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MEK/MELK inhibition and blood–brain barrier deficiencies in atypical teratoid/rhabdoid tumors
BACKGROUND: Atypical teratoid/rhabdoid tumors (AT/RT) are rare, but highly aggressive. These entities are of embryonal origin occurring in the central nervous system (CNS) of young children. Molecularly these tumors are driven by a single hallmark mutation, resulting in inactivation of SMARCB1 or SM...
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| Publicat a: | Neuro Oncol |
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| Autors principals: | , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6954444/ https://ncbi.nlm.nih.gov/pubmed/31504799 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noz151 |
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