T
Thomas F. Lüscher
Researcher at University of Zurich
Publications - 1613
Citations - 88517
Thomas F. Lüscher is an academic researcher from University of Zurich. The author has contributed to research in topics: Endothelium & Myocardial infarction. The author has an hindex of 134, co-authored 1560 publications receiving 79034 citations. Previous affiliations of Thomas F. Lüscher include University of Texas Southwestern Medical Center & Durham University.
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Journal ArticleDOI
AngiomiR-126 expression and secretion from circulating CD34(+) and CD14(+) PBMCs: role for proangiogenic effects and alterations in type 2 diabetics.
Pavani Mocharla,Sylvie Briand,Giovanna Giannotti,Carola Dörries,Philipp Jakob,Francesco Paneni,Thomas F. Lüscher,Ulf Landmesser +7 more
TL;DR: The present findings provide a novel molecular mechanism underlying increased proangiogenic effects of CD34(+) PBMCs, that is, angiomiR-126 expression/secretion.
Journal ArticleDOI
Proceedings from the European clinical consensus conference for renal denervation: considerations on future clinical trial design.
Felix Mahfoud,Michael Böhm,Michel Azizi,Atul Pathak,Isabelle Durand Zaleski,Sebastian Ewen,Kostantinos Tsioufis,Bert Andersson,Peter J. Blankestijn,Michel Burnier,Gilles Chatellier,Sameer Gafoor,Guido Grassi,Michael Joner,Sverre E. Kjeldsen,Sverre E. Kjeldsen,Thomas F. Lüscher,Melvin D. Lobo,Chaim Lotan,Gianfranco Parati,Josep Redon,Luis M. Ruilope,Isabella Sudano,Christian Ukena,Evert van Leeuwen,Massimo Volpe,Stephan Windecker,Adam Witkowski,William Wijns,Thomas Zeller,Roland E. Schmieder +30 more
TL;DR: Clinical evidence in support of RDN as an effective interventional technique in patients with resistant hypertension is conflicting; a number of observational studies and three randomized, controlled trials support both safety and efficacy of this new therapy but some smaller studies and the large, single-blind, randomized, sham-controlled symplicity HTN-3 trial failed to show superiority ofRDN when compared with medical therapy alone.
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Final Common Molecular Pathways of Aging and Cardiovascular Disease Role of the p66Shc Protein
Francesco Cosentino,Pietro Francia,Giovanni G. Camici,Pier Giuseppe Pelicci,Thomas F. Lüscher +4 more
TL;DR: The evidence so far reported and here discussed supports the concept that pharmacological modulation of p66(Shc) expression and activity may be a novel and effective target for the treatment of atherosclerotic vascular disease as well as myocardial adaptation to hypertrophic, inflammatory and neuro-hormonal stimuli in the overloaded heart.
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Endothelin-1 Potentiates Human Smooth Muscle Cell Growth to PDGF Effects of ETA and ETB Receptor Blockade
TL;DR: In human SMCs,ET-1 markedly potentiates proliferation to PDGF, mainly via ETA receptors, which may represent an important function of ET-1 for vascular structural changes in patients and provide new therapeutic opportunities for ET- 1 receptor antagonists.
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Five-Year Clinical and Angiographic Outcomes of a Randomized Comparison of Sirolimus-Eluting and Paclitaxel-Eluting Stents Results of the Sirolimus-Eluting Versus Paclitaxel-Eluting Stents for Coronary Revascularization LATE Trial
Lorenz Räber,Lea Wohlwend,Mathias Wigger,Mario Togni,Simon Wandel,Peter Wenaweser,Stéphane Cook,Aris Moschovitis,Rolf Vogel,Bindu Kalesan,Christian Seiler,Franz R. Eberli,Thomas F. Lüscher,Bernhard Meier,Peter Jüni,Stephan Windecker +15 more
TL;DR: In this paper, the authors investigated clinical and angiographic outcomes of sirolimus-eluting (SES) and paclitaxel-ELuting stents (PES) at 5 years as part of the SIRTAX LATE study and found no differences between SES and PES in terms of cardiac death (5.8% versus 5.7% of SES-and 21.4% of PES-treated patients), myocardial infarction (6.6% versus 6.9%; P=0.51