Hochschulschrift
Producing lentiviral vectors for ex vivo organ gene therapy
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Maße
-
30 cm
- Umfang
-
78 Blätter
- Sprache
-
Englisch
- Anmerkungen
-
Illustrationen, Diagramme
Medizinische Hochschule Hannover, Dissertation, 2020
- Ereignis
-
Veröffentlichung
- (wo)
-
Hannover
- (wann)
-
2019
- Urheber
- Beteiligte Personen und Organisationen
-
Blasczyk, Rainer
Medizinische Hochschule Hannover
Medizinische Hochschule Hannover. Institut für Transfusionsmedizin
- Inhaltsverzeichnis
- Rechteinformation
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Letzte Aktualisierung
-
11.06.2025, 13:51 MESZ
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.
Objekttyp
- Hochschulschrift
Beteiligte
- Jin, Zhu
- Blasczyk, Rainer
- Medizinische Hochschule Hannover
- Medizinische Hochschule Hannover. Institut für Transfusionsmedizin
Entstanden
- 2019
Ähnliche Objekte (12)
Vectors for Algernon: Receptor-Targeted Lentiviral and Adeno-Associated Vectors in Syngeneic Mouse Models of In Vivo Gene Therapy
Lentiviral vectors : with 8 tables
Targeted cell entry of lentiviral vectors
CD3-targeted lentiviral vectors : combining T cell-specific activation and in vivo gene delivery
Targeted lentiviral vectors pseudotyped with the Tupaia paramyxovirus glycoproteins
Downstream processing of lentiviral vectors with focus on steric exclusion chromatography
Measles virus glycoprotein-based lentiviral targeting vectors that avoid neutralizing antibodies
Optimized lentiviral gene therapeutic vectors for prolonged and stable transgene expression
Epigenetic regulation of lentiviral and retroviral vectors in murine embryonic stem (ES) cells and genetic modification of ES cells with lentiviral vectors for application in regenerative medicine
Epigenetic regulation of lentiviral and retroviral vectors in murine embryonic stem (ES) cells and genetic modification of ES cells with lentiviral vectors for application in regenerative medicine
Development of DC-specific lentiviral vectors: novel DC-targeting strategies for immunomodulation
Development of DC-specific lentiviral vectors : novel DC-targeting strategies for immunomodulation
Vectors for Algernon: Receptor-Targeted Lentiviral and Adeno-Associated Vectors in Syngeneic Mouse Models of In Vivo Gene Therapy
Lentiviral vectors : with 8 tables
Targeted cell entry of lentiviral vectors
CD3-targeted lentiviral vectors : combining T cell-specific activation and in vivo gene delivery
Targeted lentiviral vectors pseudotyped with the Tupaia paramyxovirus glycoproteins
Downstream processing of lentiviral vectors with focus on steric exclusion chromatography
Measles virus glycoprotein-based lentiviral targeting vectors that avoid neutralizing antibodies
Optimized lentiviral gene therapeutic vectors for prolonged and stable transgene expression
Epigenetic regulation of lentiviral and retroviral vectors in murine embryonic stem (ES) cells and genetic modification of ES cells with lentiviral vectors for application in regenerative medicine
Epigenetic regulation of lentiviral and retroviral vectors in murine embryonic stem (ES) cells and genetic modification of ES cells with lentiviral vectors for application in regenerative medicine
Development of DC-specific lentiviral vectors: novel DC-targeting strategies for immunomodulation
Development of DC-specific lentiviral vectors : novel DC-targeting strategies for immunomodulation
Vectors for Algernon: Receptor-Targeted Lentiviral and Adeno-Associated Vectors in Syngeneic Mouse Models of In Vivo Gene Therapy
Lentiviral vectors : with 8 tables
Targeted cell entry of lentiviral vectors
CD3-targeted lentiviral vectors : combining T cell-specific activation and in vivo gene delivery
Targeted lentiviral vectors pseudotyped with the Tupaia paramyxovirus glycoproteins
Downstream processing of lentiviral vectors with focus on steric exclusion chromatography
Measles virus glycoprotein-based lentiviral targeting vectors that avoid neutralizing antibodies
Optimized lentiviral gene therapeutic vectors for prolonged and stable transgene expression
Epigenetic regulation of lentiviral and retroviral vectors in murine embryonic stem (ES) cells and genetic modification of ES cells with lentiviral vectors for application in regenerative medicine
Epigenetic regulation of lentiviral and retroviral vectors in murine embryonic stem (ES) cells and genetic modification of ES cells with lentiviral vectors for application in regenerative medicine
Development of DC-specific lentiviral vectors: novel DC-targeting strategies for immunomodulation