SIRCHIA, SILVIA MARIA

SIRCHIA, SILVIA MARIA  

Dipartimento di Scienze della Salute  

Mostra records
Risultati 1 - 20 di 102 (tempo di esecuzione: 0.003 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 1-set-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 24-nov-2018 Paganini, LedaCHETTA, MASSIMILIANORovina, DavideFontana, LauraColapietro, PatriziaBonaparte, EleonoraPezzani, LidiaMarchisio, PaolaTabano, Silvia MSirchia, Silvia MRiboni, LauraMilani, DonatellaMiozzo, Monica + Article (author) -
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes 1-mar-2016 S. TabanoM. MiozzoS. SirchiaP. FinelliL. Larizza + Article (author) -
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome 1-giu-2018 Paganini, LedaPesenti, ChiaraMilani, DonatellaFontana, LauraMotta, SilviaSirchia, Silvia MariaScuvera, GiuliettaMarchisio, PaolaCinnante, Claudia MariaTabano, Silvia MariaMiozzo, Monica Rosa + Article (author) -
A perspective on diet, epigenetics and complex diseases: where is the field headed next? 1-ott-2022 Pileggi, SilvanaSirchia, Silvia Maria + Article (author) -
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected 1-lug-1997 G. SimoniSACCHI, LAURAS.M. SirchiaI.M. GaragiolaT. PersicoG. PardiA.E. Semprini + Article (author) -
An epigenetic event may underlies the TSC features in TSC2 ASM cells 1-set-2009 E. LesmaS. AnconaS.M. SirchiaV. GrandeE. ChiaramonteS. BosariA.M. Di GiulioA. Gorio Conference Object -
Analisi del metiloma negli ultralongevi e nei loro figli e stato di salute 1-ott-2011 D. MariS.M. SirchiaS. TabanoG. Vitale + Article (author) -
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva 1-gen-2005 B. GentilinF.R. GratiP. InvernizziC. SelmiS.M. SirchiaF. RossellaG. SimoniM. Miozzo + Book Part (author) -
Aneuploid correction and confined placental mosaicism 1-gen-1996 G. SimoniS.M. Sirchia + Article (author) -
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 1-gen-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) -
Assessment of X chromosome Inactivation pattern in BRCA mutation carriers : evidence for an effect of chemotherapy 1-mag-2008 M. MiozzoS.M. TabanoP. AntonazzoS.M. Sirchia + Article (author) -
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi 1-gen-2015 L. PaganiniL. FontanaR. SilipigniS. FioriA. CeredaS. SirchiaM. MiozzoS. Tabano + Article (author) -
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies 1-gen-2004 F.R. GratiS.M. SirchiaB. GentilinF. RossellaL. RamoscelliG. BulfamanteI. CetinG. SimoniM. Miozzo + Article (author) -
Blood fetal microchimerism in primary biliary cirrhosis 1-dic-2000 S.M. SirchiaP.M. BattezzatiM. ZuinF. RossellaF. PeregoM. BignottoM. Podda + Article (author) -
Characterization of four microsatellites in an Italian population and their application to paternity testing 1-apr-1996 S.M. SirchiaI. Garagiola + Article (author) -
Characterization of human TSC2 cells derived from a TSC/LAM patient chylous effusion 1-set-2011 E. LesmaS. AnconaS.M. SirchiaE. OrpianesiA.M. Di GiulioA. Gorio + Conference Object -
Characterization of LAM/TSC cells isolated from patient chylous 13-apr-2010 E. LesmaS. AnconaV. GrandeS.M. SirchiaE. ChiaramonteS. BosariA.M. Di GiulioA. Gorio Conference Object -
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders 1-gen-2018 L. FontanaP. D'UrsiS. SirchiaM. MiozzoS. Tabano + Article (author) -
Chromatin remodeling of the RAR gene in the pathogenesis and retinoid resistance to breast cancer 1-giu-2002 S.M. SirchiaG. SomenziR. GhidoniN. Sacchi + Article (author) -