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Synthetic riboswitches for external regulation of genes transferred by replication-deficient and oncolytic adenoviruses

Nucleic acids research, 2012-11, Vol.40 (21), p.e167

2012

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Engineered adenoviruses combine enhanced oncolysis with improved virus production by mesenchymal stromal carrier cells

International journal of cancer, 2015-08, Vol.137 (4), p.978-990

2015

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Transcriptional Targeting of Mature Dendritic Cells with Adenoviral Vectors via a Modular Promoter System for Antigen Expression and Functional Manipulation

Journal of Immunology Research, 2016-01, Vol.2016, p.6078473-17

2016

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Tropism Modification of Adenovirus Vectors by Peptide Ligand Insertion into Various Positions of the Adenovirus Serotype 41 Short-Fiber Knob Domain

Journal of Virology, 2007-03, Vol.81 (6), p.2688-2699

2007

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Evaluation of twenty human adenoviral types and one infectivity-enhanced adenovirus for the therapy of soft tissue sarcoma

Human gene therapy, 2007-01, Vol.18 (1), p.51

2007

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Enhanced Adenovirus Infection of Melanoma Cells by Fiber-Modification: Incorporation of RGD Peptide or Ad5/3 Chimerism

Cancer biology & therapy, 2003-09, Vol.2 (5), p.511-515

2003

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Genetic replacement of the adenovirus shaft fiber reduces liver tropism in ovarian cancer gene therapy

Human gene therapy, 2004-05, Vol.15 (5), p.509-518

2004

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Selectivity and efficiency of late transgene expression by transcriptionally targeted oncolytic adenoviruses are dependent on the transgene insertion strategy

Human gene therapy, 2011-04, Vol.22 (4), p.389

2011

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Generation of human dendritic cells that simultaneously secrete IL-12 and have migratory capacity by adenoviral gene transfer of hCD40L in combination with IFN-gamma

Journal of immunotherapy, 2009-06, Vol.32 (5), p.524-538

2009

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Targeting of Adenovirus to Endothelial Cells by a Bispecific Single-Chain Diabody Directed against the Adenovirus Fiber Knob Domain and Human Endoglin (CD105)

Molecular therapy, 2001-06, Vol.3 (6), p.882-891

2001

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Retargeting of adenoviral infection to melanoma: Combining genetic ablation of native tropism with a recombinant bispecific single‐chain diabody (scDb) adapter that binds to fiber knob and HMWMAA

International journal of cancer, 2004-01, Vol.108 (1), p.136-145

2004

Volltextzugriff (PDF)

Mode of transgene expression after fusion to early or late viral genes of a conditionally replicating adenovirus via an optimized internal ribosome entry site in vitro and in vivo

Virology (New York, N.Y.), 2004-03, Vol.320 (1), p.121-134

2004

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Modulation of viability and maturation of human monocyte‐derived dendritic cells by oncolytic adenoviruses

International journal of cancer, 2008-01, Vol.122 (1), p.219-229

2008

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Employment of microarray analysis to characterize biologic differences associated with tropism-modified adenoviral vectors: utilization of non-native cellular entry pathways

Cancer gene therapy, 2005-02, Vol.12 (2), p.162-174

2005

Volltextzugriff (PDF)

TUMOR-BUSTING VIRUSES

Scientific American, 2003-10, Vol.289 (4), p.68-75

2003

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Synthetic riboswitches for external regulation of genes transferred by replication-deficient and oncolytic adenoviruses

Engineered adenoviruses combine enhanced oncolysis with improved virus production by mesenchymal stromal carrier cells

Transcriptional Targeting of Mature Dendritic Cells with Adenoviral Vectors via a Modular Promoter System for Antigen Expression and Functional Manipulation

Tropism Modification of Adenovirus Vectors by Peptide Ligand Insertion into Various Positions of the Adenovirus Serotype 41 Short-Fiber Knob Domain

Evaluation of twenty human adenoviral types and one infectivity-enhanced adenovirus for the therapy of soft tissue sarcoma

Enhanced Adenovirus Infection of Melanoma Cells by Fiber-Modification: Incorporation of RGD Peptide or Ad5/3 Chimerism

Genetic replacement of the adenovirus shaft fiber reduces liver tropism in ovarian cancer gene therapy

Selectivity and efficiency of late transgene expression by transcriptionally targeted oncolytic adenoviruses are dependent on the transgene insertion strategy

Generation of human dendritic cells that simultaneously secrete IL-12 and have migratory capacity by adenoviral gene transfer of hCD40L in combination with IFN-gamma

Targeting of Adenovirus to Endothelial Cells by a Bispecific Single-Chain Diabody Directed against the Adenovirus Fiber Knob Domain and Human Endoglin (CD105)

Retargeting of adenoviral infection to melanoma: Combining genetic ablation of native tropism with a recombinant bispecific single‐chain diabody (scDb) adapter that binds to fiber knob and HMWMAA

Mode of transgene expression after fusion to early or late viral genes of a conditionally replicating adenovirus via an optimized internal ribosome entry site in vitro and in vivo

Modulation of viability and maturation of human monocyte‐derived dendritic cells by oncolytic adenoviruses

Employment of microarray analysis to characterize biologic differences associated with tropism-modified adenoviral vectors: utilization of non-native cellular entry pathways

TUMOR-BUSTING VIRUSES

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