Zobrazeno 1 - 9
of 9
pro vyhledávání: '"CyP, cyclophilin"'
Autor:
Robert Thimme, Volker Lohmann, K. Nitschke, Katharina Esser-Nobis, Christoph Neumann-Haefelin, Julia Schmidt
Publikováno v:
Journal of Hepatology
Graphical abstract
Background & Aims Cyclophilin-inhibitors have potent antiviral activity against Hepatitis C virus (HCV) and are promising candidates for broad-spectrum antiviral therapy. Cyclosporine A (CsA) acts immunosuppressive by blocking
Background & Aims Cyclophilin-inhibitors have potent antiviral activity against Hepatitis C virus (HCV) and are promising candidates for broad-spectrum antiviral therapy. Cyclosporine A (CsA) acts immunosuppressive by blocking
Autor:
Fabio Di Lisa, Paolo Bernardi
Publikováno v:
Journal of Molecular and Cellular Cardiology
The mitochondrial permeability transition (PT) – an abrupt increase permeability of the inner membrane to solutes – is a causative event in ischemia–reperfusion injury of the heart, and the focus of intense research in cardioprotection. The PT
Publikováno v:
Redox Biology
Redox Biology, Vol 13, Iss C, Pp 170-181 (2017)
Redox Biology, Vol 13, Iss C, Pp 170-181 (2017)
Liver failure induced by systemic inflammatory response (SIRS) is often associated with mitochondrial dysfunction but the mechanism linking SIRS and mitochondria-mediated liver failure is still a matter of discussion. Current hypotheses suggest that
Publikováno v:
Biochimica et Biophysica Acta
A prolonged period of ischaemia followed by reperfusion irreversibly damages the heart. Such reperfusion injury (RI) involves opening of the mitochondrial permeability transition pore (MPTP) under the conditions of calcium overload and oxidative stre
Autor:
Henry Dube, Michela Capano, Michela I. Simone, Sylvanie Malouitre, Martin Crompton, David L. Selwood
Publikováno v:
Biochemical Journal
Mitochondrial CyP-D (cyclophilin-D) catalyses formation of the PT (permeability transition) pore, a key lesion in the pathogenesis of I/R (ischaemia/reperfusion) injury. There is evidence [Malouitre, Dube, Selwood and Crompton (2010) Biochem. J. 425,
Publikováno v:
Biochemical Journal, 425 (1) pp. 137-148. (2009)
Biochemical Journal
Biochemical Journal
CsA (cyclosporin A) is a hydrophobic undecapeptide that inhibits CyPs (cyclophilins), a family of PPIases (peptidylprolyl cis–trans isomerases). In some experimental models, CsA offers partial protection against lethal cell injury brought about by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f2d69f30d30190847179c0a3479a03d
https://discovery.ucl.ac.uk/id/eprint/20029/
https://discovery.ucl.ac.uk/id/eprint/20029/
Autor:
Udayan Chatterji, S. Phillips, Shilpa Chokshi, Roger Williams, Philippe Gallay, Antonio Riva, Michael Bobardt, Nikolai V. Naoumov
Publikováno v:
Gastroenterology
Background & Aims Cyclophilins are host factors required for hepatitis C virus replication. Cyclophilin inhibitors such as alisporivir have shown strong anti–hepatitis C virus activity in vitro and in clinical studies. However, little is known abou
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