TURCO, Alberto
TURCO, Alberto
DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1)
1996-01-01 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
2001-01-01 S., Rugolotto; T., Bardaro; T., Esposito; F., Soli; Turco, Alberto; Pignatti, Pierfranco; M., D'Urso
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome
1995-01-01 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
1995-01-01 Turco, Alberto; S., Rossetti; E., Bresin; S., Corra; L., Gammaro; Maschio, Giuseppe; Pignatti, Pierfranco
Alport syndrome--is there a genotype-phenotype relationship? [editorial]
1997-01-01 Turco, Alberto; A., Renieri; M., De Marchi
Alport syndrome: the point of view of a pediatric nephrologist
1997-01-01 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
1996-01-01 Turco, Alberto; M., Clementi; S., Rossetti; R., Tenconi; Pignatti, Pierfranco
Analysis of published PKD1 gene sequence variants.
2007-01-01 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
2011-01-01 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.
2007-01-01 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.
2014-01-01 Gomez, Maria Macarena; Ferronato, Silvia; Malerba, Giovanni; Santinami, M; Maurichi, A; Sangalli, Antonella; Turco, Alberto; Perego, P; Rodolfo, M.
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts.
2014-01-01 Gomez, Maria Macarena; Ferronato, Silvia; Malerba, Giovanni; M., Santinami; A., Maurichi; Sangalli, Antonella; Turco, Alberto; P., Perego; M., Rodolfo
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
1996-01-01 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.
2000-01-01 Turco, Alberto; Passigato, S.; Fazion, M.; Soli, F.
Autosomal dominant polycystic kidney disease: clinical and genetic aspects
1997-01-01 A., Sessa; G. M., Ghiggeri; Turco, Alberto
Capitolo 1: Genetica umana: una prospettiva
2014-01-01 Turco, Alberto
Capitolo 2: Le cellule e la divisione cellulare
2014-01-01 Turco, Alberto
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes
1995-01-01 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
1991-01-01 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
1995-01-01 S., Rossetti; S., Corra; M. O., Biasi; Turco, Alberto; Pignatti, Pierfranco
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 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. | |
| Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. | 1-gen-2014 | Gomez, Maria Macarena; Ferronato, Silvia; Malerba, Giovanni; M., Santinami; A., Maurichi; Sangalli, Antonella; Turco, Alberto; P., Perego; M., Rodolfo | |
| 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 | A., Sessa; G. M., Ghiggeri; Turco, Alberto | |
| Capitolo 1: Genetica umana: una prospettiva | 1-gen-2014 | Turco, Alberto | |
| Capitolo 2: Le cellule e la divisione cellulare | 1-gen-2014 | Turco, Alberto | |
| 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 |