Showing results (111-120 of 247) with videos related to
Sort By:
Pageof 25
Clinical Epigenetics|August 15, 2019
DNA methylation signature is prognostic of choroid plexus tumor aggressivenessMalgorzata Pienkowska, Sanaa Choufani, Andrei L Turinsky, et al.Clinical Epigenetics|October 23, 2019
Correction to: DNA methylation signature is prognostic of choroid plexus tumor aggressivenessMalgorzata Pienkowska, Sanaa Choufani, Andrei L Turinsky, et al.The Journal of Allergy and Clinical Immunology|July 30, 2015
An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiationTangui Le Guen, Fabien Touzot, Isabelle André-Schmutz, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|November 14, 2014
The role of resection alone in select children with intracranial ependymoma: the Canadian Pediatric Brain Tumour Consortium experienceTamir Ailon, Christopher Dunham, Anne-Sophie Carret, et al.Genome Biology|December 9, 2023
Pediatric glioma histone H3.3 K27M/G34R mutations drive abnormalities in PML nuclear bodiesHsiao P J Voon, Linda Hii, Andrew Garvie, et al.Neuro-Oncology|August 1, 2023
Phase I trial of panobinostat in children with diffuse intrinsic pontine glioma: A report from the Pediatric Brain Tumor Consortium (PBTC-047)Michelle Monje, Tabitha Cooney, John Glod, et al.The EMBO Journal|November 1, 2025
Concurrence of FGFR1 mutations modulates oncogenesis in glioneuronal tumorsJacopo Boni, Míriam Fernández-González, HyeRim Han, et al.Journal of Neuro-Oncology|July 8, 2020
Pontine gliomas a 10-year population-based study: a report from The Canadian Paediatric Brain Tumour Consortium (CPBTC)Adriana Fonseca, Samina Afzal, Lynette Bowes, et al.Cancer|January 15, 2015
EZH2 expression is a prognostic factor in childhood intracranial ependymoma: a Canadian Pediatric Brain Tumor Consortium studyAmanda M Li, Christopher Dunham, Uri Tabori, et al.Journal of Medical Genetics|March 9, 2021
De novo <i>TRPV4</i> Leu619Pro variant causes a new channelopathy characterised by giant cell lesions of the jaws and skull, skeletal abnormalities and polyneuropathyAviel Ragamin, Carolina C Gomes, Karen Bindels-de Heus, et al.Pageof 25