Yuda Wei
Linyi, China
Last Updated: 09/26/2026
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Found 18 publications
Selenoprotein H Functions as a PPARα Coactivator to Link Selenium Homeostasis to Hepatic Lipid Metabolism and Protect against Steatohepatitis.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: October 03, 2025
Biallelic GSPT1 variants are associated with a syndromic neurodevelopmental disorder characterized by intellectual disability and microcephaly.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: May 23, 2025
Deleterious, protein-altering variants in GSPT2 are putatively associated with an X-linked neurodevelopmental disorder with intellectual disability, language impairment, autism, and epilepsy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 09, 2025
Two Nonsense GLI3 Variants Are Identified in Two Chinese Families With Polydactyly.
Journal: Molecular genetics & genomic medicine
Published: September 20, 2024
Targeting NECTIN-1 Based on CRISPR/Cas9 System Attenuated the Herpes Simplex Virus Infection in Human Corneal Epithelial Cells In Vitro.
Journal: Translational vision science & technology
Published: February 04, 2022
Acute liver steatosis translationally controls the epigenetic regulator MIER1 to promote liver regeneration in a study with male mice.
Journal: Nature communications
Published: February 02, 2022
In Situ Saturating Mutagenesis Screening Identifies a Functional Genomic Locus that Regulates Ucp1 Expression.
Journal: Phenomics (Cham, Switzerland)
Published: August 19, 2020
Glyburide Regulates UCP1 Expression in Adipocytes Independent of KATP Channel Blockade.
Journal: iScience
Published: April 23, 2020
Last Updated: 09/26/2026