Abnormal differentiation of intestinal epithelium and intestinal barrier dysfunction in diabetic mice associated with depressed Notch/NICD transduction in Notch/Hes1 signal pathway

Cell Biology International

Volumn 38, Issue 10, 2014, Pages 1194-1204

  Min, Xiao Hui ^a   Yu, Tao ^a   Qing, Qing ^a   Yuan, Yu Hong ^a   Zhong, Wa ^a   Chen, Guang Cheng ^a   Zhao, Li Na ^a   Deng, Na ^a   Zhang, Li Fa ^a   Chen, Qi Kui ^a  

^a SUN YAT SEN UNIVERSITY   (China)

Author keywords

Diabetes mellitus; Differentiation; Intestinal barrier function; Intestinal epithelial cells; Notch pathway

Indexed keywords

DELTA LIKE 1 PROTEIN; IMMUNOGLOBULIN J RECOMBINATION SIGNAL SEQUENCE BINDING PROTEIN; MATH1 PROTEIN; NOTCH INTRACELLULAR DOMAIN PROTEIN; NOTCH RECEPTOR; OCCLUDIN; PROTEIN ZO1; STREPTOZOCIN; TRANSCRIPTION FACTOR HES 1; UNCLASSIFIED DRUG; BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; HES1 PROTEIN, MOUSE; HOMEODOMAIN PROTEIN; MSI1H PROTEIN, MOUSE; NERVE PROTEIN; NOTCH1 RECEPTOR; RNA BINDING PROTEIN;

ABSORPTIVE CELL; AEROBIC BACTERIUM; ANAEROBIC BACTERIUM; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BODY WEIGHT; CELL PROLIFERATION; CELLS BY BODY ANATOMY; CONTROLLED STUDY; DIABETES MELLITUS; DISEASE ASSOCIATION; DOWN REGULATION; ENTEROPATHY; HYPERGLYCEMIA; HYPERPLASIA; INTESTINAL BARRIER DYSFUNCTION; INTESTINE EPITHELIUM CELL; MOUSE; NONHUMAN; PANETH CELL; PATHOGENESIS; PROTEIN DEFICIENCY; PROTEIN EXPRESSION; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; SMALL INTESTINE; TIGHT JUNCTION; TREND STUDY; UPREGULATION; ANIMAL; C57BL MOUSE; CELL DIFFERENTIATION; CELL MEMBRANE PERMEABILITY; CHEMICALLY INDUCED; CYTOLOGY; EXPERIMENTAL DIABETES MELLITUS; GENETICS; INTESTINE MUCOSA; METABOLISM; PATHOLOGY;

ANIMALS; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; CELL DIFFERENTIATION; CELL MEMBRANE PERMEABILITY; DIABETES MELLITUS, EXPERIMENTAL; DOWN-REGULATION; HOMEODOMAIN PROTEINS; INTESTINAL MUCOSA; MICE; MICE, INBRED C57BL; NERVE TISSUE PROTEINS; RECEPTOR, NOTCH1; RNA-BINDING PROTEINS; SIGNAL TRANSDUCTION;

EID: 84907873515     PISSN: 10656995     EISSN: 10958355     Source Type: Journal    
DOI: 10.1002/cbin.10323     Document Type: Article

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