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Achievement of long term gene expression via adenoviral vector-mediated delivery of CRISPR/Cas9 for in vivo editing and gene knock-in

Cytotherapy (Oxford, England), 2019-05, Vol.21 (5), p.S14-S15

2019

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Adenovirus platform enhances transduction efficiency of human mesenchymal stem cells: An opportunity for cellular carriers of targeted TRAIL-based TR3 therapeutics in ovarian cancer

Gynecologic oncology, 2017-06, Vol.145, p.91-91

2017

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Cell-based therapy in ovarian cancer: Improved adenoviral transduction strategy of human mesenchymal stem cells as tumor-homing drug factories

Gynecologic oncology, 2015-04, Vol.137, p.64-64

2015

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Utilizing camelid-derived single domain antibodies to enhance immunotherapy of ovarian cancer

Gynecologic oncology, 2015-04, Vol.137, p.133-133

2015

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Incorporation of porcine adenovirus 4 fiber protein enhances infectivity of adenovirus vector on dendritic cells: Implications for immune-mediated cancer therapy

Gynecologic oncology, 2014-06, Vol.133, p.104-105

2014

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Evolving gene therapy approaches for osteosarcoma using viral vectors: Review

Bone (New York, N.Y.), 2007-04, Vol.40 (4), p.797-812

2007

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STEM CELL DELIVERED ONCOLYTIC VIRO-IMMUNOTHERAPY FOR TREATMENT OF GLIOMA AND OVARIAN CANCER: BENCH TO BEDSIDE

Cytotherapy (Oxford, England), 2024-06, Vol.26 (6), p.S149-S149

2024

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Targeting adenoviral gene therapy vectors towards human endometrial cells

Fertility and sterility, 2009, Vol.92 (3), p.S123-S123

2009

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Characterization of infectivity of knob-modified adenoviral vectors in glioma

Cancer biology & therapy, 2008-05, Vol.7 (5), p.786-793

2008

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Targeting adenoviral vectors for enhanced gene therapy of uterine leiomyomas

Human reproduction (Oxford), 2013-09, Vol.28 (9), p.2398-2406

2013

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Gene therapy for radioprotection

Cancer gene therapy, 2015-04, Vol.22 (4), p.172-180

2015

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An Immunomagnetic-Based Method for the Purification of Ovarian Cancer Cells from Patient-Derived Ascites

Gynecologic oncology, 2001-07, Vol.82 (1), p.57-63

2001

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Therapeutic adenoviral gene transfer of a glycosyltransferase for prevention of peritoneal dissemination and metastasis of gastric cancer

Cancer gene therapy, 2014-10, Vol.21 (10), p.427-433

2014

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A myeloid cell-binding adenovirus efficiently targets gene transfer to the lung and escapes liver tropism

Gene therapy, 2013-07, Vol.20 (7), p.733-741

2013

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Augmented adenovirus transduction of murine T lymphocytes utilizing a bi-specific protein targeting murine interleukin 2 receptor

Cancer gene therapy, 2013-08, Vol.20 (8), p.445-452

2013

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Enhanced delivery of mda-7/IL-24 using a serotype chimeric adenovirus (Ad.5/3) improves therapeutic efficacy in low CAR prostate cancer cells

Cancer gene therapy, 2010-07, Vol.17 (7), p.447-456

2010

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Experimental virotherapy of chemoresistant pancreatic carcinoma using infectivity-enhanced fiber-mosaic oncolytic adenovirus

Cancer gene therapy, 2014-07, Vol.21 (7), p.264-274

2014

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A conditionally replicative adenovirus, CRAd-S-pK7, can target endometriosis with a cell-killing effect

Human reproduction (Oxford), 2010-08, Vol.25 (8), p.2068-2083

2010

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A cancer terminator virus eradicates both primary and distant human melanomas

Cancer gene therapy, 2008-05, Vol.15 (5), p.293-302

2008

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The therapeutic efficacy of adenoviral vectors for cancer gene therapy is limited by a low level of primary adenovirus receptors on tumour cells

