Pubblicazioni

Expression of the e5 oncoprotein of hpv16 impacts on the molecular profiles of emt-related and differentiation genes in ectocervical low-grade lesions

2021 - INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Ranieri, D.; French, D.; Raffa, S.; Guttieri, L.; Torrisi, M. R.; Belleudi, F.

Exome Sequencing in Individuals with Isolated Biliary Atresia

2020 - SCIENTIFIC REPORTS

Rajagopalan, R.; Tsai, E. A.; Grochowski, C. M.; Kelly, S. M.; Loomes, K. M.; Spinner, N. B.; Devoto, M.

Genetics of rotator cuff tears: No association of col5a1 gene in a case-control study

2018 - BMC MEDICAL GENETICS

Longo, U. G.; Margiotti, K.; Petrillo, S.; Rizzello, G.; Fusilli, C.; Maffulli, N.; De Luca, A.; Denaro, V.

Analysis of fibulin-3 after exposure to asbestos-like fibers

2017 - ENVIRONMENTAL RESEARCH

Rapisarda, Venerando; Caltabiano, Rosario; Musumeci, Giuseppe; Castrogiovanni, Paola; Ferrante, Margherita; Ledda, Caterina; Lombardo, Claudia; Graziano, Adriana Carol Eleonora; Cardile, Venera; Loreto, Carla

Interferon lambda 4 rs368234815 TT>Î´G variant is associated with liver damage in patients with nonalcoholic fatty liver disease.

2017 - HEPATOLOGY

Petta, S; Valenti, Laura; Tuttolomondo, A; Dongiovanni, P; Pipitone, Rm; CammÃ , C; Cabibi, D; Di Marco, V; Fracanzani, Al; Badiali, S; Nobili, V; Fargion, S; Grimaudo, S; CraxÃ¬, A.

Low-dose clofarabine in combination with a standard remission induction in patients aged 18-60 years with previously untreated intermediate and bad-risk acute myeloid leukemia or high-risk myelodysplastic syndrome: Combined phase I/II results of the EORTC/GIMEMA AML-14A trial

2017 - HAEMATOLOGICA

Selleslag, Dominik; Suciu, Stefan; Meloni, Giovanna; Muus, Petra; Halkes, Constantijn J. M.; Venditti, Adriano; Ramadan, Safaa M.; Pruijt, Hans; Meert, Liv; Vignetti, Marco; Marie, Jean-Pierre; Wittnebel, SÃ©bastian; de Witte, Theo; Amadori, Sergio; Willemze, Roelof; Baron, FrÃ©dÃ©ric

Variability in a three-generation family with pierre robin sequence, acampomelic campomelic dysplasia, and intellectual disability due to a novel â¼1 Mb deletion upstream of SOX9, and including KCNJ2 and KCNJ16

2016 - BIRTH DEFECTS RESEARCH. PART A, CLINICAL AND MOLECULAR TERATOLOGY

CASTORI, MARCO; BOTTILLO, IRENE; Morlino, Silvia; BARONE, CHIARA; Cascone, Piero; Grammatico, Paola; Laino, Luigi; Polimeni, Antonella; Pizzuti, Antonio; Silvestri, Alessandro; Roggini, Mario; Tarani, Luigi; Papoff, Paola; Giancotti, Antonella; Manganaro, Lucia; Lenzi, Jacopo; Sforzolini, Giovanna Scassellati