Yunjia Liu
Daping, 400042, China
Last Updated: 09/26/2026
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Found 17 publications
NLRP3 Deficiency Attenuates Secondary Degeneration of Visual Cortical Neurons Following Optic Nerve Injury.
Journal: Neuroscience bulletin
Published: April 07, 2019
Association of T-Bet, GATA-3, RORC, and FOXP3 Copy Number Variations With Acute Anterior Uveitis With or Without Ankylosing Spondylitis in Chinese Han.
Journal: Investigative ophthalmology & visual science
Published: April 16, 2016
Association of ATG5 Gene Polymorphisms With Behçet's Disease and ATG10 Gene Polymorphisms With VKH Syndrome in a Chinese Han Population.
Journal: Investigative ophthalmology & visual science
Published: January 10, 2016
Association of ERAP1 Gene Polymorphisms With Behçet's Disease in Han Chinese.
Journal: Investigative ophthalmology & visual science
Published: September 23, 2015
Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome.
Journal: Scientific reports
Published: December 11, 2014
FoxO1 gene confers genetic predisposition to acute anterior uveitis with ankylosing spondylitis.
Journal: Investigative ophthalmology & visual science
Published: November 22, 2014
Interleukin-10 gene polymorphisms are associated with Behcet's disease but not with Vogt-Koyanagi-Harada syndrome in the Chinese Han population.
Journal: Molecular vision
Published: October 28, 2014
Decreased interleukin-37 expression in Vogt-Koyanagi-Harada disease and upregulation following immunosuppressive treatment.
Journal: Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research
Published: October 25, 2014
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.
Journal: Nature genetics
Published: April 03, 2014
Last Updated: 09/26/2026