Di Gregorio C - Search Results

1

A rare MSH2 mutation causes defective binding to hMSH6, normal hMSH2 staining, and loss of hMSH6 at advanced cancer stage.

Loconte DC, Patruno M, Lastella P, Di Gregorio C, Grossi V, Forte G, Ingravallo G, Varvara D, Bagnulo R, Simone C, Resta N, Stella A. Loconte DC, et al. Among authors: di gregorio c. Hum Pathol. 2014 Oct;45(10):2162-7. doi: 10.1016/j.humpath.2014.05.019. Epub 2014 Jun 30. Hum Pathol. 2014. PMID: 25106712

2

Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation.

Lastella P, Patruno M, Forte G, Montanaro A, Di Gregorio C, Sabbà C, Suppressa P, Piepoli A, Panza A, Andriulli A, Resta N, Stella A. Lastella P, et al. Among authors: di gregorio c. Fam Cancer. 2011 Jun;10(2):285-95. doi: 10.1007/s10689-011-9419-0. Fam Cancer. 2011. PMID: 21286823

3

Analysis of telomere dynamics in peripheral blood cells from patients with Lynch syndrome.

Bozzao C, Lastella P, Ponz de Leon M, Pedroni M, Di Gregorio C, D'Ovidio FD, Resta N, Prete F, Guanti G, Stella A. Bozzao C, et al. Among authors: di gregorio c. Cancer. 2011 Sep 15;117(18):4325-35. doi: 10.1002/cncr.26022. Epub 2011 Mar 8. Cancer. 2011. PMID: 21387278 Free article.

4

Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.

Resta N, Pierannunzio D, Lenato GM, Stella A, Capocaccia R, Bagnulo R, Lastella P, Susca FC, Bozzao C, Loconte DC, Sabbà C, Urso E, Sala P, Fornasarig M, Grammatico P, Piepoli A, Host C, Turchetti D, Viel A, Memo L, Giunti L, Stigliano V, Varesco L, Bertario L, Genuardi M, Lucci Cordisco E, Tibiletti MG, Di Gregorio C, Andriulli A, Ponz de Leon M; AIFEG. Resta N, et al. Among authors: di gregorio c. Dig Liver Dis. 2013 Jul;45(7):606-11. doi: 10.1016/j.dld.2012.12.018. Epub 2013 Feb 15. Dig Liver Dis. 2013. PMID: 23415580

5

Relationship between MUC5AC and altered expression of MLH1 protein in mucinous and non-mucinous colorectal carcinomas.

Losi L, Scarselli A, Benatti P, Ponz de Leon M, Roncucci L, Pedroni M, Borghi F, Lamberti I, Rossi G, Marino M, Ponti G, Zangardi G, Menigatti M, Di Gregorio C. Losi L, et al. Among authors: di gregorio c. Pathol Res Pract. 2004;200(5):371-7. doi: 10.1016/j.prp.2004.01.008. Pathol Res Pract. 2004. PMID: 15239345

6

Microsatellite instability and mismatch-repair protein expression in hereditary and sporadic colorectal carcinogenesis.

Pedroni M, Sala E, Scarselli A, Borghi F, Menigatti M, Benatti P, Percesepe A, Rossi G, Foroni M, Losi L, Di Gregorio C, De Pol A, Nascimbeni R, Di Betta E, Salerni B, de Leon MP, Roncucci L. Pedroni M, et al. Among authors: di betta e, di gregorio c. Cancer Res. 2001 Feb 1;61(3):896-9. Cancer Res. 2001. PMID: 11221877

7

Neutrophil gelatinase-associated lipocalin: a new prognostic marker in stage I colorectal carcinoma?

Barresi V, Di Gregorio C, Reggiani-Bonetti L, Ieni A, Ponz-De Leon M, Barresi G. Barresi V, et al. Among authors: di gregorio c. Hum Pathol. 2011 Nov;42(11):1720-6. doi: 10.1016/j.humpath.2010.05.031. Epub 2011 Mar 21. Hum Pathol. 2011. PMID: 21420718

8

A mononucleotide markers panel to identify hMLH1/hMSH2 germline mutations.

Pedroni M, Roncari B, Maffei S, Losi L, Scarselli A, Di Gregorio C, Marino M, Roncucci L, Benatti P, Ponti G, Rossi G, Menigatti M, Viel A, Genuardi M, de Leon MP. Pedroni M, et al. Among authors: di gregorio c. Dis Markers. 2007;23(3):179-87. doi: 10.1155/2007/703129. Dis Markers. 2007. PMID: 17473388 Free PMC article.

9

Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC.

Roncari B, Pedroni M, Maffei S, Di Gregorio C, Ponti G, Scarselli A, Losi L, Benatti P, Roncucci L, De Gaetani C, Camellini L, Lucci-Cordisco E, Tricarico R, Genuardi M, Ponz de Leon M. Roncari B, et al. Among authors: di gregorio c. Clin Genet. 2007 Sep;72(3):230-7. doi: 10.1111/j.1399-0004.2007.00856.x. Clin Genet. 2007. PMID: 17718861

10

Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis.

Di Gregorio C, Frattini M, Maffei S, Ponti G, Losi L, Pedroni M, Venesio T, Bertario L, Varesco L, Risio M, Ponz de Leon M. Di Gregorio C, et al. Gastroenterology. 2006 Aug;131(2):439-44. doi: 10.1053/j.gastro.2006.05.049. Gastroenterology. 2006. PMID: 16890597

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