Circadian glucose homeostasis requires compensatory interference between brain and liver clocks

Proceedings of the National Academy of Sciences of the United States of America

Volumn 105, Issue 39, 2008, Pages 14753-14754

  Gatfield, David ^a   Schibler, Ueli ^a  

^a UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME; GLUCOSE TRANSPORTER 2; PER1 PROTEIN; PER2 PROTEIN; PROTEIN BMAL1; TRANSCRIPTION FACTOR CLOCK; BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; GLUCOSE; TRANSACTIVATOR PROTEIN;

BIOLOGICAL RHYTHM; BODY TEMPERATURE; BRAIN FUNCTION; CARBOHYDRATE METABOLISM; CELL TYPE; CIRCADIAN RHYTHM; GENE EXPRESSION; GLUCONEOGENESIS; GLUCOSE BLOOD LEVEL; GLUCOSE HOMEOSTASIS; LIGHT DARK CYCLE; LIPID METABOLISM; LIVER CELL; LIVER FUNCTION; METABOLISM; MOLECULAR CLOCK; NONHUMAN; NOTE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN METABOLISM; SIGNAL TRANSDUCTION; SUPRACHIASMATIC NUCLEUS; TISSUE CULTURE; TRANSCRIPTOMICS; XENOBIOTIC METABOLISM; ANIMAL; BRAIN; GENETICS; HOMEOSTASIS; LIVER; MOUSE; MOUSE MUTANT; PHYSIOLOGY;

ANIMALS; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; BRAIN; CIRCADIAN RHYTHM; GLUCOSE; HOMEOSTASIS; LIVER; MICE; MICE, KNOCKOUT; TRANS-ACTIVATORS;

EID: 54449096059     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0807861105     Document Type: Note

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