Lijie Gu
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
Publications
28
Citations
642
Est. group size
~4
Recurring co-author estimate
Active years
18
Publishing since 2009
Lijie Gu's research focuses on how the liver and metabolism are regulated at the molecular level, particularly involving bile acids (compounds made by the liver that help digest fats and also act as signaling molecules) and a protein degradation system called cullin-RING ligases. This work aims to understand and potentially treat conditions like cholestasis (impaired bile flow), fatty liver disease, insulin resistance, and obesity. An earlier line of work also examined microRNAs (small regulatory RNA molecules) in muscle biology, including muscle wasting and regeneration.
Publication output has been generally steady to slightly increasing over the last decade, with a shift from muscle biology topics (2017-2019) toward liver and metabolic disease research (2021-2025), and an average of about 3-4 papers per year in the last five years.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Adipose cullin 3 mediates the antiobesity effect of pan neddylation inhibitors
Proceedings of the National Academy of Sciences · 2025
- A Gly-β-muricholic acid and FGF15 combination therapy synergistically reduces “humanized” bile acid pool toxicity in cholestasis mice
Journal of Lipid Research · 2025
- Bile acids regulation of cellular stress responses in liver physiology and diseases
eGastroenterology · 2024
- Cullin 3 RING E3 ligase inactivation causes NRF2-dependent NADH reductive stress, hepatic lipodystrophy, and systemic insulin resistance
Proceedings of the National Academy of Sciences · 2024
- Gly-β-MCA is a potent anti-cholestasis agent against “human-like” hydrophobic bile acid-induced biliary injury in mice
Journal of Lipid Research · 2024
- Deletion of hepatocyte cysteine dioxygenase type 1, a bile acid repressed gene, enhances glutathione synthesis and ameliorates acetaminophen hepatotoxicity
Biochemical Pharmacology · 2024
- Combining ASBT inhibitor and FGF15 treatments enhances therapeutic efficacy against cholangiopathy in female but not male Cyp2c70 KO mice
Journal of Lipid Research · 2023
- EZH2 promotes angiogenesis in peritoneal dialysis by epigenetically activating SP4 expression in the IL-6/sIL-6R signalling pathway
International Journal of Medical Sciences · 2023
- Glycine-β-Muricholic Acid Improves Liver Fibrosis and Gut Barrier Function by Reducing Bile Acid Pool Size and Hydrophobicity in Male Cyp2c70 Knockout Mice
Cells · 2023
- Cullin neddylation inhibitor attenuates hyperglycemia by enhancing hepatic insulin signaling through insulin receptor substrate stabilization
Proceedings of the National Academy of Sciences · 2022
- Effects of apical sodium-bile acid transporter inhibitor and obeticholic acid co-treatment in experimental non-alcoholic steatohepatitis
Liver Research · 2022
- Pharmacological Inhibition of Cullin Neddylation Improves Hepatic Insulin Sensitivity
The FASEB Journal · 2022
- Combined ASBT Inhibitor and FGF15 Treatment Improves Therapeutic Efficacy in Experimental Nonalcoholic Steatohepatitis
Cellular and Molecular Gastroenterology and Hepatology · 2021
- MiR-29ab1 Cluster Resists Muscle Atrophy Through Inhibiting MuRF1
DNA and Cell Biology · 2021
- miR-29a/b1 Inhibits Hair Follicle Stem Cell Lineage Progression by Spatiotemporally Suppressing WNT and BMP Signaling
Cell Reports · 2019
- Proceedings of the National Academy of Sciences×3
- Journal of Lipid Research×3
- Cell Reports×2
- Cells×2
- The FASEB Journal×2
- Nicolas Wein
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- K. Flanigan
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- E. Frair
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Liubov V. Gushchina
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Scott Q. Harper
Biochemistry, Genetics and Molecular Biology · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 20, 2026.
Claim or correct this profile