Yantao Bao
Shenzhen, 518040, China
Last Updated: 09/26/2026
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Found 10 publications
NAALAD2 mutations disrupt the fate of photoreceptor cells and retinal pigment epithelial cells during early retinal development.
Journal: Pharmacological research
Published: December 14, 2024
Deficiency in the conserved ECHS1 gene causes Leigh syndrome by impairing mitochondrial respiration efficiency and suppressing ADRB2-PKA signaling.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: September 10, 2024
Increased HA/CD44/TGFβ signaling implicates in renal fibrosis of a Col4a5 mutant Alport mice.
Journal: Molecular medicine (Cambridge, Mass.)
Published: August 21, 2024
Genetic epidemiology of thalassemia in couples of childbearing age: over 6 years of a thalassemia intervention project.
Journal: Molecular biology reports
Published: September 11, 2023
SETD2-mediated H3K14 trimethylation promotes ATR activation and stalled replication fork restart in response to DNA replication stress.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 02, 2021
UNG2 deacetylation confers cancer cell resistance to hydrogen peroxide-induced cytotoxicity.
Journal: Free radical biology & medicine
Published: May 10, 2020
A specific assay for JmjC domain-containing lysine demethylase and its application to inhibitor screening.
Journal: Science China. Life sciences
Published: April 20, 2019
GLP-catalyzed H4K16me1 promotes 53BP1 recruitment to permit DNA damage repair and cell survival.
Journal: Nucleic acids research
Published: March 20, 2019
p53 cooperates with SIRT6 to regulate cardiolipin de novo biosynthesis.
Journal: Cell death & disease
Published: April 13, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026