about
A functional variant of PTPN22 confers risk for Vogt-Koyanagi-Harada syndrome but not for ankylosing spondylitis.Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's disease and VKH syndromeThe Association of Chemokine Gene Polymorphisms with VKH and Behcet's Disease in a Chinese Han Population.Genetic polymorphisms of C-type lectin receptors in Behcet's disease in a Chinese Han population.Lack of association of miR-146a and Ets-1 gene polymorphisms with Fuchs uveitis syndrome in Chinese Han patients.Two Genetic Variations in the IRF8 region are associated with Behçet's disease in Han Chinese.Genetic Variations of NLR family genes in Behcet's Disease.Genetic polymorphisms of cell adhesion molecules in Behcet's disease in a Chinese Han populationAnalysis of receptor tyrosine kinase genetics identifies two novel risk loci in GAS6 and PROS1 in Behçet's disease.Genetic analysis of innate immunity in Behcet's disease identifies an association with IL-37 and IL-18RAP.Lack of Association between Genetic Polymorphisms of JAK-STAT Signaling Pathway Genes and Acute Anterior Uveitis in Han Chinese.The role of mitochondria-associated reactive oxygen species in the amyloid β induced production of angiogenic factors by ARPE-19 cells.Promoter Hypermethylation of GATA3, IL-4, and TGF-β Confers Susceptibility to Vogt-Koyanagi-Harada Disease in Han Chinese.Association of ATG5 Gene Polymorphisms With Behçet's Disease and ATG10 Gene Polymorphisms With VKH Syndrome in a Chinese Han Population.Association of ERAP1 Gene Polymorphisms With Behçet's Disease in Han Chinese.Association of Genetic Variations in TNFSF15 With Acute Anterior Uveitis in Chinese Han.Ocular Behcet's disease is associated with aberrant methylation of interferon regulatory factor 8 (IRF8) in monocyte-derived dendritic cells.Phylogeny and evolutionary history of the silkworm.Aberrant DNA methylation of GATA binding protein 3 (GATA3), interleukin-4 (IL-4), and transforming growth factor-β (TGF-β) promoters in Behcet's disease.IL-1β triggered by peptidoglycan and lipopolysaccharide through TLR2/4 and ROS-NLRP3 inflammasome-dependent pathways is involved in ocular Behçet's disease.Berberine suppresses Th17 and dendritic cell responses.Polymorphisms in genetics of vitamin D metabolism confer susceptibility to ocular Behçet disease in a Chinese Han population.Identification of a novel MYO7A mutation in Usher syndrome type 1.Identification of susceptibility SNPs in IL10 and IL23R-IL12RB2 for Behçet's disease in Han Chinese.Association of genetic variations in PTPN2 and CD122 with ocular Behcet's disease.FAS Gene Copy Numbers are Associated with Susceptibility to Behçet Disease and VKH Syndrome in Han Chinese.FoxO1 gene confers genetic predisposition to acute anterior uveitis with ankylosing spondylitis.Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182.Dynamic DNA Methylation Changes of and during Experimental Autoimmune Uveitis in MiceThe Antitumor Immunity and Tumor Responses of Chemotherapy with or without DC-CIK for Non-Small-Cell Lung Cancer in China: A Meta-Analysis of 28 Randomized Controlled TrialsIncreased Notch pathway activation in Behçet's diseaseGenome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.TNFSF15 Polymorphisms are Associated with Graves' Disease and Graves' Ophthalmopathy in a Han Chinese PopulationEpigenome-wide association study identifies Behçet's disease-associated methylation loci in Han ChineseThe association between genetic polymorphisms of interleukin 23 receptor gene and the risk of rheumatoid arthritis: An updated meta-analysis
P50
Q33591011-AD9C4AAF-ECDB-4612-9D27-5B329708D504Q33654910-293FAE40-C528-4109-B797-D235934F0B58Q33654910-A4A7778F-FBFE-4EAB-A7C9-5BBD048E0A8AQ33734201-EAE7221D-5FF3-425C-A695-E62C3A99D665Q33903233-988B8B7B-6CAB-489E-8F0B-9C6BF142E277Q35768502-E568972A-6682-4CF8-89A8-C5B9445D84FEQ36501135-018907A2-6E62-4A48-8698-04DADE509357Q36527734-F19C616D-0C21-4F71-858D-2E83E99D4F98Q36830250-B31ABA6D-7562-4380-9CEE-FA5C0F97482DQ36933960-33208B1D-3BEB-4EE2-A84B-317ED9A04141Q37360271-6012A4AD-B6A8-44C3-8B86-4E63C32FF963Q37443554-36960027-AA09-4250-8105-4192359F6AFAQ38706595-BB577C32-F35F-4AAE-B0DF-5EAC31C54799Q40299723-2A8E3556-FE4B-485D-8829-13DDEA764300Q40989623-8D4EF9FB-10EB-4C30-B53D-830D2E6A446FQ41335450-A6D03667-8FB5-4FF9-8741-8D5A61CD4163Q41559678-8F4D4178-D0FB-4A09-8937-05775B04D2EBQ41612737-ABCC8A3A-BABA-4C2B-A504-B9689111859AQ42012569-A72D8FA4-CDDD-4B8C-A88C-F0E59892C472Q42362787-147A66F5-9E07-478C-8269-AC3CFE756B6DQ44376518-B4E9FD9C-A009-4E8D-B0EC-E6BF556E79A1Q45125155-8CF9D349-B481-4DAD-A093-3751ECD99AE8Q48917650-7D5F17DE-9CF8-427B-B8D6-46D652A7C7BCQ49764448-B749A436-5D75-4139-A381-B62FB3A4666EQ51612430-25457518-6AD4-41A0-BBFE-7019505CA5EBQ52675584-0D3DF815-B023-4CAC-B39B-DE700E66ACD4Q53443485-930549DF-A1C7-4564-83A6-23A12B42D920Q54184339-1ED1F995-6802-4F57-AED3-174C67CE2736Q54210124-64B10A27-31DF-4BA9-A655-4700FA688762Q58764490-5F73771F-EF3A-4A15-951A-4CA0D23447DAQ60956972-FF50FA14-10F2-4D6F-AB9F-F36A56631D29Q87135504-74A5CD39-78D1-49D6-B078-F0D803F7A4F3Q87535357-BDC30028-F336-48E0-9CE6-35B3A1F142C2Q92204625-67EDC5E8-BC81-460E-A39C-2D75BED1087EQ92317327-632012C0-0EAC-4108-98A8-C4FEE3F460BAQ92728526-1E99CCD5-835F-409C-BDB9-6D2EAAEE68E5
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Hongsong Yu
@ast
Hongsong Yu
@en
Hongsong Yu
@es
Hongsong Yu
@nl
Hongsong Yu
@sl
type
label
Hongsong Yu
@ast
Hongsong Yu
@en
Hongsong Yu
@es
Hongsong Yu
@nl
Hongsong Yu
@sl
prefLabel
Hongsong Yu
@ast
Hongsong Yu
@en
Hongsong Yu
@es
Hongsong Yu
@nl
Hongsong Yu
@sl
P1053
J-9106-2014
P106
P2038
Hongsong_Yu
P31
P3829
P496
0000-0002-1209-2104
P569
2000-01-01T00:00:00Z