Juhua Yang

发表

VarfromPDB: An Automated and Integrated Tool to Mine Disease-Gene-Variant Relations from the Public Databases and Literature

Lei Wang, Zongfu Cao, Yilu Chen, 2017 .

Identification of miRNAs associated with tumorigenesis of retinoblastoma by miRNA microarray analysis

J. Cheng, Juhua Yang, Jianhua Xu, 2008, Child's Nervous System.

Analysis of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature

Juhua Yang, Xu Ma, Yihua Zhu, 2010, Molecular vision.

The recombinant anti-TNF-α fusion protein ameliorates rheumatoid arthritis by the protective role of autophagy

R. Liu, Juhua Yang, Zhiwei Liu, 2020, Bioscience reports.

Novel mutations in CRB1 gene identified in a chinese pedigree with retinitis pigmentosa by targeted capture and next generation sequencing

Juhua Yang, Xizhen Wang, Xuyang Liu, 2016, Oncotarget.

Renoprotective Effect of the Recombinant Anti-IL-6R Fusion Proteins by Inhibiting JAK2/STAT3 Signaling Pathway in Diabetic Nephropathy

R. Liu, Juhua Yang, Juan Lin, 2021, Frontiers in Pharmacology.

A novel mutation impairing the tertiary structure and stability of γC‐crystallin (CRYGC) leads to cataract formation in humans and zebrafish lens

P. Li, Juhua Yang, Yong-Bin Yan, 2012, Human mutation.

Mutation screening of crystallin genes in Chinese families with congenital cataracts

Zongfu Cao, Juhua Yang, Lijuan Liu, 2019, Molecular vision.

The therapeutic effect of a novel anti-TNF-α/IL-6R triple-specific fusion protein under experimental septic condition

Juhua Yang, Xiaole Chen, He Wang, 2021 .

A novel de novo duplication mutation of PAX6 in a Chinese family with aniridia and other ocular abnormalities

Juhua Yang, Kanxing Zhao, Yihua Zhu, 2014, Scientific Reports.

No Association of Pri-miR-143 rs41291957 Polymorphism with the Risk of Congenital Heart Disease in a Chinese Population

Juhua Yang, Xu Ma, Guican Zhang, 2014, Pediatric Cardiology.

Overexpression of AQP5 Was Detected in Axillary Sweat Glands of Primary Focal Hyperhidrosis Patients

Juhua Yang, Jian-Feng Chen, Y. Tu, 2016, Dermatology.

Identification of candidate cancer genes involved in human retinoblastoma by data mining

Wei Xiong, W. Xiong, Juhua Yang, 2008, Child's Nervous System.

Novel mutations in HSF4 cause congenital cataracts in Chinese families

Zongfu Cao, Juhua Yang, Lijuan Liu, 2018, BMC Medical Genetics.

Mitochondrial quality control protects photoreceptors against oxidative stress in the H2O2-induced models of retinal degeneration diseases

Juhua Yang, Yihua Zhu, Xiaole Chen, 2021, Cell Death & Disease.

No association of functional variant in pri-miR-218 and risk of congenital heart disease in a Chinese population.

Xiaozhong Peng, Juhua Yang, Xu Ma, 2013, Gene.

A novel frameshift mutation in FRMD7 causing X-linked idiopathic congenital nystagmus.

Feng Gu, Juhua Yang, Xu Ma, 2008, Genetic testing.

Identifcation of a Novel Mutation p.I240T in the FRMD7 gene in a Family with Congenital Nystagmus

Feng Gu, Z. Wang, Juhua Yang, 2013, Scientific Reports.

A Dual Target-Directed Single Domain-Based Fusion Protein Against Interleukin-6 Receptor Decelerate Experimental Arthritis Progression Via Modulating JNK Expression

Juhua Yang, Xiaole Chen, Ningning Zheng, 2021, Inflammation.

A recognition survey of granular corneal dystrophy type 2 genetic detection in China.

Juhua Yang, He Wang, Qingmei Zheng, 2020, International journal of ophthalmology.

Novel A14841G mutation is associated with high penetrance of LHON/C4171A family.

Juhua Yang, Xu Ma, Yihua Zhu, 2009, Biochemical and biophysical research communications.

Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation.

Juhua Yang, Lijuan Liu, Xu Ma, 2009, Biochemical and biophysical research communications.

Protective Effects of Nicotinamide Riboside on H2O2-induced Oxidative Damage in Lens Epithelial Cells

Juhua Yang, Yihua Zhu, Xiaole Chen, 2020, Current eye research.

A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract

Zongfu Cao, Feng Gu, Juhua Yang, 2008, Molecular vision.

A recurrent G367R mutation in MYOC associated with juvenile open angle glaucoma in a large Chinese family.

Juhua Yang, Yi-hua Yao, Yi-hua Zhu, 2018, International journal of ophthalmology.

Structure‒function‒pathogenicity analysis of C-terminal myocilin missense variants based on experiments and 3D models

Juhua Yang, Yihua Zhu, Xiaojiang Lin, 2022, Frontiers in Genetics.

The novel G10680A mutation is associated with complete penetrance of the LHON/T14484C family.

Zongfu Cao, Juhua Yang, Xu Ma, 2009, Mitochondrion.

[A novel PAX6 mutation (c.1286delC) in the patients with hereditary congenital aniridia.].

Juhua Yang, Xu Ma, Y. Tong, 2008, Yi chuan = Hereditas.

The Therapeutic Effect of an Anti-TNF-α/HSA/IL-6R Triple-Specific Fusion Protein Under Experimental Septic Conditions

Juhua Yang, Xiaole Chen, He Wang, 2022, Inflammation.

Proteomics & Bioinformatics

Lei Wang, Zongfu Cao, Yilu Chen, 2022 .

Overexpression of AQP5 Was Detected in Axillary Sweat Glands of Primary Focal Hyperhidrosis Patients

Juhua Yang, Jian-Feng Chen, Y. Tu, 2016, Dermatology.