CINECA IRIS Institutional Research Information System

IRIS è la soluzione IT che facilita la raccolta e la gestione dei dati relativi alle attività e ai prodotti della ricerca. Fornisce a ricercatori, amministratori e valutatori gli strumenti per monitorare i risultati della ricerca, aumentarne la visibilità e allocare in modo efficace le risorse disponibili.

Prodotti recenti

Metabolic heterogeneity on baseline 18FDG-PET/CT scan is a predictor of outcome in primary mediastinal B-cell lymphoma

An important unmet need in the management of primary mediastinal B-cell lymphoma (PMBCL) is to identify the patients for whom first line therapy will fail, in order to intervene before the lymphoma becomes refractory. High heterogeneity of intratumoral 18F-fluorodeoxyglucose (18FDG) uptake d...

Study of dezincification in orichalcum Roman coins

A group of orichalcum Roman coins, from private collections, have been studied for this research. Numismatic examination indicated that they are asses, sestertium and dupondius, minted from Julius Caesar to Nero. Orichalcum is an ancient copper based alloy with a variable percentage of&...

New 6- and 7-heterocyclyl-1H-indole derivatives as potent tubulin assembly and cancer cell growth inhibitors

3-Arylthio- and 3-aroyl-1H-indoles are potent inhibitors of tubulin polymerization and of cancer cell growth, by binding the colchicine site on β-tubulin. Several compounds of this class were more potent than colchicine, combretastatin A-4, vinblastine, and paclitaxel. Herein, we designed and&#x...

Adventitious root formation and xylogenesis in Arabidopsis thaliana: new insights

The role of indole-3-acetic acid (IAA) and indole-3-butyric acid (IBA) and of the auxin-interacting phytohormone ethylene on xylogenesis is still little known, even if a xylogenic promotion by auxins has been reported. In particular, auxin/ethylene-target tissue(s), modality of the de novo&#...

Anesthetic management of a patient with freeman-sheldon syndrome in thoracic surgery

Freeman-Sheldon Syndrome (FSS), recently reclassified as distal arthrogryposis type 2, is a rare congenital syndrome characterized by skeletal malformations, craniofacial deformities and progressive myopathy causing multiple body contractures and respiratory muscles involvement. The literature concerning about ...