Polycythemia is associated with bone loss and reduced osteoblast activity in mice
Oikonomidou, P. R., Casu, C., Yang, Z., Crielaard, B., Shim, J. H., Rivella, S., Vogiatzi, M. G.
Published in Osteoporosis international (01.04.2016)
Published in Osteoporosis international (01.04.2016)
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P1520: AN ACTIVIN RECEPTOR IIB LIGAND TRAP, IN COMBINATION WITH TMPRSS6 INDUCED IRON‐RESTRICTION, IS A SUPERIOR TREATMENT FOR CORRECTING Β‐THALASSEMIA IN MICE
Guerra, A., Demsko, P., Sinha, S., McVeigh, P., Castruccio Castracani, C., Breda, L., Casu, C., Guo, S., Rivella, S.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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S102: OBLIGATE N‐TERMINAL BUT NOT C‐TERMINAL MONOFERRIC TRANSFERRIN AMELIORATES ANEMIA IN β‐THALASSEMIC MICE
Guerra, A., Parrow, N.L., McVeigh, P., Fleming, R.E., Ginzburg, Y.Z., Rivella, S.
Published in HemaSphere (01.01.2022)
Published in HemaSphere (01.01.2022)
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Journal Article
S101: COMBINATION OF A LUSPATERCEPT‐LIKE DRUG (RAP‐GRL) AND TMPRSS6‐ASO IS SUPERIOR TO EITHER DRUG ALONE FOR CORRECTING β‐THALASSEMIA
Guerra, A., Demsko, P., Sinha, S., McVeigh, P., Castruccio Castracani, C., Breda, L., Casu, C., Rivella, S.
Published in HemaSphere (01.01.2022)
Published in HemaSphere (01.01.2022)
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Journal Article
P1509: BONE MARROW TFR2 GENETIC DELETION ABROGATES BLOOD TRANFUSION REQUIREMENT IN THE HBBTH1/TH2 Β‐THALASSEMIC MURINE MODEL
Di Modica, S. M., Tanzi, E., Olivari, V., Lidonnici, M. R., Pettinato, M., Pagani, A., Tiboni, F., Ferrari, G., Silvestri, L., Rivella, S., Nai, A.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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P1521: A SEVERE MOUSE MODEL OF ALPHA‐THALASSEMIA SHOWS ABNORMAL IRON METABOLISM, ERYTHROPOIESIS AND COAGULATION, AND CAN BE RESCUED BY A NOVEL GENE THERAPY APPROACH
Rivella, S., Chappell, M., Jarocha, D., Breda, L., Ghiaccio, V., Fedorky, M., Triebwasser, M., Guerra, A., Gollomp, K., Teawtrakul, N., Glentis, S., Kattamis, A., Abdulmalik, O.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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Journal Article
S104: A SEVERE MOUSE MODEL OF ALPHA‐THALASSEMIA SHOWS ABNORMAL IRON METABOLISM, ERYTHROPOIESIS AND COAGULATION, AND CAN BE RESCUED BY A NOVEL GENE THERAPY APPROACH
Chappell, M, Breda, L, Guerra, A, Ghiaccio, V, Fedorky, M, Jarocha, D, Gollomp, K, Teawtrakul, N, Glentis, S, Kattamis, A, Rivella, S
Published in HemaSphere (01.01.2022)
Published in HemaSphere (01.01.2022)
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Journal Article
Non-transfusion-dependent thalassemias
Musallam, Khaled M, Rivella, Stefano, Vichinsky, Elliott, Rachmilewitz, Eliezer A
Published in Haematologica (Roma) (01.06.2013)
Published in Haematologica (Roma) (01.06.2013)
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Transcriptional Organization of a 450-kb Region of the Human X Chromosome in Xq28
Bione, S., Tamanini, F., Maestrini, E., Tribioli, C., Poustka, A., Torri, G., Rivella, S., Toniolo, D.
