Grati FR - Search Results

1

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

2

Incidence of sex chromosome aneuploidy in a prenatal population: 27-year longitudinal study in Northern Italy.

Samango-Sprouse CA, Grati FR, Brooks M, Hamzik MP, Khaksari K, Gropman A, Taylor A, Malvestiti F, Grimi B, Liuti R, Milani S, Chinetti S, Trotta A, Agrati C, Repetti E, Martin KA. Samango-Sprouse CA, et al. Among authors: grati fr. Ultrasound Obstet Gynecol. 2023 Aug;62(2):266-272. doi: 10.1002/uog.26201. Ultrasound Obstet Gynecol. 2023. PMID: 36929222 Free article.

3

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

4

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

5

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

6

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

7

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

8

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

9

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.

10

Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.

Grati FR, Grimi B, Frascoli G, Di Meco AM, Liuti R, Milani S, Trotta A, Dulcetti F, Grosso E, Miozzo M, Maggi F, Simoni G. Grati FR, et al. Eur J Hum Genet. 2006 Mar;14(3):282-8. doi: 10.1038/sj.ejhg.5201564. Eur J Hum Genet. 2006. PMID: 16418738

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