficient mice and rhesus monkeys.

Carbonaro Sarracino D, Tarantal AF, Lee CC, Martinez M, Jin X, Wang X, Hardee CL, Geiger S, Kahl CA, Kohn DB.

Mol Ther. 2014 Oct;22(10):1803-16. doi: 10.1038/mt.2014.88. Epub 2014 Jun 13.


Cigarette smoke exposure during pregnancy alters fetomaternal cell trafficking leading to retention of microchimeric cells in the maternal lung.

Vogelgesang A, Scapin C, Barone C, Tam E, Blumental Perry A, Dammann CE.

PLoS One. 2014 May 15;9(5):e88285. doi: 10.1371/journal.pone.0088285. eCollection 2014.


Correction of methylmalonic aciduria in vivo using a codon-optimized lentiviral vector.

Wong ES, McIntyre C, Peters HL, Ranieri E, Anson DS, Fletcher JM.

Hum Gene Ther. 2014 Jun;25(6):529-38. doi: 10.1089/hum.2013.111. Epub 2014 Apr 2.


Integration-deficient lentiviral vectors expressing codon-optimized R338L human FIX restore normal hemostasis in Hemophilia B mice.

Suwanmanee T, Hu G, Gui T, Bartholomae CC, Kutschera I, von Kalle C, Schmidt M, Monahan PE, Kafri T.

Mol Ther. 2014 Mar;22(3):567-74. doi: 10.1038/mt.2013.188. Epub 2013 Aug 14.


Specific transfection of inflamed brain by macrophages: a new therapeutic strategy for neurodegenerative diseases.

Haney MJ, Zhao Y, Harrison EB, Mahajan V, Ahmed S, He Z, Suresh P, Hingtgen SD, Klyachko NL, Mosley RL, Gendelman HE, Kabanov AV, Batrakova EV.

PLoS One. 2013 Apr 19;8(4):e61852. doi: 10.1371/journal.pone.0061852. Print 2013.


Targeting lentiviral vectors for cancer immunotherapy.

Arce F, Breckpot K, Collins M, Escors D.

Curr Cancer Ther Rev. 2011 Nov;7(4):248-260.


Fetal microchimeric cells in a fetus-treats-its-mother paradigm do not contribute to dystrophin production in serially parous mdx females.

Seppanen EJ, Hodgson SS, Khosrotehrani K, Bou-Gharios G, Fisk NM.

Stem Cells Dev. 2012 Oct 10;21(15):2809-16. doi: 10.1089/scd.2012.0047. Epub 2012 Aug 6.


Gene transfer to chicks using lentiviral vectors administered via the embryonic chorioallantoic membrane.

Hen G, Yosefi S, Shinder D, Or A, Mygdal S, Condiotti R, Galun E, Bor A, Sela-Donenfeld D, Friedman-Einat M.

PLoS One. 2012;7(5):e36531. doi: 10.1371/journal.pone.0036531. Epub 2012 May 11. Erratum in: PLoS One. 2012;7(7). doi:10.1371/annotation/1cdd9e97-8652-415e-a79b-1caa5298c684. PLoS One. 2015;10(9):e0138629.


Entry of herpes simplex virus type 1 (HSV-1) into the distal axons of trigeminal neurons favors the onset of nonproductive, silent infection.

Hafezi W, Lorentzen EU, Eing BR, Müller M, King NJ, Klupp B, Mettenleiter TC, Kühn JE.

PLoS Pathog. 2012;8(5):e1002679. doi: 10.1371/journal.ppat.1002679. Epub 2012 May 10.


Effect of nuclear factor κB inhibition on serotype 9 adeno-associated viral (AAV9) minidystrophin gene transfer to the mdx mouse.

Reay DP, Niizawa GA, Watchko JF, Daood M, Reay JC, Raggi E, Clemens PR.

Mol Med. 2012 May 9;18:466-76. doi: 10.2119/molmed.2011.00404.


Antiviral RNAi: translating science towards therapeutic success.

Shah PS, Schaffer DV.

Pharm Res. 2011 Dec;28(12):2966-82. doi: 10.1007/s11095-011-0549-8. Epub 2011 Aug 9. Review.


K-Cl cotransporter gene expression during human and murine erythroid differentiation.

Pan D, Kalfa TA, Wang D, Risinger M, Crable S, Ottlinger A, Chandra S, Mount DB, Hübner CA, Franco RS, Joiner CH.

J Biol Chem. 2011 Sep 2;286(35):30492-503. doi: 10.1074/jbc.M110.206516. Epub 2011 Jul 6.


A microRNA-regulated and GP64-pseudotyped lentiviral vector mediates stable expression of FVIII in a murine model of Hemophilia A.

Matsui H, Hegadorn C, Ozelo M, Burnett E, Tuttle A, Labelle A, McCray PB Jr, Naldini L, Brown B, Hough C, Lillicrap D.

Mol Ther. 2011 Apr;19(4):723-30. doi: 10.1038/mt.2010.290. Epub 2011 Feb 1.


Gene delivery of a mutant TGFβ3 reduces markers of scar tissue formation after cutaneous wounding.

Waddington SN, Crossley R, Sheard V, Howe SJ, Buckley SM, Coughlan L, Gilham DE, Hawkins RE, McKay TR.

Mol Ther. 2010 Dec;18(12):2104-11. doi: 10.1038/mt.2010.174. Epub 2010 Aug 24.


Lentiviral vectors for immune cells targeting.

Froelich S, Tai A, Wang P.

Immunopharmacol Immunotoxicol. 2010 Jun;32(2):208-18. doi: 10.3109/08923970903420582. Review. Erratum in: Immunopharmacol Immunotoxicol. 2010 Sep;32(3):532.


Reprogramming erythroid cells for lysosomal enzyme production leads to visceral and CNS cross-correction in mice with Hurler syndrome.

Wang D, Zhang W, Kalfa TA, Grabowski G, Davies S, Malik P, Pan D.

Proc Natl Acad Sci U S A. 2009 Nov 24;106(47):19958-63. doi: 10.1073/pnas.0908528106. Epub 2009 Nov 10.

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