Approaches to improving the kinetics of adenovirus-delivered genes and gene products.
暂无分享,去创建一个
H. Mizuguchi | T. Hayakawa | F. Sakurai | K. Kawabata | T. Hosono | Teruhide Yamaguchi | Yoshiteru Watanabe | Zhi-Li Xu | N. Koizumi
[1] Florian Kreppel,et al. Long-Term Transgene Expression in Proliferating Cells Mediated by Episomally Maintained High-Capacity Adenovirus Vectors , 2004, Journal of Virology.
[2] H. Mizuguchi,et al. Reduction of Natural Adenovirus Tropism to Mouse Liverby Fiber-Shaft Exchange in Combination with both CAR- andαv Integrin-BindingAblation , 2003, Journal of Virology.
[3] G. Nemerow,et al. Transductional and transcriptional targeting of cancer cells using genetically engineered viral vectors. , 2003, Cancer letters.
[4] H. Mizuguchi,et al. A soluble CAR‐SCF fusion protein improves adenoviral vector‐mediated gene transferto c‐Kit‐positive hematopoietic cells , 2003, The journal of gene medicine.
[5] H. Mizuguchi,et al. Characterization of in vitro and in vivo gene transfer properties of adenovirus serotype 35 vector. , 2003, Molecular therapy : the journal of the American Society of Gene Therapy.
[6] P. Robbins,et al. Human adenovirus type 35: nucleotide sequence and vector development , 2003, Gene Therapy.
[7] A. Gaggar,et al. CD46 is a cellular receptor for group B adenoviruses , 2003, Nature Medicine.
[8] Cameron S. Osborne,et al. LMO2-Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1 , 2003, Science.
[9] M. Kay,et al. A gene-deleted adenoviral vector results in phenotypic correction of canine hemophilia B without liver toxicity or thrombocytopenia. , 2003, Blood.
[10] P. Lowenstein,et al. Adenovirus expression of IL-1 and NF-kappaB inhibitors does not inhibit acute adenoviral-induced brain inflammation, but delays immune system-mediated elimination of transgene expression. , 2003, Molecular therapy : the journal of the American Society of Gene Therapy.
[11] J. Atkinson,et al. Adenovirus Type 11 Uses CD46 as a Cellular Receptor , 2003, Journal of Virology.
[12] S. Kostense,et al. Replication-Deficient Human Adenovirus Type 35 Vectors for Gene Transfer and Vaccination: Efficient Human Cell Infection and Bypass of Preexisting Adenovirus Immunity , 2003, Journal of Virology.
[13] K. Ozawa,et al. Positive and negative effects of adeno-associated virus Rep on AAVS1-targeted integration. , 2003, The Journal of general virology.
[14] M. Kaleko,et al. Development of adenovirus serotype 35 as a gene transfer vector. , 2003, Virology.
[15] Theresa A. Storm,et al. AAV serotype 2 vectors preferentially integrate into active genes in mice , 2003, Nature Genetics.
[16] T. Mayumi,et al. Woodchuck hepatitis virus post-transcriptional regulation element enhances transgene expression from adenovirus vectors. , 2003, Biochimica et biophysica acta.
[17] H. Mizuguchi,et al. Efficient gene transfer into human CD34+ cells by an adenovirus type 35 vector , 2003, Gene Therapy.
[18] Qiang Liu,et al. Molecular basis of the inflammatory response to adenovirus vectors , 2003, Gene Therapy.
[19] N. Chirmule,et al. Immunity to adenovirus and adeno-associated viral vectors: implications for gene therapy , 2003, Gene Therapy.
[20] J. Bromberg,et al. Adaptive and innate immune responses to gene transfer vectors: role of cytokines and chemokines in vector function , 2003, Gene Therapy.
[21] G. Nemerow,et al. Adenovirus serotype 5 fiber shaft influences in vivo gene transfer in mice. , 2003, Human gene therapy.
