Junli Yang

Yantai, 264100, China

Last Updated: 09/26/2026

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Found 8 publications

Sugiol Alleviates Cerebral Ischemia/Reperfusion Injury in the Early Phase Involving the LRRK2/NF-κB Pathway.

Sugiol Alleviates Cerebral Ischemia/Reperfusion Injury in the Early Phase Involving the LRRK2/NF-κB Pathway.

Journal: Cell biochemistry and biophysics

Published: April 13, 2026

PRC1 as an independent adverse prognostic factor in Wilms tumor via integrated bioinformatics and experimental validation.

PRC1 as an independent adverse prognostic factor in Wilms tumor via integrated bioinformatics and experimental validation.

Journal: Scientific reports

Published: December 16, 2024

YTHDF1 gene inhibits epilepsy progression by epigenetic activation of PTEN gene.

YTHDF1 gene inhibits epilepsy progression by epigenetic activation of PTEN gene.

Journal: Heliyon

Published: July 08, 2024

Neuroprotective effects of quinpirole on lithium chloride pilocarpine-induced epilepsy in rats and its underlying mechanisms.

Neuroprotective effects of quinpirole on lithium chloride pilocarpine-induced epilepsy in rats and its underlying mechanisms.

Journal: European journal of medical research

Published: December 18, 2023

Hemophagocytic lymphohistiocytosis in a neonate with neck skin abscess and thrombocytopenia.

Hemophagocytic lymphohistiocytosis in a neonate with neck skin abscess and thrombocytopenia.

Journal: Pediatrics and neonatology

Published: June 07, 2023

Clinical Feature, Treatment, and KCNH5 Mutations in Epilepsy.

Clinical Feature, Treatment, and KCNH5 Mutations in Epilepsy.

Journal: Frontiers in pediatrics

Published: January 19, 2022

Novel and de novo point and large microdeletion mutation in PRRT2-related epilepsy.

Novel and de novo point and large microdeletion mutation in PRRT2-related epilepsy.

Journal: Brain and behavior

Published: December 05, 2019

A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.

A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.

Journal: Molecular genetics & genomic medicine

Published: January 03, 2018

Showing 1-8 of 8

Last Updated: 09/26/2026