ROSSELLA, FRANCA

ROSSELLA, FRANCA  

Dipartimento di Scienze della Salute  

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Risultati 1 - 17 di 17 (tempo di esecuzione: 0.003 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Solid-State Color Centers for Single-Photon Generation 2024 S. DonatiL. FrontiniV. LiberaliF. RossellaM. SalvatoA. StabileG. TruccoV. Vitali + Article (author) -
IDENTIFICAZIONE DEI GENI TARGET DEL miR-182 NELLA LINEA CELLULARE KASUMI-1, MODELLO DI LEUCEMIA MIELOIDE ACUTA (AML), E NELLE SUE SOTTOPOPOLAZIONI 2010 G. NegriC. GervasiniF. MottadelliI. MagnaniF. RossellaM. VenturinP. RivaP. PelicciL. Larizza + Book Part (author) -
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34(+)38(-) compartment 2010 PEDRANZINI, LAURAF. MottadelliF. RossellaI. MagnaniG. RoversiP. ColapietroP.G. PelicciL. Larizza + Article (author) -
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction 2010 S. TabanoP. ColapietroI. CetinC. MandòF. RossellaL. LarizzaS.M. SirchiaM. Miozzo + Article (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) -
Three cases with de novo 6q imbalance and variable prenatal phenotype 2005 FR GratiB GentilinF RossellaI CetinG SimoniM Miozzo + 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) -
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) -
Ruolo di ESX1L nella spermatogenesi umana 2005 F.R. GratiS. M. SirchiaF. RossellaG. SimoniM. Miozzo + Book Part (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) -
Blood fetal microchimerism in primary biliary cirrhosis 2000 S.M. SirchiaP.M. BattezzatiM. ZuinF. RossellaF. PeregoM. BignottoM. Podda + Article (author) -
Loss of heterozigosity of chromosomal region 4q32-35 in basal cell carcinomas 2000 S. SirchiaA. CerriF. RossellaF. GratiG. Simoni + Article (author) -
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas 2000 F.R. GratiS.M. SirchiaI. GaragiolaE. SironiF. RossellaR. BrusatiG. Simoni + Article (author) -
Losses of heterozygosity in endometrial adenocarcinomas : positive correlations with histopathological parameters 2000 S.M. SirchiaF.R. GratiI. GaragiolaF. RossellaG. PardiG. Simoni + Article (author) -
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma 1997 S.M. SirchiaF. RossellaI. GaragiolaG. BulfamanteG. Simoni + Article (author) -
Genetic amniocentesis in biamniotic twin pregnancies by a single transabdominal insertion of the needle 1995 A.M.MarconiM.G.GrimoldiF.Rossella + Article (author) -