Sfoglia per Autore  TAMPELLA, Giacomo

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Mostrati risultati da 1 a 14 di 14
Titolo Data di pubblicazione Autore(i) File
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 1-gen-2009 Giambra, V; Cianci, R; Lolli, S; Mattioli, C; Tampella, Giacomo; Cattalini, Marco; Kilic, Ss; Pandolfi, F; Plebani, Alessandro; Frezza, D.
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. 1-gen-2011 Tampella, Giacomo; Baronio, Manuela; Vitali, Massimiliano; Soresina, A; Badolato, Raffaele; Giliani, Silvia Clara; Plebani, Alessandro; Lougaris, Vassilios
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 1-gen-2012 Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Soresina, A; Badolato, Raffaele; Plebani, Alessandro
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 1-gen-2012 Lopez Herrera, G.; Tampella, Giacomo; Pan Hammarstrom, Q.; Herholz, P.; Trujillo Vargas, C. M.; Phadwalk, ; Simon, A. K.; Moutschen, M.; Etzioni, A.; Mory, A.; Srugo, I.; Melamed, D.; Hultenby, K.; Liu, C.; Baronio, Manuela; Vitali, Massimiliano; Philippet, P.; Dideberg, V.; Aghamohammadi, A.; Rezaei, N.; Enright, V.; Du, L.; Salzer, U.; Eibel, H.; Pfeifer, D.; Veelken, H.; Stauss, H.; Lougaris, Vassilios; Plebani, Alessandro; Gertz, E. M.; Schaffer, A. A.; Hammarstrom, L.; Grimbacher, B.
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 1-gen-2014 Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Moratto, D; Tampella, Giacomo; Biasini, A; Badolato, Raffaele; Plebani, Alessandro
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 1-gen-2014 Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Cattalini, Marco; Tassone, L; Soresina, A; Badolato, Raffaele; Plebani, Alessandro
BAFF-R mutations in Good's syndrome. 1-gen-2014 Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Tampella, Giacomo; Plebani, Alessandro
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency 1-gen-2015 Gualdi, G; Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Moratto, D; Tanghetti, P; Monari, P; CALZAVARA PINTON, Piergiacomo; Plebani, Alessandro
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 1-gen-2015 Lougaris, Vassilios; Baronio, Manuela; Masneri, Stefania; Lorenzini, Tiziana; Cattivelli, Kim; Tampella, Giacomo; Soresina, Annarosa; Moratto, Daniele; Plebani, Alessandro
The tec kinase-regulated phosphoproteome reveals a mechanism for the regulation of inhibitory signals in murine macrophages 1-gen-2015 Tampella, Giacomo; Kerns, Hannah M.; Niu, Deqiang; Singh, Swati; Khim, Socheath; Bosch, Katherine A.; Garrett, Meghan E.; Moguche, Albanus; Evans, Erica; Browning, Beth; Jahan, Tahmina A.; Nacht, Mariana; Wolf Yadlin, Alejandro; Plebani, Alessandro; Hamerman, Jessica A.; Rawlings, David J.; James, Richard G.
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 1-gen-2015 Lougaris, Vassilios; Tabellini, Giovanna; Vitali, Massimiliano; Baronio, Manuela; Patrizi, Ornella; Tampella, Giacomo; Biasini, Augusto; Moratto, Daniele; Parolini, Silvia; Plebani, Alessandro
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 1-gen-2016 Lougaris, Vassilios; Moratto, Daniele; Baronio, Manuela; Tampella, Giacomo; van der Meer, Jos W. M; Badolato, Raffaele; Fliegauf, Manfred; Plebani, Alessandro
P85α is an intrinsic regulator of human natural killer cell effector functions 1-gen-2016 Lougaris, Vassilios; Patrizi, Ornella; Baronio, Manuela; Tabellini, Giovanna; Tampella, Giacomo; Lanzi, Gaetana; Salvini, Filippo; Trizzino, Antonino; Parolini, Silvia; Plebani, Alessandro
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 1-gen-2019 Lougaris, Vassilios; Baronio, Manuela; Moratto, Daniele; Tampella, Giacomo; Gazzurelli, Luisa; Facchetti, Mattia; Martire, Baldassarre; Cardinale, Fabio; Lanzarotto, Francesco; Bondioni, Maria Pia; Villanacci, Vincenzo; Grimbacher, Bodo; Plebani, Alessandro
Mostrati risultati da 1 a 14 di 14
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