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Items: 1 to 20 of 146


Exclusive Transduction of Human CD4+ T Cells upon Systemic Delivery of CD4-Targeted Lentiviral Vectors.

Zhou Q, Uhlig KM, Muth A, Kimpel J, Lévy C, Münch RC, Seifried J, Pfeiffer A, Trkola A, Coulibaly C, von Laer D, Wels WS, Hartwig UF, Verhoeyen E, Buchholz CJ.

J Immunol. 2015 Sep 1;195(5):2493-501. doi: 10.4049/jimmunol.1500956. Epub 2015 Jul 31.


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 1;101(9):3416-23. Epub 2003 Jan 2.


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. Epub 2005 Sep 15.


Targeted gene therapy to antigen-presenting cells in the central nervous system using hematopoietic stem cells.

Lesniak MS, Kelleher E, Pardoll D, Cui Y.

Neurol Res. 2005 Dec;27(8):820-6.


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. doi: 10.1016/j.exphem.2013.07.002. Epub 2013 Aug 14.


T-cell receptor gene transfer exclusively to human CD8(+) cells enhances tumor cell killing.

Zhou Q, Schneider IC, Edes I, Honegger A, Bach P, Schönfeld K, Schambach A, Wels WS, Kneissl S, Uckert W, Buchholz CJ.

Blood. 2012 Nov 22;120(22):4334-42. doi: 10.1182/blood-2012-02-412973. Epub 2012 Aug 16.


Tumor protection following vaccination with low doses of lentivirally transduced DCs expressing the self-antigen erbB2.

Mossoba ME, Walia JS, Rasaiah VI, Buxhoeveden N, Head R, Ying C, Foley JE, Bramson JL, Fowler DH, Medin JA.

Mol Ther. 2008 Mar;16(3):607-17. doi: 10.1038/ Epub 2008 Jan 8.


Baboon envelope pseudotyped lentiviral vectors efficiently transduce human B cells and allow active factor IX B cell secretion in vivo in NOD/SCIDγc-/- mice.

Levy C, Fusil F, Amirache F, Costa C, Girard-Gagnepain A, Negre D, Bernadin O, Garaulet G, Rodriguez A, Nair N, Vandendriessche T, Chuah M, Cosset FL, Verhoeyen E.

J Thromb Haemost. 2016 Dec;14(12):2478-2492. doi: 10.1111/jth.13520. Epub 2016 Nov 8.


[Construction and expression of the self-inactivating lentiviral vector containing Murine Foxp3 gene].

Cao J, Chen C, Xu KL, Pan XY, Li ZY, Zeng LY.

Sichuan Da Xue Xue Bao Yi Xue Ban. 2009 Mar;40(2):199-202. Chinese.


Restriction of transgene expression to the B-lymphoid progeny of human lentivirally transduced CD34+ cells.

Moreau T, Bardin F, Imbert J, Chabannon C, Tonnelle C.

Mol Ther. 2004 Jul;10(1):45-56.


Development of an enhanced B-specific lentiviral vector expressing BTK: a tool for gene therapy of XLA.

Moreau T, Barlogis V, Bardin F, Nunes JA, Calmels B, Chabannon C, Tonnelle C.

Gene Ther. 2008 Jun;15(12):942-52. doi: 10.1038/gt.2008.17. Epub 2008 Mar 6.


Abrogated cryptic activation of lentiviral transfer vectors.

Luche RM, Enssle J, Kiem HP.

Sci Rep. 2012;2:438. doi: 10.1038/srep00438. Epub 2012 Jun 1.


A novel lentiviral vector targets gene transfer into human hematopoietic stem cells in marrow from patients with bone marrow failure syndrome and in vivo in humanized mice.

Frecha C, Costa C, Nègre D, Amirache F, Trono D, Rio P, Bueren J, Cosset FL, Verhoeyen E.

Blood. 2012 Feb 2;119(5):1139-50. doi: 10.1182/blood-2011-04-346619. Epub 2011 Nov 23.


Lentiviral vector transduction of NOD/SCID repopulating cells results in multiple vector integrations per transduced cell: risk of insertional mutagenesis.

Woods NB, Muessig A, Schmidt M, Flygare J, Olsson K, Salmon P, Trono D, von Kalle C, Karlsson S.

Blood. 2003 Feb 15;101(4):1284-9. Epub 2002 Oct 17.


Optimization of lentiviral vector transduction into peripheral blood mononuclear cells in combination with the fibronectin fragment CH-296 stimulation.

Chono H, Goto Y, Yamakawa S, Tanaka S, Tosaka Y, Nukaya I, Mineno J.

J Biochem. 2011 Mar;149(3):285-92. doi: 10.1093/jb/mvq135. Epub 2010 Nov 23.


Immunotherapy of established tumors using bone marrow transplantation with antigen gene--modified hematopoietic stem cells.

Cui Y, Kelleher E, Straley E, Fuchs E, Gorski K, Levitsky H, Borrello I, Civin CI, Schoenberger SP, Cheng L, Pardoll DM, Whartenby KA.

Nat Med. 2003 Jul;9(7):952-8.


Lentiviral vector transduction of hematopoietic stem cells that mediate long-term reconstitution of lethally irradiated mice.

Chen W, Wu X, Levasseur DN, Liu H, Lai L, Kappes JC, Townes TM.

Stem Cells. 2000;18(5):352-9.


A highly efficient short hairpin RNA potently down-regulates CCR5 expression in systemic lymphoid organs in the hu-BLT mouse model.

Shimizu S, Hong P, Arumugam B, Pokomo L, Boyer J, Koizumi N, Kittipongdaja P, Chen A, Bristol G, Galic Z, Zack JA, Yang O, Chen IS, Lee B, An DS.

Blood. 2010 Feb 25;115(8):1534-44. doi: 10.1182/blood-2009-04-215855. Epub 2009 Dec 17.

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