AKT1 E17K mutation profiling in breast cancer: prevalence, concurrent oncogenic alterations, and blood-based detection
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2407
- 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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AKT1 E17K mutation profiling in breast cancer: prevalence, concurrent oncogenic alterations, and blood-based detection ; volume:16 ; number:1 ; day:11 ; month:8 ; year:2016 ; pages:1-12 ; date:12.2016
BMC cancer ; 16, Heft 1 (11.8.2016), 1-12, 12.2016
- Creator
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Rudolph, Marion
- Contributor
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Anzeneder, Tobias
Schulz, Anke
Beckmann, Georg
Byrne, Annette T.
Jeffers, Michael
Pena, Carol
Politz, Oliver
Köchert, Karl
Vonk, Richardus
Reischl, Joachim
SpringerLink (Online service)
- DOI
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10.1186/s12885-016-2626-1
- URN
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urn:nbn:de:1111-2016090922852
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:50 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
- Rudolph, Marion
- Anzeneder, Tobias
- Schulz, Anke
- Beckmann, Georg
- Byrne, Annette T.
- Jeffers, Michael
- Pena, Carol
- Politz, Oliver
- Köchert, Karl
- Vonk, Richardus
- Reischl, Joachim
- SpringerLink (Online service)
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Oncogenic activation revealed by FGFR2 genetic alterations in intrahepatic cholangiocarcinomas
Proteomic alterations in extracellular vesicles induced by oncogenic PIK3CA mutations
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AKT1 Mutationsanalyse in Meningeomen : AKT1 E17K Mutationen und ihre Verteilung in Bezug auf Grad, Subtyp und Lokalisation
Hexokinase 2 promoted cell motility and proliferation by activating Akt1/p-Akt1 in human ovarian cancer cells
Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT
Rare oncogenic alterations in NSCLC—focus on atypical EGFR mutations : Invited short review
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Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants
Akt1 and dCIZ1 promote cell survival from apoptotic caspase activation during regeneration and oncogenic overgrowth
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Oncogenic activation revealed by FGFR2 genetic alterations in intrahepatic cholangiocarcinomas
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Concurrent inhibition of oncogenic and wild-type RAS-GTP for cancer therapy
AKT1 Mutationsanalyse in Meningeomen : AKT1 E17K Mutationen und ihre Verteilung in Bezug auf Grad, Subtyp und Lokalisation
Hexokinase 2 promoted cell motility and proliferation by activating Akt1/p-Akt1 in human ovarian cancer cells
Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT
Rare oncogenic alterations in NSCLC—focus on atypical EGFR mutations : Invited short review