- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
Frankfurt am Main, Johann Wolfgang Goethe-Univ., Diss., 2014
- Keyword
-
Allergie
Immunkrankheit
- Event
-
Veröffentlichung
- (where)
-
Frankfurt am Main
- (who)
-
Univ.-Bibliothek Frankfurt am Main
- (when)
-
2014
- Creator
- Contributor
-
Schnierle, Barbara
Marschalek, Rolf
Klein, Jochen
Fürst, Robert
- URN
-
urn:nbn:de:hebis:30:3-346687
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:49 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
- Büchner, Sarah Manon
- Schnierle, Barbara
- Marschalek, Rolf
- Klein, Jochen
- Fürst, Robert
- Univ.-Bibliothek Frankfurt am Main
Time of origin
- 2014
Other Objects (12)
Humanized mice as preclinical model for HIV infections
Humanized mice
Humanized mice
Modeling human cytomegalovirus infections in humanized mice for preclinical development of novel cellular and antibody-based therapies
Highly Significant Antiviral Activity of HIV-1 LTR-Specific Tre-Recombinase in Humanized Mice
Induction of functional human macrophages in humanized mice
Generation of a neonatal sepsis model in humanized mice
Generation of a neonatal sepsis model in humanized mice
Strategies for the development of a preclinical humanized mouse model of experimental colitis.
UDP-glucuronosyltransferase polymorphisms affect diethylnitrosamine-induced carcinogenesis in humanized transgenic mice
Next-generation humanized NSG-SGM3 mice are highly susceptible to Staphylococcus aureus infection
Susceptibility of humanized mice to Staphylococcus aureus in a localized deep-tissue abscess model
Humanized mice as preclinical model for HIV infections
Humanized mice
Humanized mice
Modeling human cytomegalovirus infections in humanized mice for preclinical development of novel cellular and antibody-based therapies
Highly Significant Antiviral Activity of HIV-1 LTR-Specific Tre-Recombinase in Humanized Mice
Induction of functional human macrophages in humanized mice
Generation of a neonatal sepsis model in humanized mice
Generation of a neonatal sepsis model in humanized mice
Strategies for the development of a preclinical humanized mouse model of experimental colitis.
UDP-glucuronosyltransferase polymorphisms affect diethylnitrosamine-induced carcinogenesis in humanized transgenic mice
Next-generation humanized NSG-SGM3 mice are highly susceptible to Staphylococcus aureus infection
Susceptibility of humanized mice to Staphylococcus aureus in a localized deep-tissue abscess model
Humanized mice as preclinical model for HIV infections
Humanized mice
Humanized mice
Modeling human cytomegalovirus infections in humanized mice for preclinical development of novel cellular and antibody-based therapies
Highly Significant Antiviral Activity of HIV-1 LTR-Specific Tre-Recombinase in Humanized Mice
Induction of functional human macrophages in humanized mice
Generation of a neonatal sepsis model in humanized mice
Generation of a neonatal sepsis model in humanized mice
Strategies for the development of a preclinical humanized mouse model of experimental colitis.
UDP-glucuronosyltransferase polymorphisms affect diethylnitrosamine-induced carcinogenesis in humanized transgenic mice
Next-generation humanized NSG-SGM3 mice are highly susceptible to Staphylococcus aureus infection