Zobrazeno 1 - 10
of 460
pro vyhledávání: '"Magrini, U."'
Autor:
Paulli, M. *, Arcaini, L., Lucioni, M., Boveri, E., Capello, D., Passamonti, F., Merli, M., Rattotti, S., Rossi, D., Riboni, R., Berti, E., Magrini, U., Bruno, R., Gaidano, G., Lazzarino, M.
Publikováno v:
In Annals of Oncology June 2010 21(6):1189-1195
Autor:
Boveri, E. *, Arcaini, L., Merli, M., Passamonti, F., Rizzi, S., Vanelli, L., Rumi, E., Rattotti, S., Lucioni, M., Picone, C., Castello, A., Pascutto, C., Magrini, U., Lazzarino, M., Paulli, M.
Publikováno v:
In Annals of Oncology January 2009 20(1):129-136
Publikováno v:
British Medical Journal (Clinical Research Edition), 1984 Mar 01. 288(6418), 668-669.
Externí odkaz:
https://www.jstor.org/stable/29514260
Publikováno v:
The British Medical Journal, 1971 Dec . 4(5790), 812-812.
Externí odkaz:
https://www.jstor.org/stable/25417092
Akademický článek
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Autor:
Pennucci, V, Zini, R, Norfo, R, Guglielmelli, P, Bianchi, E, Salati, S, Sacchi, G, Prudente, Z, Tenedini, E, Ruberti, S, Paoli, C, Fanelli, T, Mannarelli, C, Tagliafico, E, Ferrari, S, Vannucchi, Am, Manfredini, R, on behalf of Associazione Italiana per la Ricerca sul Cancro Gruppo Italiano Malattie Mieloproliferative Investigators Collaborators Vannucchi AM, Balliu, M, Bartalucci, N, Bogani, C, Bosi, A, Fjerza, R, Martinelli, S, Pancrazzi, A, Pieri, L, Bisognin, Andrea, Bortoluzzi, Stefania, Coppe, Alessandro, Saccoman, Claudia, Masciulli, A, Giovani, B, Azzan, C, Badalucco, S, Balduini, A, Bonetti, E, Campanelli, R, Catarsi, P, Isgrò, Ma, Lupo, Ml, Magrini, U, Massa, M, Poletto, V, Rosti, V, Villani, L, Cazzola, M, Ambaglio, I, Bernasconi, P, Casetti, Ic, Catricalà, S, Elena, C, Fugazza, E, Gallì, A, Malcovati, L, Milanesi, C, Pascutto, C, Pietra, D, Ripamonti, F, Rossi, M, Rumi, E, Dejana, E, Breviario, F, Corada, M, Erba, Bg, Rambaldi, A, Barbui, T, Ferrari, Ml, Finazzi, G, Finazzi, Mc, Gritti, G, Belotti, C, Boroni, C, Salmoiraghi, S, Amaru, A, Golay, J, Cilloni, D, Campia, V, Carturan, S, Guerrasio, A, Montanari, M, Zini, R.
Long non-coding RNAs (lncRNAs), an emerging group of gene expression regulators in normal and cancer cells, are defined as endogenous RNAs consisting of more than 200 nucleotides and lacking an ope...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01e32bcbe88b1bad6daf18f6012e5b49
https://hdl.handle.net/11380/1060249
https://hdl.handle.net/11380/1060249
Autor:
Pecci A, Biino G, Fierro T, Bozzi V, Mezzasoma A, Patrizia Noris, Ramenghi U, Loffredo G, Fabris F, Momi S, Magrini U, Pirastu M, Savoia A, Balduini C, Gresele P, Myh, Italian Registry For -Releated Diseases
Publikováno v:
Europe PubMed Central
PloS one 7 (2012). doi:10.1371/journal.pone.0035986
info:cnr-pdr/source/autori:Pecci A, Biino G, Fierro T, Bozzi V, Mezzasoma A, Noris P, Ramenghi U, Loffredo G, Fabris F, Momi S, Magrini U, Pirastu M, Savoia A, Balduini C, Gresele P; for the Italian Registry for MYH9-releated diseases/titolo:Alteration of Liver Enzymes Is a Feature of the Myh9-Related Disease Syndrome/doi:10.1371%2Fjournal.pone.0035986/rivista:PloS one/anno:2012/pagina_da:/pagina_a:/intervallo_pagine:/volume:7
PLoS ONE
PLoS ONE, Vol 7, Iss 4, p e35986 (2012)
PloS one 7 (2012). doi:10.1371/journal.pone.0035986
