Oligoarginine-PEG-lipid particles for gene delivery
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[1] H Harashima,et al. Stearylated arginine-rich peptides: a new class of transfection systems. , 2001, Bioconjugate chemistry.
[2] A. Prochiantz,et al. The third helix of the Antennapedia homeodomain translocates through biological membranes. , 1994, The Journal of biological chemistry.
[3] Y. Maitani,et al. Calcium enhanced delivery of tetraarginine-PEG-lipid-coated DNA/protamine complexes. , 2009, International journal of pharmaceutics.
[4] K. Sakurai,et al. Transition from a normal to inverted cylinder for an amidine-bearing lipid/pDNA complex and its excellent transfection. , 2005, Bioconjugate chemistry.
[5] K. Ulbrich,et al. Polymer‐coated polyethylenimine/DNA complexes designed for triggered activation by intracellular reduction , 2004, The journal of gene medicine.
[6] M. Giacca,et al. Cell membrane lipid rafts mediate caveolar endocytosis of HIV-1 Tat fusion proteins. , 2004, The Journal of biological chemistry.
[7] D. Porteous,et al. HIV-1 Tat protein transduction domain peptide facilitates gene transfer in combination with cationic liposomes. , 2004, Journal of controlled release : official journal of the Controlled Release Society.
[8] Steven F Dowdy,et al. Cationic TAT peptide transduction domain enters cells by macropinocytosis. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[9] Steven F. Dowdy,et al. Cell Penetrating Peptides in Drug Delivery , 2004, Pharmaceutical Research.
[10] Y. Tseng,et al. Translocation of liposomes into cancer cells by cell-penetrating peptides penetratin and tat: a kinetic and efficacy study. , 2002, Molecular pharmacology.
[11] H Akita,et al. Development of a novel systemic gene delivery system for cancer therapy with a tumor-specific cleavable PEG-lipid , 2007, Gene Therapy.
[12] S. Schwarze,et al. In vivo protein transduction: delivery of a biologically active protein into the mouse. , 1999, Science.
[13] Yaping Li,et al. Arginine-chitosan/DNA self-assemble nanoparticles for gene delivery: In vitro characteristics and transfection efficiency. , 2008, International journal of pharmaceutics.
[14] M. Conese,et al. Gene Transfer by Means of Lipo- and Polyplexes: Role of Clathrin and Caveolae-Mediated Endocytosis , 2006, Journal of liposome research.
[15] S. W. Kim,et al. Cholesteryl oligoarginine delivering vascular endothelial growth factor siRNA effectively inhibits tumor growth in colon adenocarcinoma. , 2006, Molecular therapy : the journal of the American Society of Gene Therapy.
[16] R. Schwendener,et al. Enhanced heparan sulfate proteoglycan-mediated uptake of cell-penetrating peptide-modified liposomes , 2004, Cellular and Molecular Life Sciences CMLS.
[17] L. Tönges,et al. Stearylated octaarginine and artificial virus-like particles for transfection of siRNA into primary rat neurons. , 2006, RNA.
[18] Jong-sang Park,et al. Arginine-conjugated polypropylenimine dendrimer as a non-toxic and efficient gene delivery carrier. , 2007, Biomaterials.
[19] E. Vivés. Cellular uptake [correction of utake] of the Tat peptide: an endocytosis mechanism following ionic interactions. , 2003, Journal of molecular recognition : JMR.
[20] B. Davidson,et al. Transvascular delivery of small interfering RNA to the central nervous system , 2007, Nature.
[21] K. Leong,et al. Biodegradable polyphosphoester micelles for gene delivery. , 2004, Journal of pharmaceutical sciences.
[22] Norased Nasongkla,et al. Functionalized Micellar Systems for Cancer Targeted Drug Delivery , 2007, Pharmaceutical Research.
[23] Sandra L. Schmid,et al. Regulated portals of entry into the cell , 2003, Nature.
[24] T. Niidome,et al. Gene Therapy Progress and Prospects: Nonviral vectors , 2002, Gene Therapy.
[25] Y. Mély,et al. Gene transfer by cationic surfactants is essentially limited by the trapping of the surfactant/DNA complexes onto the cell membrane: a fluorescence investigation. , 2000, Biochimica et biophysica acta.
[26] I. Khalil,et al. Novel lipidated sorbitol-based molecular transporters for non-viral gene delivery. , 2009, Journal of controlled release : official journal of the Controlled Release Society.
[27] V. Torchilin,et al. siRNA-containing liposomes modified with polyarginine effectively silence the targeted gene , 2006, Journal of Controlled Release.
[28] G. Zuber,et al. Monomolecular DNA nanoparticles for intravenous delivery of genes. , 2005, Journal of the American Chemical Society.
[29] G. Elliott,et al. Intercellular Trafficking and Protein Delivery by a Herpesvirus Structural Protein , 1997, Cell.
[30] C. Contag,et al. Gene transfer via reversible plasmid condensation with cysteine-flanked, internally spaced arginine-rich peptides. , 2003, Human gene therapy.
[31] U. Greber,et al. Adenovirus triggers macropinocytosis and endosomal leakage together with its clathrin-mediated uptake , 2002, The Journal of cell biology.
