Shishi Li
158 Shangtang Road
Hangzhou, 310014, China
Hangzhou, 310014, China
Last Updated: 09/26/2026
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Found 14 publications
Lactate metabolism and lactylation in female reproductive diseases: From metabolic rewiring to biomarkers and translational therapeutics.
Journal: Clinical and translational medicine
Published: March 11, 2026
Pla2g7 regulates bone homeostasis via Alox12/12-HETE/Gpr31 signaling axis.
Journal: Nature communications
Published: January 20, 2025
Methyl 3,4-dihydroxybenzoate alleviates oxidative damage in granulosa cells by activating Nrf2 antioxidant pathway.
Journal: Journal of ovarian research
Published: January 05, 2024
Novel MEI1 mutations cause chromosomal and DNA methylation abnormalities leading to embryonic arrest and implantation failure.
Journal: Molecular genetics and genomics : MGG
Published: October 07, 2023
Dual laser-assisted hatching: an effective technique to salvage low-grade cleavage-stage embryos and harvest day 7 blastocysts.
Journal: Lasers in medical science
Published: March 30, 2023
The Role of Peritoneal Immunity in Peritoneal Endometriosis and Related Infertility.
Journal: Frontiers in bioscience (Landmark edition)
Published: November 12, 2022
Iron overload in endometriosis peritoneal fluid induces early embryo ferroptosis mediated by HMOX1.
Journal: Cell death discovery
Published: July 22, 2021
Iron overload compromises preimplantation mouse embryo development.
Journal: Reproductive toxicology (Elmsford, N.Y.)
Published: May 01, 2021
Laser-assisted hatching in lower grade cleavage stage embryos improves blastocyst formation: results from a retrospective study.
Journal: Journal of ovarian research
Published: December 24, 2020
Mitochondrial Dysfunctions Contribute to Hypertrophic Cardiomyopathy in Patient iPSC-Derived Cardiomyocytes with MT-RNR2 Mutation.
Journal: Stem cell reports
Published: May 14, 2017
Mitochondrial Disease-Specific Induced Pluripotent Stem Cell Models: Generation and Characterization.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: February 04, 2015
The novel mitochondrial 16S rRNA 2336T>C mutation is associated with hypertrophic cardiomyopathy.
Journal: Journal of medical genetics
Published: December 25, 2013
Last Updated: 09/26/2026