[22] M. Rots,et al. A mosaic adenovirus possessing serotype Ad5 and serotype Ad3 knobs exhibits expanded tropism. , 2003, Virology.
[23] Stefan Fischer,et al. Impact of human interleukin-10 on vector-induced inflammation and early graft function in rat lung transplantation. , 2003, American journal of respiratory cell and molecular biology.
[24] Yasuo Yoshioka,et al. Site-specific PEGylation of a lysine-deficient TNF-α with full bioactivity , 2003, Nature Biotechnology.
[25] H. Mizuguchi,et al. Generation of fiber‐modified adenovirus vectors containing heterologous peptides in both the HI loop and C terminus of the fiber knob , 2003, The journal of gene medicine.
[26] K. Kawamoto,et al. A Glucocorticoid Reduces Adverse Effects of Adenovirus Vectors in the Cochlea , 2003, Audiology and Neurotology.
[27] S. Kochanek,et al. Therapeutic factor VIII levels and negligible toxicity in mouse and dog models of hemophilia A following gene therapy with high-capacity adenoviral vectors. , 2003, Blood.
[28] H. Hamada,et al. Reduction of Natural Adenovirus Tropism to the Liver by both Ablation of Fiber-Coxsackievirus and Adenovirus Receptor Interaction and Use of Replaceable Short Fiber , 2003, Journal of Virology.
[29] D. Kayda,et al. Optimization of the generation and propagation of gutless adenoviral vectors. , 2003, Human gene therapy.
[30] E. Marshall. Second Child in French Trial Is Found to Have Leukemia , 2003, Science.
[31] A. Segerman,et al. There Are Two Different Species B Adenovirus Receptors: sBAR, Common to Species B1 and B2 Adenoviruses, and sB2AR, Exclusively Used by Species B2 Adenoviruses , 2003, Journal of Virology.
[32] Jianghuai Wang,et al. Integration efficiency of a hybrid adenoretroviral vector. , 2003, Biochemical and biophysical research communications.
[33] M. Perricaudet,et al. Genetic manipulations of adenovirus type 5 fiber resulting in liver tropism attenuation , 2003, Gene Therapy.
[34] Erika Check,et al. Gene therapy: A tragic setback , 2002, Nature.
[35] James M. Wilson,et al. PEGylation of E1-deleted adenovirus vectors allows significant gene expression on readministration to liver. , 2002, Human gene therapy.
[36] M. Mizuno,et al. Cationic liposomes conjugation to recombinant adenoviral vectors containing herpes simplex virus thymidine kinase gene followed by ganciclovir treatment reduces viral antigenicity and maintains antitumor activity in mouse experimental glioma models , 2002, Cancer Gene Therapy.
[37] M. Kay,et al. Transposition from a gutless adeno-transposon vector stabilizes transgene expression in vivo , 2002, Nature Biotechnology.
[38] D. Curiel,et al. Dual targeting of adenoviral vectors at the levels of transduction and transcription enhances the specificity of gene expression in cancer cells. , 2002, Molecular therapy : the journal of the American Society of Gene Therapy.
[39] M. Rollence,et al. In vivo hepatic adenoviral gene delivery occurs independently of the coxsackievirus-adenovirus receptor. , 2002, Molecular therapy : the journal of the American Society of Gene Therapy.
[40] H. Mizuguchi,et al. CAR- or αv integrin-binding ablated adenovirus vectors, but not fiber-modified vectors containing RGD peptide, do not change the systemic gene transfer properties in mice , 2002, Gene Therapy.
[41] M. Kay,et al. A new adenoviral helper-dependent vector results in long-term therapeutic levels of human coagulation factor IX at low doses in vivo. , 2002, Blood.
[42] M. Goldberg,et al. Correction of the nonlinear dose response improves the viability of adenoviral vectors for gene therapy of Fabry disease. , 2002, Human gene therapy.
[43] T. Mayumi,et al. Strength evaluation of transcriptional regulatory elements for transgene expression by adenovirus vector. , 2002, Journal of controlled release : official journal of the Controlled Release Society.
