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Results: 1-15 |
Results: 15
Detection of occult melanoma cells in paraffin-embedded histologically negative sentinel lymph nodes using a reverse transcriptase polymerase chain reaction assay
Authors: Palmieri, G Ascierto, PA Cossu, A Mozzillo, N Motti, ML Satriano, SMR Botti, G Caraco, C Celentano, E Satriano, RA Lissia, A Tanda, F Pirastu, M
Citation: G. Palmieri et al., Detection of occult melanoma cells in paraffin-embedded histologically negative sentinel lymph nodes using a reverse transcriptase polymerase chain reaction assay, J CL ONCOL, 19(5), 2001, pp. 1437-1443
Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traits
Authors: Angius, A Melis, PM Morelli, L Petretto, E Casu, G Maestrale, GB Fraumene, C Bebbere, D Forabosco, P Pirastu, M
Citation: A. Angius et al., Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traits, HUM GENET, 109(2), 2001, pp. 198-209
Identification of a new candidate locus for uric acid nephrolithiasis
Authors: Ombra, MN Forabosco, P Casula, S Angius, A Maestrale, G Petretto, E Casu, G Colussi, G Usai, E Melis, P Pirastu, M
Citation: Mn. Ombra et al., Identification of a new candidate locus for uric acid nephrolithiasis, AM J HU GEN, 68(5), 2001, pp. 1119-1129
Microsatellite analysis at 10q25-q26 in Sardinian patients with sporadic endometrial carcinoma - Identification of specific patterns of genetic alteration
Authors: Palmieri, G Manca, A Cossu, A Ruiu, G Pisano, M Cherchi, P Dessole, S Pintus, A Massarelli, G Tanda, F Pirastu, M
Citation: G. Palmieri et al., Microsatellite analysis at 10q25-q26 in Sardinian patients with sporadic endometrial carcinoma - Identification of specific patterns of genetic alteration, CANCER, 89(8), 2000, pp. 1773-1782
Definition of the role of chromosome 9p21 in sporadic melanoma through genetic analysis of primary tumours and their metastases
Authors: Palmieri, G Cossu, A Ascierto, PA Botti, G Strazzullo, M Lissia, A Colombino, M Casula, M Floris, C Tanda, F Pirastu, M Castello, G
Citation: G. Palmieri et al., Definition of the role of chromosome 9p21 in sporadic melanoma through genetic analysis of primary tumours and their metastases, BR J CANC, 83(12), 2000, pp. 1707-1714
Identification of a founder BRCA2 mutation in Sardinia
Authors: Pisano, M Cossu, A Persico, I Palmieri, G Angius, A Casu, G Palomba, G Sarobba, MG Rocca, PCO Dedola, MF Olmeo, N Pasca, A Budroni, M Marras, V Pisano, A Farris, A Massarelli, G Pirastu, M Tanda, F
Citation: M. Pisano et al., Identification of a founder BRCA2 mutation in Sardinia, BR J CANC, 82(3), 2000, pp. 553-559
A novel spontaneous missense mutation in VMD2 gene is a cause of a best macular dystrophy sporadic case
Authors: Palomba, G Rozzo, C Angius, A Pierrottet, CO Orzalesi, N Pirastu, M
Citation: G. Palomba et al., A novel spontaneous missense mutation in VMD2 gene is a cause of a best macular dystrophy sporadic case, AM J OPHTH, 129(2), 2000, pp. 260-262
Activation of the delta-globin gene by the beta-globin gene CACCC motif
Authors: Ristaldi, MS Casula, S Porcu, S Marongiu, MF Pirastu, M Cao, A
Citation: Ms. Ristaldi et al., Activation of the delta-globin gene by the beta-globin gene CACCC motif, BL CELL M D, 25(14), 1999, pp. 193-209
Population choice in mapping genes for complex diseases
Authors: Wright, AF Carothers, AD Pirastu, M
Citation: Af. Wright et al., Population choice in mapping genes for complex diseases, NAT GENET, 23(4), 1999, pp. 397-404
Molecular characterization of Wilson disease in the Sardinian population -Evidence of a founder effect
Authors: Loudianos, G Dessi, V Lovicu, M Angius, A Figus, A Lilliu, F De Virgiliis, S Nurchi, AM Deplano, A Moi, P Pirastu, M Cao, AO
Citation: G. Loudianos et al., Molecular characterization of Wilson disease in the Sardinian population -Evidence of a founder effect, HUM MUTAT, 14(4), 1999, pp. 294-303
Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family
Authors: Rozzo, C Fossarello, M Galleri, G Miano, MG Ciccodicola, A Sole, G Pirastu, M
Citation: C. Rozzo et al., Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family, EUR J HUM G, 7(5), 1999, pp. 574-578
Haplotype and mutation analysis in Mediterranean patients with Wilson disease
Authors: Loudianos, G Dessi, V Lovicu, M Angius, A Pirastu, M Cao, A
Citation: G. Loudianos et al., Haplotype and mutation analysis in Mediterranean patients with Wilson disease, J TR EL EXP, 12(4), 1999, pp. 315-319
Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency
Authors: Battisti, C Loudianos, G Rufa, A Dotti, MT Sangiorgi, S Dessi, V Lovicu, M Pirastu, M Federico, A
Citation: C. Battisti et al., Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency, AM J MED G, 85(2), 1999, pp. 175-178
Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations
Authors: Loudianos, G Dessi, V Lovicu, M Angius, A Altuntas, B Giacchino, R Marazzi, M Marcellini, M Sartorelli, MR Sturniolo, GC Kocak, N Yuce, A Akar, N Pirastu, M Cao, A
Citation: G. Loudianos et al., Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations, J MED GENET, 36(11), 1999, pp. 833-836
Molecular basis of open-angle glaucoma in Italy
Authors: Angius, A Pisano, M Manca, A Casu, G Persico, I Pitzalis, S De Gioia, E Grignolo, FM Loi, A Sole, G Cao, A Spinelli, P Ghillotti, G Bonomi, L Fossarello, M Serra, A Gandolfi, S Alberti, G Maraini, G Serru, A Orzalesi, N Pirastu, M
Citation: A. Angius et al., Molecular basis of open-angle glaucoma in Italy, ACT OPHTH S, 76, 1998, pp. 16-17
Risultati: 1-15 |