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Chinese Journal of Cancer ; (12): 442-449, 2011.
Artigo em Inglês | WPRIM | ID: wpr-294502

RESUMO

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.


Assuntos
Animais , Humanos , Camundongos , Neoplasias Cerebelares , Genética , Metabolismo , Patologia , Modelos Animais de Doenças , Engenharia Genética , Proteínas Hedgehog , Metabolismo , Meduloblastoma , Genética , Metabolismo , Patologia , Camundongos Transgênicos , Mutação , Receptores Patched , Interferência de RNA , RNA Interferente Pequeno , Genética , Receptores de Superfície Celular , Genética , Metabolismo , Receptores Acoplados a Proteínas G , Metabolismo , Transdução de Sinais , Receptor Smoothened , Proteína Supressora de Tumor p53 , Genética , Metabolismo
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