[44] J. Douglas,et al. Targeted adenoviral vectors , 2002 .
[45] K. Mitani,et al. Adenovirus as an integrating vector. , 2002, Current gene therapy.
[46] S. Keshavjee,et al. Transplant immunosuppression enhances efficiency of adenoviral-mediated gene retransfection: inhibition of interferon-gamma and immunoglobin G. , 2002, The Annals of thoracic surgery.
[47] H. Mizuguchi,et al. Enhanced antitumor effect and reduced vector dissemination with fiber-modified adenovirus vectors expressing herpes simplex virus thymidine kinase , 2002, Cancer Gene Therapy.
[48] J. Isner. Myocardial gene therapy , 2002, Nature.
[49] W. F. Anderson. Assessment of adenoviral vector safety and toxicity: Report of the National Institutes of Health Recombinant DNA Advisory Committee , 2002 .
[50] A. Beaudet,et al. Lethal toxicity, severe endothelial injury, and a threshold effect with high doses of an adenoviral vector in baboons. , 2002, Human gene therapy.
[51] D. Kayda,et al. Sustained human factor VIII expression in hemophilia A mice following systemic delivery of a gutless adenoviral vector. , 2002, Molecular therapy : the journal of the American Society of Gene Therapy.
[52] R. M. Burnett,et al. Replication-Defective Vector Based on a Chimpanzee Adenovirus , 2001, Journal of Virology.
[53] I. Kovesdi,et al. Reducing the Native Tropism of Adenovirus Vectors Requires Removal of both CAR and Integrin Interactions , 2001, Journal of Virology.
[54] G. Nemerow,et al. Ablating adenovirus type 5 fiber-CAR binding and HI loop insertion of the SIGYPLP peptide generate an endothelial cell-selective adenovirus. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[55] H. Mizuguchi,et al. Efficient gene transfer by fiber-mutant adenoviral vectors containing RGD peptide. , 2001, Biochimica et biophysica acta.
[56] M. Dewhirst,et al. Systemic vector leakage and transgene expression by intratumorally injected recombinant adenovirus vectors. , 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.
[57] T. Mayumi,et al. Efficient antigen gene transduction using Arg-Gly-Asp fiber-mutant adenovirus vectors can potentiate antitumor vaccine efficacy and maturation of murine dendritic cells. , 2001, Cancer research.
[58] In-Hoo Kim,et al. Lifetime correction of genetic deficiency in mice with a single injection of helper-dependent adenoviral vector , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[59] S. Kochanek,et al. High-capacity 'gutless' adenoviral vectors. , 2001, Current opinion in molecular therapeutics.
[60] A. Herrmann,et al. Targeting of high-capacity adenoviral vectors. , 2001, Human gene therapy.
[61] M. Chilosi,et al. Heparan Sulfate Glycosaminoglycans Are Receptors Sufficient To Mediate the Initial Binding of Adenovirus Types 2 and 5 , 2001, Journal of Virology.
[62] M. Kolb,et al. Budesonide enhances repeated gene transfer and expression in the lung with adenoviral vectors. , 2001, American journal of respiratory and critical care medicine.
[63] R. Alemany,et al. CAR-binding ablation does not change biodistribution and toxicity of adenoviral vectors , 2001, Gene Therapy.
[64] D. Curiel,et al. Combined transductional and transcriptional targeting improves the specificity of transgene expression in vivo , 2001, Nature Biotechnology.
[65] J. Ellis,et al. Silencing of gene expression: implications for design of retrovirus vectors , 2001, Reviews in medical virology.
[66] G. Stamatoyannopoulos,et al. A capsid-modified adenovirus vector devoid of all viral genes: assessment of transduction and toxicity in human hematopoietic cells. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[67] G. Nemerow,et al. Integrin αvβ1 Is an Adenovirus Coreceptor , 2001, Journal of Virology.
