Phosphorylation Is a Central Mechanism for Circadian Control of Metabolism and Physiology

Cell Metabolism

Volumn 25, Issue 1, 2017, Pages 118-127

  Robles, Maria S ^a   Humphrey, Sean J ^a   Mann, Matthias ^a  

^a MAX PLANCK INSTITUTE OF BIOCHEMISTRY   (Germany)

Author keywords

circadian clock; mass spectrometry; metabolism; rhythmic phosphorylation; signal transduction

Indexed keywords

CELL NUCLEUS RECEPTOR; EPIDERMAL GROWTH FACTOR RECEPTOR; GLUCOCORTICOID RECEPTOR; HEPATOCYTE NUCLEAR FACTOR 4ALPHA; LIVER X RECEPTOR ALPHA; MAMMALIAN TARGET OF RAPAMYCIN; MINERALOCORTICOID RECEPTOR; MITOGEN ACTIVATED PROTEIN KINASE; PHOSPHOPEPTIDE; PHOSPHOTRANSFERASE; PROTEIN KINASE B; STRESS ACTIVATED PROTEIN KINASE; TRANSCRIPTION FACTOR CLOCK; PHOSPHOPROTEIN; PROTEIN KINASE; PROTEOME;

ANIMAL TISSUE; ARTICLE; CIRCADIAN RHYTHM; ENZYME ACTIVATION; FATTY ACID SYNTHESIS; FEMALE; GENE TARGETING; GLYCOGEN SYNTHESIS; IN VIVO STUDY; LIPOGENESIS; LIVER; MALE; MOLECULAR CLOCK; MOUSE; NONHUMAN; PHYSIOLOGY; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN PHOSPHORYLATION; PROTEIN SYNTHESIS; AMINO ACID SEQUENCE; ANIMAL; BIOLOGICAL MODEL; C57BL MOUSE; CHEMISTRY; METABOLISM; PHOSPHORYLATION; SIGNAL TRANSDUCTION; TIME FACTOR;

AMINO ACID SEQUENCE; ANIMALS; CIRCADIAN CLOCKS; CIRCADIAN RHYTHM; CLOCK PROTEINS; ENZYME ACTIVATION; FEMALE; LIVER; MALE; METABOLIC NETWORKS AND PATHWAYS; MICE; MICE, INBRED C57BL; MODELS, BIOLOGICAL; PHOSPHOPROTEINS; PHOSPHORYLATION; PROTEIN KINASES; PROTEOME; SIGNAL TRANSDUCTION; TIME FACTORS;

EID: 85006165459     PISSN: 15504131     EISSN: 19327420     Source Type: Journal    
DOI: 10.1016/j.cmet.2016.10.004     Document Type: Article

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