UCP2 mRNA expression is dependent on glucose metabolism in pancreatic islets

Biochemical and Biophysical Research Communications

Volumn 417, Issue 1, 2012, Pages 495-500

  Dalgaard, Louise T ^a,b  

^a BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

^b ROSKILDE UNIVERSITY   (Denmark)

Author keywords

Cell; Glucokinase; Hexokinase IV; Insulin secretion; Islet of Langerhans; MODY2; Uncoupling Protein 2

Indexed keywords

ADENOSINE TRIPHOSPHATE; GLUCOKINASE; GLUCOSE; MESSENGER RNA; SUPEROXIDE DISMUTASE; UNCOUPLING PROTEIN 2;

ARTICLE; CONTROLLED STUDY; DISEASE COURSE; DOWN REGULATION; GLUCOSE METABOLISM; GLUCOSE TOLERANCE; HETEROZYGOSITY; INSULIN RELEASE; MOUSE; NONHUMAN; PANCREAS ISLET; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; UPREGULATION;

ADENOSINE TRIPHOSPHATE; ANIMALS; DIABETES MELLITUS, TYPE 2; GLUCOKINASE; GLUCOSE; GLUCOSE TOLERANCE TEST; INSULIN; ION CHANNELS; ISLETS OF LANGERHANS; MALE; MICE; MICE, KNOCKOUT; MITOCHONDRIAL PROTEINS; RNA, MESSENGER; SUPEROXIDES;

MUS;

EID: 84855821583     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2011.11.148     Document Type: Article

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