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Identification of RUNX1T1 as a potential epigenetic modifier in small‐cell lung cancer
Small‐cell lung cancer (SCLC) can be subgrouped into common ‘pure’ and rare ‘combined’ SCLC (c‐SCLC). c‐SCLC features a mixed tumor histology of both SCLC and non–small‐cell lung cancer (NSCLC). We performed targeted exome sequencing on 90 patients with SCLC, including two with c‐SCLC, and discovere...
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| Publicado no: | Mol Oncol |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7782087/ https://ncbi.nlm.nih.gov/pubmed/33084222 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/1878-0261.12829 |
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