Chai, Y., Lee, H., Shaik, A. A., Nkhata, K., Xing, C., Zhang, J., . . . Lü, J. (2010). Penta-O-galloyl-β-D-glucose induces G(1 )arrest and DNA replicative S-phase arrest independently of P21 cyclin-dependent kinase inhibitor 1A, P27 cyclin-dependent kinase inhibitor 1B and P53 in human breast cancer cells and is orally active against triple-negative xenograft growth. BioMed Central.
Citação norma ChicagoChai, Yubo, Hyo-Jeong Lee, Ahmad Ali Shaik, Katai Nkhata, Chengguo Xing, Jinhui Zhang, Soo-Jin Jeong, Sung-Hoon Kim, and Junxuan Lü. Penta-O-galloyl-β-D-glucose Induces G(1 )arrest and DNA Replicative S-phase Arrest Independently of P21 Cyclin-dependent Kinase Inhibitor 1A, P27 Cyclin-dependent Kinase Inhibitor 1B and P53 in Human Breast Cancer Cells and Is Orally Active against Triple-negative Xenograft Growth. BioMed Central, 2010.
MLA CitationChai, Yubo, et al. Penta-O-galloyl-β-D-glucose Induces G(1 )arrest and DNA Replicative S-phase Arrest Independently of P21 Cyclin-dependent Kinase Inhibitor 1A, P27 Cyclin-dependent Kinase Inhibitor 1B and P53 in Human Breast Cancer Cells and Is Orally Active against Triple-negative Xenograft Growth. BioMed Central, 2010.