Published in Proceedings of the National Academy of Sciences - PNAS (01.12.1993)
Published in Proceedings of the National Academy of Sciences - PNAS (01.12.1993)
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Combination of Tmprss6- ASO and the iron chelator deferiprone improves erythropoiesis and reduces iron overload in a mouse model of beta-thalassemia intermedia
Casu, Carla, Aghajan, Mariam, Oikonomidou, Paraskevi Rea, Guo, Shuling, Monia, Brett P, Rivella, Stefano
Published in Haematologica (Roma) (01.01.2016)
Published in Haematologica (Roma) (01.01.2016)
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The murine growth differentiation factor 15 is not essential for systemic iron homeostasis in phlebotomized mice
Casanovas, Guillem, Vujić Spasic, Maja, Casu, Carla, Rivella, Stefano, Strelau, Jens, Unsicker, Klaus, Muckenthaler, Martina U
Published in Haematologica (Roma) (01.03.2013)
Published in Haematologica (Roma) (01.03.2013)
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Journal Article
Mapping of two genes encoding isoforms of the actin binding protein ABP-280, a dystrophin like protein, to Xq28 and to chromosome 7
Maestrini, E, Patrosso, C, Mancini, M, Rivella, S, Rocchi, M, Repetto, M, Villa, A, Frattini, A, Zoppè, M, Vezzoni, P
Published in Human molecular genetics (01.06.1993)
Published in Human molecular genetics (01.06.1993)
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Isolation of new genes in distal Xq28: transcriptional map and identification of a human homologue of the ARD1 N-acetyl transferase of Saccharomyces cerevisiae
Tribioli, C, Mancini, M, Plassart, E, Bione, S, Rivella, S, Sala, C, Torri, G, Toniolo, D
Published in Human molecular genetics (01.07.1994)
Published in Human molecular genetics (01.07.1994)
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Journal Article
Hepcidin is regulated by promoter-associated histone acetylation and HDAC3
Pasricha, Sant-Rayn, Lim, Pei Jin, Duarte, Tiago L., Casu, Carla, Oosterhuis, Dorenda, Mleczko-Sanecka, Katarzyna, Suciu, Maria, Da Silva, Ana Rita, Al-Hourani, Kinda, Arezes, João, McHugh, Kirsty, Gooding, Sarah, Frost, Joe N., Wray, Katherine, Santos, Ana, Porto, Graça, Repapi, Emmanouela, Gray, Nicki, Draper, Simon J., Ashley, Neil, Soilleux, Elizabeth, Olinga, Peter, Muckenthaler, Martina U., Hughes, Jim R., Rivella, Stefano, Milne, Thomas A., Armitage, Andrew E., Drakesmith, Hal
Published in Nature communications (01.09.2017)
Published in Nature communications (01.09.2017)
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A novel murine model of Cooley anemia and its rescue by lentiviral-mediated human β-globin gene transfer
Rivella, Stefano, May, Chad, Chadburn, Amy, Rivière, Isabelle, Sadelain, Michel
Published in Blood (15.04.2003)
Published in Blood (15.04.2003)
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Recent trends in the gene therapy of β-thalassemia
Finotti, Alessia, Breda, Laura, Lederer, Carsten W, Bianchi, Nicoletta, Zuccato, Cristina, Kleanthous, Marina, Rivella, Stefano, Gambari, Roberto
Published in Journal of Blood Medicine (01.01.2015)
Published in Journal of Blood Medicine (01.01.2015)
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Book Review
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)
ROUSSEAU, F, VINCENT, A, TONIOLO, D, OBERLE, I, RIVELLA, S, HEITZ, D, TRIBOLI, C, MAESTRINI, E, WARREN, S. T, SUTHERS, G. K, GOODFELLOW, P, MANDEL, J. L
Published in American journal of human genetics (1991)
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Published in American journal of human genetics (1991)
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