MiR-9 promotes microglial activation by targeting MCPIP1

Nature Communications

Volumn 5, Issue , 2014, Pages

  Yao, Honghong ^a   Ma, Rong ^b   Yang, Lu ^b   Hu, Guoku ^b   Chen, Xufeng ^c   Duan, Ming ^d   Kook, Yeonhee ^b   Niu, Fang ^b   Liao, Ke ^b   Fu, Minggui ^e   Hu, Gang ^c   Kolattukudy, Pappachan ^f   Buch, Shilpa ^b  

^a MEDICAL SCHOOL OF SOUTHEAST UNIVERSITY   (China)

^b UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^c NANJING MEDICAL UNIVERSITY   (China)

^d JILIN UNIVERSITY   (China)

^e UNIVERSITY OF MISSOURI KANSAS CITY SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF CENTRAL FLORIDA COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA CATENIN; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INDUCIBLE NITRIC OXIDE SYNTHASE; INTERLEUKIN 1BETA; INTERLEUKIN 6; LAMIN B; LIPOPOLYSACCHARIDE; MICRORNA 9; MONOCYTE CHEMOTACTIC PROTEIN 1; MONOCYTE CHEMOTACTIC PROTEIN INDUCED PROTEIN 1; TRANSFORMING GROWTH FACTOR BETA; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG; MICRORNA; MIRN9 MICRORNA, MOUSE; MIRN9 MICRORNA, RAT; RIBONUCLEASE; ZC3H12A PROTEIN, MOUSE;

3' UNTRANSLATED REGION; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL ACTIVATION; CONTROLLED STUDY; DOWN REGULATION; FLOW CYTOMETRY; FLUORESCENCE IN SITU HYBRIDIZATION; IN VITRO STUDY; IN VIVO STUDY; INNATE IMMUNITY; INTRACELLULAR SIGNALING; MALE; MICROGLIA; MICROGLIAL ACTIVATION; MOUSE; NEWBORN; NONHUMAN; PROMOTER REGION; PROTEIN EXPRESSION; PROTEIN TARGETING; REAL TIME POLYMERASE CHAIN REACTION; REPORTER GENE; UPREGULATION; ANIMAL; C57BL MOUSE; GENETICS; IN SITU HYBRIDIZATION; METABOLISM; NORTHERN BLOTTING; PHYSIOLOGY; RAT; SIGNAL TRANSDUCTION; SPRAGUE DAWLEY RAT; WESTERN BLOTTING;

ANIMALS; BETA CATENIN; BLOTTING, NORTHERN; BLOTTING, WESTERN; FLOW CYTOMETRY; IN SITU HYBRIDIZATION; MALE; MICE; MICE, INBRED C57BL; MICROGLIA; MICRORNAS; NF-KAPPA B; RATS; RATS, SPRAGUE-DAWLEY; REAL-TIME POLYMERASE CHAIN REACTION; RIBONUCLEASES; SIGNAL TRANSDUCTION;

EID: 84904466465     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms5386     Document Type: Article

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