نتایج جستجو برای: metalloprotease

تعداد نتایج: 3114  

Journal: :Mechanisms of Development 1999
Fiona C Wardle Jennifer V Welch Leslie Dale

Bone morphogenetic protein 1 (BMP1) is a metalloprotease that ventralises dorsal mesoderm when overexpressed in early Xenopus embryos. Here we show that Xenopus BMP1 blocks the dorsalising activity of chordin, but not noggin or DeltaxBMPR, when coexpressed in the ventral marginal zone and degrades chordin protein in vitro. We also show that a dominant-negative mutation for XBMP1 (dnBMP1) dorsal...

Journal: :Biochemical and biophysical research communications 2003
James C Burnett James J Schmidt Robert G Stafford Rekha G Panchal Tam L Nguyen Ann R Hermone Jonathan L Vennerstrom Connor F McGrath Douglas J Lane Edward A Sausville Daniel W Zaharevitz Rick Gussio Sina Bavari

Botulinum neurotoxins (BoNTs) are among the most lethal biological substances to have been weaponized and are listed as biodefense category A agents. Currently, no small molecule (non-peptidic) therapeutics exist to counter this threat; hence, identifying and developing compounds that inhibit BoNTs is a high priority. In the present study, a high-throughput assay was used to identify small mole...

Journal: :Trends in cell biology 2001
C Chang Z Werb

Metalloproteases are important in many aspects of biology, ranging from cell proliferation, differentiation and remodeling of the extracellular matrix (ECM) to vascularization and cell migration. These events occur several times during organogenesis in both normal development and during tumor progression. Mechanisms of metalloprotease action underlying these events include the proteolytic cleav...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Joshua Muia Jian Zhu Garima Gupta Sandra L Haberichter Kenneth D Friedman Hendrik B Feys Louis Deforche Karen Vanhoorelbeke Lisa A Westfield Robyn Roth Niraj Harish Tolia John E Heuser J Evan Sadler

The metalloprotease ADAMTS13 cleaves von Willebrand factor (VWF) within endovascular platelet aggregates, and ADAMTS13 deficiency causes fatal microvascular thrombosis. The proximal metalloprotease (M), disintegrin-like (D), thrombospondin-1 (T), Cys-rich (C), and spacer (S) domains of ADAMTS13 recognize a cryptic site in VWF that is exposed by tensile force. Another seven T and two complement ...

Journal: :Blood 1999
R M van der Plas M E Schiphorst E G Huizinga R J Hené L F Verdonck J J Sixma R Fijnheer

Thrombotic thrombocytopenic purpura (TTP) after bone marrow transplantation (BMT) differs from classic TTP in its clinical course and therapy. A characteristic of classic TTP is the inhibition of a plasma protease that specifically cleaves von Willebrand factor (vWF), thus reducing its multimeric size. We investigated whether this protease was also inhibited in BMT-associated TTP. Plasma from p...

2012
Sawako Yoshina Kenjiro Sakaki Aki Yonezumi-Hayashi Keiko Gengyo-Ando Hideshi Inoue Yuichi Iino Shohei Mitani

A disintegrin-like and metalloprotease with thrombospondin type I motif (ADAMTS9) is a member of the secreted metalloprotease family that is believed to digest extracellular matrix (ECM) proteins outside of cells. Its Caenorhabditis elegans orthologue, GON-1, is involved in ECM degradation and is required for gonad morphogenesis. ADAMTS9 and GON-1 have similar domain structures, and both have a...

Journal: :The Journal of Experimental Medicine 2006
Anil K. Chauhan David G. Motto Colin B. Lamb Wolfgang Bergmeier Michael Dockal Barbara Plaimauer Friedrich Scheiflinger David Ginsburg Denisa D. Wagner

The metalloprotease ADAMTS13 (a disintegrin-like and metalloprotease with thrombospondin type I repeats 13) cleaves highly adhesive large von Willebrand factor (VWF) multimers after their release from the endothelium. ADAMTS13 deficiency is linked to a life-threatening disorder, thrombotic thrombocytopenic purpura (TTP), characterized by platelet-rich thrombi in the microvasculature. Here, we s...

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