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Li Peng

Researcher at University of Texas Southwestern Medical Center

Publications -  10
Citations -  3738

Li Peng is an academic researcher from University of Texas Southwestern Medical Center. The author has contributed to research in topics: Pregnane X receptor & Constitutive androstane receptor. The author has an hindex of 9, co-authored 10 publications receiving 3323 citations.

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Fibroblast growth factor 15 functions as an enterohepatic signal to regulate bile acid homeostasis

TL;DR: It is demonstrated that fibroblast growth factor 15 signals from intestine to liver to repress the gene encoding cholesterol 7alpha-hydroxylase (CYP7A1), which catalyzes the first and rate-limiting step in the classical bile acid synthetic pathway.
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Regulation of antibacterial defense in the small intestine by the nuclear bile acid receptor.

TL;DR: Findings reveal a central role for FXR in protecting the distal small intestine from bacterial invasion and suggest that FXR agonists may prevent epithelial deterioration and bacterial translocation in patients with impaired bile flow.
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Orphan Nuclear Receptor LRH-1 Is Required To Maintain Oct4 Expression at the Epiblast Stage of Embryonic Development

TL;DR: In vitro and in vivo results show that LRH-1 plays an essential role in the maintenance of Oct4 expression in ES cells at the epiblast stage of embryonic development, thereby maintaining pluripotence at this crucial developmental stage prior to segregation of the primordial germ cell lineage at gastrulation.
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Identification of a hormonal basis for gallbladder filling

TL;DR: It is demonstrated that fibroblast growth factor-15, a hormone made by the distal small intestine in response to bile acids, is required for gallbladder filling and suggested that a postprandial timing mechanism that controls gallbladders motility is suggested.
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Structural disorder in the complex of human pregnane x receptor and the macrolide antibiotic rifampicin

TL;DR: Results indicate that one wall of the PXR ligand-binding cavity can remain flexible even when the receptor is in complex with an activating ligand, highlighting the key role that structural flexibility plays in PxR's promiscuous response to xenobiotics.