COLAPIETRO, PATRIZIA

COLAPIETRO, PATRIZIA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

Risultati 1 - 14 di 14 (tempo di esecuzione: 0.035 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
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) -
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) -
(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) -
From Whole Gene Deletion to Point Mutations of EP300-Positive Rubinstein-Taybi Patients : New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks 1-feb-2016 G. NegriD. MilaniP. ColapietroD. RusconiM. CrippaP. FinelliL. LarizzaC. Gervasini + Article (author) -
IMPACT OF KIT MUTATIONS IN ACUTE MYELOID LEUKAEMIA WITH INV(16) 1-gen-2008 A. BeghiniP. Colapietro + Article (author) -
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi Syndrome patients 1-gen-2015 S. SpenaD. MilaniD. RusconiG. NegriP. ColapietroL. LarizzaC. Gervasini + Article (author) -
Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorfism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation 1-set-2008 A. BeghiniP. Colapietro + Article (author) -
NEW POINTMUTATIONS AND EXON DELETIONS OF THE EP300 GENE IN PATIENTS WITH RUBINSTEIN-TAYBI SYNDROME 8-giu-2013 G. NegriP. ColapietroD. RusconiD. MilaniL. ConsonniP. FinelliS. SpenaL. LarizzaC. Gervasini + Book Part (author) -
NUOVE MUTAZIONI PUNTIFORMI E DELEZIONI ESONICHE DEL GENE EP300 IN PAZIENTI CON SINDROME DI RUBINSTEIN-TAYBI 25-ago-2013 G. NegriP. ColapietroD. RusconiD. MilaniL. ConsonniP. FinelliS. SpenaL. LarizzaC. Gervasini + Book Part (author) -
Prevalence and prognostic impact of KIT mutations in acute myeloid leukaemia with inv(16). A retrospective study 1-nov-2007 A. BeghiniP. Colapietro + Article (author) -
Sodium coupled Neutral Aminoacid Transporter 2 (SNAT2) Intron1 methylation levels and Single Nucleotide Polymorphism in IUGR placentas 1-mar-2010 C. MandòS.M. TabanoP. ColapietroA.M. MarinoP.PileriM.R. MiozzoI.Cetin Conference Object -
Transferrin Receptor 1 protein expression and localization in human IntraUterine Growth Restriction placentas 1-mar-2010 C. MandòS. TabanoP. ColapietroA. MarinoP. PileriF. ParisiL. AvaglianoG. BulfamanteM. MiozzoI. Cetin Conference Object -