Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
about
ROS and Brain Gliomas: An Overview of Potential and Innovative Therapeutic StrategiesNeutralizing the EGF receptor in glioblastoma cells stimulates cell migration by activating uPAR-initiated cell signaling.Mechanisms of glioma formation: iterative perivascular glioma growth and invasion leads to tumor progression, VEGF-independent vascularization, and resistance to antiangiogenic therapy.Bevacizumab treatment induces metabolic adaptation toward anaerobic metabolism in glioblastomasPhosphorylated SATB1 is associated with the progression and prognosis of glioma.Phase 2 study of bosutinib, a Src inhibitor, in adults with recurrent glioblastoma.Pro-Tumorigenic Phosphorylation of p120 Catenin in Renal and Breast Cancer.Src family kinases differentially influence glioma growth and motilityPhosphorylation and isoform use in p120-catenin during development and tumorigenesisEstablishment of human iPSC-based models for the study and targeting of glioma initiating cellsThe Effect of Chemoradiotherapy with SRC Tyrosine Kinase Inhibitor, PP2 and Temozolomide on Malignant Glioma Cells In Vitro and In Vivop120catenin alteration in cancer and its role in tumour invasion.SDF-1 Blockade Enhances Anti-VEGF Therapy of Glioblastoma and Can Be Monitored by MRI.Genomic analyses reveal broad impact of miR-137 on genes associated with malignant transformation and neuronal differentiation in glioblastoma cells.VEGF-VEGFR Signals in Health and Disease.Molecular targets in glioblastoma.Src Family Kinases in Brain Edema After Acute Brain Injury.EGFRvIII mutations can emerge as late and heterogenous events in glioblastoma development and promote angiogenesis through Src activation.Reprogramming strategies for the establishment of novel human cancer models.PTPIP51 levels in glioblastoma cells depend on inhibition of the EGF-receptor.EGFR and EGFRvIII Promote Angiogenesis and Cell Invasion in Glioblastoma: Combination Therapies for an Effective Treatment.Orphan Nuclear Receptor TR3/Nur77 is a Specific Therapeutic Target for Hepatic Cancers.
P2860
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P2860
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
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2013 nî lūn-bûn
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2013 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年论文
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name
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
@ast
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
@en
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
@nl
type
label
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
@ast
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
@en
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
@nl
prefLabel
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
@ast
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
@en
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
@nl
P2093
P2860
P1433
P1476
Targeting Src family kinases inhibits bevacizumab-induced glioma cell invasion
@en
P2093
Brett L Carlson
Caterina Giannini
Deborah Huveldt
Fausto Rodriguez
Jann N Sarkaria
Laura J Lewis-Tuffin
Mark A Schroeder
Panos Z Anastasiadis
P2860
P304
P356
10.1371/JOURNAL.PONE.0056505
P407
P577
2013-02-14T00:00:00Z