FONTANA, LAURA

FONTANA, LAURA  

Dipartimento di Scienze della Salute  

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Risultati 1 - 20 di 48 (tempo di esecuzione: 0.011 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 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 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 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 novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability : a case report 2021 Moresco G.Rondinone O.Grilli F.Prada E.Marchisio P.Miozzo M.Fontana L.Milani D. + Article (author) -
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome 2018 Paganini, LedaPesenti, ChiaraMilani, DonatellaFontana, LauraMotta, SilviaSirchia, Silvia MariaScuvera, GiuliettaMarchisio, PaolaCinnante, Claudia MariaTabano, Silvia MariaMiozzo, Monica Rosa + Article (author) -
A zebrafish model of Poikiloderma with Neutropenia recapitulates the human syndrome hallmarks and traces back neutropenia to the myeloid progenitor 2015 E.A. ColomboS. CarraL. FontanaE. BrescianiF. CotelliL. Larizza Article (author) -
ANALISI SEMIQUANTITATIVA DELL’ESPRESSIONE DELLE ISOFORME DEL GENE C16orf57 IN UN PANNELLO DI LINEE CELLULARI E TESSUTI ED IN PAZIENTI CON POICHILODERMA CON NEUTROPENIA 2012 L. FontanaG. NegriE.A. ColomboL. Larizza Book Part (author) -
Analysis of BRCA1 and RAD51C promoter methylation in italian families at high-risk of breast and ovarian cancer 2020 Tabano S.Azzollini J.Fontana L.Miozzo M. + Article (author) -
Angiogenesis in human brain tumors : screening of drug response through a patient-specific cell platform for personalized therapy 2018 L. GuarnacciaA. CherubiniF. CrisàM. MiozzoL. FontanaM. LocatelliL. RiboniG. Marfia + 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) -
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi 2015 L. PaganiniL. FontanaR. SilipigniS. FioriA. CeredaS. SirchiaM. MiozzoS. Tabano + Article (author) -
Case report: Chorea and cognitive decline in a young woman: instrumental and genetic assessment of a case originally diagnosed as multiple sclerosis 2023 Moresco G.Rondinone O.Vitali P.Fontana L.Miozzo M. + Article (author) -
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders 2018 L. FontanaP. D'UrsiS. SirchiaM. MiozzoS. Tabano + 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) -
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) -
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) -
Decreased serum level of sphingosine-1-phosphate: a novel predictor of clinical severity in COVID-19 2021 Marfia, G.Guarnaccia, L.Mondoni, M.Barassi, A.Fontana, L.Chiumello, D.Miozzo, M.Centanni, S.Riboni, L. + Article (author) -
Differential signature of the centrosomal MARK4 isoforms in glioma 2011 I. MagnaniC. NovielliL. FontanaS. TabanoD. RovinaD. BauerE.A. ColomboG. TedeschiL. MontiS. BosariL. BelloL. Larizza + Article (author) -
Epigenetics of functional hypothalamic amenorrhea 2022 Fontana L.Garzia E.Marfia G.Galiano V.Miozzo M. Article (author) -
Expanding the role of the splicing USB1 gene from Poikiloderma with Neutropenia to acquired myeloid neoplasms 2015 G. NegriE.A. ColomboL. FontanaC. GervasiniL. Larizza + Article (author) -