Netea, M G <br/><br/>
NOD2 3020insC mutation and the pathogenesis of Crohn's disease: impaired IL-1beta production points to a loss-of-function phenotype.  [electronic resource] 

 -  The Netherlands journal of medicine  Sep 2005 
 - 305-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0300-2977 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acetylmuramyl-Alanyl-Isoglutamine--administration & dosage<br/>Alleles<br/>Case-Control Studies<br/>Crohn Disease--genetics<br/>Gene Expression Regulation<br/>Genetic Predisposition to Disease<br/>Homozygote<br/>Humans<br/>Interleukin-1--biosynthesis<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>Leukocytes, Mononuclear--immunology<br/>Lipopeptides<br/>Mutation<br/>Nod2 Signaling Adaptor Protein<br/>Oligopeptides--administration & dosage<br/>Peptidoglycan--administration & dosage<br/>Polymerase Chain Reaction<br/>Signal Transduction--genetics<br/>Toll-Like Receptor 2--genetics