Qinghong X. Li
Groningen, GR, Netherlands
Last Updated: 09/26/2026
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Found 9 publications
A Molecular Mechanism of Intrahepatic Cholestasis in Osteo-Oto-Hepato-Enteric Syndrome.
Journal: Cellular and molecular gastroenterology and hepatology
Published: February 10, 2026
Uncovering the Relationship Between Genes and Phenotypes Beyond the Gut in Microvillus Inclusion Disease.
Journal: Cellular and molecular gastroenterology and hepatology
Published: June 02, 2023
A Functional Relationship Between UNC45A and MYO5B Connects Two Rare Diseases With Shared Enteropathy.
Journal: Cellular and molecular gastroenterology and hepatology
Published: December 23, 2021
Letter to the Editor: Liver Cell Models for Premature Termination Codon Readthrough Analyses.
Journal: Hepatology (Baltimore, Md.)
Published: December 14, 2020
Congenital microvillus inclusion disease in a child
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: October 29, 2020
Unequal Effects of Myosin 5B Mutations in Liver and Intestine Determine the Clinical Presentation of Low-Gamma-Glutamyltransferase Cholestasis.
Journal: Hepatology (Baltimore, Md.)
Published: January 15, 2020
Loss of MYO5B expression deregulates late endosome size which hinders mitotic spindle orientation.
Journal: PLoS biology
Published: June 25, 2019
A Molecular Mechanism Underlying Genotype-Specific Intrahepatic Cholestasis Resulting From MYO5B Mutations.
Journal: Hepatology (Baltimore, Md.)
Published: April 15, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026