LOVICU, MARIO

LOVICU, MARIO  

Istituto di Ricerca Genetica e Biomedica - IRGB  

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Risultati 1 - 20 di 32 (tempo di esecuzione: 0.039 secondi).
Titolo Data di pubblicazione Autore(i) File
PRF1 mutation alters immune system activation, inflammation, and risk of autoimmunity 1-gen-2020 Sidore, C; Orru, V; Cocco, E; Steri, M; Inshaw, Jrj; Pitzalis, M; Mulas, A; Mcgurnaghan, S; Frau, J; Porcu, E; Busonero, F; Dei, M; Lai, S; Sole, G; Virdis, F; Serra, V; Poddie, F; Delitala, A; Marongiu, M; Deidda, F; Pala, M; Floris, M; Masala, M; Onengutgumuscu, S; Robertson, Cc; Leoni, L; Frongia, A; Ricciardi, Mr; Chessa, M; Olla, N; Lovicu, M; Loizedda, A; Maschio, A; Mereu, L; Ferrigno, P; Curreli, N; Balaci, L; Loi, F; Ferreli, Lap; Pilia, Mg; Pani, A; Marrosu, Mg; Abecasis, Gr; Rich, Ss; Colhoun, H; Todd, Ja; Schlessinger, D; Fiorillo, E; Cucca, F; Zoledziewska, M
FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice 1-gen-2015 Marongiu, Mara; Marcia, Loredana; Pelosi, Emanuele; Lovicu, Mario; Deiana, Manila; Zhang, Yonqing; Puddu, Alessandro; Loi, Angela; Uda, Manuela; Forabosco, Antonino; Schlessinger, David; Crisponi, Laura
Genome-wide association study of susceptibility loci for breast cancer in Sardinian population 1-gen-2015 Palomba G.; Loi A.; Porcu E.; Cossu A.; Zara I.; Budroni M.; Dei M.; Lai S.; Mulas A.; Olmeo N.; Ionta M.T.; Atzori F.; Cuccuru G.; Pitzalis M.; Zoledziewska M.; Olla N.; Lovicu M.; Pisano M.; Abecasis G.R.; Uda M.; Tanda F.; Michailidou K.; Easton D.F.; Chanock S.J.; Hoover R.N.; Hunter D.J.; Schlessinger D.; Sanna S.; Crisponi L.; Palmieri G.
A role of BRCA1 and BRCA2 germline mutations in breast cancer susceptibility within Sardinian population 1-gen-2009 Palomba, G; Loi, A; Uras, A; Fancello, P; Piras, G; Gabbas, A; Cossu, A; Budroni, M; Contu, A; Tanda, F; Farris, A; Orrù, S; Floris, C; Pisano, M; Lovicu, M; Santona, Mc; Landriscina, G; Crisponi, L; Palmieri, G; Monne, M
Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin. 1-gen-2007 Lepori, Mb; Lovicu, M; Dessì, V; Zappu, A; Incollu, S; Zancan, L; Giacchino, R; Vajro, P; Maggiore, G; Marcellini, M; Barbera, C; Pellecchia, Mt; Simonetti, R; Kostic, V; Farci, Am; Solinas, A; De Virgiliis, S; Cao, A; Loudianos, G
Direct diagnosis of Wilson disease by molecular genetics. 1-gen-2006 Caprai S; Loudianos G; Massei F; Gori L; Lovicu M; Maggiore G.
The canine copper toxicosis gene MURR1 is not implicated in the pathogenesis of Wilson disease. 1-gen-2006 Lovicu, M; Dessì, V; Lepori, Mb; Zappu, A; Zancan, L; Giacchino, R; Marazzi, Mg; Iorio, R; Vegnente, A; Vajro, P; Maggiore, G; Marcellini, M; Barbera, C; Kostic, V; Farci, Am; Solinas, A; Altuntas, B; Yuce, A; Kocak, N; Tsezou, A; De Virgiliis, S; Cao, A; Loudianos, G
