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Genetic variations in the IL-12B gene in association with IL-23 and IL-12p40 serum levels in ankylosing spondylitis

https://doi.org/10.1007/s00296-018-4204-0
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1529-0131(199801)41:1<58::aid-art8>3.0.co;2-gopenalex-snapshot
Prevalence of spondylarthropathies in HLA-B27 positive and negative blood donors
inferredcites →https://doi.org/10.1002/art.1780270401openalex-snapshot
Evaluation of Diagnostic Criteria for Ankylosing Spondylitis
inferredcites →https://doi.org/10.1002/art.24128openalex-snapshot
Investigation of association of the IL12B and IL23R genes with psoriatic arthritis
inferredcites →https://doi.org/10.1007/s00296-010-1547-6openalex-snapshot
Functional genetic polymorphisms in interleukin-12B gene in association with systemic lupus erythematosus
inferredcites →https://doi.org/10.1016/j.cyto.2009.02.003openalex-snapshot
Cytokine SNPs: Comparison of allele frequencies by race and implications for future studies☆
inferredcites →https://doi.org/10.1016/j.immuni.2006.01.001openalex-snapshot
TGFβ in the Context of an Inflammatory Cytokine Milieu Supports De Novo Differentiation of IL-17-Producing T Cells
inferredcites →https://doi.org/10.1016/s0140-6736(73)91360-3openalex-snapshot
ANKYLOSING SPONDYLITIS AND HL-A 27
inferredcites →https://doi.org/10.1016/s0198-8859(02)00440-8openalex-snapshot
Frequency of cytokine polymorphisms in populations from western Europe, Africa, Asia, the Middle East and South America
inferredcites →https://doi.org/10.1038/ng.2007.17openalex-snapshot
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
inferredcites →https://doi.org/10.1038/ng.513openalex-snapshot
Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci
inferredcites →https://doi.org/10.1038/ng.873openalex-snapshot
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
inferredcites →https://doi.org/10.1038/sj.gene.6363645openalex-snapshot
Cytokine gene polymorphism in human disease: on-line databases
inferredcites →https://doi.org/10.1056/nejm197304052881403openalex-snapshot
High Association of an HL-A Antigen, W27, with Ankylosing Spondylitis
inferredcites →https://doi.org/10.1074/jbc.m207577200openalex-snapshot
Interleukin-23 Promotes a Distinct CD4 T Cell Activation State Characterized by the Production of Interleukin-17
inferredcites →https://doi.org/10.1093/rheumatology/kes254openalex-snapshot
Exploring ankylosing spondylitis-associated ERAP1, IL23R and IL12B gene polymorphisms in subphenotypes of psoriatic arthritis
inferredcites →https://doi.org/10.1111/cei.12670openalex-snapshot
The interleukin (IL)-23/IL-17 axis in ankylosing spondylitis: new advances and potentials for treatment
inferredcites →https://doi.org/10.1136/ard.2003.011023openalex-snapshot
Cytokines in the seronegative spondyloarthropathies and their modification by TNF blockade: a brief report and literature review
inferredcites →https://doi.org/10.1136/ard.2008.094870openalex-snapshot
Development of an ASAS-endorsed disease activity score (ASDAS) in patients with ankylosing spondylitis
inferredcites →https://doi.org/10.1136/ard.2008.100826openalex-snapshot
ASDAS, a highly discriminatory ASAS-endorsed disease activity score in patients with ankylosing spondylitis
inferredcites →https://doi.org/10.1136/ard.2010.138594openalex-snapshot
Ankylosing Spondylitis Disease Activity Score (ASDAS): defining cut-off values for disease activity states and improvement scores
inferredcites →https://doi.org/10.1136/ard.44.6.359openalex-snapshot
Prevalence of ankylosing spondylitis in males and females in a young middle-aged population of Tromsø, northern Norway.
inferredcites →https://doi.org/10.1136/ard.55.4.268openalex-snapshot
HLA class I associations of ankylosing spondylitis in the white population in the United Kingdom.
