AbstractThe aim of this study was to determine if endothelin converting enzyme-1 (ECE-1) like other members of this metalloprotease family undergoes ectodomain shedding. The release/shedding of catalytically active ECE-1 was measured by monitoring the fluorescence resulting from the cleavage of a specific quenched fluorescent substrate. Catalytically active ECE-1 was detected in the media of human umbilical vein endothelial cells, and was confirmed by mass spectrometry based assays. Specificity of cleavage was confirmed by using both narrow and broad specificity inhibitors. In conclusion we demonstrate and characterize for the first time, ECE-1 shedding from the surface of endothelial cells
AbstractEndothelin-converting-enzyme-1 (ECE-1) belongs to the family of zinc metallopeptidases and i...
A number of studies using endothelin (ET) precursors, commonly termed big ETs, have revealed the pre...
grantor: University of TorontoEndothelin converting enzyme-1 (ECE-1) catalyzes the convers...
AbstractThe aim of this study was to determine if endothelin converting enzyme-1 (ECE-1) like other ...
AbstractA membrane-bound protease activity that specifically converts Big endothelin-1 has been puri...
Abstract—We have previously reported the intracellular localization of the endothelin-converting enz...
International audienceEndothelin-converting enzyme-1 (ECE-1) cleaves big endothelins, as well as bra...
International audienceEndothelin-converting enzyme (ECE) is a membrane metalloprotease that generate...
AbstractEndothelin Converting Enzyme-1 (ECE-1) plays a significant role in the regulation of vascula...
AbstractEndothelin-converting enzyme-1 (ECE-1) is a critical enzyme in the biosynthesis of the poten...
International audienceEndothelin-converting enzyme (ECE)-1 cleaves big endothelins, as well as brady...
NoEndothelln-converting enzyme (ECE-1) is a critical enzyme in the production of the potent vasocons...
AIM: This study was designed to characterize the endothelin pathway in an immortalized human adenoca...
Endothelin-converting-enzyme-1 (ECE-1) belongs to the family of zinc metallopeptidases and is respon...
Human endothelin-converting enzyme (ECE-1) has been shown to exist as three isoforms (ECE-1a, ECE-1b...
AbstractEndothelin-converting-enzyme-1 (ECE-1) belongs to the family of zinc metallopeptidases and i...
A number of studies using endothelin (ET) precursors, commonly termed big ETs, have revealed the pre...
grantor: University of TorontoEndothelin converting enzyme-1 (ECE-1) catalyzes the convers...
AbstractThe aim of this study was to determine if endothelin converting enzyme-1 (ECE-1) like other ...
AbstractA membrane-bound protease activity that specifically converts Big endothelin-1 has been puri...
Abstract—We have previously reported the intracellular localization of the endothelin-converting enz...
International audienceEndothelin-converting enzyme-1 (ECE-1) cleaves big endothelins, as well as bra...
International audienceEndothelin-converting enzyme (ECE) is a membrane metalloprotease that generate...
AbstractEndothelin Converting Enzyme-1 (ECE-1) plays a significant role in the regulation of vascula...
AbstractEndothelin-converting enzyme-1 (ECE-1) is a critical enzyme in the biosynthesis of the poten...
International audienceEndothelin-converting enzyme (ECE)-1 cleaves big endothelins, as well as brady...
NoEndothelln-converting enzyme (ECE-1) is a critical enzyme in the production of the potent vasocons...
AIM: This study was designed to characterize the endothelin pathway in an immortalized human adenoca...
Endothelin-converting-enzyme-1 (ECE-1) belongs to the family of zinc metallopeptidases and is respon...
Human endothelin-converting enzyme (ECE-1) has been shown to exist as three isoforms (ECE-1a, ECE-1b...
AbstractEndothelin-converting-enzyme-1 (ECE-1) belongs to the family of zinc metallopeptidases and i...
A number of studies using endothelin (ET) precursors, commonly termed big ETs, have revealed the pre...
grantor: University of TorontoEndothelin converting enzyme-1 (ECE-1) catalyzes the convers...