TURCO, Alberto

TURCO, Alberto  

DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO  

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A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 1-gen-1996 Bresin, E.; Rossetti, S.; Englisch, S.; Corra, S.; Pignatti, P. F.; Turco, A. E.
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 1-gen-2001 S., Rugolotto; T., Bardaro; T., Esposito; F., Soli; Turco, Alberto; Pignatti, Pierfranco; M., D'Urso
A novel frameshift deletion in type IV collagen alpha 5 gene in a juvenile-type Alport syndrome patient: an adenine deletion (2940/2943 del A) in exon 34 of COL4A5 1-gen-1994 Peissel, B.; Rossetti, S.; Renieri, A.; Galli, L.; De Marchi, M.; Battini, G.; Meroni, M.; Sessa, A.; Schiavano, S.; Pignatti, P. F.; Turco, A. E.
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 1-gen-1995 Turco, Alberto; S., Rossetti; M. O., Biasi; G., Rizzoni; L., Massella; N. H., Saarinen; A., Renieri; Pignatti, Pierfranco; M., De Marchi
A novel nonsense mutation in the PKD1 gene (C3817T) is associated with autosomal dominant polycystic kidney disease (ADPKD) in a large three-generation Italian family 1-gen-1995 Turco, Alberto; S., Rossetti; E., Bresin; S., Corra; L., Gammaro; Maschio, Giuseppe; Pignatti, Pierfranco
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 1-gen-1997 Turco, Alberto; A., Renieri; M., De Marchi
Alport syndrome: the point of view of a pediatric nephrologist 1-gen-1997 G., Rizzoni; L., Massella; T., Faraggiana; P., Barsotti; A., Renieri; T., Neri; Turco, Alberto
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 1-gen-1996 Turco, Alberto; M., Clementi; S., Rossetti; R., Tenconi; Pignatti, Pierfranco
Analysis of published PKD1 gene sequence variants. 1-gen-2007 Gout, A. M.; ADPKD Gene Variant, Consortium; Ravine, D.; Harris, P. C.; Rossetti, S.; Peters, D.; Breuning, M.; Henske, E. P.; Koizumi, A.; Inoue, S.; Shimizu, Y.; Thongnoppakhun, W.; Yenchitsomanus, P. T.; Deltas, C.; Sandford, R.; Torra, R.; Turco, Alberto; Jeffery, S.; Fontes, M.; Somlo, S.; Furu, L. M.; Smulders, Y. M.; Mercier, B.; Ferec, C.; Burtey, S.; Pei, Y.; Kalaydjieva, L.; Bogdanova, N.; Mccluskey, M.; Geon, L. J.; Wouters, C. H.; Reiterova, J.; Stekrová, J.; San Millan, J. L.; Aguiari, G.; Del Senno, L.
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 1-gen-2011 Gomez, Maria Macarena; Tessari, Gianpaolo; Mazzola, Silvia; Malerba, Giovanni; Rugiu, Carlo; Naldi, L; Nacchia, Francesco; Valerio, F; Anna, B; Forni, Alberto; Boschiero, Luigino; Sandrini, S; Faggian, Giuseppe; Girolomoni, Giampiero; Turco, Alberto
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 1-gen-2007 Gomez, Maria Macarena; Mazzola, Silvia; Tessari, Gianpaolo; Malerba, Giovanni; Ortombina, M.; Naldi, L.; Remuzzi, G.; Boschiero, Luigino; Forni, Alberto; Rugiu, Carlo; Piaserico, S.; Girolomoni, Giampiero; Turco, Alberto
Association of promoter polymorphism -765G>C in the PTGS2 gene with malignant melanoma in Italian patients and its correlation to gene expression in dermal fibroblasts. 1-gen-2014 Gomez, Maria Macarena; Ferronato, Silvia; Malerba, Giovanni; Santinami, M; Maurichi, A; Sangalli, Antonella; Turco, Alberto; Perego, P; Rodolfo, M.
Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 Gene 1-gen-1996 S., Rossetti; E., Bresin; G., Restagno; A., Carbonara; S., Corra; O., De Prisco; Pignatti, Pierfranco; Turco, Alberto
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 1-gen-2000 Turco, Alberto; Passigato, S.; Fazion, M.; Soli, F.
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 1-gen-1997 Sessa, A.; Ghiggeri, G. M.; Turco, A. E.
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes 1-gen-1995 Turco, Alberto; S., Rossetti; B., Peissel; L., Gammaro; Maschio, Giuseppe; Pignatti, Pierfranco
Clinical value of PCR in diagnosis and follow-up of leukaemia and lymphoma: report of the Third Workshop of the Molecular Biology/BMT Study Group 1-gen-1991 T. P., Hughes; Ambrosetti, Achille; V., Barbu; C., Bartram; R., Battista; A., Biondi; A., Chiamenti; G., Cimino; P., Ernst; F., Frassoni; Gasparini, Paolo; I., Gentilini; E., Gluckman; G., Grosveld; A., Guerrasio; S., Hegewich; J. W. G., Janssen; A., Keating; F., LO COCO; P., Martiat; G., Martinelli; K., Mills; G., Morgan; G., Nadali; P. G., Pelicci; G., Perona; Pignatti, Pierfranco; P., Richard; G., Saglio; Trabetti, Elisabetta; Turco, Alberto; D., Veneri; A., Zaccaria; A., Zander; J. M., Goldman
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 1-gen-1995 S., Rossetti; S., Corra; M. O., Biasi; Turco, Alberto; Pignatti, Pierfranco
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 1-gen-1996 M., Rossato; M., Rigotti; M., Grazia; Turco, Alberto; L., Bonomi
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 1-gen-2018 Ferronato, Silvia; Scuro, Alberto; Gomez-Lira, Macarena; Mazzucco, Sara; Olivato, Silvia; Turco, Alberto; Orlandi, Elisa; Malerba, Giovanni; Romanelli, Maria Grazia