Notch-TNF signalling is required for development and homeostasis of arterial valves

European Heart Journal

Volumn 38, Issue 9, 2017, Pages 675-686

  Wang, Yidong ^a   Wu, Bingruo ^a   Farrar, Emily ^b   Lui, Wendy ^a   Lu, Pengfei ^a   Zhang, Donghong ^a   Alfieri, Christina M ^c   Mao, Kai ^a   Chu, Ming ^d   Yang, Di ^d   Xu, Di ^d   Rauchman, Michael ^e   Taylor, Verdon ^f   Conway, Simon J ^g   Yutzey, Katherine E ^c   Butcher, Jonathan T ^b   Zhou, Bin ^a,d  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^b School of Operations Research and Industrial Engineering   (United States)

^c Cincinnati Childrens Hosp Med Ctr   (United States)

^d THE FIRST AFFILIATED HOSPITAL OF NANJING MEDICAL UNIVERSITY   (China)

^e SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF BASEL   (Switzerland)

^g INDIANA UNIVERSITY   (United States)

Author keywords

Congenital anomalies of arterial valves; Notch; TNF; Valvar aortic stenosis

Indexed keywords

NOTCH RECEPTOR; TUMOR NECROSIS FACTOR; NOTCH1 PROTEIN, MOUSE; NOTCH1 RECEPTOR; TUMOR NECROSIS FACTOR RECEPTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; BICUSPID AORTIC VALVE; CELL PROLIFERATION; CONTROLLED STUDY; EMBRYO; EPITHELIAL MESENCHYMAL TRANSITION; HEART VALVE STENOSIS; HOMEOSTASIS; IN VIVO STUDY; MOUSE; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; SIGNAL TRANSDUCTION; VALVAR INTERSTITIAL CELL; VASCULAR ENDOTHELIAL CELL; ABNORMALITIES; ANIMAL; AORTIC VALVE; AORTIC VALVE STENOSIS; DISEASE MODEL; EMBRYOLOGY; ENDOTHELIUM CELL; KNOCKOUT MOUSE; MESENCHYMAL STROMA CELL; METABOLISM; PATHOPHYSIOLOGY; PHYSIOLOGY;

ANIMALS; AORTIC VALVE; AORTIC VALVE STENOSIS; APOPTOSIS; DISEASE MODELS, ANIMAL; ENDOTHELIAL CELLS; HOMEOSTASIS; MESENCHYMAL STROMAL CELLS; MICE, KNOCKOUT; RECEPTOR, NOTCH1; RECEPTORS, TUMOR NECROSIS FACTOR; SIGNAL TRANSDUCTION; TUMOR NECROSIS FACTOR-ALPHA;

EID: 85016219115     PISSN: 0195668X     EISSN: 15229645     Source Type: Journal    
DOI: 10.1093/eurheartj/ehv520     Document Type: Article

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