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Suppression of Cholesterol 7a-Hydroxylase Transcription and Bile Acid Synthesis by an a1-Antitrypsin Peptide via Interaction with a1-Fetoprotein Transcription Factor


Suppression of Cholesterol 7a-Hydroxylase Transcription and Bile Acid Synthesis by an a1-Antitrypsin Peptide via Interaction with a1-Fetoprotein Transcription Factor



The Journal of Biological Chemistry 277(45): 973-80




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Related references

Suppression of cholesterol 7alpha-hydroxylase transcription and bile acid synthesis by an alpha1-antitrypsin peptide via interaction with alpha1-fetoprotein transcription factor. Journal of Biological Chemistry 277(45): 42973-42980, 2002

A1-fetoprotein transcription factor is required for the expression of sterol 12a-hydroxylase, the specific enzyme for cholic acid synthesis. Potential role in the bile acid-mediated regulation of gene transcription. The Journal of Biological Chemistry 275(23): 793-9, 2000

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The negative effects of bile acids and tumor necrosis factor-alpha on the transcription of cholesterol 7alpha-hydroxylase gene (CYP7A1) converge to hepatic nuclear factor-4: a novel mechanism of feedback regulation of bile acid synthesis mediated by nuclear receptors. Journal of Biological Chemistry 276(33): 30708-30716, 2001

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The Role of a 1-Fetoprotein Transcription Factor/LRH-1 in Bile Acid Biosynthesis. A Known Nuclear Receptor Activator that can Act as a Suppressor of Bile Acid Biosynthesis. The Journal of Biological Chemistry 279(16): 813-21, 2004

Bile acids exert negative feedback control on bile acid synthesis in cultured pig hepatocytes by suppression of cholesterol 7 alpha-hydroxylase activity. Hepatology 12(5): 1209-1215, 1990