[68] R. Kontermann,et al. Targeting of adenovirus to endothelial cells by a bispecific single-chain diabody directed against the adenovirus fiber knob domain and human endoglin (CD105). , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[69] B. Delmas,et al. Construction of Avian Adenovirus CELO Recombinants in Cosmids , 2001, Journal of Virology.
[70] James M. Wilson,et al. “Stealth” Adenoviruses Blunt Cell-Mediated and Humoral Immune Responses against the Virus and Allow for Significant Gene Expression upon Readministration in the Lung , 2001, Journal of Virology.
[71] J. Wilson,et al. Acute cytokine response to systemic adenoviral vectors in mice is mediated by dendritic cells and macrophages. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[72] J. Wilson,et al. Activation of innate immunity in nonhuman primates following intraportal administration of adenoviral vectors. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[73] P. Quax,et al. Improved Adenovirus Vectors for Infection of Cardiovascular Tissues , 2001, Journal of Virology.
[74] D. Curiel,et al. Fiber knob modifications overcome low, heterogeneous expression of the coxsackievirus-adenovirus receptor that limits adenovirus gene transfer and oncolysis for human rhabdomyosarcoma cells. , 2001, Cancer research.
[75] T. Mayumi,et al. Efficient gene delivery into dendritic cells by fiber-mutant adenovirus vectors. , 2001, Biochemical and biophysical research communications.
[76] D. Curiel,et al. Efficient Gene Transduction by RGB‐fiber Modified Recombinant Adenovirus into Dendritic Cells , 2001, Japanese journal of cancer research : Gann.
[77] P. Goossens,et al. Infection efficiency of type 5 adenoviral vectors in synovial tissue can be enhanced with a type 16 fiber. , 2001, Arthritis and rheumatism.
[78] M. Kaleko,et al. Generation and characterization of E1/E2a/E3/E4-deficient adenoviral vectors encoding human factor VIII. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[79] J. Grill,et al. Combined targeting of adenoviruses to integrins and epidermal growth factor receptors increases gene transfer into primary glioma cells and spheroids. , 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.
[80] T. Sawamura,et al. Identification of Peptides That Target the Endothelial Cell–Specific LOX-1 Receptor , 2001, Hypertension.
[81] D. Curiel,et al. Selective transduction of murine myelomonocytic leukemia cells (WEHI-3B) with regular and RGD-adenoviral vectors. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[82] P. Lowenstein,et al. Acute direct adenoviral vector cytotoxicity and chronic, but not acute, inflammatory responses correlate with decreased vector-mediated transgene expression in the brain. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[83] S. Fawell,et al. Sequestration of adenoviral vector by Kupffer cells leads to a nonlinear dose response of transduction in liver. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[84] S. Cusack,et al. Influence of adenoviral fiber mutations on viral encapsidation, infectivity and in vivo tropism , 2001, Gene Therapy.
[85] D. Curiel,et al. A targetable, injectable adenoviral vector for selective gene delivery to pulmonary endothelium in vivo. , 2000, Molecular therapy : the journal of the American Society of Gene Therapy.
[86] A. Lieber,et al. Dependence of Adenovirus Infectivity on Length of the Fiber Shaft Domain , 2000, Journal of Virology.
[87] R. Alemany,et al. Blood clearance rates of adenovirus type 5 in mice. , 2000, The Journal of general virology.
[88] Inder M. Verma,et al. Gene therapy: trials and tribulations , 2000, Nature Reviews Genetics.
[89] P. Lowenstein,et al. Strong promoters are the key to highly efficient, noninflammatory and noncytotoxic adenoviral-mediated transgene delivery into the brain in vivo. , 2000, Molecular therapy : the journal of the American Society of Gene Therapy.
[90] M. Weitzman,et al. Molecular adaptors for vascular-targeted adenoviral gene delivery. , 2000, Human gene therapy.
[91] J. Bergelson,et al. The dual impact of coxsackie and adenovirus receptor expression on human prostate cancer gene therapy. , 2000, Cancer research.
