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A kinase-deficient NTRK2 splice variant predominates in glioma and amplifies several oncogenic signaling pathways
Independent scientific achievements have led to the discovery of aberrant splicing patterns in oncogenesis, while more recent advances have uncovered novel gene fusions involving neurotrophic tyrosine receptor kinases (NTRKs) in gliomas. The exploration of NTRK splice variants in normal and neoplast...
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| Veröffentlicht in: | Nat Commun |
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| Hauptverfasser: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Nature Publishing Group UK
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7293284/ https://ncbi.nlm.nih.gov/pubmed/32532995 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-020-16786-5 |
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