248 related articles for article (PubMed ID: 19741733)
1. Foamy combinatorial anti-HIV vectors with MGMTP140K potently inhibit HIV-1 and SHIV replication and mediate selection in vivo.
Kiem HP; Wu RA; Sun G; von Laer D; Rossi JJ; Trobridge GD
Gene Ther; 2010 Jan; 17(1):37-49. PubMed ID: 19741733
[TBL] [Abstract][Full Text] [Related]
2. Stem cell selection in vivo using foamy vectors cures canine pyruvate kinase deficiency.
Trobridge GD; Beard BC; Wu RA; Ironside C; Malik P; Kiem HP
PLoS One; 2012; 7(9):e45173. PubMed ID: 23028826
[TBL] [Abstract][Full Text] [Related]
3. Protection of stem cell-derived lymphocytes in a primate AIDS gene therapy model after in vivo selection.
Trobridge GD; Wu RA; Beard BC; Chiu SY; Muñoz NM; von Laer D; Rossi JJ; Kiem HP
PLoS One; 2009 Nov; 4(11):e7693. PubMed ID: 19888329
[TBL] [Abstract][Full Text] [Related]
4. Foamy virus vectors expressing anti-HIV transgenes efficiently block HIV-1 replication.
Taylor JA; Vojtech L; Bahner I; Kohn DB; Laer DV; Russell DW; Richard RE
Mol Ther; 2008 Jan; 16(1):46-51. PubMed ID: 17955023
[TBL] [Abstract][Full Text] [Related]
5. Foamy virus vectors for HIV gene therapy.
Olszko ME; Trobridge GD
Viruses; 2013 Oct; 5(10):2585-600. PubMed ID: 24153061
[TBL] [Abstract][Full Text] [Related]
6. Large animal models for foamy virus vector gene therapy.
Trobridge GD; Horn PA; Beard BC; Kiem HP
Viruses; 2012 Dec; 4(12):3572-88. PubMed ID: 23223198
[TBL] [Abstract][Full Text] [Related]
7. In vivo selection of hematopoietic stem cells transduced at a low multiplicity-of-infection with a foamy viral MGMT(P140K) vector.
Cai S; Ernstberger A; Wang H; Bailey BJ; Hartwell JR; Sinn AL; Eckermann O; Linka Y; Goebel WS; Hanenberg H; Pollok KE
Exp Hematol; 2008 Mar; 36(3):283-92. PubMed ID: 18279716
[TBL] [Abstract][Full Text] [Related]
8. Transduction of human CD34+ hematopoietic progenitor cells by a retroviral vector expressing an RRE decoy inhibits human immunodeficiency virus type 1 replication in myelomonocytic cells produced in long-term culture.
Bahner I; Kearns K; Hao QL; Smogorzewska EM; Kohn DB
J Virol; 1996 Jul; 70(7):4352-60. PubMed ID: 8676458
[TBL] [Abstract][Full Text] [Related]
9. Inhibition of simian/human immunodeficiency virus replication in CD4+ T cells derived from lentiviral-transduced CD34+ hematopoietic cells.
Braun SE; Wong FE; Connole M; Qiu G; Lee L; Gillis J; Lu X; Humeau L; Slepushkin V; Binder GK; Dropulic B; Johnson RP
Mol Ther; 2005 Dec; 12(6):1157-67. PubMed ID: 16168713
[TBL] [Abstract][Full Text] [Related]
10. Foamy viral vector integration sites in SCID-repopulating cells after MGMTP140K-mediated in vivo selection.
Olszko ME; Adair JE; Linde I; Rae DT; Trobridge P; Hocum JD; Rawlings DJ; Kiem HP; Trobridge GD
Gene Ther; 2015 Jul; 22(7):591-5. PubMed ID: 25786870
[TBL] [Abstract][Full Text] [Related]
11. Inhibition of human immunodeficiency virus-1 (HIV-1) replication after transduction of granulocyte colony-stimulating factor-mobilized CD34+ cells from HIV-1-infected donors using retroviral vectors containing anti-HIV-1 genes.
