Blau syndrome polymorphisms in NOD2 identify nucleotide hydrolysis and helical domain 1 as signalling regulators

FEBS Letters

Volumn 588, Issue 18, 2014, Pages 3382-3389

  Parkhouse, Rhiannon ^a   Boyle, Joseph P ^a   Monie, Tom P ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

Blau syndrome; containing 2; Innate immunity; NACHT; Nucleotide oligomerisation domain; Nucleotide binding, leucine rich repeat containing receptor; Single nucleotide polymorphisms

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15; CASPASE RECRUITMENT DOMAIN PROTEIN 4; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; NOD1 PROTEIN, HUMAN; NOD2 PROTEIN, HUMAN;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; BLAU SYNDROME; CHEMICAL STRUCTURE; CRANIAL NEUROPATHY; ENZYMOLOGY; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETICS; HEK293 CELL LINE; HUMAN; HYDROLYSIS; INNATE IMMUNITY; METABOLISM; MOLECULAR GENETICS; NACHT; NUCLEOTIDE OLIGOMERISATION DOMAIN CONTAINING 2; NUCLEOTIDE-BINDING, LEUCINE-RICH REPEAT CONTAINING RECEPTOR; PHYSIOLOGY; PROTEIN SECONDARY STRUCTURE; PROTEIN TERTIARY STRUCTURE; PROTEIN TRANSPORT; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISMS; SYNOVITIS; UVEITIS;

BLAU SYNDROME; INNATE IMMUNITY; NACHT; NUCLEOTIDE OLIGOMERISATION DOMAIN CONTAINING 2; NUCLEOTIDE-BINDING, LEUCINE-RICH REPEAT CONTAINING RECEPTOR; SINGLE NUCLEOTIDE POLYMORPHISMS;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; CRANIAL NERVE DISEASES; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HEK293 CELLS; HUMANS; HYDROLYSIS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; NF-KAPPA B; NOD1 SIGNALING ADAPTOR PROTEIN; NOD2 SIGNALING ADAPTOR PROTEIN; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; SIGNAL TRANSDUCTION; SYNOVITIS; UVEITIS;

EID: 84909952195     PISSN: 00145793     EISSN: 18733468     Source Type: Journal    
DOI: 10.1016/j.febslet.2014.07.029     Document Type: Article

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