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10.1038/srep36315

http://scihub22266oqcxt.onion/10.1038/srep36315
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suck abstract from ncbi


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pmid27819323
      Sci+Rep 2016 ; 6 (ä): 36315
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  • Donor and recipient genetic variants in NLRP3 associate with early acute rejection following kidney transplantation #MMPMID27819323
  • Dessing MC ; Kers J ; Damman J ; Navis GJ ; Florquin S ; Leemans JC
  • Sci Rep 2016[Nov]; 6 (ä): 36315 PMID27819323 show ga
  • NLRP3 (NOD-like receptor family, pyrin domain containing 3) is a member of the inflammasome family and is of special interest in renal disease. Experimental studies have shown that Nlrp3 plays a significant role in the induction of renal damage and dysfunction in acute and chronic renal injury. However, the role of NLRP3 in human renal disease is completely unknown. From a retrospective cohort study, we determined in 1271 matching donor and recipient samples if several NLRP3 single nucelotide polymorphisms (SNPs) were associated with primary non-function (PNF), delayed graft function (DGF), biopsy-proven acute rejection (BPAR) and death-censored graft and patient survival. NLRP3 gain-of-function SNP (rs35829419) in donors was associated with an increased risk of BPAR while NLRP3 loss-of-function SNP (rs6672995) in the recipient was associated with a decreased risk of BPAR in the first year following renal transplantation (HR 1.91, 95% CI 1.38-2.64, P?
  • |*Polymorphism, Single Nucleotide [MESH]
  • |Adult [MESH]
  • |Biopsy [MESH]
  • |Delayed Graft Function [MESH]
  • |Female [MESH]
  • |Graft Rejection/*genetics/pathology [MESH]
  • |Humans [MESH]
  • |Kidney Diseases/genetics/*therapy [MESH]
  • |Kidney Transplantation [MESH]
  • |Male [MESH]
  • |Middle Aged [MESH]
  • |NLR Family, Pyrin Domain-Containing 3 Protein/*genetics [MESH]
  • |Retrospective Studies [MESH]


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