Peijun Li
Wenzhou, China
Last Updated: 09/26/2026
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Found 18 publications
GABA(A) Receptor Subunit (γ2, δ, β1-3) Variants in Genetic Epilepsy: A Comprehensive Summary of 206 Clinical Cases.
Journal: Journal of child neurology
Published: September 04, 2024
The de novo missense mutation F224S in GABRB2, identified in epileptic encephalopathy and developmental delay, impairs GABAAR function.
Journal: Neuroscience
Published: March 01, 2024
Clock knockout in inhibitory neurons reduces predisposition to epilepsy and influences anxiety-like behaviors in mice.
Journal: Neurobiology of disease
Published: October 23, 2023
FGF9 is required for Purkinje cell development and function in the cerebellum.
Journal: iScience
Published: September 19, 2023
Catalpol alleviates hypoxia ischemia-induced brain damage by inhibiting ferroptosis through the PI3K/NRF2/system Xc-/GPX4 axis in neonatal rats.
Journal: European journal of pharmacology
Published: July 18, 2023
Neonatal di-(2-ethylhexyl)phthalate exposure induces permanent alterations in secretory CRH neuron characteristics in the hypothalamus paraventricular region of adult male rats.
Journal: Experimental neurology
Published: May 11, 2023
microRNA profilings identify plasma biomarkers and targets associated with pediatric epilepsy patients.
Journal: Pediatric research
Published: March 22, 2023
11β-HSD1 participates in epileptogenesis and the associated cognitive impairment by inhibiting apoptosis in mice.
Journal: Journal of translational medicine
Published: June 15, 2022
Disrupted myelination network in the cingulate cortex of Parkinson's disease.
Journal: IET systems biology
Published: December 28, 2021
Last Updated: 09/26/2026