Sfoglia per Autore
Griseofulvin: a potential agent of chromosomal segregation in cultured cells
1974 L. Larizza, G. Simoni, F. Tredici, L. De Carli
A family with three sibs carrying trisomy 21
1975 F. Nuzzo, M. Stefanini, G. Simoni, L. Larizza, A. Mottura, E. Reali, P. Franceschini
Detection of aneuploid cells in fibroblast cultures from the father of two trisomy 21 patients
1976 G. Simoni, A. Mottura, M. Stefanini, L. Larizza, P. Maraschio, F. Nuzzo
Chromosome lesions in amniotic fluid cell cultures
1979 G. Simoni, L. Larizza, N. Sacchi, G. Della Valle, F. Dambrosio, L. De Carli
Spontaneous and griseofulvin-induced segregation for 8-azaguanine resistance in hybrids from a human heteroploid line
1979 L. Larizza, G. Simoni, M. Stefanini, L. de Carli
Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotype
1994 S.M. Sirchia, C. De Andreis, S. Pariani, M.G. Grimoldi, A. Molinari, M. Buscaglia, G. Simoni
Confined placental mosaicism
1994 G. Simoni, S.M. Sirchia
Aneuploid correction and confined placental mosaicism
1996 G. Simoni, S.M. Sirchia, M. Fraccaro
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma
1997 S.M. Sirchia, S. Pariani, F. Rossella, I. Garagiola, C. De Andreis, G. Bulfamante, E. Zannoni, U. Radaelli, G. Simoni
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected
1997 C. De Andreis, G. Simoni, C. Castagna, L. Sacchi, S.M. Sirchia, I.M. Garagiola, T. Persico, P. Serafini, G. Pardi, A.E. Semprini
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism
1998 S.M. Sirchia, I. Garagiola, G. Colucci, S. Guerneri, F. Lalatta, M.G. Grimoldi, G. Simoni
Highly sensitive chemiluminescent method for the detection of cell contamination
1998 S.M. Sirchia, I. Garagiola, C. De Andreis, L. Pedranzini, F. Poli, F.R. Grati, B. Diomelli, G. Simoni
Loss of heterozigosity of chromosomal region 4q32-35 in basal cell carcinomas
2000 E. Sironi, S. Sirchia, A. Cerri, F. Rossella, F. Grati, R. Calcaterra, D. Tomasini, G. Simoni
Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery
2000 A.E. Semprini, C. De Andreis, S. Fiore, I. Garagiola, S.M. Sirchia, V. Savasi, M.L. Newell, G. Simoni
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas
2000 F.R. Grati, S.M. Sirchia, I. Garagiola, E. Sironi, S. Galioto, F. Rossella, P. Serafini, F. Dulcetti, A. Bozzetti, R. Brusati, G. Simoni
Losses of heterozygosity in endometrial adenocarcinomas : positive correlations with histopathological parameters
2000 S.M. Sirchia, E. Sironi, F.R. Grati, P. Serafini, I. Garagiola, F. Rossella, F. Dulcetti, G. Pardi, S. Garsia, G. Simoni
Post-zygotic origin of complete maternal chromosome 7 isodysomy and consequent loss of placental PEG1/MEST expression
2001 M. Miozzo, F. Grati, G. Bulfamante, F. Rossella, M. Cribiu, T. Radaelli, B. Cassani, T. Persico, E. Ferrazzi, I. Cetin, G. Pardi, G. Simoni
Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries
2001 F.R. Grati, G. Ghilardi, S.M. Sirchia, F. Massaro, B. Cassani, R. Scorza, C. De Andreis, E. Sironi, G. Simoni
The role of imprinted genes in fetal growth
2002 M. Miozzo, G. Simoni
Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes
2004 E. Sironi, A. Cerri, D.Tomasini, S.M. Sirchia, G. Porta, F. Rossella, F.R. Grati, G. Simoni
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