Human Amnion Mesenchyme Harbors Cells with Allogeneic T‐Cell Suppression and Stimulation Capabilities von Magatti, Marta, De Munari, Silvia, Vertua, Elsa, Gibelli, Lucia, Wengler, Georg S., Parolini, Ornella

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Isolation and characterization of mesenchymal cells from human fetal membranes von Soncini, Maddalena, Vertua, Elsa, Gibelli, Lucia, Zorzi, Fausto, Denegri, Marco, Albertini, Alberto, Wengler, Georg S., Parolini, Ornella

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Transplantation of Allogeneic and Xenogeneic Placenta-Derived Cells Reduces Bleomycin-Induced Lung Fibrosis von Cargnoni, Anna, Gibelli, Lucia, Tosini, Alessandra, Signoroni, Patrizia Bonassi, Nassuato, Claudia, Arienti, Davide, Lombardi, Guerino, Albertini, Alberto, Wengler, Georg S., Parolini, Ornella

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Amniotic Mesenchymal Tissue Cells Inhibit Dendritic Cell Differentiation of Peripheral Blood and Amnion Resident Monocytes von Magatti, Marta, De Munari, Silvia, Vertua, Elsa, Nassauto, Claudia, Albertini, Alberto, Wengler, Georg S., Parolini, Ornella

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Engraftment potential of human amnion and chorion cells derived from term placenta von Bailo, Marco, Soncini, Maddalena, Vertua, Elsa, Signoroni, Patrizia Bonassi, Sanzone, Silvia, Lombardi, Guerino, Arienti, Davide, Calamani, Francesca, Zatti, Daniela, Paul, Petra, Albertini, Alberto, Zorzi, Fausto, Cavagnini, Angelo, Candotti, Fabio, Wengler, Georg S, Parolini, Ornella

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Molecular signature detection of circulating tumor cells using a panel of selected genes von Gervasoni, Annalisa, Monasterio Muñoz, Rina M, Wengler, Georg S, Rizzi, Anna, Zaniboni, Alberto, Parolini, Ornella

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In-utero transplantation of parental CD34 haematopoietic progenitor cells in a patient with X-linked severe combined immunodeficiency (SCIDX1) von Wengler, Georg S, Lanfranchi, Arnalda, Frusca, Tiziana, Verardi, Rosanna, Neva, Arabella, Brugnoni, Duilio, Giliani, Silvia, Fiorini, Maurilia, Mella, Patrizia, Guandalini, Fabiola, Mazzolari, Evelina, Notarangelo, LD, Pecorelli, Sergio, Porta, Fulvio, Ugazio, AG

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In utero transplantation of human cord blood cells into rabbits von Wengler, Georg S, Lombardi, Guerino, Frusca, Tiziana, Alberti, Daniele, Albertini, Alberto, Parolini, Ornella

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Conditioning of neonatal pigs using low-dose chemotherapy and murine fetal tissue before murine hybridoma transplantation von WENGIER, Georg S, BROCCHI, Emiliana, LOMBARDI, Guerino, BAILO, Marco, BONASSI, Patrizia, ARIENTI, Davide, ALBERTINI, Alberto, ALBERTI, Daniele, ZANINI, Roberto, PAROLINI, Ornella

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Use of highly sensitive mitochondrial probes to detect microchimerism in xenotransplantation models von Soncini, Maddalena, Signoroni, Patrizia Bonassi, Bailo, Marco, Zatti, Daniela, Gregori, Alessandra, Lombardi, Guerino, Albertini, Alberto, Wengler, Georg S., Parolini, Ornella

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Feasibility and potential of in utero foetal membrane-derived cell transplantation von Caruso, Maddalena, Bonassi Signoroni, Patrizia, Zanini, Roberto, Ressel, Lorenzo, Vertua, Elsa, Bonelli, Piero, Dattena, Maria, Varoni, Maria Vittoria, Wengler, Georg, Parolini, Ornella

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A PCR-based non-radioactive X-chromosome inactivation assay for genetic counseling in X-linked primary immunodeficiencies von Wengler, Georg S., Parolini, Ornella, Fiorini, Maurilia, Mella, Patrizia, Smith, Hedy, Ugazio, Alberto G., Notarangelo, Luigi D.

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Nonrandom inactivation of the X chromosome in early lineage hematopoietic cells in carriers of Wiskott-Aldrich syndrome von WENGLER, G, GORLIN, J. B, WILLIAMSON, J. M, ROSEN, F. S, BING, D. H

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In-Utero Transplantation of Parental CD34 Haematopoietic Progenitor Cells in a Patient With X-Linked Severe Combined Immunodeficiency (SCIDXI) von Wengler, Georg S, Lanfranchi, Arnalda, Frusca, Tiziana, Verardi, Rosanna, Neva, Arabella, Brugnoni, Duilio, Giliani, Silvia, Fiorini, Maurilia, Mella, Patrizia, Guandalini, Fabiola, Mazzolari, Evelina, Pecorelli, Sergio, Notarangelo, Luigi D, Porta, Fulvio, Ugazio, Alberto G

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High Prevalence of Nonsense, Frame Shift, and Splice-Site Mutations in 16 Patients With Full-Blown Wiskott-Aldrich Syndrome von Wengler, Georg S., Notarangelo, Luigi D., Berardelli, Stefania, Pollonni, Gabriella, Mella, Patrizia, Fasth, Anders, Ugazio, Alberto G., Parolini, Ornella

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Nonrandom X chromosome inactivation in natural killer cells from obligate carriers of X-linked severe combined immunodeficiency von Wengler, GS, Allen, RC, Parolini, O, Smith, H, Conley, ME

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Engraftment potential of human amnion and chorion cells derived from term placenta. Commentary von BAILO, Marco, SONCINI, Maddalena, ALBERTINI, Alberto, ZORZI, Fausto, CAVAGNINI, Angelo, CANDOTTI, Fabio, WENGLER, Georg S, PAROLINI, Ornella, HEEGER, Peter S, VERTUA, Elsa, BONASSI SIGNORONI, Patrizia, SANZONE, Silvia, LOMBARDI, Guerino, ARIENTI, Davide, CALAMANI, Francesca, ZATTI, Daniela, PAUL, Petra

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Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1) von WENGLER, G. S, GILIANI, S, PAROLINI, O, FIORINI, M, MELLA, P, MANTUANO, E, ZANOLA, A, POLLONINI, G, EIBL, M. M, UGAZIO, A. G, NOTARANGELO, L. D

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Mutation analysis by a non‐radioactive single‐strand conformation polymorphism assay in nine families with X‐linked severe combined immunodeficiency (SCIDX1) von Wengler, Georg S., Giliani, Silvia, Fiorini, Maurilia, Mella, Patrizia, Mantuano, Elide, Zanola, Alessandra, Pollonini, Gabriella, Eibl, Martha M., Ugazio, Alberto G., Notarangelo, Luigi D., Parolini, Ornella

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Mutation analysis in Wiskott Aldrich syndrome on chorionic villus DNA von Wengler, GeorgS, Notarangelo, LuigiD, Giliani, Silvia, Pirastru, MariaG, Ugazio, AlbertoG, Parolini, Ornella

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