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Mouse models of medulloblastoma

Medulloblastoma is the most common malignant pediatric brain tumor. Despite its prevalence and importance in pediatric neuro-oncology, the genes and pathways responsible for its initiation, maintenance, and progression remain poorly understood. Genetically engineered mouse models are an essential to...

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Detalles Bibliográficos
Autores principales: Wu, Xiaochong, Northcott, Paul A., Croul, Sidney, Taylor, Michael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sun Yat-sen University Cancer Center 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013419/
https://www.ncbi.nlm.nih.gov/pubmed/21718590
http://dx.doi.org/10.5732/cjc.011.10040
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author Wu, Xiaochong
Northcott, Paul A.
Croul, Sidney
Taylor, Michael D.
author_facet Wu, Xiaochong
Northcott, Paul A.
Croul, Sidney
Taylor, Michael D.
author_sort Wu, Xiaochong
collection PubMed
description Medulloblastoma is the most common malignant pediatric brain tumor. Despite its prevalence and importance in pediatric neuro-oncology, the genes and pathways responsible for its initiation, maintenance, and progression remain poorly understood. Genetically engineered mouse models are an essential tool for uncovering the molecular and cellular basis of human diseases, including cancer, and serve a valuable role as preclinical models for testing targeted therapies. In this review, we summarize how such models have been successfully applied to the study of medulloblastoma over the past decade and what we might expect in the coming years.
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spelling pubmed-40134192014-05-15 Mouse models of medulloblastoma Wu, Xiaochong Northcott, Paul A. Croul, Sidney Taylor, Michael D. Chin J Cancer Review Medulloblastoma is the most common malignant pediatric brain tumor. Despite its prevalence and importance in pediatric neuro-oncology, the genes and pathways responsible for its initiation, maintenance, and progression remain poorly understood. Genetically engineered mouse models are an essential tool for uncovering the molecular and cellular basis of human diseases, including cancer, and serve a valuable role as preclinical models for testing targeted therapies. In this review, we summarize how such models have been successfully applied to the study of medulloblastoma over the past decade and what we might expect in the coming years. Sun Yat-sen University Cancer Center 2011-07 /pmc/articles/PMC4013419/ /pubmed/21718590 http://dx.doi.org/10.5732/cjc.011.10040 Text en Chinese Journal of Cancer http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Review
Wu, Xiaochong
Northcott, Paul A.
Croul, Sidney
Taylor, Michael D.
Mouse models of medulloblastoma
title Mouse models of medulloblastoma
title_full Mouse models of medulloblastoma
title_fullStr Mouse models of medulloblastoma
title_full_unstemmed Mouse models of medulloblastoma
title_short Mouse models of medulloblastoma
title_sort mouse models of medulloblastoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013419/
https://www.ncbi.nlm.nih.gov/pubmed/21718590
http://dx.doi.org/10.5732/cjc.011.10040
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