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Publications by Gerhard Jungwirth
Intraventricular Meningiomas Frequently Harbor NF2 Mutations but Lack Common Genetic Alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT
Acta neuropathologica communications
Forensic Medicine
Molecular Neuroscience
Pathology
Neurology
Cellular
Related publications
PI3K Signaling Pathway Is Activated by PIK3CA mRNA Overexpression and Copy Gain in Prostate Tumors, but PIK3CA, BRAF, KRAS and AKT1 Mutations Are Infrequent Events
Modern Pathology
Forensic Medicine
Pathology
Genetic Mutations Predict SMO Inhibitor Response in SHH Medulloblastoma
Cancer Discovery
Oncology
PIK3CA Mutations Are Common in Lobular Carcinoma in Situ, but Are Not a Biomarker of Progression
Breast Cancer Research
Cancer Research
Oncology
SMARCB1 Mutations Are Not a Common Cause of Multiple Meningiomas
Journal of Medical Genetics
Genetics
Knock in of the AKT1 E17K Mutation in Human Breast Epithelial Cells Does Not Recapitulate Oncogenic PIK3CA Mutations
Oncogene
Cancer Research
Genetics
Molecular Biology
PIK3CA Mutations Frequently Coexist With EGFR/KRAS Mutations in Non-Small Cell Lung Cancer and Suggest Poor Prognosis in EGFR/KRAS Wildtype Subgroup
PLoS ONE
Multidisciplinary
Bevacizumab Treatment for Meningiomas in NF2: A Retrospective Analysis of 15 Patients
PLoS ONE
Multidisciplinary
Absence of AKT1 Mutations in Glioblastoma
PLoS ONE
Multidisciplinary
Frequently Oral Alterations in Diabetic Patients
