SIGIRR genetic variants in premature infants with necrotizing enterocolitis

Pediatrics

Volumn 135, Issue 6, 2015, Pages e1530-e1534

  Sampath, Venkatesh ^a   Menden, Heather ^a   Helbling, Daniel ^a   Li, Keguo ^a   Gastonguay, Adam ^a   Ramchandran, Ramani ^a   Dimmock, David P ^a  

^a MEDICAL COLLEGE OF WISCONSIN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIUM LIPOPOLYSACCHARIDE; TOLL LIKE RECEPTOR 4; INTERLEUKIN 1 RECEPTOR; TIR8 PROTEIN, HUMAN;

ARTICLE; CLINICAL ARTICLE; EMBRYO; EXOME; FEMALE; GENE; GENE DELETION; GENE MUTATION; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HUMAN; HUMAN CELL; INFANT; INFLAMMATION; LOSS OF FUNCTION MUTATION; MALE; MISSENSE MUTATION; NECROTIZING ENTEROCOLITIS; PREMATURITY; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SIGIRR GENE; SPLICING DEFECT; STOP MUTATION; GENETICS; MUTATION; NEWBORN;

ENTEROCOLITIS, NECROTIZING; FEMALE; GENETIC VARIATION; HUMANS; INFANT, NEWBORN; INFANT, PREMATURE; MALE; MUTATION; RECEPTORS, INTERLEUKIN-1;

EID: 84930607947     PISSN: 00314005     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.2014-3386     Document Type: Article

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