The autophagy regulator Rubicon is a feedback inhibitor of CARD9-mediated host innate immunity

Cell Host and Microbe

Volumn 11, Issue 3, 2012, Pages 277-289

  Yang, Chul Su ^a   Rodgers, Mary ^a   Min, Chan Ki ^a   Lee, Jong Soo ^a,b   Kingeter, Lara ^c   Lee, June Yong ^a   Jong, Ambrose ^d   Kramnik, Igor ^e   Lin, Xin ^c   Jung, Jae U ^a  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b Chungnam National University   (South Korea)

^c UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER   (United States)

^d CHILDREN S HOSPITAL LOS ANGELES   (United States)

^e BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BECLIN 1; CASPASE RECRUITMENT DOMAIN 9; CASPASE RECRUITMENT DOMAIN SIGNALING PROTEIN; DECTIN; MALT1 PROTEIN; PATTERN RECOGNITION RECEPTOR; PROTEIN BCL 10; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE; REGULATOR PROTEIN; RETINOIC ACID INDUCIBLE PROTEIN I; RUBICON PROTEIN; T LYMPHOCYTE RECEPTOR; UNCLASSIFIED DRUG;

ANTIMICROBIAL ACTIVITY; ANTIVIRAL ACTIVITY; ARTICLE; AUTOPHAGY; COMPLEX FORMATION; CONTROLLED STUDY; CYTOKINE PRODUCTION; FEEDBACK SYSTEM; HUMAN; HUMAN CELL; IMMUNE RESPONSE; INFLAMMATION; INNATE IMMUNITY; LYMPHOCYTE ACTIVATION; NONHUMAN; PHAGOCYTOSIS; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN INDUCTION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM; SIGNAL TRANSDUCTION;

14-3-3 PROTEINS; ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ANIMALS; BINDING, COMPETITIVE; CANDIDA ALBICANS; CANDIDIASIS; CARD SIGNALING ADAPTOR PROTEINS; CASPASES; CELLS, CULTURED; CYTOKINES; FEEDBACK, PHYSIOLOGICAL; HOST-PATHOGEN INTERACTIONS; HUMANS; IMMUNITY, INNATE; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MACROPHAGES; MICE; MICE, TRANSGENIC; MICROBIAL VIABILITY; MULTIPROTEIN COMPLEXES; NEOPLASM PROTEINS; ORTHOMYXOVIRIDAE INFECTIONS; PHOSPHORYLATION; PROTEIN BINDING; PROTEIN INTERACTION DOMAINS AND MOTIFS; SIGNAL TRANSDUCTION;

EID: 84863354715     PISSN: 19313128     EISSN: 19346069     Source Type: Journal    
DOI: 10.1016/j.chom.2012.01.019     Document Type: Article

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