UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Antibody-epitope conjugates deliver immunogenic T-cell epitopes more efficiently when close to cell surfaces

mAbs, 2024, Vol.16 (1), p.2329321-2329321

2024

Volltextzugriff (PDF)

Correction of murine Rag1 deficiency by self-inactivating lentiviral vector-mediated gene transfer

Leukemia, 2011-09, Vol.25 (9), p.1471-1483

2011

Volltextzugriff (PDF)

Developing a potentially immunologically inert tetracycline-regulatable viral vector for gene therapy in the peripheral nerve

Gene therapy, 2014-06, Vol.21 (6), p.549-557

2014

Volltextzugriff (PDF)

The chicken chorioallantoic membrane tumor assay as model for qualitative testing of oncolytic adenoviruses

Cancer gene therapy, 2012-01, Vol.19 (1), p.58-68

2012

Volltextzugriff (PDF)

How not to be seen: immune-evasion strategies in gene therapy

Gene therapy, 2008-02, Vol.15 (4), p.239-246

2008

Volltextzugriff (PDF)

A transductionally retargeted adenoviral vector for virotherapy of Her2/neu-expressing prostate cancer

Human gene therapy, 2012-01, Vol.23 (1), p.70-82

2012

Volltextzugriff (PDF)

A strategy for genetic modification of the spike-encoding segment of human reovirus T3D for reovirus targeting

Gene therapy, 2008-12, Vol.15 (24), p.1567-1578

2008

Volltextzugriff (PDF)

Efficient incorporation of a functional hyper-stable single-chain antibody fragment protein-IX fusion in the adenovirus capsid

Gene therapy, 2007-04, Vol.14 (8), p.664-670

2007

Volltextzugriff (PDF)

Characterization of an immune-evading doxycycline-inducible lentiviral vector for gene therapy in the spinal cord

Experimental neurology, 2022-09, Vol.355, p.114120-114120, Article 114120

2022

Volltextzugriff (PDF)

A cathepsin-cleavage site between the adenovirus capsid protein IX and a tumor-targeting ligand improves targeted transduction

Gene therapy, 2012-09, Vol.19 (9), p.899-906

2012

Volltextzugriff (PDF)

Toll-like receptor triggering augments activation of human mast cells by anti-citrullinated protein antibodies

Annals of the rheumatic diseases, 2015-10, Vol.74 (10), p.1915-1923

2015

Volltextzugriff (PDF)

Comprehensive sequence analysis of the E1A proteins of human and simian adenoviruses

Virology (New York, N.Y.), 2004-11, Vol.329 (2), p.477-492

2004

Volltextzugriff (PDF)

Highly Efficient Transduction of Human Monocyte-Derived Dendritic Cells with Subgroup B Fiber-Modified Adenovirus Vectors Enhances Transgene-Encoded Antigen Presentation to Cytotoxic T Cells

The Journal of immunology (1950), 2001-04, Vol.166 (8), p.5236-5244

2001

Volltextzugriff (PDF)

Herpesvirus microRNAs for use in gene therapy immune-evasion strategies

Gene therapy, 2017-07, Vol.24 (7), p.385-391

2017

Volltextzugriff (PDF)

Adenovirus targeting to HLA-A1 MAGE-A1-positive tumor cells by fusing a single-chain T-cell receptor with minor capsid protein IX

Gene therapy, 2008-07, Vol.15 (13), p.978-989

2008

Volltextzugriff (PDF)

Replicating reoviruses with a transgene replacing the codons for the head domain of the viral spike

Gene therapy, 2015-03, Vol.22 (3), p.267-279

2015

Volltextzugriff (PDF)

Human adenovirus type 35 vector for gene therapy of brain cancer: improved transduction and bypass of pre-existing anti-vector immunity in cancer patients

Cancer gene therapy, 2007-02, Vol.14 (2), p.211-219

2007

Volltextzugriff (PDF)

Transient infection of freshly isolated human colorectal tumor cells by reovirus T3D intermediate subviral particles

Cancer gene therapy, 2008-05, Vol.15 (5), p.284-292

2008

Volltextzugriff (PDF)

Severe hepatic dysfunction after adenovirus-mediated transfer of the herpes simplex virus thymidine kinase gene and ganciclovir administration

Gene therapy, 1998-04, Vol.5 (4), p.451-458

1998

Volltextzugriff (PDF)

Mammalian orthoreovirus T3D infects U-118 MG cell spheroids independent of junction adhesion molecule-A

Gene therapy, 2014-06, Vol.21 (6), p.609-617

2014

Volltextzugriff (PDF)

Creation of immune 'stealth' genes for gene therapy through fusion with the Gly-Ala repeat of EBNA-1

