Genetically engineered islets and alternative sources of insulin-producing cells for treating autoimmune diabetes: Quo vadis?

International Journal of Endocrinology

Volumn 2012, Issue , 2012, Pages

  Chou, Feng Cheng ^a   Huang, Shing Hwa ^b   Sytwu, Huey Kang ^a  

^a NATIONAL DEFENSE MEDICAL CENTER   (Taiwan)

^b TRI SERVICE GENERAL HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMOKINE; CYTOKINE; CYTOTOXIC T LYMPHOCYTE ANTIGEN 4; CYTOTOXIC T LYMPHOCYTE ANTIGEN 4 ANTIBODY; GAMMA INTERFERON; HEME OXYGENASE 1; INTERLEUKIN 4; INTERLEUKIN 5; PROGRAMMED DEATH 1 RECEPTOR; REACTIVE OXYGEN METABOLITE; SUPPRESSOR OF CYTOKINE SIGNALING 1; THIOREDOXIN; TRANSFORMING GROWTH FACTOR BETA;

ADULT STEM CELL; ALLOIMMUNITY; ANTIGEN EXPRESSION; APOPTOSIS; AUTOIMMUNITY; CELL FUNCTION; CELL PROTECTION; CELLULAR IMMUNITY; EFFECTOR CELL; EMBRYONIC STEM CELL; GENE OVEREXPRESSION; GENETIC ENGINEERING; GENETIC TRANSDUCTION; GENETIC TRANSFECTION; GRAFT REJECTION; GRAFT SURVIVAL; HUMAN; IMMUNOMODULATION; IMMUNOREGULATION; INSULIN DEPENDENT DIABETES MELLITUS; INSULITIS; MESENCHYMAL STEM CELL; NONHUMAN; PANCREAS ISLET BETA CELL; PANCREAS ISLET TRANSPLANTATION; PLURIPOTENT STEM CELL; PRIORITY JOURNAL; REGULATOR GENE; REVIEW; SIGNAL TRANSDUCTION; STEM CELL TRANSPLANTATION; T LYMPHOCYTE ACTIVATION; TH1 CELL; TH17 CELL; TRANSGENIC MOUSE; VIRAL GENE DELIVERY SYSTEM;

EID: 84862302007     PISSN: 16878337     EISSN: 16878345     Source Type: Journal    
DOI: 10.1155/2012/296485     Document Type: Review

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