European journal of cancer (1990), 2002-09, Vol.38 (14), p.1917-1926

2002

Volltextzugriff (PDF)

Genetic incorporation of HSV-1 thymidine kinase into the adenovirus protein IX for functional display on the virion

Virology (New York, N.Y.), 2005-08, Vol.338 (2), p.247-258

2005

Volltextzugriff (PDF)

Gene therapy strategies for carcinoma of the breast

Breast cancer research and treatment, 1997-06, Vol.44 (2), p.93-114

1997

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Towards gene therapy of postoperative adhesions: fiber and transcriptional modifications enhance adenovirus targeting towards human adhesion cells

Gynecologic and obstetric investigation, 2013-01, Vol.76 (2), p.119

2013

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A system for the propagation of adenoviral vectors with genetically modified receptor specificities

Nature biotechnology, 1999-05, Vol.17 (5), p.470-475

1999

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Toward gene therapy of uterine fibroids: targeting modified adenovirus to human leiomyoma cells

Human reproduction (Oxford), 2008-03, Vol.23 (3), p.514-524

2008

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Achievement of long term gene expression via adenoviral vector-mediated delivery of CRISPR/Cas9 for in vivo editing and gene knock-in

Adenovirus platform enhances transduction efficiency of human mesenchymal stem cells: An opportunity for cellular carriers of targeted TRAIL-based TR3 therapeutics in ovarian cancer

Cell-based therapy in ovarian cancer: Improved adenoviral transduction strategy of human mesenchymal stem cells as tumor-homing drug factories

Utilizing camelid-derived single domain antibodies to enhance immunotherapy of ovarian cancer

Incorporation of porcine adenovirus 4 fiber protein enhances infectivity of adenovirus vector on dendritic cells: Implications for immune-mediated cancer therapy

Evolving gene therapy approaches for osteosarcoma using viral vectors: Review

STEM CELL DELIVERED ONCOLYTIC VIRO-IMMUNOTHERAPY FOR TREATMENT OF GLIOMA AND OVARIAN CANCER: BENCH TO BEDSIDE

Targeting adenoviral gene therapy vectors towards human endometrial cells

Characterization of infectivity of knob-modified adenoviral vectors in glioma

Targeting adenoviral vectors for enhanced gene therapy of uterine leiomyomas

Gene therapy for radioprotection

An Immunomagnetic-Based Method for the Purification of Ovarian Cancer Cells from Patient-Derived Ascites

Therapeutic adenoviral gene transfer of a glycosyltransferase for prevention of peritoneal dissemination and metastasis of gastric cancer

A myeloid cell-binding adenovirus efficiently targets gene transfer to the lung and escapes liver tropism

Augmented adenovirus transduction of murine T lymphocytes utilizing a bi-specific protein targeting murine interleukin 2 receptor

Enhanced delivery of mda-7/IL-24 using a serotype chimeric adenovirus (Ad.5/3) improves therapeutic efficacy in low CAR prostate cancer cells

Experimental virotherapy of chemoresistant pancreatic carcinoma using infectivity-enhanced fiber-mosaic oncolytic adenovirus

A conditionally replicative adenovirus, CRAd-S-pK7, can target endometriosis with a cell-killing effect

A cancer terminator virus eradicates both primary and distant human melanomas

The therapeutic efficacy of adenoviral vectors for cancer gene therapy is limited by a low level of primary adenovirus receptors on tumour cells

Genetic incorporation of HSV-1 thymidine kinase into the adenovirus protein IX for functional display on the virion

Gene therapy strategies for carcinoma of the breast

Towards gene therapy of postoperative adhesions: fiber and transcriptional modifications enhance adenovirus targeting towards human adhesion cells

A system for the propagation of adenoviral vectors with genetically modified receptor specificities

Toward gene therapy of uterine fibroids: targeting modified adenovirus to human leiomyoma cells

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