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The genetics of Behçet's disease in a Chinese population.
- Published in:
- Frontiers of Medicine, 2012, v. 6, n. 4, p. 354, doi. 10.1007/s11684-012-0234-2
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- Publication type:
- Article
Inflammasome-targeting natural compounds in inflammatory bowel disease: Mechanisms and therapeutic potential.
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- Frontiers in Immunology, 2022, v. 13, p. 01, doi. 10.3389/fimmu.2022.963291
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- Publication type:
- Article
METTL3 inhibits inflammation of retinal pigment epithelium cells by regulating NR2F1 in an m<sup>6</sup>A-dependent manner.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.905211
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- Publication type:
- Article
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.
- Published in:
- Nature Genetics, 2014, v. 46, n. 9, p. 1007, doi. 10.1038/ng.3061
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- Article
Corrigendum: Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis.
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- Scientific Reports, 2017, p. 46785, doi. 10.1038/srep46785
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- Publication type:
- Article
Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis.
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- Scientific Reports, 2017, p. 42628, doi. 10.1038/srep42628
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- Article
Association of TNFSF4 Polymorphisms with Vogt-Koyanagi-Harada and Behcet's Disease in Han Chinese.
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- Scientific Reports, 2016, p. 37257, doi. 10.1038/srep37257
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- Article
Association between Functional MICA-TM and Behcet's Disease: A Systematic Review and Meta-analysis.
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- Scientific Reports, 2016, p. 21033, doi. 10.1038/srep21033
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- Article
miR-23a, miR-146a and miR-301a confer predisposition to Vogt-Koyanagi-Harada syndrome but not to Behcet's disease.
- Published in:
- Scientific Reports, 2016, p. 20057, doi. 10.1038/srep20057
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- Article
Two Genetic Variations in the IRF8 region are associated with Behçet's disease in Han Chinese.
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- Scientific Reports, 2016, p. 19651, doi. 10.1038/srep19651
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- Article
Aryl Hydrocarbon Receptor Regulates Apoptosis and Inflammation in a Murine Model of Experimental Autoimmune Uveitis.
- Published in:
- Frontiers in Immunology, 2018, p. N.PAG, doi. 10.3389/fimmu.2018.01713
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- Publication type:
- Article
Genetic Variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's Disease and VKH Syndrome.
- Published in:
- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0098373
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- Publication type:
- Article
A Functional Variant of PTPN22 Confers Risk for Vogt-Koyanagi-Harada Syndrome but Not for Ankylosing Spondylitis.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0096943
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- Publication type:
- Article
Association of a <i>TNIP1</i> Polymorphism with Vogt-Koyanagi-Harada Syndrome but Not with Ocular Behcet’s Disease in Han Chinese.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0095573
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- Article
MicroRNA-146a and Ets-1 Gene Polymorphisms Are Associated with Pediatric Uveitis.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0091199
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- Publication type:
- Article
TRAF5 and TRAF3IP2 Gene Polymorphisms Are Associated with Behçet's Disease and Vogt-Koyanagi-Harada Syndrome: A Case-Control Study.
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- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0084214
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- Article
FGFR1OP tagSNP but Not CCR6 Polymorphisms Are Associated with Vogt-Koyanagi-Harada Syndrome in Chinese Han.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0069358
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- Publication type:
- Article
<i>TNFAIP3</i> Gene Polymorphisms in a Chinese Han Population with Vogt–Koyanagi–Harada Syndrome.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059515
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- Publication type:
- Article
Increased Expression of IL-22 Is Associated with Disease Activity in Behcet’s Disease.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059009
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- Article
No Association of PTPN22 Polymorphisms with Susceptibility to Ocular Behcet's Disease in Two Chinese Han Populations.
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- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0031230
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- Article
Lack of an Association of PD-1 and Its Ligand Genes with Behcet's Disease in a Chinese Han Population.
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- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0025345
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- Publication type:
- Article
Label-Free Proteomics Reveals Decreased Expression of CD18 and AKNA in Peripheral CD4<sup>+</sup> T Cells from Patients with Vogt-Koyanagi-Harada Syndrome.
- Published in:
- PLoS ONE, 2011, v. 6, n. 1, p. 1, doi. 10.1371/journal.pone.0014616
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- Publication type:
- Article
A functional variant of pre-miRNA-196a2 confers risk for Behcet’s disease but not for Vogt–Koyanagi–Harada syndrome or AAU in ankylosing spondylitis.
- Published in:
- Human Genetics, 2013, v. 132, n. 12, p. 1395, doi. 10.1007/s00439-013-1346-8
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- Publication type:
- Article
Genetic variants in the JAK1 gene confer higher risk of Behcet's disease with ocular involvement in Han Chinese.
- Published in:
- Human Genetics, 2013, v. 132, n. 9, p. 1049, doi. 10.1007/s00439-013-1312-5
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- Publication type:
- Article
TNFAIP3 gene polymorphisms confer risk for Behcet's disease in a Chinese Han population.
- Published in:
- Human Genetics, 2013, v. 132, n. 3, p. 293, doi. 10.1007/s00439-012-1250-7
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- Publication type:
- Article
Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility.
- Published in:
- Human Genetics, 2012, v. 131, n. 12, p. 1841, doi. 10.1007/s00439-012-1200-4
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- Publication type:
- Article
YY1 Lactylation Aggravates Autoimmune Uveitis by Enhancing Microglial Functions via Inflammatory Genes.
