Pulling the right viral levers: Engineering, screening and application of next-generation combinatorial AAV vectors
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
Heidelberg, Universität Heidelberg, Dissertation, 2023
- Schlagwort
-
Gentherapie
Vektor
Dependoviren
Genexpression
- Ereignis
-
Veröffentlichung
- (wo)
-
Heidelberg
- (wer)
-
Universitätsbibliothek Heidelberg
- (wann)
-
2023
- Urheber
- Beteiligte Personen und Organisationen
-
Grimm, Dirk
- DOI
-
10.11588/heidok.00034091
- URN
-
urn:nbn:de:bsz:16-heidok-340911
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:49 MEZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Becker, Jonas
- Grimm, Dirk
- Universitätsbibliothek Heidelberg
Entstanden
- 2023
Ähnliche Objekte (12)
Adeno-Associated Virus (AAV) vectors in gene therapy
Engineered nanoparticles promote cardiac tropism of AAV vectors
Optimization of AAV vectors to target persistent viral reservoirs
Engineering AAV-2 targeting vectors : a new insertion site and scFv driven vectors
Engineering AAV-2 targeting vectors : a new insertion site and scFv driven vectors
Recombinant AAV Vectors for Enhanced Expression of Authentic IgG
Adeno-associated virus display : in vitro evolution of AAV retargeted vectors
Immunogenicity of Recombinant Adeno-Associated Virus (AAV) Vectors for Gene Transfer
Generation and characterization of AAV vectors for combination immunotherapy against HIV-1
Modifying the immunogenicity of AAV vectors for gene therapy and cancer immunotherapy
Pulling
Receptor-targeted viral vectors : tracking of stem cells and side by side comparison of AAV and lentiviral vectors
Adeno-Associated Virus (AAV) vectors in gene therapy
Engineered nanoparticles promote cardiac tropism of AAV vectors
Optimization of AAV vectors to target persistent viral reservoirs
Engineering AAV-2 targeting vectors : a new insertion site and scFv driven vectors
Engineering AAV-2 targeting vectors : a new insertion site and scFv driven vectors
Recombinant AAV Vectors for Enhanced Expression of Authentic IgG
Adeno-associated virus display : in vitro evolution of AAV retargeted vectors
Immunogenicity of Recombinant Adeno-Associated Virus (AAV) Vectors for Gene Transfer
Generation and characterization of AAV vectors for combination immunotherapy against HIV-1
Modifying the immunogenicity of AAV vectors for gene therapy and cancer immunotherapy
Pulling
Receptor-targeted viral vectors : tracking of stem cells and side by side comparison of AAV and lentiviral vectors
Adeno-Associated Virus (AAV) vectors in gene therapy
Engineered nanoparticles promote cardiac tropism of AAV vectors
Optimization of AAV vectors to target persistent viral reservoirs
Engineering AAV-2 targeting vectors : a new insertion site and scFv driven vectors
Engineering AAV-2 targeting vectors : a new insertion site and scFv driven vectors
Recombinant AAV Vectors for Enhanced Expression of Authentic IgG
Adeno-associated virus display : in vitro evolution of AAV retargeted vectors
Immunogenicity of Recombinant Adeno-Associated Virus (AAV) Vectors for Gene Transfer
Generation and characterization of AAV vectors for combination immunotherapy against HIV-1
Modifying the immunogenicity of AAV vectors for gene therapy and cancer immunotherapy
Pulling