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[PMID 18479293] Evaluation of IL10, IL19 and IL20 gene polymorphisms and chronic hepatitis B infection outcome.
[PMID 18520591] Sequence variants in host cell factor C1 are associated with Meniere's disease.
[PMID 18640487] Association of donor inflammation- and apoptosis-related genotypes and delayed allograft function after kidney transplantation.
[PMID 19468064] Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions.
[PMID 19503741] Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
[PMID 19505919] Toll-like receptor signaling pathway variants and prostate cancer mortality.
[PMID 19753309] SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
[PMID 19907653] Selection for genetic variation inducing pro-inflammatory responses under adverse environmental conditions in a Ghanaian population.
[PMID 20416077] Identification of type 2 diabetes-associated combination of SNPs using support vector machine.
[PMID 20525402] Analysis of eight genes modulating interferon gamma and human genetic susceptibility to tuberculosis: a case-control association study.
[PMID 20617178] Leprosy and the adaptation of human toll-like receptor 1.
[PMID 20622879] Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behcet's disease susceptibility loci.
[PMID 21532858] Association of IL10, IL10RA, and IL10RB polymorphisms with benign prostate hyperplasia in Korean population.
[PMID 22378604] Association study of IL10 and IL23R-IL12RB2 in Iranian patients with Behcet's disease.
[PMID 24040186] Relationship of serum interleukin-10 and its genetic variations with ischemic stroke in a chinese general population
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[PMID 24903972] Genetic predisposition to calcific aortic stenosis and mitral annular calcification
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