The A2A adenosine receptor is a dual coding gene: A novel mechanism of gene usage and signal transduction

Journal of Biological Chemistry

Volumn 289, Issue 3, 2014, Pages 1257-1270

  Lee, Chien Fei ^a,b   Lai, Hsin Lin ^b   Lee, Yi Chao ^b,c,d   Chien, Chen Li ^a,b,e   Chern, Yijuang ^a,b,d  

^a NATIONAL YANG MING UNIVERSITY   (Taiwan)

^b INSTITUTE OF BIOMEDICAL SCIENCES   (Taiwan)

^c TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^d TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^e TAIPEI VETERANS GENERAL HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE RECEPTOR; CODING REGION; G PROTEIN COUPLED RECEPTORS; MAMMALIAN GENOMES; MEDIATED TRANSCRIPTION; NERVE GROWTH FACTOR; POST-TRANSCRIPTIONAL REGULATIONS; UNTRANSLATED REGIONS;

AMINO ACIDS; ENCODING (SYMBOLS); GENES; PROTEINS; RATS; SIGNAL TRANSDUCTION;

TRANSCRIPTION;

ADENOSINE A2A RECEPTOR; AMINO ACID; MESSENGER RNA; MITOGEN ACTIVATED PROTEIN KINASE; NERVE GROWTH FACTOR; PROTEIN; PROTEIN UORF5; TRANSCRIPTION FACTOR AP 1; UNCLASSIFIED DRUG; 3' UNTRANSLATED REGION; 5' UNTRANSLATED REGION;

5' UNTRANSLATED REGION; ADORA2A GENE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL HYPOXIA; CODON USAGE; CONTROLLED STUDY; EMBRYO; GENE; GENE ACTIVITY; GENE EXPRESSION REGULATION; GENETIC CODE; GENETIC TRANSCRIPTION; HUMAN; HUMAN CELL; IN VIVO STUDY; NONHUMAN; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; OVERLAPPING GENE; PC12 CELL; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN PROCESSING; PROTEIN SYNTHESIS; RAT; SIGNAL TRANSDUCTION; START CODON; TRANSLATION REGULATION; UPREGULATION; 3' UNTRANSLATED REGION; ANIMAL; BIOSYNTHESIS; GENETICS; HEK293 CELL LINE; PC12 CELL LINE; PHYSIOLOGY; SPRAGUE DAWLEY RAT;

3' UNTRANSLATED REGIONS; 5' UNTRANSLATED REGIONS; ANIMALS; CELL HYPOXIA; GENE EXPRESSION REGULATION; HEK293 CELLS; HUMANS; MAP KINASE SIGNALING SYSTEM; OPEN READING FRAMES; PC12 CELLS; RATS; RATS, SPRAGUE-DAWLEY; RECEPTOR, ADENOSINE A2A; SIGNAL TRANSDUCTION;

EID: 84892643195     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.509059     Document Type: Article

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