Liu, H.-M.;                     Chang, Z.-Y.;                     Yang, C.-W.;                     Chang, H.-H.;                     Lee, T.-Y.    
        Farnesoid X Receptor Agonist GW4064 Protects Lipopolysaccharide-Induced Intestinal Epithelial Barrier Function and Colorectal Tumorigenesis Signaling through the αKlotho/βKlotho/FGFs Pathways in Mice. Int. J. Mol. Sci. 2023, 24, 16932.
    https://doi.org/10.3390/ijms242316932
    AMA Style
    
                                Liu H-M,                                 Chang Z-Y,                                 Yang C-W,                                 Chang H-H,                                 Lee T-Y.        
                Farnesoid X Receptor Agonist GW4064 Protects Lipopolysaccharide-Induced Intestinal Epithelial Barrier Function and Colorectal Tumorigenesis Signaling through the αKlotho/βKlotho/FGFs Pathways in Mice. International Journal of Molecular Sciences. 2023; 24(23):16932.
        https://doi.org/10.3390/ijms242316932
    
    Chicago/Turabian Style
    
                                Liu, Hsuan-Miao,                                 Zi-Yu Chang,                                 Ching-Wei Yang,                                 Hen-Hong Chang,                                 and Tzung-Yan Lee.        
                2023. "Farnesoid X Receptor Agonist GW4064 Protects Lipopolysaccharide-Induced Intestinal Epithelial Barrier Function and Colorectal Tumorigenesis Signaling through the αKlotho/βKlotho/FGFs Pathways in Mice" International Journal of Molecular Sciences 24, no. 23: 16932.
        https://doi.org/10.3390/ijms242316932
    
    APA Style
    
                                Liu, H.-M.,                                 Chang, Z.-Y.,                                 Yang, C.-W.,                                 Chang, H.-H.,                                 & Lee, T.-Y.        
        
        (2023). Farnesoid X Receptor Agonist GW4064 Protects Lipopolysaccharide-Induced Intestinal Epithelial Barrier Function and Colorectal Tumorigenesis Signaling through the αKlotho/βKlotho/FGFs Pathways in Mice. International Journal of Molecular Sciences, 24(23), 16932.
        https://doi.org/10.3390/ijms242316932