Genetically engineered K cells provide sufficient insulin to correct hyperglycemia in a nude murine model

Acta Biochimica et Biophysica Sinica

Volumn 40, Issue 2, 2008, Pages 149-157

  Zhang, Yiqun ^a   Yao, Liqing ^a   Shen, Kuntang ^a   Xu, Meidong ^a   Zhou, Pinghong ^a   Yang, Weige ^a   Liu, Xinyuan ^b   Qin, Xinyu ^a  

^a FUDAN UNIVERSITY   (China)

^b INSTITUTE OF BIOCHEMISTRY AND CELL BIOLOGY   (China)

Author keywords

Gene therapy; Glucose; Glucose dependent insulinotropic polypeptide; Insulin; STC 1 cell; Type 1 diabetes mellitus

Indexed keywords

INSULIN; PRIMER DNA; RECOMBINANT PROTEIN;

ANIMAL; ARTICLE; BAGG ALBINO MOUSE; BLOOD; CELL LINE; DISEASE MODEL; ENTEROENDOCRINE CELL; EXPERIMENTAL DIABETES MELLITUS; GENE EXPRESSION; GENE THERAPY; GENETIC ENGINEERING; GENETIC TRANSFECTION; GENETICS; GLUCOSE BLOOD LEVEL; GLUCOSE TOLERANCE TEST; HUMAN; HYPERGLYCEMIA; INSULIN DEPENDENT DIABETES MELLITUS; MALE; METABOLISM; MOUSE; NUCLEOTIDE SEQUENCE; NUDE MOUSE; PANCREAS ISLET; PATHOLOGY; PATHOPHYSIOLOGY; SECRETION; TRANSPLANTATION;

ANIMALS; BASE SEQUENCE; BLOOD GLUCOSE; CELL LINE; DIABETES MELLITUS, EXPERIMENTAL; DIABETES MELLITUS, TYPE 1; DISEASE MODELS, ANIMAL; DNA PRIMERS; ENTEROENDOCRINE CELLS; GENE EXPRESSION; GENE THERAPY; GENETIC ENGINEERING; GLUCOSE TOLERANCE TEST; HUMANS; HYPERGLYCEMIA; INSULIN; ISLETS OF LANGERHANS; MALE; MICE; MICE, INBRED BALB C; MICE, NUDE; RECOMBINANT PROTEINS; TRANSFECTION;

MURINAE; MUS MUSCULUS;

EID: 39749193212     PISSN: 16729145     EISSN: 17457270     Source Type: Journal    
DOI: 10.1111/j.1745-7270.2008.00387.x     Document Type: Article

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