Results 191 to 200 of about 71,273 (273)

IDH mutations are rare events in SHH medulloblastoma. [PDF]

Acta Neuropathol
Fürst A, Ruf V, Fiedler C, Rutkowski S, Sill M, Korshunov A, Gerber NU, Frank S, Hench J, Schüller U.   +9 more
europepmc   +1 more source

MBCL-20. MGMT PROTEIN EXPRESSION AND MGMT GENE PROMOTER METHYLATION AS MARKERS OF DRUG SENSITIVITY TO EPIGENETIC THERAPY IN CHILDHOOD MEDULLOBLASTOMA [PDF]

, 2018
Andrey Levashov, Д. А. Хоченков, А. М. Строганова, Marina Ryzhova, Sergey Gorelyshev, Stepan Babelyan, Natalya Subbotina, Vidmante Daylidite, И. С. Долгополов, Svetlana R. Zagidullina, G. I. Seregin, Georgy Mentkevich   +11 more
openalex   +1 more source

Interrogating molecular data for medulloblastoma risk stratification [PDF]

, 2018
Ferretti, Elisabetta, Po, Agnese
core   +1 more source

Fractal-geometry analysis of pediatric posterior fossa tumors - a preoperative tool for prediction of histopathology. [PDF]

Neurosurg Rev
Mezei T, Báskay J, Markia B, Várallyay P, Banczerowski P, Pollner P.   +5 more
europepmc   +1 more source

Pattern of Relapse and Treatment Response in WNT-Activated Medulloblastoma

, 2019
Liana Nobre, Michal Zápotocký, Sara Khan, Kohei Fukuoka, Adriana Fonseca, David Sumerauer, Aleš Vícha, Wiesława Grajkowska, Joanna Trubicka, Kay Ka Wai Li, Ho‐Keung Ng, Luca Massimi, Ji Yeoun Lee, Seung‐Ki Kim, Shayna Zelcer, Alexandre Vasiljevic, Cecile Faure-Contre, Péter Hauser, Bolesław Lach, Marie‐Lise C. van Veelen, Pim J. French, Erwin G. Van Meir, William A. Weiss, Nalin Gupta, Ian F. Pollack, Ronald L. Hamilton, Amulya Nageswara Rao, Caterina Giannini, Joshua B. Rubin, Andrew S. Moore, Lola B. Chambless, Rajeev Vibhakar, Young Seob Shin, Maura Massimino, Roger E. MacLendon, Helen Wheeler, Massimo Zollo, Veronica Ferruci, Toshihiro Kumabe, Cláudia C. Faria, Jaroslav Štěrba, Shin Jung, Enrique López‐Aguilar, Jaume Mora, Carlos Gilberto Carlotti, James M. Olson, Sarah Leary, Jason E. Cain, Lenka Krsková, Josef Zámečnı́k, Cynthia Hawkins, Uri Tabori, Annie Huang, Ute Bartels, Paul A. Northcott, Michael D. Taylor, Jordan R. Hansford, Éric Bouffet, Vijay Ramaswamy   +58 more
openalex   +1 more source

A recurrent mosaic mutation in SMO, encoding the hedgehog signal transducer smoothened, is the major cause of Curry-Jones syndrome [PDF]

, 2016
et al,, Grange, Dorothy K
core   +1 more source

Abstracts

Cancer Science, Volume 117, Issue S1, Page 1-2148, January 2026.
wiley   +1 more source

Non-WNT/non-SHH medulloblastoma in siblings: case report and literature review. [PDF]

Discov Oncol
Huang M, Li J, Liu B, Liao Y, Wang B, Liu H, Liu Y, Zhao J.   +7 more
europepmc   +1 more source

Single-Cell Heterogeneity of Epigenetic Factor Regulation Deciphers Alteration of RNA Metabolism During Proliferative SHH-Medulloblastoma. [PDF]

Cancers (Basel)
Francés R, Bonifacio-Mundaca J, Casafont Í, Desterke C, Mata-Garrido J.   +4 more
europepmc   +1 more source

Author response: Jak2-mediated phosphorylation of Atoh1 is critical for medulloblastoma growth

, 2017
Tiemo J. Klisch, Anna Vainshtein, Akash J. Patel, Huda Y. Zoghbi   +3 more
openalex   +1 more source