COLAPIETRO, PATRIZIA

COLAPIETRO, PATRIZIA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 57 (tempo di esecuzione: 0.006 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study 2023 A. PiccininiG. BarbaraM. MiozzoS. TabanoP. ColapietroS. M. SirchiaE. BattaglioliC. La Vecchia + Article (author) -
Mental health and the effects on methylation of stress-related genes in front-line versus other health care professionals during the second wave of COVID-19 pandemic: an Italian pilot study 2022 Tabano SBrescia GGaudioso GFerrara MColapietro PFontana LMiozzo MRCroci GASolbiati MTobaldini EFerrero SMontano NCostantino GBuoli M + Article (author) -
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 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) -
Circulating microRNAs Suggest Networks Associated with Biological Functions in Aggressive Refractory Type 2 Celiac Disease 2022 Doneda, LuigiaElli, LucaVaira, ValentinaColapietro, PatriziaTerranova, LeonardoVecchi, MaurizioScaramella, LuciaNandi, NicolettaRoncoroni, Leda + Article (author) -
Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia Gravis 2022 Silvia Maria TabanoPatrizia ColapietroLaura FontanaMonica Miozzo + Article (author) -
Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology 2022 Moresco, GiadaRondinone, OrnellaMauri, AlessiaColapietro, PatriziaMarfia, GiovanniGrilli, FedericoRinaldi, BerardoPrada, ElisabettaMiozzo, Monica RosaMilani, DonatellaFontana, Laura + 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 2021 Silvana PileggiElisa Adele ColomboLaura FontanaPatrizia ColapietroAnnamaria MorottiSilvia TabanoMyriam AlcalayCristina GervasiniMonica MiozzoSilvia Maria Sirchia + Article (author) -
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance 2021 Fontana L.Tabano S.Maitz S.Colapietro P.Garzia E.Sirchia S. M.Miozzo M. + Article (author) -
Extensive placental methylation profiling in normal pregnancies 2021 Rondinone O.Tabano S.Fontana L.Colapietro P.Motta S.Ferrazzi E.Bosari S.Sirchia S. M.Miozzo M. + Article (author) -
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 2020 Fontana L.Cagnoli G. A.Persico N.Colapietro P.Crippa M.Sirchia s. m.Miozzo M.Tabano S. + Article (author) -
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer 2019 Azzollini, JacopoPesenti, ChiaraFontana, LauraPlebani, MaddalenaTabano, SilviaSirchia, Silvia MariaColapietro, PatriziaVERDERIO, PAOLOMiozzo, Monica + Article (author) -
A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls 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) -
Mismatch repair protein loss is a prognostic and predictive biomarker in breast cancers regardless of microsatellite instability 2019 Fusco, N.Lopez, G.Corti, C.Pesenti, C.Colapietro, P.Gaudioso, G.Vaira, V.Miozzo, M.Ferrero, S.Bosari, S. + Conference Object -
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 2018 Paganini, LedaCHETTA, MASSIMILIANORovina, DavideFontana, LauraColapietro, PatriziaBonaparte, EleonoraPezzani, LidiaMarchisio, PaolaTabano, Silvia MSirchia, Silvia MRiboni, LauraMilani, DonatellaMiozzo, Monica + Article (author) -
Mismatch repair protein loss as a prognostic and predictive biomarker in breast cancers regardless of microsatellite instability 2018 Fusco, NicolaLopez, GianlucaCorti, ChiaraPesenti, ChiaraColapietro, PatriziaGaudioso, GabriellaFaversani, AliceVaira, ValentinaMiozzo, MonicaFerrero, StefanoBosari, Silvano + Article (author) -
From Whole Gene Deletion to Point Mutations of EP300-Positive Rubinstein-Taybi Patients : New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks 2016 G. NegriD. MilaniP. ColapietroD. RusconiM. CrippaP. FinelliL. LarizzaC. Gervasini + Article (author) -
Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome : an update of the CREBBP deletion repertoire 2015 D. RusconiG. NegriP. ColapietroS. SpenaP. FinelliL. LarizzaC. Gervasini + Article (author) -
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi Syndrome patients 2015 S. SpenaD. MilaniD. RusconiG. NegriP. ColapietroL. LarizzaC. Gervasini + Article (author) -
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene 2015 G. NegriD. MilaniP. ColapietroD. RusconiP. FinelliS. SpenaL. LarizzaC. Gervasini + Article (author) -
TSC2 epigenetic defect in primary LAM cells. Evidence of an anchorage-independent survival 2014 E. LesmaS. AnconaS.M. SirchiaE. OrpianesiV. GrandeP. ColapietroE. ChiaramonteA.M. Di GiulioA. Gorio Article (author) -