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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Mol Oncol
Päätekijät: He, Tian, Wildey, Gary, McColl, Karen, Savadelis, Alyssa, Spainhower, Kyle, McColl, Cassidy, Kresak, Adam, Tan, Aik Choon, Yang, Michael, Abbas, Ata, Dowlati, Afshin
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: John Wiley and Sons Inc. 2020
Aiheet:
Linkit: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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