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- Advanced Science, 2024, v. 11, n. 19, p. 1, doi. 10.1002/advs.202308031
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- Article
YY1 Lactylation Aggravates Autoimmune Uveitis by Enhancing Microglial Functions via Inflammatory Genes (Adv. Sci. 19/2024).
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- Advanced Science, 2024, v. 11, n. 19, p. 1, doi. 10.1002/advs.202470110
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- Article
OR11H1 Missense Variant Confers the Susceptibility to Vogt‒Koyanagi‒Harada Disease by Mediating Gadd45g Expression.
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- Advanced Science, 2024, v. 11, n. 11, p. 1, doi. 10.1002/advs.202306563
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- Publication type:
- Article
Integrative Single‐Cell Transcriptomics and Epigenomics Mapping of the Fetal Retina Developmental Dynamics.
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- Advanced Science, 2023, v. 10, n. 16, p. 1, doi. 10.1002/advs.202206623
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- Article
TNF receptor-associated factor 5 gene confers genetic predisposition to acute anterior uveitis and pediatric uveitis.
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- Arthritis Research & Therapy, 2013, v. 15, n. 5, p. 1, doi. 10.1186/ar4293
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- Article
PRKCQ rs4750316 is associated with Vogt-Koyanagi-Harada syndrome in a Han Chinese population.
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- Molecular Vision, 2019, v. 25, p. 834
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- Article
Association of a NOS3 gene polymorphism with Behçet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese.
- Published in:
- Molecular Vision, 2016, v. 22, p. 1
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- Publication type:
- Article
Increased Notch pathway activation in Behçet’s disease.
- Published in:
- Rheumatology, 2014, v. 53, n. 5, p. 810, doi. 10.1093/rheumatology/ket438
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- Article
CD40 gene polymorphisms confer risk of Behçet's disease but not of Vogt–Koyanagi–Harada syndrome in a Han Chinese population.
- Published in:
- 2012
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- Publication type:
- Journal Article
CD40 gene polymorphisms confer risk of Behçet's disease but not of Vogt–Koyanagi–Harada syndrome in a Han Chinese population.
- Published in:
- Rheumatology, 2012, v. 51, n. 1, p. 47, doi. 10.1093/rheumatology/ker345
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- Publication type:
- Article
The rs391957 variant cis-regulating oncogene GRP78 expression contributes to the risk of hepatocellular carcinoma.
- Published in:
- Carcinogenesis, 2013, v. 34, n. 6, p. 1273, doi. 10.1093/carcin/bgt061
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- Publication type:
- Article
A feedback loop driven by H3K9 lactylation and HDAC2 in endothelial cells regulates VEGF-induced angiogenesis.
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- Genome Biology, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s13059-024-03308-5
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- Article
YY1 lactylation in microglia promotes angiogenesis through transcription activation-mediated upregulation of FGF2.
- Published in:
- Genome Biology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s13059-023-02931-y
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- Article
The cancer exosomes: Clinical implications, applications and challenges.
- Published in:
- International Journal of Cancer, 2020, v. 146, n. 11, p. 2946, doi. 10.1002/ijc.32762
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- Publication type:
- Article
Small molecules targeting RORγt inhibit autoimmune disease by suppressing Th17 cell differentiation.
- Published in:
- Cell Death & Disease, 2020, v. 11, n. 8, p. 1, doi. 10.1038/s41419-020-02891-2
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- Article
Genetic Variation in the REL Gene Increases Risk of Behcet’s Disease in a Chinese Han Population but That of PRKCQ Does Not.
- Published in:
- PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0147350
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- Article
A metagenomic study of the gut microbiome in Behcet's disease.
- Published in:
- Microbiome, 2018, v. 6, n. 1, p. N.PAG, doi. 10.1186/s40168-018-0520-6
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- Publication type:
- Article
Copy number variations and gene polymorphisms of Complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome.
- Published in:
- Scientific Reports, 2015, p. 12989, doi. 10.1038/srep12989
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- Publication type:
- Article
Low Expression of YTH Domain-Containing 1 Promotes Microglial M1 Polarization by Reducing the Stability of Sirtuin 1 mRNA.
- Published in:
- Frontiers in Cellular Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fncel.2021.774305
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- Publication type:
- Article
Icariin alleviates oxygen‐induced retinopathy by targeting microglia hexokinase 2.
- Published in:
- Immunology, 2024, v. 173, n. 1, p. 141, doi. 10.1111/imm.13818
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- Publication type:
- Article
Retinal microglia: Functions and diseases.
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- Immunology, 2022, v. 166, n. 3, p. 268, doi. 10.1111/imm.13479
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- Publication type:
- Article
UVEOGENE: An SNP database for investigations on genetic factors associated with uveitis and their relationship with other systemic autoimmune diseases.
- Published in:
- Human Mutation, 2019, v. 40, n. 3, p. 258, doi. 10.1002/humu.23702
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- Article
A novel mutation of PANK4 causes autosomal dominant congenital posterior cataract.
- Published in:
- Human Mutation, 2019, v. 40, n. 4, p. 380, doi. 10.1002/humu.23696
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- Article
Genetic Variant on PDGFRL Associated with Behçet Disease in Chinese Han Populations.
- Published in:
- Human Mutation, 2013, v. 34, n. 1, p. 74, doi. 10.1002/humu.22208
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- Publication type:
- Article