Rossella F - Search Results

1

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: rossella f. J Cutan Pathol. 2004 Apr;31(4):318-22. doi: 10.1111/j.0303-6987.2004.0187.x. J Cutan Pathol. 2004. PMID: 15005689

2

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: rossella f. Cancer Genet Cytogenet. 2000 Sep;121(2):156-62. doi: 10.1016/s0165-4608(00)00240-5. Cancer Genet Cytogenet. 2000. PMID: 11063800

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. Among authors: rossella f. 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

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: rossella f. Cancer Res. 2005 Mar 15;65(6):2139-46. doi: 10.1158/0008-5472.CAN-04-3465. Cancer Res. 2005. PMID: 15781624 Free article.

5

Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies.

Grati FR, Miozzo M, Cassani B, Rossella F, Antonazzo P, Gentilin B, Sirchia SM, Mori L, Rigano S, Bulfamante G, Cetin I, Simoni G. Grati FR, et al. Among authors: rossella f. Placenta. 2005 Jan;26(1):10-8. doi: 10.1016/j.placenta.2004.04.009. Placenta. 2005. PMID: 15664406

6

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. Among authors: rossella f. Eur J Hum Genet. 2004 Apr;12(4):272-8. doi: 10.1038/sj.ejhg.5201121. Eur J Hum Genet. 2004. PMID: 14673477

7

Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma.

Sirchia SM, Pariani S, Rossella F, Garagiola I, De Andreis C, Bulfamante G, Zannoni E, Radaelli U, Simoni G. Sirchia SM, et al. Among authors: rossella f. Cancer Genet Cytogenet. 1997 Apr;94(2):113-9. doi: 10.1016/s0165-4608(96)00211-7. Cancer Genet Cytogenet. 1997. PMID: 9109939

8

Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction.

Tabano S, Colapietro P, Cetin I, Grati FR, Zanutto S, Mandò C, Antonazzo P, Pileri P, Rossella F, Larizza L, Sirchia SM, Miozzo M. Tabano S, et al. Among authors: rossella f. Epigenetics. 2010 May 16;5(4):313-24. doi: 10.4161/epi.5.4.11637. Epub 2010 May 28. Epigenetics. 2010. PMID: 20418667 Free article.

9

Blood fetal microchimerism in primary biliary cirrhosis.

Invernizzi P, De Andreis C, Sirchia SM, Battezzati PM, Zuin M, Rossella F, Perego F, Bignotto M, Simoni G, Podda M. Invernizzi P, et al. Among authors: rossella f. Clin Exp Immunol. 2000 Dec;122(3):418-22. doi: 10.1046/j.1365-2249.2000.01381.x. Clin Exp Immunol. 2000. PMID: 11122249 Free PMC article.

10

Three cases with de novo 6q imbalance and variable prenatal phenotype.

Grati FR, Lalatta F, Turolla L, Cavallari U, Gentilin B, Rossella F, Cetin I, Antonazzo P, Bellotti M, Dulcetti F, Baldo D, Tenconi R, Simoni G, Miozzo M. Grati FR, et al. Among authors: rossella f. Am J Med Genet A. 2005 Jul 30;136(3):254-8. doi: 10.1002/ajmg.a.30837. Am J Med Genet A. 2005. PMID: 15957159

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