Search Results - "Droetto, S."

Mutations of the tyrosinase gene in patients with oculocutaneous albinism from various ethnic groups in Israel by GERSHONI-BARUCH, R, ROSENMANN, A, DROETTO, S, HOLMES, S, TRIPATHI, R. K, SPRITZ, R. A

“…We have analyzed the tyrosinase (TYR) gene in 38 unrelated patients with oculocutaneous albinism (OCA), derived from several different ethnic groups of the…”
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An X chromosome-linked gene encoding a protein with characteristics of a rhoGAP predominantly expressed in hematopoietic cells by Tribioli, C, Droetto, S, Bione, S, Cesareni, G, Torrisi, M R, Lotti, L V, Lanfrancone, L, Toniolo, D, Pelicci, P

“…An increasingly large number of proteins involved in signal transduction have been identified in recent years and shown to control different steps of cell…”
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Expression of the IRTA1 receptor identifies intraepithelial and subepithelial marginal zone B cells of the mucosa-associated lymphoid tissue (MALT) by Falini, Brunangelo, Tiacci, Enrico, Pucciarini, Alessandra, Bigerna, Barbara, Kurth, Julia, Hatzivassiliou, Georgia, Droetto, Sara, Galletti, Barbara Verducci, Gambacorta, Marcello, Orazi, Attilio, Pasqualucci, Laura, Miller, Ira, Küppers, Ralf, Dalla-Favera, Riccardo, Cattoretti, Giorgio

“…IRTA1 (immunoglobulin superfamily receptor translocation-associated 1) is a novel surface B-cell receptor related to Fc receptors, inhibitory receptor…”
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Lentiviral gene transfer and ex vivo expansion of human primitive stem cells capable of primary, secondary, and tertiary multilineage repopulation in NOD/SCID mice by Piacibello, Wanda, Bruno, Stefania, Sanavio, Fiorella, Droetto, Sara, Gunetti, Monica, Ailles, Laurie, de Sio, Francesca Santoni, Viale, Andrea, Gammaitoni, Loretta, Lombardo, Angelo, Naldini, Luigi, Aglietta, Massimo

“…The ability of advanced-generation lentiviral vectors to transfer the green fluorescent protein (GFP) gene into human hematopoietic stem cells (HSCs) was…”
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Vasculogenic potential of long term repopulating cord blood progenitors by Droetto, Sara, Viale, Andrea, Primo, Luca, Jordaney, Noela, Bruno, Stefania, Pagano, Marco, Piacibello, Wanda, Bussolino, Federico, Aglietta, Massimo

“…ABSTRACT In the adult, involvement of bone marrow‐derived circulating endothelial progenitor cells (EPCs) in tissue revascularization (vasculogenesis) and the…”
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Deletion of the KIT and PDGFRA genes in a patient with piebaldism by Spritz, R A, Droetto, S, Fukushima, Y

“…We have previously shown that human piebaldism results from mutations of the KIT gene, which encodes the receptor for the mast/stem cell growth factor and is…”
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Role of T‐helper type 2 cytokines in down‐modulation of Fas mRNA and receptor on the surface of activated CD4+ T cells: molecular basis for the persistence of the allergic immune response by Spinozzi, Fabrizio, Agea, Elisabetta, Fizzotti, Marco, Bassotti, Gabrio, Russano, Anna, Droetto, Sara, Bistoni, Onelia, Grignani, Fausto, Bertotto, Alberto

“…ABSTRACT The mechanisms responsible for persistence of T lymphocytes at the sites of allergic inflammation are not completely understood. Activated T cells,…”
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Defective expression of Fas messenger RNA and Fas receptor on pulmonary T cells from patients with asthma by SPINOZZI, F, FIZZOTTI, M, AGEA, E, PIATTONI, S, DROETTO, S, RUSSANO, A, FORENZA, N, BASSOTTI, G, GRIGNANI, F, BERTOTTO, A

“…Inflammation at sites of target organs seems to be the pathologic hallmark of respiratory allergic diseases, but why this response cannot be turned off in…”
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Role of T-helper type 2 cytokines in down-modulation of Fas mRNA and receptor on the surface of activated CD4 super(+) T cells: molecular basis for the persistence of the allergic immune response by Spinozzi, F, Agea, E, Fizzotti, M, Bassotti, G, Russano, A, Droetto, S, Bistoni, O, Grignani, F, Bertotto, A

“…The mechanisms responsible for persistence of T lymphocytes at the sites of allergic inflammation are not completely understood. Activated T cells, usually…”
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Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA) by TRIPATHI, R. K, BUNDEY, S, MUSARELLA, M. A, DROETTO, S, STRUNK, K. M, HOLMES, S. A, SPRITZ, R. A

“…Oculocutaneous albinism (OCA) is a group of autosomal recessive disorders characterized by deficient synthesis of melanin pigment. Type I…”
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Mutations of the tyrosinase gene in patients with oculocultaneous albinism from various ethnic groups in Israel by Gershoni-Baruch, R, Rosenmann, A, Droetto, S, Holmes, S, Tripathi, R K, Spritz, R A

“…We have analyzed the tyrosinase (TYR) gene in 38 unrelated patients with oculocutaneous albinism (OCA), derived from several different ethnic groups of the…”
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Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinsm (OCA) by Tripathi, R.K., Droetto, S., Strunk, K.M., Holmes, S.A., Spritz, R.A., Bundey, S., Musarella, M.A.

“…Oculocutaneous albinism (OCA) is a group of autosomal recessive disorders characterized by deficient synthesis of melanin pigment. Type I…”
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