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David Castel

Showing results (71-80 of 96) with videos related to

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Briefings in Bioinformatics|September 19, 2012
A comprehensive evaluation of normalization methods for Illumina high-throughput RNA sequencing data analysisMarie-Agnès Dillies, Andrea Rau, Julie Aubert, et al.
Acta Neuropathologica|September 25, 2015
Histone H3F3A and HIST1H3B K27M mutations define two subgroups of diffuse intrinsic pontine gliomas with different prognosis and phenotypesDavid Castel, Cathy Philippe, Raphaël Calmon, et al.
Neuropathology and Applied Neurobiology|July 14, 2022
The genomic landscape of dysembryoplastic neuroepithelial tumours and a comprehensive analysis of recurrent casesMélanie Pagès, Marie-Anne Debily, Frédéric Fina, et al.
Neuro-Oncology Advances|September 5, 2024
Glioma oncogenesis in the Constitutional mismatch repair deficiency (CMMRD) syndromeLea Guerrini-Rousseau, Jane Merlevede, Philippe Denizeau, et al.
Journal of Neuropathology and Experimental Neurology|January 18, 2024
"Hemispheric pilocytic astrocytoma" revisited: A comprehensive clinicopathological and molecular series emphasizing their overlap with other glioneuronal tumorsCassandra Mariet, Jacques Grill, Yassine Ajlil, et al.
Plos One|June 16, 2017
Integrating Tenascin-C protein expression and 1q25 copy number status in pediatric intracranial ependymoma prognostication: A new model for risk stratificationFelipe Andreiuolo, Gwénaël Le Teuff, Mohamed Amine Bayar, et al.
Acta Neuropathologica|March 4, 2026
H3K27ME3 loss in diffuse midline gliomas lacking H3K27M or EZHIP expressions, a potential diagnostic pitfall!Arnault Tauziède-Espariat, David Castel, Yassine Ajlil, et al.
Acta Neuropathologica|December 8, 2023
A new subtype of diffuse midline glioma, H3 K27 and BRAF/FGFR1 co-altered: a clinico-radiological and histomolecular characterisationLucie Auffret, Yassine Ajlil, Arnault Tauziède-Espariat, et al.
Nature Genetics|April 8, 2014
Recurrent activating ACVR1 mutations in diffuse intrinsic pontine gliomaKathryn R Taylor, Alan Mackay, Nathalène Truffaux, et al.
Acta Neuropathologica Communications|November 3, 2020
The EP300:BCOR fusion extends the genetic alteration spectrum defining the new tumoral entity of "CNS tumors with BCOR internal tandem duplication"Arnault Tauziède-Espariat, Gaëlle Pierron, Aurore Siegfried, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
Briefings in Bioinformatics|September 19, 2012
A comprehensive evaluation of normalization methods for Illumina high-throughput RNA sequencing data analysisMarie-Agnès Dillies, Andrea Rau, Julie Aubert, et al.
Acta Neuropathologica|September 25, 2015
Histone H3F3A and HIST1H3B K27M mutations define two subgroups of diffuse intrinsic pontine gliomas with different prognosis and phenotypesDavid Castel, Cathy Philippe, Raphaël Calmon, et al.
Neuropathology and Applied Neurobiology|July 14, 2022
The genomic landscape of dysembryoplastic neuroepithelial tumours and a comprehensive analysis of recurrent casesMélanie Pagès, Marie-Anne Debily, Frédéric Fina, et al.
Neuro-Oncology Advances|September 5, 2024
Glioma oncogenesis in the Constitutional mismatch repair deficiency (CMMRD) syndromeLea Guerrini-Rousseau, Jane Merlevede, Philippe Denizeau, et al.
Journal of Neuropathology and Experimental Neurology|January 18, 2024
"Hemispheric pilocytic astrocytoma" revisited: A comprehensive clinicopathological and molecular series emphasizing their overlap with other glioneuronal tumorsCassandra Mariet, Jacques Grill, Yassine Ajlil, et al.
Plos One|June 16, 2017
Integrating Tenascin-C protein expression and 1q25 copy number status in pediatric intracranial ependymoma prognostication: A new model for risk stratificationFelipe Andreiuolo, Gwénaël Le Teuff, Mohamed Amine Bayar, et al.
Acta Neuropathologica|March 4, 2026
H3K27ME3 loss in diffuse midline gliomas lacking H3K27M or EZHIP expressions, a potential diagnostic pitfall!Arnault Tauziède-Espariat, David Castel, Yassine Ajlil, et al.
Acta Neuropathologica|December 8, 2023
A new subtype of diffuse midline glioma, H3 K27 and BRAF/FGFR1 co-altered: a clinico-radiological and histomolecular characterisationLucie Auffret, Yassine Ajlil, Arnault Tauziède-Espariat, et al.
Nature Genetics|April 8, 2014
Recurrent activating ACVR1 mutations in diffuse intrinsic pontine gliomaKathryn R Taylor, Alan Mackay, Nathalène Truffaux, et al.
Acta Neuropathologica Communications|November 3, 2020
The EP300:BCOR fusion extends the genetic alteration spectrum defining the new tumoral entity of "CNS tumors with BCOR internal tandem duplication"Arnault Tauziède-Espariat, Gaëlle Pierron, Aurore Siegfried, et al.
Pageof 10