Liming Wang

发表

Targeting HMGB1-NFκb Axis and miR-21 by Glycyrrhizin: Role in Amelioration of Corneal Injury in a Mouse Model of Alkali Burn

Xi Chen, Peng Hao, Xuan Li, 2022, Frontiers in Pharmacology.

Blockade of extracellular high-mobility group box 1 attenuates inflammation-mediated damage and haze grade in mice with corneal wounds.

Peng Hao, Xuan Li, Yongying Zhou, 2020, International immunopharmacology.

Nepetin inhibits IL-1β induced inflammation via NF-κB and MAPKs signaling pathways in ARPE-19 cells.

Dexin Kong, Xi Chen, Meihua Jin, 2018, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

The Potential Inhibitory Effects of miR-19b on Ocular Inflammation are Mediated Upstream of the JAK/STAT Pathway in a Murine Model of Allergic Conjunctivitis

Peng Hao, Xuan Li, Chen Guo, 2020, Investigative ophthalmology & visual science.

Upregulation of microRNA-17-5p contributes to hypoxia-induced proliferation in human pulmonary artery smooth muscle cells through modulation of p21 and PTEN

Peng Hao, Xuan Li, M. Ying, 2018, Respiratory Research.

ACE2 Expression Is Upregulated in Inflammatory Corneal Epithelial Cells and Attenuated by Resveratrol

Xi Chen, Zhi-xin Jiang, Peng Hao, 2021, Investigative ophthalmology & visual science.

Novel variants identified in a three‑generation family with concomitant exotropia

Jiaxun Li, Xuefeng Shi, Liming Wang, 2022, Experimental and therapeutic medicine.

GPR143 Gene Mutations in Five Chinese Families with X-linked Congenital Nystagmus

M. Ying, Rui-fang Han, Liming Wang, 2015, Scientific Reports.

Two Novel NYX Gene Mutations in the Chinese Families with X-linked Congenital Stationary Night Blindness

Peng Hao, M. Ying, Rui-fang Han, 2015, Scientific Reports.

The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes.

Jianqiu Xiao, R. Gbadegesin, E. Davis, 2018, Journal of the American Society of Nephrology : JASN.

Assessment of p16 expression and HPV infection in adenoid cystic carcinoma of the lacrimal gland

Yuan Tian, Peng Hao, Xuan Li, 2018, Molecular vision.

Five novel mutations of the FRMD7 gene in Chinese families with X-linked infantile nystagmus

Kanxing Zhao, J. Hejtmancik, Liming Wang, 2008, Molecular vision.

MicroRNA-34a inhibits epithelial-mesenchymal transition of lens epithelial cells by targeting Notch1.

Peng Hao, Xuan Li, Xin Tang, 2019, Experimental eye research.

Paracrine effects of mesenchymal stem cells on the activation of keratocytes

Weiyi Wang, Fang Li, Peng Hao, 2017, British Journal of Ophthalmology.

A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.

N. Katsanis, A. Shaw, Edwin C. T. Oh, 2015, Journal of the American Society of Nephrology : JASN.

Novel deletion in the pre‐mRNA splicing gene PRPF31 causes autosomal dominant retinitis pigmentosa in a large Chinese family

Qiuyun Chen, Kanxing Zhao, Lejin Wang, 2003, American journal of medical genetics. Part A.

Inherited KIF21A and PAX6 gene mutations in a boy with congenital Fibrosis of extraocular muscles and aniridia

Peng Hao, M. Ying, Rui-fang Han, 2013, BMC Medical Genetics.

A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS

G. Cavalleri, F. Hildebrandt, V. Vega-Warner, 2021, Journal of the American Society of Nephrology : JASN.

Investigation of the gene mutations in two Chinese families with X-linked infantile nystagmus

Kanxing Zhao, M. Ying, Rui-fang Han, 2011, Molecular vision.

Progressive hemifacial atrophy with characteristic ocular manifestations in a Chinese patient with a CRB1 mutation

Y. Liu, Peng Hao, Xuan Li, 2020, The Journal of international medical research.

Identification of the forkhead transcriptional factor 2 (FOXL2) gene mutations in four Chinese families with blepharophimosis syndrome

Hao Peng, M. Ying, Liming Wang, 2013, Molecular vision.

Expression of Peroxiredoxin 2 and Vascular Endothelial Growth Factor Receptor 2 in Pterygium

Peng Hao, Xuan Li, Luxia Chen, 2017, Cornea.

MicroRNA-146a negatively regulates inflammation via the IRAK1/TRAF6/NF-κB signaling pathway in dry eye

X. Chen, Peng Hao, Xuan Li, 2023, Scientific reports.

A novel mutation of RPGR gene in an X-linked Chinese family with retinitis pigmentosa.

Lili Zhang, Liming Wang, S. Dai, 2011, Molecular genetics and metabolism.

A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.

N. Katsanis, A. Shaw, Edwin C. T. Oh, 2015, Journal of the American Society of Nephrology : JASN.

Five novel mutations of the FRMD7 gene in Chinese families with X-linked infantile nystagmus

Kanxing Zhao, J. Hejtmancik, Liming Wang, 2008, Molecular vision.