COLAPIETRO, PATRIZIA

COLAPIETRO, PATRIZIA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 58 (tempo di esecuzione: 0.005 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines 2024 Pileggi S.Colombo E. A.Ancona S.Quadri R.Bernardelli C.Colapietro P.Taiana M.Fontana L.Miozzo M.Lesma E.Sirchia S. M. Article (author) -
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) -
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) -
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) -
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) -
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) -
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) -
(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) -
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 -
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) -
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) -
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) -
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) -