[32] Priscille Brodin,et al. A Truncated HIV-1 Tat Protein Basic Domain Rapidly Translocates through the Plasma Membrane and Accumulates in the Cell Nucleus* , 1997, The Journal of Biological Chemistry.
[33] S. Zeng,et al. A novel chitosan oligosaccharide-stearic acid micelles for gene delivery: properties and in vitro transfection studies. , 2006, International journal of pharmaceutics.
[34] Dong-Eun Kim,et al. Evaluation of generations 2, 3 and 4 arginine modified PAMAM dendrimers for gene delivery. , 2008, International journal of pharmaceutics.
[35] Steven F Dowdy,et al. Transducible TAT-HA fusogenic peptide enhances escape of TAT-fusion proteins after lipid raft macropinocytosis , 2004, Nature Medicine.
[36] S. Takeoka,et al. Evaluation of cationic assemblies constructed with amino acid based lipids for plasmid DNA delivery. , 2008, Bioconjugate chemistry.
[37] Jeremy C Simpson,et al. Cellular uptake of arginine-rich peptides: roles for macropinocytosis and actin rearrangement. , 2004, Molecular therapy : the journal of the American Society of Gene Therapy.
[38] W. Seeger,et al. Effects of cell‐penetrating peptides and pegylation on transfection efficiency of polyethylenimine in mouse lungs , 2008, The journal of gene medicine.
[39] W. Moerner,et al. Single-molecule motions of oligoarginine transporter conjugates on the plasma membrane of Chinese hamster ovary cells. , 2008, Journal of the American Chemical Society.
[40] M. Bally,et al. Self-Assembling DNA-Lipid Particles for Gene Transfer , 1997, Pharmaceutical Research.
[41] Y. Maitani,et al. High gene delivery in tumor by intratumoral injection of tetraarginine-PEG lipid-coated protamine/DNA. , 2008, Journal of controlled release : official journal of the Controlled Release Society.
[42] P. Searle,et al. Vectors based on reducible polycations facilitate intracellular release of nucleic acids , 2003, The journal of gene medicine.
[43] Y. Maitani,et al. Intracellular delivery of proteins in complexes with oligoarginine-modified liposomes and the effect of oligoarginine length. , 2006, Bioconjugate chemistry.
[44] V. Torchilin,et al. TAT peptide on the surface of liposomes affords their efficient intracellular delivery even at low temperature and in the presence of metabolic inhibitors , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[45] R. Raines,et al. Pathway for polyarginine entry into mammalian cells. , 2004, Biochemistry.
[46] Ü. Langel,et al. Cell-Penetrating Peptides , 2000, Methods in Molecular Biology.
[47] E. Brambilla,et al. An electron microscopy study into the mechanism of gene transfer with lipopolyamines. , 1996, Gene therapy.
[48] P. Cullis,et al. Calcium enhances the transfection potency of plasmid DNA-cationic liposome complexes. , 2000, Biochimica et biophysica acta.
[49] W. Jiskoot,et al. OVCAR-3 cells internalize TAT-peptide modified liposomes by endocytosis. , 2004, Biochimica et biophysica acta.
[50] A. Prochiantz,et al. Cell Internalization of the Third Helix of the Antennapedia Homeodomain Is Receptor-independent* , 1996, The Journal of Biological Chemistry.
[51] M. Ferrer,et al. Effects of cargo molecules on the cellular uptake of arginine-rich cell-penetrating peptides. , 2005, Biochimica et biophysica acta.
[52] H. Riezman,et al. Molecular Mechanisms of Endocytosis , 1997, Cell.
[53] D. Scherman,et al. Virus-sized self-assembling lamellar complexes between plasmid DNA and cationic micelles promote gene transfer. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[54] L. Huang,et al. Direct gene transfer to mouse melanoma by intratumor injection of free DNA. , 1996, Gene therapy.
[55] J. Northrop,et al. Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[56] H Harashima,et al. Mechanism of improved gene transfer by the N-terminal stearylation of octaarginine: enhanced cellular association by hydrophobic core formation , 2004, Gene Therapy.
[57] Shiroh Futaki,et al. High Density of Octaarginine Stimulates Macropinocytosis Leading to Efficient Intracellular Trafficking for Gene Expression* , 2006, Journal of Biological Chemistry.
[58] R. Müller,et al. Oligomers of the Arginine-rich Motif of the HIV-1 TAT Protein Are Capable of Transferring Plasmid DNA into Cells* 210 , 2003, The Journal of Biological Chemistry.
[59] M. Manning,et al. Long chain arginine esters: a new class of cationic detergents for preparation of hydrophobic ion-paired complexes. , 2000, Biochemistry and cell biology = Biochimie et biologie cellulaire.
[60] Y. Maitani,et al. Design, synthesis and gene delivery efficiency of novel oligo-arginine-linked PEG-lipids: effect of oligo-arginine length. , 2005, International journal of pharmaceutics.
[61] Dale L. Greiner,et al. T Cell-Specific siRNA Delivery Suppresses HIV-1 Infection in Humanized Mice , 2008, Cell.
