Hyperglycemia slows embryonic growth and suppresses cell cycle via cyclin D1 and p21

Diabetes

Volumn 62, Issue 1, 2013, Pages 234-242

  Scott Drechsel, Devon E ^a   Rugonyi, Sandra ^a   Marks, Daniel L ^b   Thornburg, Kent L ^b   Hinds, Monica T ^a  

^a Oregon Health and Science University Department of Biomedical Engineering   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN D1; GLUCOSE; GLUCOSE TRANSPORTER 1; PROTEIN P21;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL CYCLE ARREST; CELL PROLIFERATION; CHICKEN; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DISEASE MODEL; EMBRYO; EMBRYO GROWTH; ENDOCARDIUM CELL; ENDOTHELIUM CELL; FEMALE; GENE EXPRESSION REGULATION; GLUCOSE BLOOD LEVEL; HEART DEVELOPMENT; HEART LEFT VENTRICLE OUTFLOW TRACT; HEART MUSCLE CELL; HYPERGLYCEMIA; HYPEROSMOLARITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION;

ANIMALS; BLOOD GLUCOSE; CELL CYCLE; CELL PROLIFERATION; CHICK EMBRYO; CYCLIN D1; CYCLIN-DEPENDENT KINASE INHIBITOR P21; EMBRYONIC DEVELOPMENT; FEMALE; GLUCOSE TRANSPORTER TYPE 1; HEART DEFECTS, CONGENITAL; HUMANS; HYPERGLYCEMIA; PREGNANCY; PREGNANCY IN DIABETICS;

EID: 84872033269     PISSN: 00121797     EISSN: 1939327X     Source Type: Journal    
DOI: 10.2337/db12-0161     Document Type: Article

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