Cite
MRSA-induced endothelial permeability and acute lung injury are attenuated by FTY720 S-phosphonate.
MLA
Lichun Wang, et al. “MRSA-Induced Endothelial Permeability and Acute Lung Injury Are Attenuated by FTY720 S-Phosphonate.” American Journal of Physiology: Lung Cellular & Molecular Physiology, vol. 322, no. 1, Jan. 2022, pp. L149–61. EBSCOhost, https://doi.org/10.1152/ajplung.00100.2021.
APA
Lichun Wang, Letsiou, E., Huashan Wang, Belvitch, P., Meliton, L. N., Brown, M. E., Bandela, M., Jiwang Chen, Garcia, J. G. N., & Dudek, S. M. (2022). MRSA-induced endothelial permeability and acute lung injury are attenuated by FTY720 S-phosphonate. American Journal of Physiology: Lung Cellular & Molecular Physiology, 322(1), L149–L161. https://doi.org/10.1152/ajplung.00100.2021
Chicago
Lichun Wang, Eleftheria Letsiou, Huashan Wang, Patrick Belvitch, Lucille N. Meliton, Mary E. Brown, Mounica Bandela, Jiwang Chen, Joe G. N. Garcia, and Steven M. Dudek. 2022. “MRSA-Induced Endothelial Permeability and Acute Lung Injury Are Attenuated by FTY720 S-Phosphonate.” American Journal of Physiology: Lung Cellular & Molecular Physiology 322 (1): L149–61. doi:10.1152/ajplung.00100.2021.