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Activating Death Receptor DR5 as a Therapeutic Strategy for Rhabdomyosarcoma

Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children. It is believed to arise from skeletal muscle progenitors, preserving the expression of genes critical for embryonic myogenic development such as MYOD1 and myogenin. RMS is classified as embryonal, which is more common in youn...

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Detalles Bibliográficos
Autores principales: Kang, Zhigang, Sun, Shi-Yong, Cao, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3345273/
https://www.ncbi.nlm.nih.gov/pubmed/22577581
http://dx.doi.org/10.5402/2012/395952