inferredcites →https://doi.org/10.1136/ard.61.suppl_2.ii25openalex-snapshot
Balancing the immune system: Th1 and Th2
inferredcites →https://doi.org/10.1146/annurev-immunol-030409-101212openalex-snapshot
Differentiation of Effector CD4 T Cell Populations
inferredcites →https://doi.org/10.1186/ar4228openalex-snapshot
Microbes, the gut and ankylosing spondylitis
inferredcites →https://doi.org/10.1371/journal.pone.0130982openalex-snapshot
Association Study of IL-12B Polymorphisms Susceptibility with Ankylosing Spondylitis in Mainland Han Population
inferredcites →https://doi.org/10.3109/14397595.2016.1157282openalex-snapshot
Relationship between the IL12B (rs3212227) gene polymorphism and susceptibility to multiple autoimmune diseases: A meta-analysis
inferredcites →https://doi.org/10.3109/9780203214237-70openalex-snapshot
A new approach to defining functional ability in ankylosing spondylitis: the development of the Bath ankylosing spondylitis functional index
inferredcites →https://doi.org/10.3899/jrheum.110613openalex-snapshot
Association of IL-12B Genetic Polymorphism with the Susceptibility and Disease Severity of Ankylosing Spondylitis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4073557openalex-extracted
IL-12B and IL-17 Genes Polymorphisms are Associated with Different Susceptibility to Juvenile Idiopathic Arthritis and Juvenile-Onset Systemic Lupus Erythematosus In Chinese Children
inferred← citeshttps://doi.org/10.1007/978-981-16-4733-8_5openalex-snapshot
Association of Non-HLA Genes with Ankylosing Spondylitis
inferred← citeshttps://doi.org/10.1007/s00393-020-00804-4openalex-snapshot
Circulating interleukin-23 levels in ankylosing spondylitis and their correlation with disease activity
inferred← citeshttps://doi.org/10.1007/s10528-020-10023-wopenalex-snapshot
RETRACTED ARTICLE: Aberrant Methylation of miR-34b and IL-12B mRNA Promoters Contributes to the Reduced Severity of Ankylosing Spondylitis
inferred← citeshttps://doi.org/10.1016/j.cyto.2020.155296openalex-snapshot
Association between IL12B polymorphisms and inflammatory bowel disease in Caucasian population: A meta-analysis
inferred← citeshttps://doi.org/10.1016/j.ejogrb.2021.12.016openalex-snapshot
Association of interleukin-12B gene polymorphisms and mRNA expression with preeclampsia
inferred← citeshttps://doi.org/10.1016/j.intimp.2019.03.026openalex-snapshot
DNA methylation and transcriptome signature of the IL12B gene in ankylosing spondylitis
inferred← citeshttps://doi.org/10.1038/s12276-019-0361-9openalex-snapshot
Role of interleukin-23 in the development of nonallergic eosinophilic inflammation in a murine model of asthma
inferred← citeshttps://doi.org/10.1080/08820139.2019.1622561openalex-snapshot
Impact of IL12B Polymorphisms on Genetic Susceptibility and IL-12p40 and IL-23 Serum Levels in Rheumatoid Arthritis
inferred← citeshttps://doi.org/10.1080/14712598.2020.1737855openalex-snapshot
Role of the IL-23 pathway in the pathogenesis and treatment of enthesitis in psoriatic arthritis
inferred← citeshttps://doi.org/10.1080/21645515.2019.1680239openalex-snapshot
Genomic, proteomic, and immunologic associations with a durable complete remission of measurable metastatic melanoma induced by a patient-specific dendritic cell vaccine
inferred← citeshttps://doi.org/10.1089/dna.2020.5464openalex-snapshot
IL-12B Polymorphisms Are Associated with the Presence of Premature Coronary Artery Disease and with Cardiovascular Risk Factors: The Genetics of Atherosclerotic Disease Mexican Study
inferred← citeshttps://doi.org/10.1097/md.0000000000034477openalex-snapshot
IL12B and IL17 genes polymorphisms associated with differential susceptibility to juvenile idiopathic arthritis and juvenile-onset systemic lupus erythematosus in Chinese children
inferred← citeshttps://doi.org/10.1177/03000605221075220openalex-snapshot
Association between interleukin 12B and interleukin 23R gene polymorphisms and systemic lupus erythematosus: a meta-analysis
inferred← citeshttps://doi.org/10.1177/1759720x20934277openalex-snapshot
An update on serum biomarkers to assess axial spondyloarthritis and to guide treatment decision
inferred← citeshttps://doi.org/10.1186/s12967-024-05925-xopenalex-snapshot
Identifying prioritization of therapeutic targets for ankylosing spondylitis: a multi-omics Mendelian randomization study
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2900968/v1openalex-snapshot
IL12B and IL17 genes polymorphisms are associated with different susceptibility to Juvenile Idiopathic Arthritis and Juvenile-onset Systemic Lupus Erythematosus in Chinese children
inferred← citeshttps://doi.org/10.3389/fcell.2021.748063openalex-snapshot
The Potential Role of Genetics, Environmental Factors, and Gut Dysbiosis in the Aberrant Non-Coding RNA Expression to Mediate Inflammation and Osteoclastogenic/Osteogenic Differentiation in Ankylosing Spondylitis
inferred← citeshttps://doi.org/10.3389/fimmu.2021.681217openalex-snapshot
Testing if Micro-CT Is Capable of Quantitating the Extent of Proteoglycan-Aggrecan Induced Axial Spondyloarthritis in Mice
inferred← citeshttps://doi.org/10.3390/jcm14113677openalex-snapshot
The Genetic Background of Ankylosing Spondylitis Reveals a Distinct Overlap with Autoimmune Diseases: A Systematic Review
inferred← citeshttps://doi.org/10.35465/28.3.2020.pp25-38openalex-snapshot
Оценка на атрофията и мастната дегенерация на паравертебралната мускулатура при аксиален спондилоартрит
inferred← citeshttps://doi.org/10.3892/mmr.2023.12983openalex-snapshot
Genetic factors involved in the co‑occurrence of endometriosis with ankylosing spondylitis (Review)
inferred← citeshttps://doi.org/10.4102/ajlm.v14i1.2916openalex-snapshot
Genetic copy number variation of TLR7, T-bet, IL12B, and FcγRIIIB in Egyptian ankylosing spondylitis patients
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