Complement genetics, deficiencies, and disease associations

Protein and Cell

Volumn 3, Issue 7, 2012, Pages 487-496

  Mayilyan, Karine R ^a  

^a INSTITUTE OF MOLECULAR BIOLOGY   (Armenia)

Author keywords

complement system; deficiency; disease association; HLA III; RCA

Indexed keywords

COMPLEMENT COMPONENT C3B RECEPTOR; COMPLEMENT COMPONENT C4 BINDING PROTEIN; COMPLEMENT COMPONENT C4A; COMPLEMENT COMPONENT C4B; COMPLEMENT FACTOR H; DECAY ACCELERATING FACTOR; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 3; MANNOSE BINDING LECTIN 2; MONOCYTE CHEMOTACTIC PROTEIN;

AUTOIMMUNE DISEASE; COMPLEMENT ACTIVATION; COMPLEMENT COMPONENT C4 BINDING PROTEIN GENE; COMPLEMENT COMPONENT C4A GENE; COMPLEMENT COMPONENT C4B GENE; COMPLEMENT DEFICIENCY; COMPLEMENT FACTOR H GENE; COMPLEMENT LECTIN PATHWAY; COMPLEMENT REGULATION; COMPLEMENT SYSTEM; CR1 GENE; CR2 GENE; DAF GENE; DISEASE ASSOCIATION; GENE; GENE CLUSTER; GENE CONVERSION; GENE FUNCTION; GENE IDENTIFICATION; GENE INTERACTION; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC COMPLEMENTATION; GENETIC LOAD; GENETIC POLYMORPHISM; GENETIC RISK; GENOTYPE ENVIRONMENT INTERACTION; HLA SYSTEM; HOST RESISTANCE; HUMAN; HUMORAL IMMUNITY; INNATE IMMUNITY; INTRACELLULAR SIGNALING; MBL2 GENE; MCP GENE; NONHUMAN; PRIORITY JOURNAL; REVIEW;

ANIMALS; COMPLEMENT ACTIVATION; COMPLEMENT SYSTEM PROTEINS; HLA ANTIGENS; HUMANS; IMMUNITY, INNATE; IMMUNOLOGIC DEFICIENCY SYNDROMES; LECTINS; MULTIGENE FAMILY; RECEPTORS, COMPLEMENT;

EID: 84867000608     PISSN: 1674800X     EISSN: 16748018     Source Type: Journal    
DOI: 10.1007/s13238-012-2924-6     Document Type: Review

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