[92] J. Wilson,et al. Development of a rapid method for the PEGylation of adenoviruses with enhanced transduction and improved stability under harsh storage conditions. , 2000, Human gene therapy.
[93] D. Curiel,et al. Ectodomain of Coxsackievirus and Adenovirus Receptor Genetically Fused to Epidermal Growth Factor Mediates Adenovirus Targeting to Epidermal Growth Factor Receptor-Positive Cells , 2000, Journal of Virology.
[94] S. J. White,et al. Selective targeting of gene transfer to vascular endothelial cells by use of peptides isolated by phage display. , 2000, Circulation.
[95] C. Balagué,et al. Replicative adenoviruses for cancer therapy , 2000, Nature Biotechnology.
[96] S. Moffatt,et al. Circumvention of vector-specific neutralizing antibody response by alternating use of human and non-human adenoviruses: implications in gene therapy. , 2000, Virology.
[97] J. Grill,et al. Targeting of adenoviral vectors through a bispecific single-chain antibody , 2000, Cancer Gene Therapy.
[98] M. Mizuno,et al. Transduction efficiency of adenoviral vectors into human glioma cells increased by association with cationic liposomes. , 2000, Neurologia medico-chirurgica.
[99] F. Deist,et al. Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease. , 2000, Science.
[100] M. Mizuno,et al. Cationic Liposome Conjugation to Recombinant Adenoviral Vector Reduces Viral Antigenicity , 2000, Japanese journal of cancer research : Gann.
[101] M. Perricaudet,et al. Stable transduction of actively dividing cells via a novel adenoviral/episomal vector. , 2000, Molecular therapy : the journal of the American Society of Gene Therapy.
[102] G. Stamatoyannopoulos,et al. Efficient Gene Transfer into Human CD34+ Cells by a Retargeted Adenovirus Vector , 2000, Journal of Virology.
[103] O. Danos,et al. Canine Adenovirus Vectors: an Alternative for Adenovirus-Mediated Gene Transfer , 2000, Journal of Virology.
[104] G. Pierce,et al. Fibroblast growth factor 2-retargeted adenoviral vectors exhibit a modified biolocalization pattern and display reduced toxicity relative to native adenoviral vectors. , 2000, Human gene therapy.
[105] N. Fairweather,et al. Retargeting of adenoviral vectors to neurons using the HC fragment of tetanus toxin , 2000, Gene Therapy.
[106] E Marshall,et al. Gene Therapy Death Prompts Review of Adenovirus Vector , 1999, Science.
[107] L. Babiuk,et al. Replication-Defective Bovine Adenovirus Type 3 as an Expression Vector , 1999, Journal of Virology.
[108] M. Kay,et al. Integrating Adenovirus–Adeno-Associated Virus Hybrid Vectors Devoid of All Viral Genes , 1999, Journal of Virology.
[109] A. Beaudet,et al. Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[110] G. Pierce,et al. FGF2-targeted adenoviral vectors for systemic and local disease. , 1999, Current opinion in molecular therapeutics.
[111] A. Houtsmuller,et al. Expression of Coxsackie adenovirus receptor and alphav-integrin does not correlate with adenovector targeting in vivo indicating anatomical vector barriers , 1999, Gene Therapy.
[112] K. Kasono,et al. Selective gene delivery to head and neck cancer cells via an integrin targeted adenoviral vector. , 1999, Clinical cancer research : an official journal of the American Association for Cancer Research.
[113] D. Curiel,et al. An advanced generation of adenoviral vectors selectively enhances gene transfer for ovarian cancer gene therapy approaches. , 1999, Gynecologic oncology.
[114] C. Miller,et al. Retargeting to EGFR enhances adenovirus infection efficiency of squamous cell carcinoma. , 1999, Archives of otolaryngology--head & neck surgery.
[115] K. Spindler,et al. Mouse adenovirus (MAV-1) expression in primary human endothelial cells and generation of a full-length infectious plasmid , 1999, Gene Therapy.
