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333 related items for PubMed ID: 16539746

  • 1. Recombinant AAV-mediated HSVtk gene transfer with direct intratumoral injections and Tet-On regulation for implanted human breast cancer.
    Li ZB, Zeng ZJ, Chen Q, Luo SQ, Hu WX.
    BMC Cancer; 2006 Mar 16; 6():66. PubMed ID: 16539746
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  • 2. Suicide gene therapy of human breast cancer in SCID mice model by the regulation of Tet-On.
    Hu WX, Zeng ZJ, Luo SQ, Chen Q.
    Chin Med J (Engl); 2004 Mar 16; 117(3):434-9. PubMed ID: 15043787
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  • 3. [The construction of recombinant AAV vector expressing HSVtk gene controlled by Tet-On and the detection of its activity].
    Chen Q, Li ZB, Zeng ZJ, Luo SQ, Hu WX.
    Sheng Wu Gong Cheng Xue Bao; 2005 May 16; 21(3):360-4. PubMed ID: 16108356
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  • 4. Retrovirus-mediated tk gene therapy of implanted human breast cancer in nude mice under the regulation of Tet-On.
    Zeng ZJ, Li ZB, Luo SQ, Hu WX.
    Cancer Gene Ther; 2006 Mar 16; 13(3):290-7. PubMed ID: 16110312
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  • 8. Suicide gene therapy using AAV-HSVtk/ganciclovir in combination with irradiation results in regression of human head and neck cancer xenografts in nude mice.
    Kanazawa T, Mizukami H, Okada T, Hanazono Y, Kume A, Nishino H, Takeuchi K, Kitamura K, Ichimura K, Ozawa K.
    Gene Ther; 2003 Jan 16; 10(1):51-8. PubMed ID: 12525837
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  • 13. Transcriptional targeting of RGD fiber-mutant adenovirus vectors can improve the safety of suicide gene therapy for murine melanoma.
    Okada Y, Okada N, Mizuguchi H, Hayakawa T, Nakagawa S, Mayumi T.
    Cancer Gene Ther; 2005 Jul 16; 12(7):608-16. PubMed ID: 15746944
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  • 14. Golgi membrane protein GP73 modified-liposome mediates the antitumor effect of survivin promoter-driven HSVtk in hepatocellular carcinoma.
    Liu C, Wen C, Wang X, Wei Y, Xu C, Mu X, Zhang L, Wang X, Tian J, Ma P, Meng F, Zhang Q, Zhao N, Yu B, Gong T, Guo R, Wang H, Xie J, Sun G, Li G, Zhang H, Qin Q, Xu J, Dong X, Wang L.
    Exp Cell Res; 2019 Oct 01; 383(1):111496. PubMed ID: 31306654
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  • 15. Complete cure of established murine hepatocellular carcinoma is achievable by repeated injections of retroviruses carrying the herpes simplex virus thymidine kinase gene.
    Kuriyama S, Masui K, Kikukawa M, Sakamoto T, Nakatani T, Nagao S, Yamazaki M, Yoshiji H, Tsujinoue H, Fukui H, Yoshimatsu T, Ikenaka K.
    Gene Ther; 1999 Apr 01; 6(4):525-33. PubMed ID: 10476212
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  • 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 01; 6(3):288-99. PubMed ID: 15026990
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