A RAPID AND CONVENIENT METHOD TO ENHANCE TRANSGENIC EXPRESSION IN TARGET CELLS
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Chia-Hung Chen | Yen-Ku Liu | Yu-Ling Lin | Huai-Yao Chuang | Wei-Tung Hsu | Y. Chiu | T. Cheng | K. Liao
[1] X. Qi,et al. Development of small interfering RNA delivery system using PEI-PEG-APRPG polymer for antiangiogenic vascular endothelial growth factor tumor-targeted therapy , 2011, International journal of nanomedicine.
[2] Won Jong Kim,et al. PEI-g-PEG-RGD/small interference RNA polyplex-mediated silencing of vascular endothelial growth factor receptor and its potential as an anti-angiogenic tumor therapeutic strategy. , 2011, Oligonucleotides.
[3] Wing‐Fu Lai. In vivo nucleic acid delivery with PEI and its derivatives: current status and perspectives , 2011, Expert review of medical devices.
[4] B. Qin,et al. Silencing of the IKKε gene by siRNA inhibits invasiveness and growth of breast cancer cells , 2010, Breast Cancer Research.
[5] Wei-Yang Chang,et al. The characteristics and transfection efficiency of PEI modified by biodegradable poly(β-amino ester) , 2010, Journal of materials science. Materials in medicine.
[6] M. Bar‐eli,et al. Silencing cAMP-response Element-binding Protein (CREB) Identifies CYR61 as a Tumor Suppressor Gene in Melanoma* , 2009, The Journal of Biological Chemistry.
[7] Tomoko Ito,et al. Highly efficient in vivo gene transfection by plasmid/PEI complexes coated by anionic PEG derivatives bearing carboxyl groups and RGD peptide. , 2008, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[8] H. Ghandehari,et al. Polymeric conjugates of mono- and bi-cyclic αvβ3 binding peptides for tumor targeting , 2006 .
[9] R. Cristiano,et al. A multifunctional PEI-based cationic polyplex for enhanced systemic p53-mediated gene therapy , 2006, Gene Therapy.
[10] Y. Kaneda,et al. Non‐viral vectors for cancer therapy , 2006, Cancer science.
[11] R. Cristiano,et al. Successful in vivo tumor targeting of prostate-specific membrane antigen with a highly efficient J591/PEI/DNA molecular conjugate , 2006, Gene Therapy.
[12] D. Curiel,et al. Gene therapy for carcinoma of the breast , 2006, Cancer Gene Therapy.
[13] H. Ghandehari,et al. Polymeric conjugates of mono- and bi-cyclic alphaVbeta3 binding peptides for tumor targeting. , 2006, Journal of controlled release : official journal of the Controlled Release Society.
[14] A. Sochanik,et al. Antitumor effect of RGD-4C-GG-D(KLAKLAK)2 peptide in mouse B16(F10) melanoma model. , 2006, Acta biochimica Polonica.
[15] R. Schiffelers,et al. RGD-based strategies for selective delivery of therapeutics and imaging agents to the tumour vasculature. , 2005, Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy.
[16] A. Göpferich,et al. Polyethylenimine-based non-viral gene delivery systems. , 2005, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[17] R. Cristiano,et al. Tumor-specific gene delivery mediated by a novel peptide-polyethylenimine-DNA polyplex targeting aminopeptidase N/CD13. , 2005, Human gene therapy.
[18] Rosanna Martinelli,et al. Short and highly efficient synthetic promoters for melanoma‐specific gene expression , 2005, FEBS letters.
[19] T. Fujiwara,et al. [Gene therapy for lung cancer]. , 2002, Nihon rinsho. Japanese journal of clinical medicine.
[20] D. Nettelbeck,et al. Analyses of melanoma-targeted oncolytic adenoviruses with tyrosinase enhancer/promoter-driven E1A, E4, or both in submerged cells and organotypic cultures. , 2004, Molecular cancer therapeutics.
[21] S J White,et al. Promoters and control elements: designing expression cassettes for gene therapy. , 2004, Current gene therapy.
[22] D. Schadendorf,et al. Evaluation of combined gene regulatory elements for transcriptional targeting of suicide gene expression to malignant melanoma , 2003, Experimental dermatology.
[23] Lily Wu,et al. Transcriptionally targeted gene therapy to detect and treat cancer. , 2003, Trends in molecular medicine.
[24] D. Hirst,et al. Transcriptional Targeting in Cancer Gene Therapy , 2003, Journal of biomedicine & biotechnology.
[25] D. Fischer,et al. Low-molecular-weight polyethylenimine as a non-viral vector for DNA delivery: comparison of physicochemical properties, transfection efficiency and in vivo distribution with high-molecular-weight polyethylenimine. , 2003, Journal of controlled release : official journal of the Controlled Release Society.
[26] David A. Cheresh,et al. Role of integrins in cell invasion and migration , 2002, Nature Reviews Cancer.
[27] F. McCormick,et al. Cancer gene therapy: fringe or cutting edge? , 2001, Nature Reviews Cancer.
[28] K. Harrington,et al. Transcriptional control: an essential component of cancer gene therapy strategies? , 2000, Advanced drug delivery reviews.
[29] A. Mikos,et al. Poly(ethylenimine) and its role in gene delivery. , 1999, Journal of controlled release : official journal of the Controlled Release Society.
[30] A. Mikos,et al. Improved packing of poly(ethylenimine)/DNA complexes increases transfection efficiency , 1999, Gene Therapy.
[31] E. Brambilla,et al. In vivo delivery to tumors of DNA complexed with linear polyethylenimine. , 1999, Human gene therapy.
[32] W. Silvers,et al. Changes in expression of putative antigens encoded by pigment genes in mouse melanomas at different stages of malignant progression. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[33] D. Scherman,et al. A versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo: polyethylenimine. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[34] K. Sekiguchi,et al. Peptide ligands for integrin alpha v beta 3 selected from random phage display libraries. , 1995, Biochemistry.
[35] S. Hart,et al. Cell binding and internalization by filamentous phage displaying a cyclic Arg-Gly-Asp-containing peptide. , 1994, The Journal of biological chemistry.
[36] A. Israël,et al. The DNA binding subunit of NF-κB is identical to factor KBF1 and homologous to the rel oncogene product , 1990, Cell.