Grati FR - Search Results

1

Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells.

Sirchia SM, Ramoscelli L, Grati FR, Barbera F, Coradini D, Rossella F, Porta G, Lesma E, Ruggeri A, Radice P, Simoni G, Miozzo M. Sirchia SM, et al. Among authors: grati fr. Cancer Res. 2005 Mar 15;65(6):2139-46. doi: 10.1158/0008-5472.CAN-04-3465. Cancer Res. 2005. PMID: 15781624 Free article.

2

Highly sensitive chemiluminescent method for the detection of cell contamination.

Sirchia SM, Garagiola I, De Andreis C, Pedranzini L, Poli F, Grati FR, Diomelli B, Simoni G. Sirchia SM, et al. Among authors: grati fr. J Biolumin Chemilumin. 1998 Sep-Oct;13(5):303-5. doi: 10.1002/(SICI)1099-1271(1998090)13:5<303::AID-BIO492>3.0.CO;2-A. J Biolumin Chemilumin. 1998. PMID: 9839195

3

Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas.

Grati FR, Sirchia SM, Garagiola I, Sironi E, Galioto S, Rossella F, Serafini P, Dulcetti F, Bozzetti A, Brusati R, Simoni G. Grati FR, et al. Cancer Genet Cytogenet. 2000 Apr 1;118(1):57-61. doi: 10.1016/s0165-4608(99)00199-5. Cancer Genet Cytogenet. 2000. PMID: 10731592

4

Losses of heterozygosity in endometrial adenocarcinomas: positive correlations with histopathological parameters.

Sirchia SM, Sironi E, Grati FR, Serafini P, Garagiola I, Rossella F, Dulcetti F, Pardi G, Garsia S, Simoni G. Sirchia SM, et al. Among authors: grati fr. Cancer Genet Cytogenet. 2000 Sep;121(2):156-62. doi: 10.1016/s0165-4608(00)00240-5. Cancer Genet Cytogenet. 2000. PMID: 11063800

5

Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expression.

Miozzo M, Grati FR, Bulfamante G, Rossella F, Cribiù M, Radaelli T, Cassani B, Persico T, Cetin I, Pardi G, Simoni G. Miozzo M, et al. Among authors: grati fr. Placenta. 2001 Nov;22(10):813-21. doi: 10.1053/plac.2001.0728. Placenta. 2001. PMID: 11718568

6

Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries.

Grati FR, Ghilardi G, Sirchia SM, Massaro F, Cassani B, Scorza R, De Andreis C, Sironi E, Simoni G. Grati FR, et al. Atherosclerosis. 2001 Dec;159(2):261-7. doi: 10.1016/s0021-9150(01)00466-x. Atherosclerosis. 2001. PMID: 11730805

7

Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies.

Grati FR, Sirchia SM, Gentilin B, Rossella F, Ramoscelli L, Antonazzo P, Cavallari U, Bulfamante G, Cetin I, Simoni G, Miozzo M. Grati FR, et al. Eur J Hum Genet. 2004 Apr;12(4):272-8. doi: 10.1038/sj.ejhg.5201121. Eur J Hum Genet. 2004. PMID: 14673477

8

Frequency of monosomy X in women with primary biliary cirrhosis.

Invernizzi P, Miozzo M, Battezzati PM, Bianchi I, Grati FR, Simoni G, Selmi C, Watnik M, Gershwin ME, Podda M. Invernizzi P, et al. Among authors: grati fr. Lancet. 2004 Feb 14;363(9408):533-5. doi: 10.1016/S0140-6736(04)15541-4. Lancet. 2004. PMID: 14975617

9

Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes.

Sironi E, Cerri A, Tomasini D, Sirchia SM, Porta G, Rossella F, Grati FR, Simoni G. Sironi E, et al. Among authors: grati fr. J Cutan Pathol. 2004 Apr;31(4):318-22. doi: 10.1111/j.0303-6987.2004.0187.x. J Cutan Pathol. 2004. PMID: 15005689

10

Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.

Ruggeri A, Dulcetti F, Miozzo M, Grati FR, Grimi B, Bellato S, Natacci F, Maggi F, Simoni G. Ruggeri A, et al. Among authors: grati fr. Prenat Diagn. 2004 Dec 15;24(12):997-1000. doi: 10.1002/pd.961. Prenat Diagn. 2004. PMID: 15614836

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