Bauer G; Valdez P; Kearns K; Bahner I; Wen SF; Zaia JA; Kohn DB
Blood; 1997 Apr; 89(7):2259-67. PubMed ID: 9116267
[TBL] [Abstract][Full Text] [Related]
12. Lentivirus-mediated Gene Transfer in Hematopoietic Stem Cells Is Impaired in SHIV-infected, ART-treated Nonhuman Primates.
Younan PM; Peterson CW; Polacino P; Kowalski JP; Obenza W; Miller HW; Milless BP; Gafken P; DeRosa SC; Hu SL; Kiem HP
Mol Ther; 2015 May; 23(5):943-951. PubMed ID: 25648264
[TBL] [Abstract][Full Text] [Related]
13. High-efficiency transduction of rhesus hematopoietic repopulating cells by a modified HIV1-based lentiviral vector.
Uchida N; Hargrove PW; Lap CJ; Evans ME; Phang O; Bonifacino AC; Krouse AE; Metzger ME; Nguyen AD; Hsieh MM; Wolfsberg TG; Donahue RE; Persons DA; Tisdale JF
Mol Ther; 2012 Oct; 20(10):1882-92. PubMed ID: 22871664
[TBL] [Abstract][Full Text] [Related]
14. Sustained transgene expression by human cord blood derived CD34+ cells transduced with simian immunodeficiency virus agmTYO1-based vectors carrying the human coagulation factor VIII gene in NOD/SCID mice.
Kikuchi J; Mimuro J; Ogata K; Tabata T; Ueda Y; Ishiwata A; Kimura K; Takano K; Madoiwa S; Mizukami H; Hanazono Y; Kume A; Hasegawa M; Ozawa K; Sakata Y
J Gene Med; 2004 Oct; 6(10):1049-60. PubMed ID: 15386735
[TBL] [Abstract][Full Text] [Related]
15. Intracellular immunization of rhesus CD34+ hematopoietic progenitor cells with a hairpin ribozyme protects T cells and macrophages from simian immunodeficiency virus infection.
Rosenzweig M; Marks DF; Hempel D; Heusch M; Kraus G; Wong-Staal F; Johnson RP
Blood; 1997 Dec; 90(12):4822-31. PubMed ID: 9389699
[TBL] [Abstract][Full Text] [Related]
16. Efficacy and safety of a clinically relevant foamy vector design in human hematopoietic repopulating cells.
Everson EM; Hocum JD; Trobridge GD
J Gene Med; 2018 Jul; 20(7-8):e3028. PubMed ID: 29935087
[TBL] [Abstract][Full Text] [Related]
17. Foamy virus vectors: an awaited alternative to gammaretro- and lentiviral vectors.
Rethwilm A
Curr Gene Ther; 2007 Aug; 7(4):261-71. PubMed ID: 17969559
[TBL] [Abstract][Full Text] [Related]
18. Transduction of CD34+ hematopoietic progenitor cells with an antitat gene protects T-cell and macrophage progeny from AIDS virus infection.
Rosenzweig M; Marks DF; Hempel D; Lisziewicz J; Johnson RP
J Virol; 1997 Apr; 71(4):2740-6. PubMed ID: 9060627
[TBL] [Abstract][Full Text] [Related]
19. Optimized lentiviral vectors for HIV gene therapy: multiplexed expression of small RNAs and inclusion of MGMT(P140K) drug resistance gene.
Chung J; Scherer LJ; Gu A; Gardner AM; Torres-Coronado M; Epps EW; Digiusto DL; Rossi JJ
Mol Ther; 2014 May; 22(5):952-63. PubMed ID: 24576853
[TBL] [Abstract][Full Text] [Related]
20. Activity of TAR in inducible inhibition of HIV replication by foamy virus vector expressing siRNAs under the control of HIV LTR.
Park J; Nadeau PE; Mergia A
Virus Res; 2009 Mar; 140(1-2):112-20. PubMed ID: 19110017
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]