Zobrazeno 1 - 10
of 55
pro vyhledávání: '"C, Cirielli"'
Autor:
A Magenta, M D D'Agostino, S B Beji, S S Sileno, D L Lulli, L M Mercurio, S M Madonna, C C Cirielli, S P Pallotta, C A Albanesi, M C C Capogrossi, D A Avitabile, G M Melillo
Publikováno v:
European Heart Journal. 43
Introduction We previously showed that genotoxic stress induced an active extracellular release of nucleophosmin (NPM) in human cardiac mesenchymal progenitor cells, and that serum deprivation provokes NPM secretion from human endothelial cells, elic
Publikováno v:
Current Drug Target -Cardiovascular & Hematological Disorders. 4:295-300
In the last decade, studies of the biological mechanisms underlying angiogenesis, i.e. the development of a new vasculature from pre-existing blood vessels, have suggested a new approach to peripheral obstructive artery disease based on the treatment
Autor:
C Cirielli, Massimiliano M. Marrocco-Trischitta, S Camilli, Paolo Guerrini, Francesco Stillo, G Bandiera
Publikováno v:
European Journal of Vascular and Endovascular Surgery. 22:405-409
Objectives to prospectively evaluate the safety and efficacy of remifentanil during regional anaesthesia for carotid endarterectomy. Methods twenty-eight consecutive patients underwent carotid endarterectomy with combined superficial and deep cervica
Akademický článek
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Akademický článek
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Publikováno v:
International angiology : a journal of the International Union of Angiology. 22(1)
Our study aims to evaluate the efficiency of short-term therapy with alprostadil (a PGE molecular derivative) on patients affected by critical ischemia of the lower limbs and unsuitable for surgical revascularization. The study was carried out on two
Publikováno v:
Journal of neuro-oncology. 43(2)
Adenoviral-mediated gene transfer for the treatment of experimental intrinsic malignant brain neoplasms holds promise. The role, however, of intracellular, adenoviral-mediated p53 expression to inhibit growth of experimental human intracranial malign
Publikováno v:
Journal of neuro-oncology. 31(1-2)
Gene therapy as an anti-tumor strategy is becoming a powerful tool for cytokine delivery to inhibit the growth of many tumors. Several delivery systems are being utilized and designed for the expression of specific genes to achieve a therapeutic resu
Autor:
J, Mühlhauser, M, Jones, I, Yamada, C, Cirielli, P, Lemarchand, T R, Gloe, B, Bewig, S, Signoretti, R G, Crystal, M C, Capogrossi
Publikováno v:
Gene therapy. 3(2)
Gene transfer with replication-deficient recombinant adenovirus (Ad) vectors may provide a novel approach to the treatment of some cardiac disorders. The relative efficiency of intramyocardial vs intracoronary Ad vector injection in transducing myoca
Publikováno v:
Cancer research. 55(19)
The use of replication-deficient adenoviral vectors in gene therapy may become a powerful method to achieve efficient but safe transfer of anti-tumor agents. Introduction of the wild-type p53 gene into tumor cells has, in general, been associated wit