The Clinical Chameleon of Autoinflammatory Diseases in Children von Sangiorgi, Eugenio, Rigante, Donato

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intestinal stem cell markers Bmi1 and Lgr5 identify two functionally distinct populations von Yan, Kelley S, Chia, Luis A, Li, Xingnan, Ootani, Akifumi, Su, James, Lee, Josephine Y, Su, Nan, Luo, Yuling, Heilshorn, Sarah C, Amieva, Manuel R, Sangiorgi, Eugenio, Capecchi, Mario R, Kuo, Calvin J

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Sustained in vitro intestinal epithelial culture within a Wnt-dependent stem cell niche von Ootani, Akifumi, Li, Xingnan, Sangiorgi, Eugenio, Ho, Quoc T, Ueno, Hiroo, Toda, Shuji, Sugihara, Hajime, Fujimoto, Kazuma, Weissman, Irving L, Capecchi, Mario R, Kuo, Calvin J

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Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome von Sangiorgi, Eugenio, Azzarà, Alessia, Molinario, Clelia, Pietrobono, Roberta, Rigante, Donato, Verrecchia, Elena, Sicignano, Ludovico Luca, Genuardi, Maurizio, Gurrieri, Fiorella, Manna, Raffaele

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Bmi1 lineage tracing identifies a self-renewing pancreatic acinar cell subpopulation capable of maintaining pancreatic organ homeostasis von Sangiorgi, Eugenio, Capecchi, Mario R

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Clinical and molecular features of familial chronic lymphocytic leukemia: a pilot monocentric study von Benintende, Giulia, Innocenti, Idanna, Fresa, Alberto, Autore, Francesco, Tomasso, Annamaria, Piciocchi, Alfonso, Vuono, Florenzia, Stirparo, Luca, Mosca, Antonio, Bacigalupo, Andrea, Gattei, Valter, Efremov, Dimitar, Sangiorgi, Eugenio, Laurenti, Luca

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Results of a Gene Panel Approach in a Cohort of Patients with Incomplete Distal Renal Tubular Acidosis and Nephrolithiasis von D’Ambrosio, Viola, Azzarà, Alessia, Sangiorgi, Eugenio, Gurrieri, Fiorella, Hess, Bernhard, Gambaro, Giovanni, Ferraro, Pietro Manuel

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From Churchill to Elephants: The Role of Protective Genes against Cancer von Gazzellone, Annalisa, Sangiorgi, Eugenio

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Bmi1 is expressed in vivo in intestinal stem cells von Sangiorgi, Eugenio, Capecchi, Mario R

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P0058THE ROLE OF GENETICS IN INCOMPLETE DISTAL RENAL TUBULAR ACIDOSIS IN NEPHROLITHIASIS von D'Ambrosio, Viola, Sangiorgi, Eugenio, Hess, Bernhard, Gambaro, Giovanni, Ferraro, Pietro Manuel

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Identification of new candidate genes for spina bifida through exome sequencing von Azzarà, Alessia, Rendeli, Claudia, Crivello, Anna Maria, Brugnoletti, Fulvia, Rumore, Roberto, Ausili, Emanuele, Sangiorgi, Eugenio, Gurrieri, Fiorella

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BMI1 represses Ink4a/Arf and Hox genes to regulate stem cells in the rodent incisor von Biehs, Brian, Hu, Jimmy Kuang-Hsien, Strauli, Nicolas B., Sangiorgi, Eugenio, Jung, Heekyung, Heber, Ralf-Peter, Ho, Sunita, Goodwin, Alice F., Dasen, Jeremy S., Capecchi, Mario R., Klein, Ophir D.

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RADX Gene Variant May Predispose to Familial Asperger Syndrome von Azzarà, Alessia, Rumore, Roberto, Brugnoletti, Fulvia, Tabolacci, Elisabetta, Bottillo, Irene, Sangiorgi, Eugenio, Gurrieri, Fiorella

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IRADX/I Gene Variant May Predispose to Familial Asperger Syndrome von Azzarà, Alessia, Rumore, Roberto, Brugnoletti, Fulvia, Tabolacci, Elisabetta, Bottillo, Irene, Sangiorgi, Eugenio, Gurrieri, Fiorella

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Phenotypic effects of chronic and acute use of methiopropamine in a mouse model von Foti, Federica, Marti, Matteo, Ossato, Andrea, Bilel, Sabrine, Sangiorgi, Eugenio, Botrè, Francesco, Cerbelli, Bruna, Baldi, Alfonso, De-Giorgio, Fabio

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Base-Excision Repair Mutational Signature in Two Sebaceous Carcinomas of the Eyelid von Sangiorgi, Eugenio, Giannuzzi, Federico, Molinario, Clelia, Rapari, Giulia, Riccio, Melania, Cuffaro, Giovanni, Castri, Federica, Benvenuto, Roberta, Genuardi, Maurizio, Massi, Daniela, Savino, Gustavo

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Identification by Exome Sequencing of Predisposing Variants in Familial Cases of Autoinflammatory Recurrent Fevers von Sangiorgi, Eugenio, Azzarà, Alessia, Rumore, Roberto, Cassano, Ilaria, Verrecchia, Elena, Giacò, Luciano, Tullio, Maria Alessandra, Gurrieri, Fiorella, Manna, Raffaele

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Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura von Milillo, Annamaria, Molinario, Clelia, Costanzi, Stefano, Vischini, Gisella, La Carpia, Francesca, La Greca, Francesco, Rigante, Donato, Gambaro, Giovanni, Gurrieri, Fiorella, Sangiorgi, Eugenio

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DNA Methylation in the Diagnosis of Monogenic Diseases von Cerrato, Flavia, Sparago, Angela, Ariani, Francesca, Brugnoletti, Fulvia, Calzari, Luciano, Coppedè, Fabio, De Luca, Alessandro, Gervasini, Cristina, Giardina, Emiliano, Gurrieri, Fiorella, Lo Nigro, Cristiana, Merla, Giuseppe, Miozzo, Monica, Russo, Silvia, Sangiorgi, Eugenio, Sirchia, Silvia M, Squeo, Gabriella Maria, Tabano, Silvia, Tabolacci, Elisabetta, Torrente, Isabella, Genuardi, Maurizio, Neri, Giovanni, Riccio, Andrea

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A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy von Milillo, Annamaria, La Carpia, Francesca, Costanzi, Stefano, D'Urbano, Vanessa, Martini, Maurizio, Lanuti, Paola, Vischini, Gisella, Larocca, Luigi M, Marchisio, Marco, Miscia, Sebastiano, Amoroso, Antonio, Gurrieri, Fiorella, Sangiorgi, Eugenio

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