NF-κB and pSTAT3 synergistically drive G6PD overexpression and facilitate sensitivity to G6PD inhibition in ccRCC
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1475-2867
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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NF-κB and pSTAT3 synergistically drive G6PD overexpression and facilitate sensitivity to G6PD inhibition in ccRCC ; volume:20 ; number:1 ; day:6 ; month:10 ; year:2020 ; pages:1-19 ; date:12.2020
Cancer cell international ; 20, Heft 1 (6.10.2020), 1-19, 12.2020
- Creator
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Zhang, Qiao
Yang, Zhe
Ni, Yueli
Bai, Honggang
Han, Qiaoqiao
Yi, Zihan
Yi, Xiaojia
Agbana, Yannick Luther
Kuang, Yingmin
Zhu, Yuechun
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12935-020-01576-2
- URN
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urn:nbn:de:101:1-2020112215413165424276
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:39 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
- Zhang, Qiao
- Yang, Zhe
- Ni, Yueli
- Bai, Honggang
- Han, Qiaoqiao
- Yi, Zihan
- Yi, Xiaojia
- Agbana, Yannick Luther
- Kuang, Yingmin
- Zhu, Yuechun
- SpringerLink (Online service)
Other Objects (12)
Correction to: NF-κB and pSTAT3 synergistically drive G6PD overexpression and facilitate sensitivity to G6PD inhibition in ccRCC
Charakterisierung und Vergleich von "Mittelmeer"- ähnlichen und (A-)- ähnlichen G6PD- Varianten, Charakterisierung einer G6PD- Variante einer G6PD- defekten Maus und Einsatz der Mikroimmunoaffinitätschromatografie zur Isolierung der G6PD
Molekulargenetische G6PD-Genotypisierung und Bestimmung er Genfrequenzen polymorpher G6PD-Varianten in Südwest-Nigeria
Assessment of CareStart G6PD rapid diagnostic test and CareStart G6PD biosensor in Mauritania
Charakterisierung von G6PD-Mutanten [GPD-Mutanten]
Spectrophotometry assays to determine G6PD activity from Trinity Biotech and Pointe Scientific G6PD show good correlation
G6PD testing in support of treatment and elimination of malaria: recommendations for evaluation of G6PD tests
Molecular characterization of G6PD mutations reveals the high frequency of G6PD Aures in the Lao Theung population
Effect of neonatal reticulocytosis on glucose 6-phosphate dehydrogenase (G6PD) activity and G6PD deficiency detection: a cross-sectional study
G6PD deficiency in malaria endemic areas of Nepal
Establishing a unique specimen repository with characterized G6PD enzyme activity for the development of new G6PD point-of-care tests
Primaquine-induced haemolysis in females heterozygous for G6PD deficiency
Correction to: NF-κB and pSTAT3 synergistically drive G6PD overexpression and facilitate sensitivity to G6PD inhibition in ccRCC
Charakterisierung und Vergleich von "Mittelmeer"- ähnlichen und (A-)- ähnlichen G6PD- Varianten, Charakterisierung einer G6PD- Variante einer G6PD- defekten Maus und Einsatz der Mikroimmunoaffinitätschromatografie zur Isolierung der G6PD
Molekulargenetische G6PD-Genotypisierung und Bestimmung er Genfrequenzen polymorpher G6PD-Varianten in Südwest-Nigeria
Assessment of CareStart G6PD rapid diagnostic test and CareStart G6PD biosensor in Mauritania
Charakterisierung von G6PD-Mutanten [GPD-Mutanten]
Spectrophotometry assays to determine G6PD activity from Trinity Biotech and Pointe Scientific G6PD show good correlation
G6PD testing in support of treatment and elimination of malaria: recommendations for evaluation of G6PD tests
Molecular characterization of G6PD mutations reveals the high frequency of G6PD Aures in the Lao Theung population
Effect of neonatal reticulocytosis on glucose 6-phosphate dehydrogenase (G6PD) activity and G6PD deficiency detection: a cross-sectional study
G6PD deficiency in malaria endemic areas of Nepal
Establishing a unique specimen repository with characterized G6PD enzyme activity for the development of new G6PD point-of-care tests
Primaquine-induced haemolysis in females heterozygous for G6PD deficiency
Correction to: NF-κB and pSTAT3 synergistically drive G6PD overexpression and facilitate sensitivity to G6PD inhibition in ccRCC
Charakterisierung und Vergleich von "Mittelmeer"- ähnlichen und (A-)- ähnlichen G6PD- Varianten, Charakterisierung einer G6PD- Variante einer G6PD- defekten Maus und Einsatz der Mikroimmunoaffinitätschromatografie zur Isolierung der G6PD
Molekulargenetische G6PD-Genotypisierung und Bestimmung er Genfrequenzen polymorpher G6PD-Varianten in Südwest-Nigeria
Assessment of CareStart G6PD rapid diagnostic test and CareStart G6PD biosensor in Mauritania
Charakterisierung von G6PD-Mutanten [GPD-Mutanten]
Spectrophotometry assays to determine G6PD activity from Trinity Biotech and Pointe Scientific G6PD show good correlation
G6PD testing in support of treatment and elimination of malaria: recommendations for evaluation of G6PD tests
Molecular characterization of G6PD mutations reveals the high frequency of G6PD Aures in the Lao Theung population
Effect of neonatal reticulocytosis on glucose 6-phosphate dehydrogenase (G6PD) activity and G6PD deficiency detection: a cross-sectional study
G6PD deficiency in malaria endemic areas of Nepal
Establishing a unique specimen repository with characterized G6PD enzyme activity for the development of new G6PD point-of-care tests