GRATI, FRANCESCA ROMANA

GRATI, FRANCESCA ROMANA  

DIPARTIMENTO DI MEDICINA, CHIRURGIA E ODONTOIATRIA (attivo dal 01/01/1999 al 26/04/2012)  

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Risultati 1 - 20 di 23 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
X chromosome inactivation pattern in BRCA gene mutation carriers 2013 P. VerderioS. TabanoP. ColapietroF.R. GratiM. CalvelloS.M. SirchiaM. Miozzo + Article (author) -
Microchimerismo fetale bovino in gravidanze normali e con embryo transfer 2010 L. TurinP. InvernizziF.R. GratiF. RivaG. Tribbioli + Article (author) -
Placental IGF2 expression in normal and intrauterine growth restricted (IUGR) pregnancies 2008 P. AntonazzoG. AlvinoCOZZI, VERONICAF.R. GratiS. TabanoS. SirchiaM. MiozzoI. Cetin Article (author) -
Fetal microchimerism in normal and embryo transfer bovine pregnancies 2007 L. TurinG. TribbioliP. InvernizziF.R. GratiS. CremaF. Riva + Article (author) -
Bovine fetal microchimerism in normal and embryo transfer pregnancies and its implications for biotechnology applications in cattle 2007 L. TurinP. InvernizziF.R. GratiF. RivaG. Tribbioli + Article (author) -
Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele : new highlights on phenotype-genotype correlations in Beckwith-Wiedemann syndrome 2007 F.R. GratiM. MiozzoL. Larizza + Article (author) -
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis 2007 M.R. MiozzoC.F. SelmiB. GentilinF.R. GratiS.M. SirchiaM. ZuinM. PoddaP. Invernizzi + Article (author) -
Microchimerismo fetale in gravidanze bovine normali e con embryo transfer 2006 L. TurinG. TribbioliP. InvernizziF.R. GratiS. CremaF. Riva + Article (author) -
Placental LPL gene expression is increased in severe intrauterine growth-restricted pregnancies 2006 S.M. TabanoG. AlvinoP.G.M. AntonazzoF.R. GratiM.R. MiozzoI. Cetin Article (author) -
Three cases with de novo 6q imbalance and variable prenatal phenotype 2005 FR GratiB GentilinF RossellaI CetinG SimoniM Miozzo + Article (author) -
Ruolo di ESX1L nella spermatogenesi umana 2005 F.R. GratiS. M. SirchiaF. RossellaG. SimoniM. Miozzo + Book Part (author) -
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva 2005 B. GentilinF.R. GratiP. InvernizziC. SelmiS.M. SirchiaF. RossellaG. SimoniM. Miozzo + Book Part (author) -
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells 2005 S.M. SirchiaL. RamoscelliF.R. GratiF. RossellaE. LesmaG. SimoniM. Miozzo + Article (author) -
X chromosome monosomy : a common mechanism for autoimmune diseases 2005 P. InvernizziM. MiozzoC. SelmiL. PersaniP.M. BattezzatiM. ZuinP.L. MeroniMARASINI, BIANCAF.R. GratiG. SimoniM. Podda + Article (author) -
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies 2005 F.R. GratiM. MiozzoF. RossellaP. AntonazzoB. GentilinS.M. SirchiaS. RiganoG. BulfamanteI. CetinG. Simoni + Article (author) -
Frequency of monosomy X in women with primary biliary cirrhosis 2004 P. InvernizziM. MiozzoP.M. BattezzatiF.R. GratiG. SimoniC. SelmiM. Podda + Article (author) -
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies 2004 F.R. GratiS.M. SirchiaB. GentilinF. RossellaL. RamoscelliG. BulfamanteI. CetinG. SimoniM. Miozzo + Article (author) -
Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes 2004 A. CerriS.M. SirchiaF. RossellaF.R. GratiG. Simoni + Article (author) -
Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries 2001 F.R. GratiG. GhilardiS.M. SirchiaR. ScorzaG. Simoni + Article (author) -
Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expression 2001 M. MiozzoF. R. GratiG. BulfamanteT. RadaelliT. PersicoI. CetinG. Pardi + Article (author) -