Grati FR - Search Results

1

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

2

X chromosome monosomy: a common mechanism for autoimmune diseases.

Invernizzi P, Miozzo M, Selmi C, Persani L, Battezzati PM, Zuin M, Lucchi S, Meroni PL, Marasini B, Zeni S, Watnik M, Grati FR, Simoni G, Gershwin ME, Podda M. Invernizzi P, et al. Among authors: grati fr. J Immunol. 2005 Jul 1;175(1):575-8. doi: 10.4049/jimmunol.175.1.575. J Immunol. 2005. PMID: 15972694

3

Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis.

Miozzo M, Selmi C, Gentilin B, Grati FR, Sirchia S, Oertelt S, Zuin M, Gershwin ME, Podda M, Invernizzi P. Miozzo M, et al. Among authors: grati fr. Hepatology. 2007 Aug;46(2):456-62. doi: 10.1002/hep.21696. Hepatology. 2007. PMID: 17659578

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: 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.

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

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. Placenta. 2005 Jan;26(1):10-8. doi: 10.1016/j.placenta.2004.04.009. Placenta. 2005. PMID: 15664406

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

Misbehaviour of XIST RNA in breast cancer cells.

Sirchia SM, Tabano S, Monti L, Recalcati MP, Gariboldi M, Grati FR, Porta G, Finelli P, Radice P, Miozzo M. Sirchia SM, et al. Among authors: grati fr. PLoS One. 2009;4(5):e5559. doi: 10.1371/journal.pone.0005559. Epub 2009 May 15. PLoS One. 2009. PMID: 19440381 Free PMC article.

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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