COLAPIETRO, PATRIZIA

COLAPIETRO, PATRIZIA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

Mostra records
Risultati 1 - 20 di 57 (tempo di esecuzione: 0.003 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 1-set-2020 Fontana L.Cagnoli G. A.Persico N.Colapietro P.Crippa M.Sirchia s. m.Miozzo M.Tabano S. + Article (author) -
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 24-nov-2018 Paganini, LedaCHETTA, MASSIMILIANORovina, DavideFontana, LauraColapietro, PatriziaBonaparte, EleonoraPezzani, LidiaMarchisio, PaolaTabano, Silvia MSirchia, Silvia MRiboni, LauraMilani, DonatellaMiozzo, Monica + Article (author) -
A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls 1-gen-2019 Tabano S.Caldiroli A.Terrasi A.Colapietro P.Grassi S.Carnevali G. S.Fontana L.Serati M.Vaira V.Altamura A. C.Miozzo M.Buoli M. Article (author) -
Altered H19 and SNAT2 expression in type 1 IUGR (Intrauterine Growth Restriction) placentas 1-ago-2008 S. TabanoC. MandòP. ColapietroS. CalabreseP. PileriV. SignorelliM.R. MiozzoI. Cetin + Article (author) -
APPROCCI TECNOLOGICI MULTIPLI PER L'IDENTIFICAZIONE DI MUTAZIONI E MECCANISMI PATOGENETICI IN PAZIENTI CON SINDROME DI RUBINSTEIN-TAYBI 25-nov-2012 C. GervasiniG. NegriP. ColapietroD. Rusconi..R. TenconiP. FinelliS. SpenaL. Larizza + Book Part (author) -
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 1-gen-2022 De Cosmi V.Tabano S.Fontana L.Privitera G.Alberico D.Colapietro P.Sirchia S.Stampalija T.Tabasso C.Parazzini F.Mosca F.Ferrazzi E.Bosari S.Miozzo M.Agostoni C. + Article (author) -
Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome : an update of the CREBBP deletion repertoire 1-gen-2015 D. RusconiG. NegriP. ColapietroS. SpenaP. FinelliL. LarizzaC. Gervasini + Article (author) -
Circulating microRNAs Suggest Networks Associated with Biological Functions in Aggressive Refractory Type 2 Celiac Disease 1-gen-2022 Doneda, LuigiaElli, LucaVaira, ValentinaColapietro, PatriziaTerranova, LeonardoVecchi, MaurizioScaramella, LuciaNandi, NicolettaRoncoroni, Leda + Article (author) -
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene 1-gen-2015 G. NegriD. MilaniP. ColapietroD. RusconiP. FinelliS. SpenaL. LarizzaC. Gervasini + Article (author) -
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance 26-mar-2021 Fontana L.Tabano S.Maitz S.Colapietro P.Garzia E.Sirchia S. M.Miozzo M. + Article (author) -
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines 2-nov-2021 Silvana PileggiElisa Adele ColomboLaura FontanaPatrizia ColapietroAnnamaria MorottiSilvia TabanoMyriam AlcalayCristina GervasiniMonica MiozzoSilvia Maria Sirchia + Article (author) -
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer 9-gen-2019 Azzollini, JacopoPesenti, ChiaraFontana, LauraPlebani, MaddalenaTabano, SilviaSirchia, Silvia MariaColapietro, PatriziaVERDERIO, PAOLOMiozzo, Monica + Article (author) -
DELEZIONI IN 16p13.2 COINVOLGENTI TOTALMENTE O PARZIALMENTE IL GENE CREBBP IN PAZIENTI CON SINDROME DI RUBINSTEIN-TAYBI 25-set-2013 C. GervasiniD. RusconiP. ColapietroS. SpenaG. NegriD. MilaniP. FinelliL. Larizza + Book Part (author) -
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34(+)38(-) compartment 1-ott-2010 PEDRANZINI, LAURAF. MottadelliF. RossellaI. MagnaniG. RoversiP. ColapietroP.G. PelicciL. Larizza + Article (author) -
Distinct expression pattern of microtubule-associated protein/microtubule affinity-regulating kinase 4 in differentiated neurons 1-gen-2006 S. De BiasiP. ColapietroL. LarizzaA. Beghini + Article (author) -
Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 1-dic-1999 P. ColapietroP. RivaL.N. RossiL. Larizza + Article (author) -
Duplicazioni parziali di SHOX associate alla Sindrome di Mayer-Rokitansky-Kuster-Hauser 1-nov-2009 C. GervasiniS. TabanoP. ColapietroMAITZ, SILVIA BEATRICEL. LarizzaM. Miozzo + Conference Object -
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction 16-mag-2010 S. TabanoP. ColapietroI. CetinC. MandòF. RossellaL. LarizzaS.M. SirchiaM. Miozzo + Article (author) -
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men 1-dic-2014 A. PansaS.M. SirchiaS. MelisP. ColapietroS. FioriR. FalconeL. PaganiniE. BonaparteM. MiozzoS. Tabano + Article (author) -
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions 1-gen-2004 M. VenturinC. GervasiniF. OrzanP. ColapietroL. LarizzaP. Riva + Article (author) -