Tissue-intrinsic dysfunction of circadian clock confers transplant arteriosclerosis

Proceedings of the National Academy of Sciences of the United States of America

Volumn 108, Issue 41, 2011, Pages 17147-17152

  Cheng, Bo ^a,b   Anea, Ciprian B ^a   Yao, Lin ^a   Chen, Feng ^a   Patel, Vijay ^a   Merloiu, Ana ^a   Pati, Paramita ^a   Caldwell, R William ^a   Fulton, David J ^a   Rudic, R Daniel ^a  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

^b HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

RAG KO; Rejection; Remodeling; Vascular

Indexed keywords

CXCL9 CHEMOKINE; CYCLINE; GRANZYME B; INTERCELLULAR ADHESION MOLECULE 2; PER2 PROTEIN; PERFORIN; PROTEIN BMAL1; T LYMPHOCYTE RECEPTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; AORTA GRAFT; ARTERIAL WALL THICKNESS; ARTERIOSCLEROSIS; ARTERY DIAMETER; ARTICLE; BRAIN DYSFUNCTION; CAROTID ARTERY; CELL INFILTRATION; CIRCADIAN CLOCK DYSFUNCTION; CIRCADIAN RHYTHM; CONTROLLED STUDY; KNOCKOUT MOUSE; MACROPHAGE; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; TRANSPLANT ARTERIOSCLEROSIS; UPREGULATION; WILD TYPE;

ANIMALS; AORTA; ARNTL TRANSCRIPTION FACTORS; ARTERIOSCLEROSIS; CAROTID ARTERY, COMMON; CIRCADIAN CLOCKS; MACROPHAGES; MALE; MICE; MICE, CONGENIC; MICE, INBRED C57BL; MICE, KNOCKOUT; MUTATION; ORGAN SPECIFICITY; PERIOD CIRCADIAN PROTEINS; RECEPTORS, ANTIGEN, T-CELL; SUPRACHIASMATIC NUCLEUS; TRANSPLANTATION, ISOGENEIC; UP-REGULATION;

MUS;

EID: 80054742534     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1112998108     Document Type: Article

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