info:cnr-pdr/source/autori:Pecci A, Biino G, Fierro T, Bozzi V, Mezzasoma A, Noris P, Ramenghi U, Loffredo G, Fabris F, Momi S, Magrini U, Pirastu M, Savoia A, Balduini C, Gresele P; for the Italian Registry for MYH9-releated diseases/titolo:Alteration of Liver Enzymes Is a Feature of the Myh9-Related Disease Syndrome/doi:10.1371%2Fjournal.pone.0035986/rivista:PloS one/anno:2012/pagina_da:/pagina_a:/intervallo_pagine:/volume:7
PLoS ONE
PLoS ONE, Vol 7, Iss 4, p e35986 (2012)
BACKGROUND: MYH9-related disease (MYH9-RD) is a rare autosomal dominant genetic syndrome characterized by congenital thrombocytopenia associated with the risk of developing progressive nephropathy, sensorineural deafness, and presenile cataract. Duri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bb1b18abda4787c7f860dc65240b568
http://hdl.handle.net/11562/1064408
http://hdl.handle.net/11562/1064408
Autor:
Rumi, E, Pietra, D, Pascutto, C, Guglielmelli, P, Martínez Trillos, A, Casetti, I, Colomer, D, Pieri, L, Pratcorona, M, Rotunno, G, Sant'Antonio, E, Bellini, M, Cavalloni, C, Mannarelli, C, Milanesi, C, Boveri, E, Ferretti, V, Astori, C, Rosti, V, Cervantes, F, Barosi, G, Vannucchi, Am, Cazzola, M, Associazione Italiana per la Ricerca sul Cancro Gruppo Italiano Malattie Mieloproliferative Investigators Collaborators Vannucchi AM, Balliu, M, Bartalucci, N, Biamonte, F, Bisognin, A, Bogani, C, Bortoluzzi, S, Bosi, A, Coppe, A, Fanelli, T, Fjerza, R, Loiacono, I, Marchioli, R, Martinelli, S, Masciulli, A, Pancrazzi, A, Paoli, C, Saccoman, C, Spolverini, A, Susini, Mc, Tozzi, L, Azzan, C, Badalucco, S, Balduini, A, Bonetti, E, Campanelli, R, Catarsi, P, Isgrò, Am, Lupo, Ml, Magrini, U, Massa, M, Poletto, V, Villani, L, Ambaglio, I, Bernasconi, P, Casetti, Ic, Catricalà, S, Elena, C, Fugazza, E, Gall, A, Malcovati, L, Ripamonti, F, Rossi, M, Dejana, E, Breviario, F, Corada, M, Erba, Bg, Rambaldi, A, Amaru, A, Barbui, T, Belotti, C, Boroni, C, Ferrari, Ml, Finazzi, G, Finazzi, Mc, Golay, J, Gritti, G, Salmoiraghi, S, Cilloni, Daniela, Campia, V, Carturan, S, Guerrasio, Angelo, Manfredini, R, Bianchi, E, Salati, S, Tagliafico, E, Tenedini, E, Zini, R.
We studied the impact of driver mutations of JAK2, CALR, (calreticulin gene) or MPL on clinical course, leukemic transformation, and survival of patients with primary myelofibrosis (PMF). Of the 617 subjects studied, 399 (64.7%) carried JAK2 (V617F),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fcc20185ca75ffed69c01238001098b
https://europepmc.org/articles/PMC4133481/
https://europepmc.org/articles/PMC4133481/
Autor:
Balduini, Cl, Pecci, A, Loffredo, G, Izzo, P, Noris, P, Grosso, M, Bergamaschi, G, Rosti, V, Magrini, U, Ceresa, If, Conti, V, Poggi, V, Savoia, Anna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4fbc1e9b4a2416706b3a037d16aecee6
https://hdl.handle.net/11368/1701487
https://hdl.handle.net/11368/1701487
Autor:
SERI M, CUSANO R, GANGAROSSA S, CARIDI G, BORDO D, LO NIGRO C, GHIGGERI GM, RAVAZZOLO R, SAVINO M, DEL VECCHIO M, D'APOLITO M, ZELANTE LL, SAVOIA A, BALDUINI CL, NORIS P, MAGRINI U, BELLETTI S, HEATH KE, BABCOCK M, GLUCKSMAN MJ, ALIPRANDIS E, BIZZARO N, DESNICK RJ, MARTIGNETTI J.A., IOLASCON, ACHILLE
Publikováno v:
Nature genetics. 26(1)
The autosomal dominant, giant-platelet disorders, May-Hegglin anomaly (MHA; MIM 155100), Fechtner syndrome (FTNS; MIM 153640) and Sebastian syndrome (SBS), share the triad of thrombocytopenia, large platelets and characteristic leukocyte inclusions (