SIRCHIA, SILVIA MARIA

SIRCHIA, SILVIA MARIA  

Dipartimento di Scienze della Salute  

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Risultati 1 - 20 di 105 (tempo di esecuzione: 0.01 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Non-invasive biomarkers for sperm retrieval in non-obstructive patients: a comprehensive review 2024 Fontana L.Sirchia S. M.Pesenti C.Miozzo M. R. + Article (author) -
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) -
A perspective on diet, epigenetics and complex diseases: where is the field headed next? 2022 Silvana PileggiSilvia Maria Sirchia + Article (author) -
Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model 2022 Clara BernardelliEloisa ChiaramonteSilvia AnconaSilvia M. SirchiaAmilcare CerriElena Lesma 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) -
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) -
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) -
(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) -
DNA methylation in the diagnosis of monogenic diseases 2020 Gervasini C.Miozzo M.Sirchia S. M.Tabano S. + Article (author) -
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients 2020 Rovina D.Fontana L.Tabano S.Bodega B.Miozzo M.Sirchia S. M. + 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) -
Introduzione 2018 Anna MarozziLuca FerrariMonica MiozzoPaola RivaSilvia Sirchia + Book Part (translator) -
Introduzione al genoma umano 2018 Anna MarozziLuca FerrariMonica MiozzoAntonio PizzutiPaola RivaSilvia Sirchia + Book Part (translator) -
GDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML 2018 TARARA', LUCIABarlassina, CristinaBarcella, MatteoSirchia, SilviaPISCITELLI, ELEONORA + 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) -
Thompson & Thompson : Genetica in medicina 2018 Sirchia S.MiozzoM.Marozzi A.Riva P.Finelli P. Book Part (translator) -
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) -
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometry 2018 E. BonaparteC. PesentiL. FontanaR. FalconeL. PaganiniM. NosottiP. MendogniS. M. SirchiaS. M. TabanoS. BosariM. R. Miozzo + Article (author) -