SIMONI, GIUSEPPE
SIMONI, GIUSEPPE
DIPARTIMENTO DI MEDICINA, CHIRURGIA E ODONTOIATRIA (attivo dal 01/01/1999 al 26/04/2012)
A family with three sibs carrying trisomy 21
1975 F. Nuzzo, M. Stefanini, G. Simoni, L. Larizza, A. Mottura, E. Reali, P. Franceschini
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva
2005 B. Gentilin, F.R. Grati, P. Invernizzi, C. Selmi, P. Busatto, S.M. Sirchia, F. Rossella, G. Simoni, M. Miozzo
Aneuploid correction and confined placental mosaicism
1996 G. Simoni, S.M. Sirchia, M. Fraccaro
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies
2004 F.R. Grati, S.M. Sirchia, B. Gentilin, F. Rossella, L. Ramoscelli, P. Antonazzo, U. Cavallari , G. Bulfamante, I. Cetin , G. Simoni, M. Miozzo
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
Chromosome lesions in amniotic fluid cell cultures
1979 G. Simoni, L. Larizza, N. Sacchi, G. Della Valle, F. Dambrosio, L. De Carli
Confined placental mosaicism
1994 G. Simoni, S.M. Sirchia
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi
2006 F.R. Grati, B. Grimi, G. Frascoli, A.M. Di Meco, R. Liuti, S. Milani, A. Trotta, F. Dulcetti, E. Grosso, M. Miozzo, F. Maggi, G. Simoni
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
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
Detection of human immunodeficiency virus-1 RNA and DNA by extractive and in situ PCR in unprocessed semen and seminal fractions isolated by semen washing procedure
2006 T. Persico, V. Savasi, E. Ferrazzi, M. Oneta, A.E. Semprini, 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
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies
2005 F.R. Grati, M. Miozzo, B. Cassani, F. Rossella, P. Antonazzo, B. Gentilin, S.M. Sirchia, L. Mori, S. Rigano, G. Bulfamante, I. Cetin, G. Simoni
Frequency of monosomy X in women with primary biliary cirrhosis
2004 P. Invernizzi, M. Miozzo, P.M. Battezzati, I. Bianchi, F.R. Grati, G. Simoni, C. Selmi, M. Watnik, M.E. Gershwin, M. Podda
Griseofulvin: a potential agent of chromosomal segregation in cultured cells
1974 L. Larizza, G. Simoni, F. Tredici, L. De Carli
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
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
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
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells
2005 S.M. Sirchia, L. Ramoscelli, F.R. Grati, F. Barbera, D. Coradini, F. Rossella, G. Porta, E. Lesma, A. Ruggeri, P. Radice, G. Simoni, M. Miozzo