Frontiers in Immunology · 2020 · 21 citations · 40 references
Life SciencesGeneticsImmunologyImmunogeneticsInflammationInnate ImmunityHuman Leukocyte Antigen SystemInflammatory SignalingInnate Immune Gene PolymorphismsSickle Cell DiseaseToll-like Receptor GeneticsToll-like ReceptorsAcute Chest SyndromeCytotoxic T Lymphocyte Antigen 4Cytotoxic T-lymphocyte Antigen 4 (Ctla-4) PathwayHuman Leukocyte Antigen GenotypeHuman Leukocyte AntigensInnate Immunity Gene VariantsSingle-nucleotide PolymorphismsToll-like Receptor Gene Polymorphisms
= 0.049, in patients of same SCD genotype). These results, by uncovering susceptibility to, or protection against SCD complications, might contribute to a better understanding of the inflammatory pathways involved in SCD manifestations and to pave the way for the discovery of biomarkers that predict disease severity, which would improve SCD management.
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NKG2D-Deficient Mice Are Defective in Tumor Surveillance in Models of Spontaneous Malignancy
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