CATALOGO DEI PRODOTTI DELLA RICERCA

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Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 1-gen-1988 Turco, Alberto; Pignatti, Pierfranco
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 1-gen-1990 J. N., Dietz Band; Turco, Alberto; H. F., Willard; A., Vincent; M. H., Skolnick; D. F., Barker
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 1-gen-1990 CANNON ALBRIGHT, L. A.; Goldgar, D. E.; Wright, E. C.; Turco, Alberto; Jost, M.; Meyer, L. J.; Piepkorn, M.; Zone, J. J.; Skolnick, M. H.
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families 1-gen-1991 Turco, Alberto; B., Peissel; L., Gammaro; Maschio, Giuseppe; Pignatti, Pierfranco
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 1-gen-1991 D. F., Barker; P. R., Fain; D. E., Goldgar; J. N., Dietz Band; Turco, Alberto; C. E., Kashtan; M. C., Gregory; K., Tryggvason; M. H., Skolnick; C. L., Atkin
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
Tracking disease genes by reverse genetics 1-gen-1992 Pignatti, Pierfranco; Turco, Alberto
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 1-gen-1992 Turco, Alberto; B., Peissel; P., Quaia; R., Morandi; L., Bovicelli; Pignatti, Pierfranco
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 1-gen-1993 Turco, Alberto; B., Peissel; S., Rossetti; A., Selicorni; S., Manoukian; A., Brusasco; G., Tadini; A., Galimberti; B., Tassis; L., Turolla
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 1-gen-1994 Turco, Alberto; B., Peissel; S., Rossetti; Pignatti, Pierfranco
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
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 1-gen-1995 Turco, Alberto; S., Rossetti; E., Bressin; S., Corra
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
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
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
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
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 1-gen-1996 A., Renieri; M., Bruttini; L., Galli; P., Zanelli; T., Neri; S., Rossetti; Turco, Alberto; N., Heiskari; J., Zhou; R., Gusmano; L., Massella; G., Banfi; F., Scolari; A., Sessa; G., Rizzoni; K., Tryggvason; Pignatti, Pierfranco; M., Savi; A., Ballabio; M., De Marchi
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.
Detection of two different nonsense mutations in exon 44 of the PKD1 gene in two unrelated Italian families with severe autosomal dominant polycystic kidney disease 1-gen-1996 Turco, Alberto; S., Rossetti; E., Bresin; S., Corra; G., Restagno; A., Carbonara; O., De Prisco; L., Gammaro; Maschio, Giuseppe; Pignatti, Pierfranco
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
Mostrati risultati da 1 a 20 di 56
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