COLAPIETRO, PATRIZIA
COLAPIETRO, PATRIZIA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome
2020 L. Fontana, M.F. Bedeschi, G.A. Cagnoli, J. Costanza, N. Persico, S. Gangi, M. Porro, P. Ajmone, P. Colapietro, C. Santaniello, M. Crippa, S.M. Sirchia, M. Miozzo, S. Tabano
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins
2018 L. Paganini, L.A. Hadi, M. Chetta, D. Rovina, L. Fontana, P. Colapietro, E. Bonaparte, L. Pezzani, P. Marchisio, S.M. Tabano, J. Costanza, S.M. Sirchia, L. Riboni, D. Milani, M. Miozzo
A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls
2019 S. Tabano, A. Caldiroli, A. Terrasi, P. Colapietro, S. Grassi, G.S. Carnevali, L. Fontana, M. Serati, V. Vaira, A.C. Altamura, M. Miozzo, M. Buoli
Altered H19 and SNAT2 expression in type 1 IUGR (Intrauterine Growth Restriction) placentas
2008 S. Tabano, C. Mandò, P. Colapietro, S. Zanutto, S. Calabrese, P. Pileri, V. Signorelli, M.R. Miozzo, I. Cetin
APPROCCI TECNOLOGICI MULTIPLI PER L'IDENTIFICAZIONE DI MUTAZIONI E MECCANISMI PATOGENETICI IN PAZIENTI CON SINDROME DI RUBINSTEIN-TAYBI
2012 C. Gervasini, G. Negri, P. Colapietro, F. Forzano, M. Silengo, C. Picinelli, D. Rusconi, L. Basso Ricci, L. Garavelli, ..R. Tenconi, P. Finelli, S. Spena, L. Larizza
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes
2022 J. Costanza, M. Camanni, M.M. Ferrari, V. De Cosmi, S. Tabano, L. Fontana, T. Radaelli, G. Privitera, D. Alberico, P. Colapietro, S. Motta, S. Sirchia, T. Stampalija, C. Tabasso, P. Roggero, F. Parazzini, F. Mosca, E. Ferrazzi, S. Bosari, M. Miozzo, C. Agostoni
Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome : an update of the CREBBP deletion repertoire
2015 D. Rusconi, G. Negri, P. Colapietro, C. Picinelli, D. Milani, S. Spena, C. Magnani, M.C. Silengo, L. Sorasio, V. Curtisova, M.L. Cavaliere, P. Prontera, G. Stangoni, G.B. Ferrero, E. Biamino, R. Fischetto, M. Piccione, P. Gasparini, L. Salviati, A. Selicorni, P. Finelli, L. Larizza, C. Gervasini
Circulating microRNAs Suggest Networks Associated with Biological Functions in Aggressive Refractory Type 2 Celiac Disease
2022 N. Bianchi, L. Doneda, L. Elli, C. Taccioli, V. Vaira, A. Scricciolo, V. Lombardo, A. Terrazzan, P. Colapietro, L. Terranova, C. Bergamini, M. Vecchi, L. Scaramella, N. Nandi, L. Roncoroni
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene
2015 G. Negri, D. Milani, P. Colapietro, F. Forzano, M. Della Monica, D. Rusconi, L. Consonni, L.G. Caffi, P. Finelli, G. Scarano, C. Magnani, A. Selicorni, S. Spena, L. Larizza, C. Gervasini
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance
2021 L. Fontana, S. Tabano, S. Maitz, P. Colapietro, E. Garzia, A.G. Gerli, S.M. Sirchia, M. Miozzo
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines
2021 S. Pileggi, M. La Vecchia, E.A. Colombo, L. Fontana, P. Colapietro, D. Rovina, A. Morotti, S.M. Tabano, G. Porta, M. Alcalay, C.C.G. Gervasini, M.R. Miozzo, S.M. Sirchia
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer
2019 J. Azzollini, C. Pesenti, S. Pizzamiglio, L. Fontana, C. Guarino, B. Peissel, M. Plebani, S. Tabano, S.M. Sirchia, P. Colapietro, R. Villa, B. Paolini, P. Verderio, M. Miozzo, S. Manoukian
DELEZIONI IN 16p13.2 COINVOLGENTI TOTALMENTE O PARZIALMENTE IL GENE CREBBP IN PAZIENTI CON SINDROME DI RUBINSTEIN-TAYBI
2013 C. Gervasini, D. Rusconi, P. Colapietro, S. Spena, C. Picinelli, G. Negri, D. Milani, A. Selicorni, P. Finelli, L. Larizza
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34(+)38(-) compartment
2010 L. Pedranzini, F. Mottadelli, S. Ronzoni, F. Rossella, M. Ferracin, I. Magnani, G. Roversi, P. Colapietro, M. Negrini, P.G. Pelicci, L. Larizza
Distinct expression pattern of microtubule-associated protein/microtubule affinity-regulating kinase 4 in differentiated neurons
2006 R.F. Moroni, S. De Biasi, P. Colapietro, L. Larizza, A. Beghini
Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population
1999 F. Natacci, P. Colapietro, P. Riva, L. Corrado, L.N. Rossi, M.M. Maninetti, M.C. Casciati, C.A. Zambrino, G. Lanzi, L. Larizza
Duplicazioni parziali di SHOX associate alla Sindrome di Mayer-Rokitansky-Kuster-Hauser
2009 C. Gervasini, F. Grati, S. Tabano, P. Colapietro, S. De Toffo, S.B. Maitz, B. Gentilin, G. Frontino, L. Bernardini, B. Dallapiccola, L. Fedele, F. Lalatta, L. Larizza, M. Miozzo
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction
2010 S. Tabano, P. Colapietro, I. Cetin, F.R. Grati, S. Zanutto, C. Mandò, P. Antonazzo, P. Pileri, F. Rossella, L. Larizza, S.M. Sirchia, M. Miozzo
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men
2014 A. Pansa, S.M. Sirchia, S. Melis, D. Giacchetta, M. Castiglioni, P. Colapietro, S. Fiori, R. Falcone, L. Paganini, E. Bonaparte, G. Colpi, M. Miozzo, S. Tabano
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions
2004 M. Venturin , C. Gervasini, F. Orzan, A. Bentivegna, L. Corrado, P. Colapietro , A. Friso, R. Tenconi, M. Upadhyaya, L. Larizza, P. Riva