[116] T. Curiel,et al. Maturation of dendritic cells accompanies high-efficiency gene transfer by a CD40-targeted adenoviral vector. , 1999, Journal of immunology.
[117] D. Curiel,et al. Fibroblast growth factor 2 retargeted adenovirus has redirected cellular tropism: evidence for reduced toxicity and enhanced antitumor activity in mice. , 1999, Cancer research.
[118] M. Kay,et al. Implication of Interfering Antibody Formation and Apoptosis as Two Different Mechanisms Leading to Variable Duration of Adenovirus-Mediated Transgene Expression in Immune-Competent Mice , 1999, Journal of Virology.
[119] Alan E. Smith,et al. PEGylation of adenovirus with retention of infectivity and protection from neutralizing antibody in vitro and in vivo. , 1999, Human gene therapy.
[120] J. Isner,et al. Angiogenesis and vasculogenesis as therapeutic strategies for postnatal neovascularization. , 1999, The Journal of clinical investigation.
[121] G. Pari,et al. Expression of the primary coxsackie and adenovirus receptor is downregulated during skeletal muscle maturation and limits the efficacy of adenovirus-mediated gene delivery to muscle cells. , 1999, Human gene therapy.
[122] R. Cortese,et al. Site-specific integration mediated by a hybrid adenovirus/adeno-associated virus vector. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[123] R. Crystal,et al. CAR-dependent and CAR-independent pathways of adenovirus vector-mediated gene transfer and expression in human fibroblasts. , 1999, The Journal of clinical investigation.
[124] A. Sagalowsky,et al. Loss of adenoviral receptor expression in human bladder cancer cells: a potential impact on the efficacy of gene therapy. , 1999, Cancer research.
[125] C. Miller,et al. Differential susceptibility of primary and established human glioma cells to adenovirus infection: targeting via the epidermal growth factor receptor achieves fiber receptor-independent gene transfer. , 1998, Cancer Research.
[126] J. Gall,et al. Construction and Characterization of Hexon-Chimeric Adenoviruses: Specification of Adenovirus Serotype , 1998, Journal of Virology.
[127] M. Kay,et al. Inhibition of NF-κB Activation in Combination with Bcl-2 Expression Allows for Persistence of First-Generation Adenovirus Vectors in the Mouse Liver , 1998, Journal of Virology.
[128] D. Brough,et al. The Coxsackievirus-Adenovirus Receptor Protein Can Function as a Cellular Attachment Protein for Adenovirus Serotypes from Subgroups A, C, D, E, and F , 1998, Journal of Virology.
[129] G F Pierce,et al. Basic fibroblast growth factor enhancement of adenovirus-mediated delivery of the herpes simplex virus thymidine kinase gene results in augmented therapeutic benefit in a murine model of ovarian cancer. , 1998, Clinical cancer research : an official journal of the American Association for Cancer Research.
[130] A. van der Eb,et al. New helper cells and matched early region 1-deleted adenovirus vectors prevent generation of replication-competent adenoviruses. , 1998, Human gene therapy.
[131] M. Kaleko,et al. Circumvention of Immunity to the Adenovirus Major Coat Protein Hexon , 1998, Journal of Virology.
[132] A. Beaudet,et al. Toxicological comparison of E2a-deleted and first-generation adenoviral vectors expressing alpha1-antitrypsin after systemic delivery. , 1998, Human gene therapy.
[133] D. Fisher,et al. PEGylation of cytokines and other therapeutic proteins and peptides: the importance of biological optimisation of coupling techniques. , 1998, International journal of hematology.
[134] S. Randell,et al. Limited Entry of Adenovirus Vectors into Well-Differentiated Airway Epithelium Is Responsible for Inefficient Gene Transfer , 1998, Journal of Virology.
[135] James M. Wilson,et al. Adenovirus-mediated herpes simplex virus thymidine kinase/ganciclovir gene therapy in patients with localized malignancy: results of a phase I clinical trial in malignant mesothelioma. , 1998, Human gene therapy.
