195 related articles for article (PubMed ID: 3031683)
1. Handicapped retroviral vectors efficiently transduce foreign genes into hematopoietic stem cells.
Hawley RG; Covarrubias L; Hawley T; Mintz B
Proc Natl Acad Sci U S A; 1987 Apr; 84(8):2406-10. PubMed ID: 3031683
[TBL] [Abstract][Full Text] [Related]
2. Retroviral vector design for long-term expression in murine hematopoietic cells in vivo.
Correll PH; Colilla S; Karlsson S
Blood; 1994 Sep; 84(6):1812-22. PubMed ID: 8080986
[TBL] [Abstract][Full Text] [Related]
3. Retroviral vectors containing chimeric promoter/enhancer elements exhibit cell-type-specific gene expression.
Couture LA; Mullen CA; Morgan RA
Hum Gene Ther; 1994 Jun; 5(6):667-77. PubMed ID: 7948129
[TBL] [Abstract][Full Text] [Related]
4. Retroviral gene transfer of human adenosine deaminase in murine hematopoietic cells: effect of selectable marker sequences on long-term expression.
Apperley JF; Luskey BD; Williams DA
Blood; 1991 Jul; 78(2):310-7. PubMed ID: 2070069
[TBL] [Abstract][Full Text] [Related]
5. Clonal contributions of small numbers of retrovirally marked hematopoietic stem cells engrafted in unirradiated neonatal W/Wv mice.
Capel B; Hawley R; Covarrubias L; Hawley T; Mintz B
Proc Natl Acad Sci U S A; 1989 Jun; 86(12):4564-8. PubMed ID: 2567516
[TBL] [Abstract][Full Text] [Related]
6. Production of human glucocerebrosidase in mice after retroviral gene transfer into multipotential hematopoietic progenitor cells.
Correll PH; Fink JK; Brady RO; Perry LK; Karlsson S
Proc Natl Acad Sci U S A; 1989 Nov; 86(22):8912-6. PubMed ID: 2573069
[TBL] [Abstract][Full Text] [Related]
7. Comparative analysis of retroviral vector expression in mouse embryonal carcinoma cells.
Hawley TS; Sabourin LA; Hawley RG
Plasmid; 1989 Sep; 22(2):120-31. PubMed ID: 2560217
[TBL] [Abstract][Full Text] [Related]
8. Simplified retroviral vector gcsap with murine stem cell virus long terminal repeat allows high and continued expression of enhanced green fluorescent protein by human hematopoietic progenitors engrafted in nonobese diabetic/severe combined immunodeficient mice.
Kaneko S; Onodera M; Fujiki Y; Nagasawa T; Nakauchi H
Hum Gene Ther; 2001 Jan; 12(1):35-44. PubMed ID: 11177540
[TBL] [Abstract][Full Text] [Related]
9. Construction and characterization of a retroviral vector demonstrating efficient expression of cloned cDNA sequences.
Kirschmeier PT; Housey GM; Johnson MD; Perkins AS; Weinstein IB
DNA; 1988 Apr; 7(3):219-25. PubMed ID: 2836147
[TBL] [Abstract][Full Text] [Related]
10. Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cells.
Yu SF; von Rüden T; Kantoff PW; Garber C; Seiberg M; Rüther U; Anderson WF; Wagner EF; Gilboa E
Proc Natl Acad Sci U S A; 1986 May; 83(10):3194-8. PubMed ID: 3458176
[TBL] [Abstract][Full Text] [Related]
11. Co-packaging of non-vector RNAs generates replication-defective retroviral vector particles: a novel approach for blocking retrovirus replication.
Joshi S; Ding SF; Liem SE
Nucleic Acids Res; 1997 Aug; 25(16):3199-203. PubMed ID: 9241231
[TBL] [Abstract][Full Text] [Related]
12. Gene transduction into murine primitive hematopoietic cells with 2-gene retroviral vectors using a Transwell coculture system.
Asami N; Germeraad WT; Fujimoto S; Nagai S; Izumi T; Katsura Y
Eur J Haematol; 1996 Oct; 57(4):278-85. PubMed ID: 8982290
[TBL] [Abstract][Full Text] [Related]
13. Enhanced transgene expression in primitive hematopoietic progenitor cells and embryonic stem cells efficiently transduced by optimized retroviral hybrid vectors.
Ketteler R; Glaser S; Sandra O; Martens UM; Klingmüller U
Gene Ther; 2002 Apr; 9(8):477-87. PubMed ID: 11948372
[TBL] [Abstract][Full Text] [Related]
14. Retroviral-mediated gene transfer into mammalian cells.
Kohn DB; Kantoff PW; Eglitis MA; McLachlin JR; Moen RC; Karson E; Zwiebel JA; Nienhuis A; Karlsson S; O'Reilly R
Blood Cells; 1987; 13(1-2):285-98. PubMed ID: 3311223
[TBL] [Abstract][Full Text] [Related]
15. Expression of human glucocerebrosidase in murine macrophages: identification of efficient retroviral vectors.
Freas-Lutz DL; Correll PH; Dougherty SF; Xu L; Pluznik DH; Karlsson S
Exp Hematol; 1994 Aug; 22(9):857-65. PubMed ID: 8062885
[TBL] [Abstract][Full Text] [Related]
16. In vivo persistence of retrovirally transduced murine long-term repopulating cells is not limited by expression of foreign gene products in the fully or minimally myeloablated setting.
Kang E; Giri N; Wu T; Sellers S; Kirby M; Hanazono Y; Tisdale J; Dunbar CE
Hum Gene Ther; 2001 Sep; 12(13):1663-72. PubMed ID: 11535169
[TBL] [Abstract][Full Text] [Related]
17. In situ generation of pseudotyped retroviral progeny by adenovirus-mediated transduction of tumor cells enhances the killing effect of HSV-tk suicide gene therapy in vitro and in vivo.
Okada T; Caplen NJ; Ramsey WJ; Onodera M; Shimazaki K; Nomoto T; Ajalli R; Wildner O; Morris J; Kume A; Hamada H; Blaese RM; Ozawa K
J Gene Med; 2004 Mar; 6(3):288-99. PubMed ID: 15026990
[TBL] [Abstract][Full Text] [Related]
18. Selection of transduced CD34+ progenitors and enzymatic correction of cells from Gaucher patients, with bicistronic vectors.
Migita M; Medin JA; Pawliuk R; Jacobson S; Nagle JW; Anderson S; Amiri M; Humphries RK; Karlsson S
Proc Natl Acad Sci U S A; 1995 Dec; 92(26):12075-9. PubMed ID: 8618847
[TBL] [Abstract][Full Text] [Related]
19. High-frequency cell surface expression of a foreign protein in murine hematopoietic stem cells using a new retroviral vector.
Tumas DB; Spangrude GJ; Brooks DM; Williams CD; Chesebro B
Blood; 1996 Jan; 87(2):509-17. PubMed ID: 8555472
[TBL] [Abstract][Full Text] [Related]
20. Introduction of a selectable gene into primitive stem cells capable of long-term reconstitution of the hemopoietic system of W/Wv mice.
Dick JE; Magli MC; Huszar D; Phillips RA; Bernstein A
Cell; 1985 Aug; 42(1):71-9. PubMed ID: 4016956
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]