- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Malaria inflammation by xanthine oxidase‐produced reactive oxygen species ; volume:11 ; number:8 ; year:2019 ; extent:15
EMBO molecular medicine / European Molecular Biology Organization ; 11, Heft 8 (2019) (gesamt 15)
- Creator
-
Ty, Maureen C.
Zuniga, Marisol
Götz, Anton
Kayal, Sriti
Sahu, Praveen K.
Mohanty, Akshaya
Mohanty, Sanjib
Wassmer, Samuel C.
Rodriguez, Ana
- DOI
-
10.15252/emmm.201809903
- URN
-
urn:nbn:de:101:1-2022080307300609148158
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 15.08.2025, 7:24 AM CEST
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.
Associated
- Ty, Maureen C.
- Zuniga, Marisol
- Götz, Anton
- Kayal, Sriti
- Sahu, Praveen K.
- Mohanty, Akshaya
- Mohanty, Sanjib
- Wassmer, Samuel C.
- Rodriguez, Ana
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Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species
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Unravelling NADPH oxidase complexes and the role of reactive oxygen species as signaling components in Botrytis cinerea
Roles of neutrophil NADPH oxidase derived reactive oxygen species (ROS) in innate responses
Role of neutrophil NADPH oxidase derived reactive oxygen species (ROS) in innate immune responses
NADPH-oxidase derived Reactive Oxygen Species (ROS) regulate Staphylococcus aureus-induced autophagy through PI3K
NADPH oxidase and reactive oxygen species contribute to alcohol-induced microglial activation and neurodegeneration
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Inhibition of NADPH Oxidase-Derived Reactive Oxygen Species Decreases Expression of Inflammatory Cytokines in A549 Cells
Thymidine catabolism promotes NADPH oxidase-derived reactive oxygen species (ROS) signalling in KB and yumoto cells
Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species
Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species