These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
292 related articles for article (PubMed ID: 27930847)
1. Targeting expression to megakaryocytes and platelets by lineage-specific lentiviral vectors. Latorre-Rey LJ; Wintterle S; Dütting S; Kohlscheen S; Abel T; Schenk F; Wingert S; Rieger MA; Nieswandt B; Heinz N; Modlich U J Thromb Haemost; 2017 Feb; 15(2):341-355. PubMed ID: 27930847 [TBL] [Abstract][Full Text] [Related]
2. Glycoprotein Ibalpha promoter drives megakaryocytic lineage-restricted expression after hematopoietic stem cell transduction using a self-inactivating lentiviral vector. Lavenu-Bombled C; Izac B; Legrand F; Cambot M; Vigier A; Massé JM; Dubart-Kupperschmitt A Stem Cells; 2007 Jun; 25(6):1571-7. PubMed ID: 17379771 [TBL] [Abstract][Full Text] [Related]
3. Silencing of a targeted protein in in vivo platelets using a lentiviral vector delivering short hairpin RNA sequence. Ohmori T; Kashiwakura Y; Ishiwata A; Madoiwa S; Mimuro J; Sakata Y Arterioscler Thromb Vasc Biol; 2007 Oct; 27(10):2266-72. PubMed ID: 17872456 [TBL] [Abstract][Full Text] [Related]
4. Transcriptional targeting of lentiviral vectors by long terminal repeat enhancer replacement. Lotti F; Menguzzato E; Rossi C; Naldini L; Ailles L; Mavilio F; Ferrari G J Virol; 2002 Apr; 76(8):3996-4007. PubMed ID: 11907239 [TBL] [Abstract][Full Text] [Related]
6. Efficient expression of a transgene in platelets using simian immunodeficiency virus-based vector harboring glycoprotein Ibalpha promoter: in vivo model for platelet-targeting gene therapy. Ohmori T; Mimuro J; Takano K; Madoiwa S; Kashiwakura Y; Ishiwata A; Niimura M; Mitomo K; Tabata T; Hasegawa M; Ozawa K; Sakata Y FASEB J; 2006 Jul; 20(9):1522-4. PubMed ID: 16723382 [TBL] [Abstract][Full Text] [Related]
7. Comparison of Tetracycline-regulated Promoters in Lentiviral-based Vectors in Murine Transplantation Studies. Stahlhut M; Ha TC; Morgan M; Schambach A; Kustikova OS Curr Gene Ther; 2016; 16(4):242-248. PubMed ID: 27739375 [TBL] [Abstract][Full Text] [Related]
8. Targeting transgene expression to antigen-presenting cells derived from lentivirus-transduced engrafting human hematopoietic stem/progenitor cells. Cui Y; Golob J; Kelleher E; Ye Z; Pardoll D; Cheng L Blood; 2002 Jan; 99(2):399-408. PubMed ID: 11781219 [TBL] [Abstract][Full Text] [Related]
9. Lentiviral gene transfer regenerates hematopoietic stem cells in a mouse model for Mpl-deficient aplastic anemia. Heckl D; Wicke DC; Brugman MH; Meyer J; Schambach A; Büsche G; Ballmaier M; Baum C; Modlich U Blood; 2011 Apr; 117(14):3737-47. PubMed ID: 21289307 [TBL] [Abstract][Full Text] [Related]
10. Specific transgene expression in human and mouse CD4+ cells using lentiviral vectors with regulatory sequences from the CD4 gene. Marodon G; Mouly E; Blair EJ; Frisen C; Lemoine FM; Klatzmann D Blood; 2003 May; 101(9):3416-23. PubMed ID: 12511423 [TBL] [Abstract][Full Text] [Related]
11. Transduction of Murine Hematopoietic Stem Cells with Tetracycline-regulated Lentiviral Vectors. Stahlhut M; Schambach A; Kustikova OS Methods Mol Biol; 2016; 1448():65-76. PubMed ID: 27317173 [TBL] [Abstract][Full Text] [Related]
12. Comparison of transduction efficiency among various lentiviruses containing GFP reporter in bone marrow hematopoietic stem cell transplantation. Wang N; Rajasekaran N; Hou T; Lisowski L; Mellins ED Exp Hematol; 2013 Nov; 41(11):934-43. PubMed ID: 23954710 [TBL] [Abstract][Full Text] [Related]
13. High-level erythroid-specific gene expression in primary human and murine hematopoietic cells with self-inactivating lentiviral vectors. Moreau-Gaudry F; Xia P; Jiang G; Perelman NP; Bauer G; Ellis J; Surinya KH; Mavilio F; Shen CK; Malik P Blood; 2001 Nov; 98(9):2664-72. PubMed ID: 11675336 [TBL] [Abstract][Full Text] [Related]
14. miR-15a-5p regulates expression of multiple proteins in the megakaryocyte GPVI signaling pathway. Basak I; Bhatlekar S; Manne BK; Stoller M; Hugo S; Kong X; Ma L; Rondina MT; Weyrich AS; Edelstein LC; Bray PF J Thromb Haemost; 2019 Mar; 17(3):511-524. PubMed ID: 30632265 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. High-level transduction and gene expression in hematopoietic repopulating cells using a human immunodeficiency [correction of imunodeficiency] virus type 1-based lentiviral vector containing an internal spleen focus forming virus promoter. Demaison C; Parsley K; Brouns G; Scherr M; Battmer K; Kinnon C; Grez M; Thrasher AJ Hum Gene Ther; 2002 May; 13(7):803-13. PubMed ID: 11975847 [TBL] [Abstract][Full Text] [Related]
17. OP9 bone marrow stroma cells differentiate into megakaryocytes and platelets. Matsubara Y; Ono Y; Suzuki H; Arai F; Suda T; Murata M; Ikeda Y PLoS One; 2013; 8(3):e58123. PubMed ID: 23469264 [TBL] [Abstract][Full Text] [Related]
18. High-level transgene expression in human hematopoietic progenitors and differentiated blood lineages after transduction with improved lentiviral vectors. Salmon P; Kindler V; Ducrey O; Chapuis B; Zubler RH; Trono D Blood; 2000 Nov; 96(10):3392-8. PubMed ID: 11071633 [TBL] [Abstract][Full Text] [Related]
19. Transduction of human hematopoietic stem cells by lentiviral vectors pseudotyped with the RD114-TR chimeric envelope glycoprotein. Di Nunzio F; Piovani B; Cosset FL; Mavilio F; Stornaiuolo A Hum Gene Ther; 2007 Sep; 18(9):811-20. PubMed ID: 17824830 [TBL] [Abstract][Full Text] [Related]