MDA5 and autoimmune disease

Nature Genetics

Volumn 46, Issue 5, 2014, Pages 418-419

  Miner, Jonathan J ^a   Diamond, Michael S ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL DNA; COMPLEMENT COMPONENT C1Q; COMPLEMENT COMPONENT C2; COMPLEMENT COMPONENT C4; DOUBLE STRANDED RNA; PATTERN RECOGNITION RECEPTOR; VIRUS DNA; VIRUS RNA; DOUBLE STRANDED RNA MDA5; INTERFERON; RNA HELICASE; UNCLASSIFIED DRUG;

AICARDI GOUTIERES SYNDROME; ALLELE; AUTOIMMUNE DISEASE; DISABILITY; DYSTONIA; ENVIRONMENTAL FACTOR; GAIN OF FUNCTION MUTATION; GENE SEQUENCE; HUMAN; MYELINATED NERVE; NERVE FIBER; NONHUMAN; NUCLEIC ACID METABOLISM; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SPASTICITY; SYSTEMIC LUPUS ERYTHEMATOSUS; TRANSCRIPTION INITIATION; VIRUS INFECTION; VIRUS PATHOGENESIS; VIRUS REPLICATION; AUTOIMMUNITY; DISEASE PREDISPOSITION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC VARIABILITY; IMMUNE RESPONSE; IMMUNOPATHOGENESIS; PROTEIN PROTEIN INTERACTION; SHORT SURVEY; UPREGULATION; VIRUS MUTATION;

AUTOIMMUNE DISEASES OF THE NERVOUS SYSTEM; DEAD-BOX RNA HELICASES; HUMANS; INTERFERON TYPE I; MODELS, MOLECULAR; MUTATION; NERVOUS SYSTEM MALFORMATIONS; PHENOTYPE; SIGNAL TRANSDUCTION;

EID: 84899534322     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2959     Document Type: Review

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