Sangiorgi, Eugenio

Sangiorgi, Eugenio  

ROMA - Dipartimento di Scienze della vita e sanità pubblica  

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Data di pubblicazione Titolo Autore(i) File
1-gen-1996 A split hand-split foot (SHFM3) gene is located at 10q24-->25 Gurrieri, Fiorella; Prinos, P; Tackels, D; Kilpatrick, Mw; Allanson, J; Genuardi, M; Vuckov, A; Nanni, L; Sangiorgi, Eugenio; Garofalo, G; Nunes, Me; Neri, Giovanni; Schwartz, C; Tsipouras, P.
1-gen-2015 A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy. Sangiorgi, Eugenio; Gurrieri, Fiorella; Milillo, Annamaria; La Carpia, Francesca; Costanzi, Stefano; Martini, Maurizio; Larocca, Luigi Maria; Vischini, Gisella
1-gen-2001 Advances in the genetics of progressive myoclonus epilepsy Torrisi, L.; Sangiorgi, E.; Russo, L.; Gurrieri, F.
1-gen-2007 Applicazioni dell'ingegneria genetica in medicina Tiziano, Francesco Danilo; Sangiorgi, Eugenio
1-gen-2008 Bmi1 is expressed in vivo in intestinal stem cells Sangiorgi, Eugenio; Capecchi, Mr
1-gen-2009 Bmi1 lineage tracing identifies a self-renewing pancreatic acinar cell subpopulation capable of maintaining pancreatic organ homeostasis Sangiorgi, Eugenio; Capecchi, Mr
1-gen-2013 BMI1 represses Ink4a/Arf and Hox genes to regulate stem cells in the rodent incisor Biehs, B; Hu, Jk; Strauli, Nb; Sangiorgi, Eugenio; Jung, H; Heber, R; Ho, S; Goodwin, Af; Dasen, Js; Capecchi, Mr; Klein, Od
1-gen-2022 The clinical chameleon of autoinflammatory diseases in children Sangiorgi, E; Rigante, D
1-gen-2018 Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schonlein purpura Milillo, A; Molinario, C; Costanzi, S; Vischini, G; La Carpia, F; La Greca, F; Rigante, D; Gambaro, G; Gurrieri, F; Sangiorgi, E
1-gen-2018 Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura Milillo, A; Molinario, C; Costanzi, S; Vischini, G; La Carpia, F; La Greca, F; Rigante, D; Gambaro, G; Gurrieri, F; Sangiorgi, E.
1-gen-2007 Difetti genetici dello sviluppo embrionale Gurrieri, Fiorella; Sangiorgi, Eugenio
1-gen-2020 DNA Methylation in the Diagnosis of Monogenic Diseases. Cerrato, F; Sparago, A; Ariani, F; Brugnoletti, F; Calzari, L; Coppedè, F; De Luca, A; Gervasini, C; Giardina, E; Gurrieri, F; Lo Nigro, C; Merla, G; Miozzo, M; Russo, S; Sangiorgi, E; Sirchia, Sm; Squeo, Gm; Tabano, S; Tabolacci, E; Torrente, I; Genuardi, M; Neri, G; Riccio, A.
1-gen-2016 Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects. La Carpia, Francesca; Rendeli, Claudia; Molinario, Clelia; Milillo, Annamaria; Farroni, C.; Cannelli, Natalia; Ausili, Emanuele; Paolucci, V.; Neri, Giovanni; Romagnoli, Costantino; Sangiorgi, Eugenio; Gurrieri, Fiorella
1-gen-2016 Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects. La Carpia, Francesca; Rendeli, Claudia; Molinario, Clelia; Milillo, Annamaria; Farroni, C; Cannelli, Natalia; Ausili, Emanuele; Paolucci, V; Neri, Giovanni; Romagnoli, Costantino; Sangiorgi, Eugenio; Gurrieri, Fiorella
1-gen-2022 Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome Kozycki, Christina Torres; Kodati, Shilpa; Huryn, Laryssa; Wang, Hongying; Warner, Blake M; Jani, Priyam; Hammoud, Dima; Abu-Asab, Mones S; Jittayasothorn, Yingyos; Mattapallil, Mary J; Tsai, Wanxia Li; Ullah, Ehsan; Zhou, Ping; Tian, Xiaoying; Soldatos, Ariane; Moutsopoulos, Niki; Kao-Hsieh, Marie; Heller, Theo; Cowen, Edward W; Lee, Chyi-Chia Richard; Toro, Camilo; Kalsi, Shelley; Khavandgar, Zohreh; Baer, Alan; Beach, Margaret; Long Priel, Debra; Nehrebecky, Michele; Rosenzweig, Sofia; Romeo, Tina; Deuitch, Natalie; Brenchley, Laurie; Pelayo, Eileen; Zein, Wadih; Sen, Nida; Yang, Alexander H; Farley, Gary; Sweetser, David A; Briere, Lauren; Yang, Janine; de Oliveira Poswar, Fabiano; Schwartz, Ida Vanessa D; Silva Alves, Tamires; Dusser, Perrine; Koné-Paut, Isabelle; Touitou, Isabelle; Titah, Salah Mohamed; van Hagen, Petrus Martin; van Wijck, Rogier T A; van der Spek, Peter J; Yano, Hiromi; Benneche, Andreas; Apalset, Ellen M; Jansson, Ragnhild Wivestad; Caspi, Rachel R; Kuhns, Douglas Byron; Gadina, Massimo; Takada, Hidetoshi; Ida, Hiroaki; Nishikomori, Ryuta; Verrecchia, Elena; Sangiorgi, Eugenio; Manna, Raffaele; Brooks, Brian P; Sobrin, Lucia; Hufnagel, Robert B; Beck, David; Shao, Feng; Ombrello, Amanda K; Aksentijevich, Ivona; Kastner, Daniel L
1-gen-2021 Identification of new candidate genes for spina bifida through exome sequencing Azzara, A.; Rendeli, C.; Crivello, A. M.; Brugnoletti, F.; Rumore, R.; Ausili, E.; Sangiorgi, E.; Gurrieri, F.
1-gen-2008 In vivo evaluation of PhiC31 recombinase activity using a self-excision cassette Sangiorgi, Eugenio; Shuhua, Z; Capecchi, Mr
1-gen-2009 Morphology and immunophenotyping of a monolateral ovotestis in a 46,XderY/45,X mosaic individual with ambiguous genitalia Zannoni, G. F; Vellone, G; Cordisco, E. L; Sangiorgi, Eugenio; Grimaldi, Maria Eufemia; Neri, Caterina; Nanni, L; Neri, Giovanni
1-gen-2010 Morphology and immunophenotyping of a monolateral ovotestis in a 46,XderY/45,X mosaic individual with ambiguous genitalia Zannoni, Gf; Vellone, Vg; Cordisco, El; Sangiorgi, Eugenio; Grimaldi, Me; Neri, C; Nanni, L; Neri, G.
1-gen-1999 Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13 Gurrieri, Fiorella; Battaglia, A; Torrisi, L; Tancredi, R; Cavallaro, C; Sangiorgi, Eugenio; Neri, Giovanni