Direct diagnosis of Wilson disease by molecular genetics. 1-gen-2005 Caprai, S; Loudianos, G; Massei, F; Gori, L; Lovicu, M; Maggiore, G
Mutation analysis of ATP7B gene in Wilson disease patients of Turkish origin. 1-gen-2004 Loudianos, G; Lovicu, M; Dessì, V; Lepori, Mb; Zappu, A; Dessì, V; Altuntas, B; Yuce, A; Kocak, N; Ozsoylu, S; Kayseril, H; Akar, N; De Virgiliis, S; Pirastu, M; Cao, A
The development appropriate strategies and methods for mutation analysis in the ATP7B gene. 1-gen-2004 Loudianos, G; Lovicu, M; Dessì, V; Lepori, M; Zappu, A; Zancan, L; Giacchino, R Iorio R; Vajro, P; Maggiore, G; Marcellini, M; Barbera, C; Pellecchia, M; Simonetti, R; Kostic, V; Majumdar, R; Eapen, C; De Virgiliis, S; Cao, A
Characterization of the molecular defect and genotype-phenotype analysis in Wilson disease patients from Yugoslavia. 1-gen-2003 Loudianos, G; Kostic, V; Solinas, P; Lovicu, M; Svetel, M; Major, T; Cao, A
Efficient strategy for molecular diagnosis of Wilson disease in the sardinian population. 1-gen-2003 Lovicu, M; Dessì, V; Zappu, A; De Virgiliis, S; Cao, A; Loudianos, G
Abnormal m RNA splicing resulting from consensus sequence splicing mutations of ATP7B. 1-gen-2002 Loudianos G.; Lovicu M.; Dessi V.; Tzetis M.; Kanavakis E.; Zancan L.; Zelante L.; GalvizGalviz C.; Cao A.
Haplotype and mutation analysis in Mediterranean patients with Wilson disease 1-gen-1999 Loudianos, G; Dessi, V; Lovicu, M; Angius, A; Pirastu, M; Cao, A
Molecular characterization of Wilson disease in the Sardinian population. Evidence of a founder effect 1-gen-1999 Loudianos, G; Dessì, V; Lovicu, M; Angius, A; Figus, Al; Lilliu, F; De Virgiliis, S; Nurchi, A; Deplano, A; Pirastu, M; Cao, A
Mutation analysis in patients of Mediterranean descent with Wilson disease. Identification of 19 novel mutations. 1-gen-1999 G Loudianos; V Dessi; M Lovicu; A Angius; B Altuntas; R Giacchino; M Marazzi; M Marcellini; MR Sartorelli; GC Sturniolo; N Kocak; A Yuce; N Akar; M Pirastu; A Cao.
Early and severe neurological features in a Wilson disease patient compound heterozygous for two frameshift mutations. 1-gen-1998 A Angius; V Dessì; M Lovicu; S De Virgiliis; M Pirastu; A Cao.
Further delineation of the molecular pathology of Wilson disease in the Mediterranean population. 1-gen-1998 G Loudianos; V Dessì; M Lovicu; A Angius; S De Virgiliis; A Nurchi; A Solinas; M Marcellini; L Zancan; C Barbera; N Akar; R Yagci; A Vegnente; A Cao; M Pirastu.
Haplotype and mutation analysis in Greek patients with Wilson disease 1-gen-1998 Loudianos, G; Dessi, V; Lovicu, M; Angius, A; Kanavakis, E; Tzetis, M; Kattamis, C; Manolaki, N; Vassiliki, G; Karpathios, T; Cao, A; Pirastu, M
The -75 A>C substitution in the 5' UTR of the Wilson disease gene is a sequence polymorphism in the Mediterranean population 1-gen-1998 G Loudianos; V Dessì; M Lovicu; A Angius; A Cao; M Pirastu