Gene therapy, 2003-11, Vol.10 (24), p.2020-2028

2003

Volltextzugriff (PDF)

Heterogeneous reovirus susceptibility in human glioblastoma stem-like cell cultures

Cancer gene therapy, 2013-09, Vol.20 (9), p.507-513

2013

Volltextzugriff (PDF)

Polycistronic lentivirus induced pluripotent stem cells from skin biopsies after long term storage, blood outgrowth endothelial cells and cells from milk teeth

Differentiation (London), 2013-02, Vol.85 (3), p.101-109

2013

Volltextzugriff (PDF)

Recombinant adenoviral vectors have adjuvant activity and stimulate T cell responses against tumor cells

Gene therapy, 2000-08, Vol.7 (16), p.1410-1416

2000

Volltextzugriff (PDF)

A comparative study between catalase gene therapy and the cardioprotector monohydroxyethylrutoside (MonoHER) in protecting against doxorubicin-induced cardiotoxicity in vitro

British journal of cancer, 2003-12, Vol.89 (11), p.2140-2146

2003

Volltextzugriff (PDF)

1 – 25 von 194

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(187)
Mit Volltextzugriff
(159)

Publikationsform

Artikel
(192)
Tagungsberichte
(2)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(143)
Life Sciences & Biomedicine
(124)
Humans
(101)
Animals
(65)
Gene Therapy
(49)
Biological And Medical Sciences
(48)
Genetics & Heredity
(44)
Medicine, Research & Experimental
(44)
Research & Experimental Medicine
(44)
Biotechnology & Applied Microbiology
(42)
Mice
(34)
Adenoviridae - Genetics
(33)
Fundamental And Applied Biological Sciences. Psychology
(32)
Female
(30)
Male
(29)
Medical Sciences
(29)
Adenovirus
(28)
Genetic Therapy - Methods
(28)
Gene Expression
(27)
Biochemistry & Molecular Biology
(26)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Antibody-epitope conjugates deliver immunogenic T-cell epitopes more efficiently when close to cell surfaces

Correction of murine Rag1 deficiency by self-inactivating lentiviral vector-mediated gene transfer

Developing a potentially immunologically inert tetracycline-regulatable viral vector for gene therapy in the peripheral nerve

The chicken chorioallantoic membrane tumor assay as model for qualitative testing of oncolytic adenoviruses

How not to be seen: immune-evasion strategies in gene therapy

A transductionally retargeted adenoviral vector for virotherapy of Her2/neu-expressing prostate cancer

A strategy for genetic modification of the spike-encoding segment of human reovirus T3D for reovirus targeting

Efficient incorporation of a functional hyper-stable single-chain antibody fragment protein-IX fusion in the adenovirus capsid

Characterization of an immune-evading doxycycline-inducible lentiviral vector for gene therapy in the spinal cord

A cathepsin-cleavage site between the adenovirus capsid protein IX and a tumor-targeting ligand improves targeted transduction

Toll-like receptor triggering augments activation of human mast cells by anti-citrullinated protein antibodies

Comprehensive sequence analysis of the E1A proteins of human and simian adenoviruses

Highly Efficient Transduction of Human Monocyte-Derived Dendritic Cells with Subgroup B Fiber-Modified Adenovirus Vectors Enhances Transgene-Encoded Antigen Presentation to Cytotoxic T Cells

Herpesvirus microRNAs for use in gene therapy immune-evasion strategies

Adenovirus targeting to HLA-A1 MAGE-A1-positive tumor cells by fusing a single-chain T-cell receptor with minor capsid protein IX

Replicating reoviruses with a transgene replacing the codons for the head domain of the viral spike

Human adenovirus type 35 vector for gene therapy of brain cancer: improved transduction and bypass of pre-existing anti-vector immunity in cancer patients

Transient infection of freshly isolated human colorectal tumor cells by reovirus T3D intermediate subviral particles

Severe hepatic dysfunction after adenovirus-mediated transfer of the herpes simplex virus thymidine kinase gene and ganciclovir administration

Mammalian orthoreovirus T3D infects U-118 MG cell spheroids independent of junction adhesion molecule-A

Creation of immune 'stealth' genes for gene therapy through fusion with the Gly-Ala repeat of EBNA-1

Heterogeneous reovirus susceptibility in human glioblastoma stem-like cell cultures

Polycistronic lentivirus induced pluripotent stem cells from skin biopsies after long term storage, blood outgrowth endothelial cells and cells from milk teeth

Recombinant adenoviral vectors have adjuvant activity and stimulate T cell responses against tumor cells

A comparative study between catalase gene therapy and the cardioprotector monohydroxyethylrutoside (MonoHER) in protecting against doxorubicin-induced cardiotoxicity in vitro

Suchergebnisse filtern