[136] M. Lusky,et al. In Vitro and In Vivo Biology of Recombinant Adenovirus Vectors with E1, E1/E2A, or E1/E4 Deleted , 1998, Journal of Virology.
[137] L. Turka,et al. Blunting of immune responses to adenoviral vectors in mouse liver and lung with CTLA4Ig , 1998, Gene Therapy.
[138] C. Miller,et al. Characterization of an Adenovirus Vector Containing a Heterologous Peptide Epitope in the HI Loop of the Fiber Knob , 1998, Journal of Virology.
[139] S. Efstathiou,et al. High adenoviral loads stimulate NFκB-dependent gene expression in human vascular smooth muscle cells , 1998, Gene Therapy.
[140] R. Plasterk,et al. Molecular Reconstruction of Sleeping Beauty , a Tc1-like Transposon from Fish, and Its Transposition in Human Cells , 1997, Cell.
[141] D. Brough,et al. Increased in vitro and in vivo gene transfer by adenovirus vectors containing chimeric fiber proteins , 1997, Journal of virology.
[142] M. Kay,et al. The role of Kupffer cell activation and viral gene expression in early liver toxicity after infusion of recombinant adenovirus vectors , 1997, Journal of virology.
[143] R. Hawkins,et al. The ‘adenobody’ approach to viral targeting: specific and enhanced adenoviral gene delivery , 1997, Gene Therapy.
[144] R. Crystal,et al. Tumor necrosis factor α plays a central role in immune-mediated clearance of adenoviral vectors , 1997 .
[145] J. Zabner,et al. Lack of high affinity fiber receptor activity explains the resistance of ciliated airway epithelia to adenovirus infection. , 1997, The Journal of clinical investigation.
[146] J. Marshall,et al. Integrin alpha5beta1-mediated adenovirus infection is enhanced by the integrin-activating antibody TS2/16 , 1997, Journal of virology.
[147] M. Rollence,et al. Selective targeting of human cells by a chimeric adenovirus vector containing a modified fiber protein , 1997, Journal of virology.
[148] Guido Kroemer,et al. The proto-oncogene Bcl-2 and its role in regulating apoptosis , 1997, Nature Medicine.
[149] A. Gown,et al. Transient immunomodulation with anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus-mediated gene transfer into mouse liver. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[150] D. Curiel,et al. Targeted gene delivery to Kaposi's sarcoma cells via the fibroblast growth factor receptor. , 1997, Cancer research.
[151] L. Philipson,et al. HCAR and MCAR: the human and mouse cellular receptors for subgroup C adenoviruses and group B coxsackieviruses. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[152] B. Davidson,et al. Complexes of Adenovirus with Polycationic Polymers and Cationic Lipids Increase the Efficiency of Gene Transfer in Vitro and in Vivo* , 1997, The Journal of Biological Chemistry.
[153] J. Bergelson,et al. Isolation of a Common Receptor for Coxsackie B Viruses and Adenoviruses 2 and 5 , 1997, Science.
[154] B. Harvey,et al. Enhancement of in vivo adenovirus-mediated gene transfer and expression by prior depletion of tissue macrophages in the target organ , 1997, Journal of virology.
[155] M. Hitt,et al. Human adenovirus vectors for gene transfer into mammalian cells. , 1997, Advances in pharmacology.
[156] R. Crystal,et al. Innate immune mechanisms dominate elimination of adenoviral vectors following in vivo administration. , 1997, Human gene therapy.
[157] M. Rudnicki,et al. A helper-dependent adenovirus vector system: removal of helper virus by Cre-mediated excision of the viral packaging signal. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[158] Marty W. Mayo,et al. TNF- and Cancer Therapy-Induced Apoptosis: Potentiation by Inhibition of NF-κB , 1996, Science.
[159] Seamus J. Martin,et al. Suppression of TNF-α-Induced Apoptosis by NF-κB , 1996, Science.
