Sfoglia per SSD
UDP exerts cytostatic and cytotoxic actions in human neuroblastoma SH-SY5Y cells over-expressing P2Y6 receptor
2010 Apolloni, S; Finocchi, P; D'Agnano, I; Alloisio, S; Nobile, M; D'Ambrosi, Nadia; Volonté, C.
[Ultrastructural observations on choroid neurons of ciliary ganglia]
1980 Olivieri Sangiacomo, C; Del Fa' Gangitano, Aurora
Umbilical cord versus bone marrow-derived mesenchymal stromal cells
2012 Huang, Yong Can; Parolini, Ornella; La Rocca, Giampiero; Deng, Li
Use of highly sensitive mitochondrial probes to detect microchimerism in xenotransplantation models
2006 Soncini, Maddalena; Signoroni, Patrizia Bonassi; Bailo, Marco; Zatti, Daniela; Gregori, Alessandra; Lombardi, Guerino; Albertini, Alberto; Wengler, Georg S; Parolini, Ornella
The Use of Placenta-Derived Cells in Autoimmune Disorders
2016 Antonietta Rosa, Silini; Parolini, Ornella; Mario, Delgado
Use of the highly polymorphic DNA marker CRI-S232 for monitoring of engraftment and chimerism following bone marrow transplantation
1991 Notarangelo, L. D; Parolini, Ornella; Porta, F; Arrighini, Alberto; Basagni, G; Candotti, F; Cavagna, Anna; Cossandi, Gianmarco; Crescini, C; Faustini, R.
The Wiskott-Aldrich syndrome (WAS) gene is expressed prior to the granulocyte-macrophage colony forming unit (GM-CFU) stage of hematopoietic differentiation
1993 Mantuano, E; Notarangelo, Ld; Candotti, F; Giliani, S; Lusardi, M; Parolini, Ornella; Porta, F; Ugazio, Ag
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27ß
1992 De Saint Basile, G; Notarangelo, Ld; Bonaiti Pellie, C; Doussau, M; Parolini, Ornella; Craig, Iw; Ugazio, A; Griscelli, C; Fischer, A.
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty
1994 Buzi, F; Notarangelo, L. D; Plebani, A; Duse, M; Parolini, Ornella; Monteleone, M; Ugazio, A. G.
X-linked agammaglobulinemia: new approaches to old questions based on the identification of the defective gene
1994 Conley, M E; Parolini, Ornella; Rohrer, J; Campana, D
X-linked Wiskott-Aldrich syndrome in a girl
1998 Parolini, Ornella; Ressmann, G; Haas, O. A; Pawlowsky, J; Gadner, H; Knapp, W; Holter, W.
XRCC1 Arg399Gln gene polymorphism and hepatocellular carcinoma risk in the Italian population
2017 Santonocito, Concetta; Scapaticci, Margherita; Nedovic, Bojan; Annicchiarico, Eleonora B; Guarino, Donatella; Leoncini, Emanuele; Boccia, Stefania; Gasbarrini, Antonio; Capoluongo, Ettore Domenico
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2010 | UDP exerts cytostatic and cytotoxic actions in human neuroblastoma SH-SY5Y cells over-expressing P2Y6 receptor | Apolloni, S; Finocchi, P; D'Agnano, I; Alloisio, S; Nobile, M; D'Ambrosi, Nadia; Volonté, C. | |
| 1-gen-1980 | [Ultrastructural observations on choroid neurons of ciliary ganglia] | Olivieri Sangiacomo, C; Del Fa' Gangitano, Aurora | |
| 1-gen-2012 | Umbilical cord versus bone marrow-derived mesenchymal stromal cells | Huang, Yong Can; Parolini, Ornella; La Rocca, Giampiero; Deng, Li | |
| 1-gen-2006 | Use of highly sensitive mitochondrial probes to detect microchimerism in xenotransplantation models | Soncini, Maddalena; Signoroni, Patrizia Bonassi; Bailo, Marco; Zatti, Daniela; Gregori, Alessandra; Lombardi, Guerino; Albertini, Alberto; Wengler, Georg S; Parolini, Ornella | |
| 1-gen-2016 | The Use of Placenta-Derived Cells in Autoimmune Disorders | Antonietta Rosa, Silini; Parolini, Ornella; Mario, Delgado | |
| 1-gen-1991 | Use of the highly polymorphic DNA marker CRI-S232 for monitoring of engraftment and chimerism following bone marrow transplantation | Notarangelo, L. D; Parolini, Ornella; Porta, F; Arrighini, Alberto; Basagni, G; Candotti, F; Cavagna, Anna; Cossandi, Gianmarco; Crescini, C; Faustini, R. | |
| 1-gen-1993 | The Wiskott-Aldrich syndrome (WAS) gene is expressed prior to the granulocyte-macrophage colony forming unit (GM-CFU) stage of hematopoietic differentiation | Mantuano, E; Notarangelo, Ld; Candotti, F; Giliani, S; Lusardi, M; Parolini, Ornella; Porta, F; Ugazio, Ag | |
| 1-gen-1992 | Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27ß | De Saint Basile, G; Notarangelo, Ld; Bonaiti Pellie, C; Doussau, M; Parolini, Ornella; Craig, Iw; Ugazio, A; Griscelli, C; Fischer, A. | |
| 1-gen-1994 | X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty | Buzi, F; Notarangelo, L. D; Plebani, A; Duse, M; Parolini, Ornella; Monteleone, M; Ugazio, A. G. | |
| 1-gen-1994 | X-linked agammaglobulinemia: new approaches to old questions based on the identification of the defective gene | Conley, M E; Parolini, Ornella; Rohrer, J; Campana, D | |
| 1-gen-1998 | X-linked Wiskott-Aldrich syndrome in a girl | Parolini, Ornella; Ressmann, G; Haas, O. A; Pawlowsky, J; Gadner, H; Knapp, W; Holter, W. | |
| 1-gen-2017 | XRCC1 Arg399Gln gene polymorphism and hepatocellular carcinoma risk in the Italian population | Santonocito, Concetta; Scapaticci, Margherita; Nedovic, Bojan; Annicchiarico, Eleonora B; Guarino, Donatella; Leoncini, Emanuele; Boccia, Stefania; Gasbarrini, Antonio; Capoluongo, Ettore Domenico |
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