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Titolo Data di pubblicazione Autore(i) File
MESENCHYMAL STEM CELLS EXPANSION BY PLATING WHOLE BONE MARROW AT LOW CELLULAR DENSITY: A MORE ADVANTAGEOUS METHOD FOR CLINICAL USE 1-gen-2010 Mareschi, Katia; Rustichelli, Deborah; Gunetti, Monica; Sanavio, Fiorella; Errichiello, Edoardo; Ferrero, Ivana; Fagioli, Franca
Potential and immuno-modulant proprieties of mesenchymal stem cells from amniotic fluid 1-gen-2011 Mareschi, K.; Rustichelli, D.; Muraro, M.; Castiglia, S.; Errichiello, E.; Signorino, E.; Fagioli, F.
Ex vivo-expanded bone marrow CD34(+) for acute myocardial infarction treatment: in vitro and in vivo studies 1-gen-2011 Gunetti, M; Noghero, A; Molla, F; Staszewsky, Li; de Angelis, N; Soldo, A; Russo, I; Errichiello, E; Frasson, C; Rustichelli, D; Ferrero, I; Gualandris, A; Berger, M; Geuna, M; Scacciatella, P; Basso, G; Marra, S; Bussolino, F; Latini, R; Fagioli, F.
Ex vivo expanded bone marrow CD34+ for acute myocardial infarction treatment: in vitro and in vivo studies 1-gen-2011 Gunetti, M; Ferrero, I; Noghero, A; Staszewsky, L; De Angelis, N; Soldo, A; Russo, I; Errichiello, E; Rustichelli, D; Berger, M; Marra, S; Bussolino, F; Latini, R; Fagioli, F
Myogenic potential of whole bone marrow mesenchymal stem cells in vitro and in vivo for usage in urinary incontinence 1-gen-2012 Gunetti, M; Tomasi, S; Giammò, A; Boido, M; Rustichelli, D; Mareschi, K; Errichiello, E; Parola, M; Ferrero, I; Fagioli, F; Vercelli, A; Carone, R
Systemic AA amyloidosis as a unique manifestation of a combined mutation of TNFRSF1A and MEFV genes 1-gen-2013 Mereuta, Om; Baldovino, S; Errichiello, E; Binello, Gb; Restagno, G; Battaglia, Gg; Mazzucco, G; Roccatello, D
Oxidative DNA damage drives carcinogenesis in MUTYH-associated-polyposis by specific mutations of mitochondrial and MAPK genes. 1-gen-2013 Venesio, T; Balsamo, A; Errichiello, Edoardo; Ranzani, Gn; Risio, M.
A genome-wide association study of myasthenia gravis 1-gen-2015 Renton, Ae; Pliner, Ha; Provenzano, C; Evoli, A; Ricciardi, R; Nalls, Ma; Marangi, G; Abramzon, Y; Arepalli, S; Chong, S; Hernandez, Dg; Johnson, Jo; Bartoccioni, E; Scuderi, F; Maestri, M; Gibbs, Jr; Errichiello, E; Chiò, A; Restagno, G; Sabatelli, M; Macek, M; Scholz, Sw; Corse, A; Chaudhry, V; Benatar, M; Barohn, Rj; Mcvey, A; Pasnoor, M; Dimachkie, Mm; Rowin, J; Kissel, J; Freimer, M; Kaminski, Hj; Sanders, Db; Lipscomb, B; Massey, Jm; Chopra, M; Howard JF, Jr; Koopman, Wj; Nicolle, Mw; Pascuzzi, Rm; Pestronk, A; Wulf, C; Florence, J; Blackmore, D; Soloway, A; Siddiqi, Z; Muppidi, S; Wolfe, G; Richman, D; Mezei, Mm; Jiwa, T; Oger, J; Drachman, Db; Traynor, Bj.
Mitochondrial variants in MT-CO2 and D-loop instability are involved in MUTYH-associated polyposis 1-gen-2015 Errichiello, E; Balsamo, A; Cerni, M; Venesio, T
TBK1 is associated with ALS and ALS-FTD in Sardinian patients. 1-gen-2016 Borghero, G; Pugliatti, M; Marrosu, F; Marrosu, Mg; Murru, Mr; Floris, G; Cannas, A; Occhineri, P; Cau, Tb; Loi, D; Ticca, A; Traccis, S; Manera, U; Canosa, A; Moglia, C; Calvo, A; Barberis, M; Brunetti, M; Gibbs, Jr; Renton, Ae; Errichiello, E; Zoledziewska, M; Mulas, A; Qian, Y; Din, J; Pliner, Ha; Traynor, Bj; Chiò, A; ITALSGEN and SARDINALS, Consortia.
A Data Fusion Approach to Enhance Association Study in Epilepsy 1-gen-2016 Marini, Simone; Limongelli, Ivan; Rizzo, Ettore; Malovini, ALBERTO LUIGI; Errichiello, Edoardo; Vetro, Annalisa; Da, Tan; Zuffardi, Orsetta; Bellazzi, Riccardo
Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature 1-gen-2016 Errichiello, E; Novara, F; Cremante, Anna; Verri, A; Galli, J; Fazzi, E; Bellotti, D; Losa, Laura; Cisternino, M; Zuffardi, O
SMARCA4 inactivating mutations cause concomitant Coffin-Siris syndrome, microphthalmia and small-cell carcinoma of the ovary hypercalcaemic type 1-gen-2017 Errichiello, Edoardo; Mustafa, NOOR HUSSEIN MOHAMMAD; Vetro, Annalisa; Notarangelo, Lucia Dora; DE JONGE, Hugo; Rinaldi, Berardo; Vergani, Debora; Giglio, SABRINA RITA; Morbini, Patrizia; Zuffardi, Orsetta
Patologia ereditaria da gain of function 1-gen-2017 Errichiello, E; Casati, Beatrice; Zuffardi, O
Mitochondrial DNA variants in colorectal carcinogenesis: Drivers or passengers? 1-gen-2017 Errichiello, E; Venesio, T
Whole exome sequencing in the differential diagnosis of Diamond-Blackfan anemia: Clinical and molecular study of three patients with novel RPL5 and mosaic RPS19 mutations 1-gen-2017 Errichiello, E; Vetro, A; Mina, T; Wischmeijer, A; Berrino, E; Carella, Miriam; Romagnoli, M; Sacchini, P; Venesio, T; Zecca, M; Zuffardi, O
A donor splice site mutation in CISD2 generates multiple truncated, non-functional isoforms in Wolfram syndrome type 2 patients 1-gen-2017 Cattaneo, M; La Sala, L; Rondinelli, M; Errichiello, E; Zuffardi, O; Puca, Aa; Genovese, S; Ceriello, A
SOX2: Not always eye malformations. Severe genital but no major ocular anomalies in a female patient with the recurrent c.70del20 variant 1-gen-2018 Errichiello, E; Gorgone, C; Giuliano, L; Iadarola, B; Cosentino, E; Rossato, M; Kurtas, Ne; Delledonne, M; Mattina, T; Zuffardi, O
Mitochondrial DNA variations in tumours: Drivers or passengers? 1-gen-2018 Errichiello, E; Venesio, T
Confini e medicina di precisione in coppie consanguinee di migranti: la ricezione della consulenza genetica successiva all'identificazione di patologie fetali 1-gen-2018 Berlincioni, V.; Catania, CRISTINA GRAZIA; Acerbi, F.; Spinillo, A.; Arossa, A.; Kurtas, EDIBE NEHIR; Errichiello, E.; Zuffardi, O.
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