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Felix Sahm

Showing results (391-400 of 451) with videos related to

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Acta Neuropathologica|December 15, 2020
Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1Philipp Sievers, Martin Sill, Christina Blume, et al.
Acta Neuropathologica|October 11, 2025
Molecular characterization and clinical features of diffuse midline glioma in the pediatric precision oncology registry INFORMElke Pfaff, Kathrin Schramm, Mirjam Blattner-Johnson, et al.
Neuro-Oncology|January 22, 2025
The clinical and molecular landscape of diffuse hemispheric glioma, H3 G34-mutantEmilie Le Rhun, Andrea Bink, Joerg Felsberg, et al.
The Journal of Molecular Diagnostics : JMD|July 30, 2023
Implementation of DNA Methylation Array Profiling in Pediatric Central Nervous System Tumors: The AIM BRAIN Project: An Australian and New Zealand Children's Haematology/Oncology Group StudyChristine L White, Kathryn M Kinross, Molly K Moore, et al.
Acta Neuropathologica|August 2, 2025
PLAG1 fusions define a third subtype of CNS embryonal tumor with PLAG family gene alterationMichaela-Kristina Keck, Maysa Al-Hussaini, Nisreen Amayiri, et al.
Nature Medicine|August 21, 2024
Molecular classification to refine surgical and radiotherapeutic decision-making in meningiomaJustin Z Wang, Vikas Patil, Alexander P Landry, et al.
Acta Neuropathologica|April 20, 2021
Glioblastomas with primitive neuronal component harbor a distinct methylation and copy-number profile with inactivation of TP53, PTEN, and RB1Abigail K Suwala, Damian Stichel, Daniel Schrimpf, et al.
Acta Neuropathologica|February 14, 2019
Papillary glioneuronal tumor (PGNT) exhibits a characteristic methylation profile and fusions involving PRKCAYanghao Hou, Jorge Pinheiro, Felix Sahm, et al.
Acta Neuropathologica Communications|January 11, 2022
Pleomorphic xanthoastrocytoma is a heterogeneous entity with pTERT mutations prognosticating shorter survivalAzadeh Ebrahimi, Andrey Korshunov, Guido Reifenberger, et al.
Neuro-Oncology|April 19, 2023
LOGGIC Core BioClinical Data Bank: Added clinical value of RNA-Seq in an international molecular diagnostic registry for pediatric low-grade glioma patientsEmily C Hardin, Simone Schmid, Alexander Sommerkamp, et al.
Pageof 46

Showing results (391-400 of 451) with videos related to

Sort By:
Pageof 46
Acta Neuropathologica|December 15, 2020
Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1Philipp Sievers, Martin Sill, Christina Blume, et al.
Acta Neuropathologica|October 11, 2025
Molecular characterization and clinical features of diffuse midline glioma in the pediatric precision oncology registry INFORMElke Pfaff, Kathrin Schramm, Mirjam Blattner-Johnson, et al.
Neuro-Oncology|January 22, 2025
The clinical and molecular landscape of diffuse hemispheric glioma, H3 G34-mutantEmilie Le Rhun, Andrea Bink, Joerg Felsberg, et al.
The Journal of Molecular Diagnostics : JMD|July 30, 2023
Implementation of DNA Methylation Array Profiling in Pediatric Central Nervous System Tumors: The AIM BRAIN Project: An Australian and New Zealand Children's Haematology/Oncology Group StudyChristine L White, Kathryn M Kinross, Molly K Moore, et al.
Acta Neuropathologica|August 2, 2025
PLAG1 fusions define a third subtype of CNS embryonal tumor with PLAG family gene alterationMichaela-Kristina Keck, Maysa Al-Hussaini, Nisreen Amayiri, et al.
Nature Medicine|August 21, 2024
Molecular classification to refine surgical and radiotherapeutic decision-making in meningiomaJustin Z Wang, Vikas Patil, Alexander P Landry, et al.
Acta Neuropathologica|April 20, 2021
Glioblastomas with primitive neuronal component harbor a distinct methylation and copy-number profile with inactivation of TP53, PTEN, and RB1Abigail K Suwala, Damian Stichel, Daniel Schrimpf, et al.
Acta Neuropathologica|February 14, 2019
Papillary glioneuronal tumor (PGNT) exhibits a characteristic methylation profile and fusions involving PRKCAYanghao Hou, Jorge Pinheiro, Felix Sahm, et al.
Acta Neuropathologica Communications|January 11, 2022
Pleomorphic xanthoastrocytoma is a heterogeneous entity with pTERT mutations prognosticating shorter survivalAzadeh Ebrahimi, Andrey Korshunov, Guido Reifenberger, et al.
Neuro-Oncology|April 19, 2023
LOGGIC Core BioClinical Data Bank: Added clinical value of RNA-Seq in an international molecular diagnostic registry for pediatric low-grade glioma patientsEmily C Hardin, Simone Schmid, Alexander Sommerkamp, et al.
Pageof 46