- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
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MicroRNAs as the pivotal regulators of Temozolomide resistance in glioblastoma ; volume:17 ; number:1 ; day:2 ; month:7 ; year:2024 ; pages:1-12 ; date:12.2024
Molecular brain ; 17, Heft 1 (2.7.2024), 1-12, 12.2024
- Creator
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Palizkaran Yazdi, Mahsa
Barjasteh, Amirhosein
Moghbeli, Meysam
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13041-024-01113-6
- URN
-
urn:nbn:de:101:1-2409202142081.853966569675
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:20 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Palizkaran Yazdi, Mahsa
- Barjasteh, Amirhosein
- Moghbeli, Meysam
- SpringerLink (Online service)
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Temozolomide promotes genomic and phenotypic changes in glioblastoma cells
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p53/E2F7 axis promotes temozolomide chemoresistance in glioblastoma multiforme
Considering the experimental use of temozolomide in glioblastoma research
Integrins as the pivotal regulators of cisplatin response in tumor cells
Multivalent protein–protein interactions are pivotal regulators of eukaryotic Hsp70 complexes
MicroRNAs as the pivotal regulators of cisplatin resistance in head and neck cancers
Accelerated hyperfractionation plus temozolomide in glioblastoma
Deubiquitinases as pivotal regulators of T cell functions
Pivotal regulators of tissue homeostasis and cancer: macrophages
Long noncoding RNAs: pivotal regulators in acute myeloid leukemia
MicroRNAs: regulators of oncogenesis and stemness
microRNAs: important regulators of stem cells
Temozolomide promotes genomic and phenotypic changes in glioblastoma cells
p53/E2F7 axis promotes temozolomide chemoresistance in glioblastoma multiforme
Considering the experimental use of temozolomide in glioblastoma research
Integrins as the pivotal regulators of cisplatin response in tumor cells