This study was stopped early due to the frequency and magnitude of the elevation in ALT in the treatment group relative to controls, although none of the participants expressed symptoms of liver disease
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Pharmacol.,38MAPK, and SAPK/JNK activation
After combining the amounts measured for the known FXR-antagonistic BAs, we also showed that the percentage of T(/)MCA, (T/G)UDCA, and (T)HDCA in the gallbladder bile was significantly increased in MMI + T3-5d mice compared to MMI mice (Fig