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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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Détails bibliographiques
Auteurs principaux: Kang, Zhigang, Sun, Shi-Yong, Cao, Liang
Format: Artigo
Langue:Inglês
Publié: International Scholarly Research Network 2012
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3345273/
https://ncbi.nlm.nih.gov/pubmed/22577581
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5402/2012/395952
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