XIN TONG

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University of Michigan

United States

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Role and Mechanisms of E4BP4 over-activation in diet-induced fatty liver disease

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Articles (8)

Year:

2025

Year:

2024

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2023

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2021

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2021

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2020

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2020

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2020

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chunaram choudhary

Professor

University of Copenhagen

DENMARK

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XIN TONG

Research Interests

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Recent Grants

Articles (8)

The Non‐Canonical ChREBPα Activity Suppresses the Activation of Hepatic Stellate Cells and Liver Fibrosis by Antagonizing TGF‐β‐E2F1 Axis

OPN‐Mediated Crosstalk Between Hepatocyte E4BP4 and Hepatic Stellate Cells Promotes MASH‐Associated Liver Fibrosis

Fructose as a novel nutraceutical for acetaminophen (APAP)-induced hepatotoxicity

Fructose Protects Against Acetaminophen‐Induced Hepatotoxicity Mainly by Activating the Carbohydrate‐Response Element‐Binding Protein α–Fibroblast Growth Factor 21 Axis in Mice

Hepatic metabolic regulation by nuclear factor E4BP4.

Histone Acetyltransferase MOF Blocks Acquisition of Quiescence in Ground-State ESCs through Activating Fatty Acid Oxidation.

Hepatic E4BP4 induction promotes lipid accumulation by suppressing AMPK signaling in response to chemical or diet‐induced ER stress

DDB1 E3 ligase controls dietary fructose-induced ChREBPα stabilization and liver steatosis via CRY1

Collaborators (1)

chunaram choudhary

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