Identification of therapeutic targets in chordoma through comprehensive genomic and transcriptomic analyses

Chordoma is a rare, orphan cancer arising from embryonal precursors of bone. Surgery and radiotherapy (RT) provide excellent local control, often at the price of significant morbidity because of the structures involved and the need for relatively high doses of RT; however, recurrence remains high. A...

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Detalles Bibliográficos
Autores principales: Liang, Winnie S., Dardis, Christopher, Helland, Adrienne, Sekar, Shobana, Adkins, Jonathan, Cuyugan, Lori, Enriquez, Daniel, Byron, Sara, Little, Andrew S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2018
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318766/
https://www.ncbi.nlm.nih.gov/pubmed/30322893
http://dx.doi.org/10.1101/mcs.a003418

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318766/
https://www.ncbi.nlm.nih.gov/pubmed/30322893
http://dx.doi.org/10.1101/mcs.a003418

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