[160] D. Curiel,et al. Targeted gene delivery by tropism-modified adenoviral vectors , 1996, Nature Biotechnology.
[161] D. Brough,et al. Adenovirus targeted to heparan-containing receptors increases its gene delivery efficiency to multiple cell types , 1996, Nature Biotechnology.
[162] J. Gebert,et al. Adenovirus-assisted lipofection: efficient in vitro gene transfer of luciferase and cytosine deaminase to human smooth muscle cells. , 1996, Atherosclerosis.
[163] S. McGuire,et al. Adenovirus-mediated gene transfer of herpes simplex virus thymidine kinase in an ascites model of human breast cancer. , 1996, Human gene therapy.
[164] L. Leinwand,et al. Adenovirus type 5 and 7 capsid chimera: fiber replacement alters receptor tropism without affecting primary immune neutralization epitopes , 1996, Journal of virology.
[165] A. Houweling,et al. Characterization of 911: a new helper cell line for the titration and propagation of early region 1-deleted adenoviral vectors. , 1996, Human gene therapy.
[166] Xiang Gao,et al. Cationic liposome-mediated gene transfer. , 1995, Gene therapy.
[167] D. Curiel,et al. Addition of a short peptide ligand to the adenovirus fiber protein. , 1995, Gene therapy.
[168] J. Naftilan,et al. Enhancement of liposome-mediated gene transfer into vascular tissue by replication deficient adenovirus. , 1995, Gene therapy.
[169] G. Nemerow,et al. Upregulation of integrins alpha v beta 3 and alpha v beta 5 on human monocytes and T lymphocytes facilitates adenovirus-mediated gene delivery , 1995, Journal of virology.
[170] H. Ertl,et al. Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses , 1995, Journal of virology.
[171] M. Kay,et al. Strain related variations in adenovirally mediated transgene expression from mouse hepatocytes in vivo: comparisons between immunocompetent and immunodeficient inbred strains. , 1995, Gene therapy.
[172] F. Graham,et al. An efficient and flexible system for construction of adenovirus vectors with insertions or deletions in early regions 1 and 3. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[173] R. Crystal,et al. Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis , 1994, Nature Genetics.
[174] J. Deisenhofer,et al. Characterization of the knob domain of the adenovirus type 5 fiber protein expressed in Escherichia coli , 1994, Journal of virology.
[175] P. Kitts,et al. Cell-binding domain of adenovirus serotype 2 fiber , 1994, Journal of virology.
[176] Gooding Lr. Regulation of TNF-mediated cell death and inflammation by human adenoviruses. , 1994 .
[177] Y. Inada,et al. [7] Modification of proteins with polyethylene glycol derivatives , 1994 .
[178] Ari Helenius,et al. Stepwise dismantling of adenovirus 2 during entry into cells , 1993, Cell.
[179] F. Graham,et al. Packaging capacity and stability of human adenovirus type 5 vectors , 1993, Journal of virology.
[180] G. Nemerow,et al. Integrins α v β 3 and α v β 5 promote adenovirus internalization but not virus attachment , 1993, Cell.
[181] B. Talbot,et al. The orientation of the adenovirus fiber and its anchor domain identified through molecular mimicry. , 1989, Virology.
[182] I. Pastan,et al. Role of a low-pH environment in adenovirus enhancement of the toxicity of a Pseudomonas exotoxin-epidermal growth factor conjugate , 1984, Journal of virology.
[183] N M Green,et al. Evidence for a repeating cross‐beta sheet structure in the adenovirus fibre. , 1983, The EMBO journal.
[184] A. Kirn,et al. Interaction of viruses with sinusoidal cells. , 1982, Progress in liver diseases.
[185] P. Jahrling,et al. Comparisons among members of the Venezuelan encephalitis virus complex using hydroxylapatite column chromatography. , 1977, American journal of epidemiology.
[186] F. Graham,et al. Characteristics of a human cell line transformed by DNA from human adenovirus type 5. , 1977, The Journal of general virology.