The Lancet Oncology, ISSN 1470-2045, 10/2017, Volume 18, Issue 10, pp. 1373 - 1385
Rindopepimut (also known as CDX-110), a vaccine targeting the deletion mutation EGFRvIII, consists of an EGFRvIII-specific peptide conjugated to keyhole limpet...
GLIOMAS | ONCOLOGY | RECURSIVE PARTITIONING ANALYSIS | GROWTH-FACTOR | RADIOTHERAPY | CANCER | PEPTIDE | ADJUVANT TEMOZOLOMIDE | Dacarbazine - adverse effects | Antineoplastic Combined Chemotherapy Protocols - administration & dosage | Follow-Up Studies | Humans | Middle Aged | Brain Neoplasms - pathology | ErbB Receptors - genetics | Gene Expression Regulation, Neoplastic | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Male | Patient Selection | Dose-Response Relationship, Drug | Young Adult | Glioblastoma - genetics | Time Factors | Dacarbazine - analogs & derivatives | Adult | Female | Vaccines, Subunit - adverse effects | Brain Neoplasms - mortality | Dacarbazine - administration & dosage | Double-Blind Method | Drug Administration Schedule | Cancer Vaccines - administration & dosage | Kaplan-Meier Estimate | Proportional Hazards Models | Brain Neoplasms - genetics | Cancer Vaccines - adverse effects | Treatment Outcome | Brain Neoplasms - drug therapy | Disease-Free Survival | Internationality | Vaccines, Subunit - administration & dosage | Glioblastoma - pathology | Survival Analysis | Aged | Temozolomide | Glioblastoma - drug therapy | Glioblastoma - mortality | Antimitotic agents | Clinical trials | Care and treatment | Product development | Antineoplastic agents | Glioblastoma multiforme | Analysis
GLIOMAS | ONCOLOGY | RECURSIVE PARTITIONING ANALYSIS | GROWTH-FACTOR | RADIOTHERAPY | CANCER | PEPTIDE | ADJUVANT TEMOZOLOMIDE | Dacarbazine - adverse effects | Antineoplastic Combined Chemotherapy Protocols - administration & dosage | Follow-Up Studies | Humans | Middle Aged | Brain Neoplasms - pathology | ErbB Receptors - genetics | Gene Expression Regulation, Neoplastic | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Male | Patient Selection | Dose-Response Relationship, Drug | Young Adult | Glioblastoma - genetics | Time Factors | Dacarbazine - analogs & derivatives | Adult | Female | Vaccines, Subunit - adverse effects | Brain Neoplasms - mortality | Dacarbazine - administration & dosage | Double-Blind Method | Drug Administration Schedule | Cancer Vaccines - administration & dosage | Kaplan-Meier Estimate | Proportional Hazards Models | Brain Neoplasms - genetics | Cancer Vaccines - adverse effects | Treatment Outcome | Brain Neoplasms - drug therapy | Disease-Free Survival | Internationality | Vaccines, Subunit - administration & dosage | Glioblastoma - pathology | Survival Analysis | Aged | Temozolomide | Glioblastoma - drug therapy | Glioblastoma - mortality | Antimitotic agents | Clinical trials | Care and treatment | Product development | Antineoplastic agents | Glioblastoma multiforme | Analysis
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 12/2019, Volume 138, Issue 6, pp. 1033 - 1052
Glioblastomas (GBMs) are malignant central nervous system (CNS) neoplasms with a very poor prognosis. They display cellular hierarchies containing...
Pathology | Neurosciences | Glioma stem cell (GSC) commitment | Medicine & Public Health | Glioblastoma (GBM) | MES-like GBM | Dystroglycan (DG) | Perivascular niche | MAPK signalling | EphA3 | Integrin-α6 | Dystroglycan | Mesenchyme | Glioma cells | Central nervous system | Stem cells | Extracellular signal-regulated kinase | Extracellular matrix | MAP kinase | Tumors | Original Paper
Pathology | Neurosciences | Glioma stem cell (GSC) commitment | Medicine & Public Health | Glioblastoma (GBM) | MES-like GBM | Dystroglycan (DG) | Perivascular niche | MAPK signalling | EphA3 | Integrin-α6 | Dystroglycan | Mesenchyme | Glioma cells | Central nervous system | Stem cells | Extracellular signal-regulated kinase | Extracellular matrix | MAP kinase | Tumors | Original Paper
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 4902 - 14
Low-passage, serum-free cell lines cultured from patient tumour tissue are the gold-standard for preclinical studies and cellular investigations of...
HETEROGENEITY | STEM-CELLS | PHOSPHORYLATION | SUBTYPES | MULTIDISCIPLINARY SCIENCES | INHIBITORS | TUMORIGENICITY | EXPRESSION | RADIATION | CULTURE | TEMOZOLOMIDE | Gold | CRISPR | Cell culture | Mesenchyme | Plasmids | Glioblastoma | Cell lines | Xenografts | Labelling | Tumor cell lines | Gene expression | Tumors
HETEROGENEITY | STEM-CELLS | PHOSPHORYLATION | SUBTYPES | MULTIDISCIPLINARY SCIENCES | INHIBITORS | TUMORIGENICITY | EXPRESSION | RADIATION | CULTURE | TEMOZOLOMIDE | Gold | CRISPR | Cell culture | Mesenchyme | Plasmids | Glioblastoma | Cell lines | Xenografts | Labelling | Tumor cell lines | Gene expression | Tumors
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2016, Volume 34, Issue 15_suppl, pp. 6589 - 6589
Journal Article
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