ROVIDA, ERMANNA

ROVIDA, ERMANNA  

Istituto di Ricerca Genetica e Biomedica - IRGB - Sede Secondaria Milano  

Mostra records
Risultati 1 - 20 di 39 (tempo di esecuzione: 0.05 secondi).
Titolo Data di pubblicazione Autore(i) File
Enhanced Antitumoral Activity and Photoacoustic Imaging Properties of AuNP-Enriched Endothelial Colony Forming Cells on Melanoma 1-gen-2021 Armanetti, P.; Chilla, A.; Margheri, F.; Biagioni, A.; Menichetti, L.; Margheri, G.; Ratto, F.; Centi, S.; Bianchini, F.; Severi, M.; Traversi, R.; Bani, D.; Lulli, M.; Del Rosso, T.; Mocali, A.; Rovida, E.; Del Rosso, M.; Fibbi, G.; Laurenzana, A.
Neuroferritinopathy: From ferritin structure modification to pathogenetic mechanism 1-gen-2015 Levi, S; Rovida, E
BRCA1 point mutations in premenopausal breast cancer patients from Central Sudan 1-gen-2014 Biunno I.; Aceto G.; Awadelkarim K.D.; Morgano A.; Elhaj A.; Eltayeb E.A.; Abuidris D.O.; Elwali N.E.; Spinelli C.; De Blasio P.; Rovida E.; MarianiCostantini R.
Molecular chaperons as therapeutic targets to counteract proteostasis defects 1-gen-2012 Cattaneo, Monica; Dominici, Roberto; Cardano, Marina; Diaferia, Giuseppe; Rovida, Ermanna; IDA BIUNNO, And
Study of FTMT and ABCA4 genes in a patient affected by age-related macular degeneration: identification and analysis of new mutations 1-gen-2012 Stenirri, S; Santambrogio, P; Setaccioli, M; Erba, Bg; Manitto, Mp; Rovida, E; Ferrari, M; Levi, S; Cremonesi, L
Exploring the role of the phospholipid ligand in Endothelial Protein C Receptor: a molecular dynamics study 1-gen-2010 Chiappori, F; Merelli, I; Milanesi, L; Rovida, E
A Docking Procedure for the identification of potential Bisphenol A protein targhets and characterization of the major environmental matrix involved in their pathways 1-gen-2009 Lazzati Z.; DUrsi P.; Rovida E.; Gambaro A.; Zangrando R.; Chiappori F.; Milanesi L.; Bolzacchini E.
In silico saturation mutagenesis and docking screening for the analysis of protein-ligand interaction: the Endothelial Protein C Receptor case study 1-gen-2009 Chiappori, F; D'Ursi, P; Merelli, I; Milanesi, L; Rovida, E
The role of iron in mitochondrial function 1-gen-2009 Levi S; Rovida E
Virtual screening pipeline and ligand modelling for H5N1 neuraminidase 1-gen-2009 D'Ursi, P; Chiappori, F; Merelli, I; Cozzi, P; Rovida, E; Milanesi, L
3D-Structure Prediction of the Modular Protein Sialoadhesin Using a Multi-step Modelling Strategy 1-gen-2008 Corrada Dario; Pasqualina DUrsi; Sara Botti; Aldo Luperini; Luciano Milanesi;Ermanna Rovida
A pipeline for saturation mutagenesis and docking, applied to the endothelial protein C receptor . 1-gen-2008 Chiappori Federica; Pasqualina DUrsi; Ivan Merelli; Marco Salina; Ermanna Rovida; Luciano Milanesi.
Comparison of protein-protein algorithms for the study of Proteinase-3 Endothelial Protein C Receptor complex. 1-gen-2008 Federica, Chiappori; Merelli, Ivan; Milanesi, Luciano; Rovida, Ermanna
Pipeline for saturation mutagenesis and docking screening in the study of protein-ligand interaction: the Endothelial Protein C Receptor (EPCR) 1-gen-2008 Chiappori F.; P. DUrsi ; I. Merelli; E. Rovida; L. Milanesi
Grid docking simulation for comparative ligand binding of Neurominidase structures 1-gen-2007 Dursi, P Chiappori F; Salvi, E; Merelli, I; Rovida, E; Milanesi, L
Identification and computationally-based structural interpretation of naturally occurring variants of human protein C. 1-gen-2007 Rovida E; Merati G; D'Ursi P; Zanardelli S; Marino F; Fontana G; Castaman G; Faioni EM
Identification and computionally-based structural interpretation of naturally occuring variants of human protein C 1-gen-2007 Rovida, Ermanna; Merati, Giuliana; D'Ursi, Pasqualina; Zanardelli, Sara; Marino, Francesca; Fontana, Gessica; Giancarlocastaman, ; M Faioni, Elena
Identification of a Novel Frameshift Mutation in the Kir6.2 gene in a population of Italian patients affected by Hyprinsulinism of Infancy 1-gen-2007 Biagiotti, L; Proverbio, Mc; Bosio, L; Gervasi, F; Rovida, E; Cerioni, V; Mora, S; Chiumello, G; Biunno, I
Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy. 1-gen-2007 Biagiotti, L; Proverbio, Mc; Bosio, L; Gervasi, F; Rovida, E; Cerioni, V; Bove, M; Valin, Ps; Albarello, L; Zamproni, I; Grassi, S; Doglioni, C; Mora, S; Chiumello, G; Biunno, I
ProCMD: a database and 3D web resource for protein C mutants. 1-gen-2007 D'Ursi P; Marino F; Caprera A; Milanesi L; Faioni EM; Rovida E.