[62] W. Seeger,et al. Nano-carriers for DNA delivery to the lung based upon a TAT-derived peptide covalently coupled to PEG-PEI. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[63] P. Reynier,et al. In Vitro and In Vivo Transfection of Melanoma Cells B16-F10 Mediated by Cholesterol-based Cationic Liposomes , 2002, Journal of drug targeting.
[64] Y. Maitani,et al. Decaarginine-PEG-liposome enhanced transfection efficiency and function of arginine length and PEG. , 2009, International journal of pharmaceutics.
[65] A. Rees,et al. Studies on the Internalization Mechanism of Cationic Cell-penetrating Peptides* , 2003, Journal of Biological Chemistry.
[66] M. Pooga,et al. Cell penetration by transportan. , 1998, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[67] L. Medina-Kauwe,et al. Intracellular trafficking of nonviral vectors , 2005, Gene Therapy.
[68] K. Hruska,et al. Protein transduction: unrestricted delivery into all cells? , 2000, Trends in cell biology.
[69] R. Fischer,et al. A quantitative validation of fluorophore-labelled cell-permeable peptide conjugates: fluorophore and cargo dependence of import. , 2002, Biochimica et biophysica acta.
[70] D. Scherman,et al. Design, synthesis, and evaluation of gadolinium cationic lipids as tools for biodistribution studies of gene delivery complexes. , 2003, Bioconjugate chemistry.
[71] B. Franc,et al. Intracellular cargo delivery by an octaarginine transporter adapted to target prostate cancer cells through cell surface protease activation. , 2006, Bioconjugate chemistry.
[72] E. Vivés. Cellular utake of the Tat peptide: an endocytosis mechanism following ionic interactions , 2003 .
[73] D. Pezzoli,et al. A dimerizable cationic lipid with potential for gene delivery , 2008, The journal of gene medicine.
[74] B. Deurs,et al. Phorbol myristate acetate selectively stimulates apical endocytosis via protein kinase C in polarized MDCK cells. , 1995, Experimental cell research.
[75] M. Morris,et al. A peptide carrier for the delivery of biologically active proteins into mammalian cells , 2001, Nature Biotechnology.
[76] Yasuhiro Tsume,et al. Bile acid-oligopeptide conjugates interact with DNA and facilitate transfection. , 2007, Molecular pharmaceutics.
[77] R. Fischer,et al. A Stepwise Dissection of the Intracellular Fate of Cationic Cell-penetrating Peptides* , 2004, Journal of Biological Chemistry.
[78] E Marshall,et al. Gene Therapy Death Prompts Review of Adenovirus Vector , 1999, Science.
[79] K. Pattabiraman,et al. The design, synthesis, and evaluation of molecules that enable or enhance cellular uptake: peptoid molecular transporters. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[80] K. L. Douglas. Toward Development of Artificial Viruses for Gene Therapy: A Comparative Evaluation of Viral and Non‐viral Transfection , 2008, Biotechnology progress.
[81] Ralph Weissleder,et al. Tat peptide-derivatized magnetic nanoparticles allow in vivo tracking and recovery of progenitor cells , 2000, Nature Biotechnology.
[82] J. Rothbard,et al. Polyarginine enters cells more efficiently than other polycationic homopolymers. , 2000, The journal of peptide research : official journal of the American Peptide Society.
[83] J. Behr,et al. Dimerizable cationic detergents with a low cmc condense plasmid DNA into nanometric particles and transfect cells in culture. , 2001, Journal of the American Chemical Society.
[84] D. Song,et al. Marked transfection enhancement by the DPL (DNA/peptide/lipid) complex. , 2007, International journal of molecular medicine.
[85] S. W. Kim,et al. Arginine-grafted bioreducible poly(disulfide amine) for gene delivery systems. , 2009, Biomaterials.
[86] K. Nagayama,et al. Decaarginine-PEG-artificial lipid/DNA complex for gene delivery: nanostructure and transfection efficiency. , 2008, Journal of nanoscience and nanotechnology.
[87] T. Chen,et al. Transfection properties of stabilized plasmid-lipid particles containing cationic PEG lipids. , 2003, Biochimica et biophysica acta.
[88] Hans P Merkle,et al. On the biomedical promise of cell penetrating peptides: limits versus prospects. , 2008, Journal of pharmaceutical sciences.
[89] D. Friend,et al. Endocytosis and intracellular processing accompanying transfection mediated by cationic liposomes. , 1996, Biochimica et biophysica acta.
[90] A. Sochanik,et al. A new cholesterol derivative suitable for transfecting certain type of cells in the presence of 10% serum , 2000, Cancer Gene Therapy.
[91] K. Sandvig,et al. Membrane ruffling and macropinocytosis in A431 cells require cholesterol. , 2002, Journal of cell science.
[92] H Akita,et al. Octaarginine-modified multifunctional envelope-type nanoparticles for gene delivery , 2007, Gene Therapy.
[93] B. Wiesner,et al. Cellular uptake of an alpha-helical amphipathic model peptide with the potential to deliver polar compounds into the cell interior non-endocytically. , 1998, Biochimica et biophysica acta.