P2RX7 genotype association in severe sepsis identified by a novel Multi-Individual Array for rapid screening and replication of risk SNPs

Clinica Chimica Acta

Volumn 413, Issue 1-2, 2012, Pages 39-47

  Geistlinger, J ^a   Du, W ^b   Groll, J ^c,f   Liu, F ^b   Hoegel, J ^d   Foehr, K J ^b   Pasquarelli, A ^e   Schneider, E M ^b  

^a Array On GmbH   (Germany)

^b UNIVERSITY HOSPITAL ULM   (Germany)

^c RWTH AACHEN UNIVERSITY   (Germany)

^d Department of Human Genetics ^*  (Germany)

^e UNIVERSITY OF ULM   (Germany)

^f UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

Functional SNPs; Hemophagocytic syndromes; HLH; MAS; Multi Individual Array (MIA); P2RX7

Indexed keywords

ANALYTIC METHOD; ARTICLE; CONTROLLED STUDY; DENDRITIC CELL; DISEASE PREDISPOSITION; DISEASE SEVERITY; GENE; GENE IDENTIFICATION; GENE MUTATION; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MULTI INDIVIDUAL ARRAY; MUTATIONAL ANALYSIS; P2RX7 GENE; PRIORITY JOURNAL; PYROSEQUENCING; SEPSIS; SEPTIC SHOCK; SINGLE NUCLEOTIDE POLYMORPHISM;

BASE SEQUENCE; DNA PRIMERS; GENOTYPE; HUMANS; PHENOTYPE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, PURINERGIC P2X7; SEPSIS;

EID: 82955213043     PISSN: 00098981     EISSN: 18733492     Source Type: Journal    
DOI: 10.1016/j.cca.2011.05.023     Document Type: Article

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