https://www.selleckchem.com/pr....oducts/polyethylenim
ACC is extremely rare; it is difficult to observe a specific genetic pattern and NGS can provide a lot of information about the genetic causes of this disease. Our work shows that the MET p.Thr1010Ile mutation can be associated with the hereditary occurrence of ACC. The current study was designed to investigate the functionality of lncRNA CCHE1 in nasopharyngeal carcinoma. MiRNA levels of lncRNA CCHE1 were examined by RT-qPCR. CCK8 assay and colony formation assay were together performed to detect cell proliferation viability.
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