Ceccarelli C - Search Results

1

Human papillomavirus infection and pathogenic mitochondrial DNA mutation in bilateral multinodular oncocytic hyperplasia of the parotid.

Kurelac I, Salfi NC, Ceccarelli C, Alessandrini F, Cricca M, Caliceti U, Gasparre G. Kurelac I, et al. Among authors: ceccarelli c. Pathology. 2014 Apr;46(3):250-3. doi: 10.1097/PAT.0000000000000079. Pathology. 2014. PMID: 24614700 No abstract available.

2

Differentiation pathways in primary invasive breast carcinoma as suggested by intermediate filament and biopathological marker expression.

Santini D, Ceccarelli C, Taffurelli M, Pileri S, Marrano D. Santini D, et al. Among authors: ceccarelli c. J Pathol. 1996 Aug;179(4):386-91. doi: 10.1002/(SICI)1096-9896(199608)179:4<386::AID-PATH631>3.0.CO;2-V. J Pathol. 1996. PMID: 8869285

3

The basal-like breast carcinoma phenotype is regulated by SLUG gene expression.

Storci G, Sansone P, Trere D, Tavolari S, Taffurelli M, Ceccarelli C, Guarnieri T, Paterini P, Pariali M, Montanaro L, Santini D, Chieco P, Bonafé M. Storci G, et al. Among authors: ceccarelli c. J Pathol. 2008 Jan;214(1):25-37. doi: 10.1002/path.2254. J Pathol. 2008. PMID: 17973239

4

An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells.

Gasparre G, Iommarini L, Porcelli AM, Lang M, Ferri GG, Kurelac I, Zuntini R, Mariani E, Pennisi LF, Pasquini E, Pasquinelli G, Ghelli A, Bonora E, Ceccarelli C, Rugolo M, Salfi N, Romeo G, Carelli V. Gasparre G, et al. Among authors: ceccarelli c. Hum Mutat. 2009 Mar;30(3):391-6. doi: 10.1002/humu.20870. Hum Mutat. 2009. PMID: 19086058

5

The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization.

Porcelli AM, Ghelli A, Ceccarelli C, Lang M, Cenacchi G, Capristo M, Pennisi LF, Morra I, Ciccarelli E, Melcarne A, Bartoletti-Stella A, Salfi N, Tallini G, Martinuzzi A, Carelli V, Attimonelli M, Rugolo M, Romeo G, Gasparre G. Porcelli AM, et al. Among authors: ceccarelli c. Hum Mol Genet. 2010 Mar 15;19(6):1019-32. doi: 10.1093/hmg/ddp566. Epub 2009 Dec 22. Hum Mol Genet. 2010. PMID: 20028790

6

Placing mitochondrial DNA mutations within the progression model of type I endometrial carcinoma.

Guerra F, Kurelac I, Cormio A, Zuntini R, Amato LB, Ceccarelli C, Santini D, Cormio G, Fracasso F, Selvaggi L, Resta L, Attimonelli M, Gadaleta MN, Gasparre G. Guerra F, et al. Among authors: ceccarelli c. Hum Mol Genet. 2011 Jun 15;20(12):2394-405. doi: 10.1093/hmg/ddr146. Epub 2011 Apr 5. Hum Mol Genet. 2011. PMID: 21470976

7

Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva.

Bartoletti-Stella A, Salfi NC, Ceccarelli C, Attimonelli M, Romeo G, Gasparre G. Bartoletti-Stella A, et al. Among authors: ceccarelli c. Arch Ophthalmol. 2011 May;129(5):664-6. doi: 10.1001/archophthalmol.2011.95. Arch Ophthalmol. 2011. PMID: 21555623 No abstract available.

8

Mitochondrial DNA genotyping reveals synchronous nature of simultaneously detected endometrial and ovarian cancers.

Guerra F, Kurelac I, Magini P, Cormio A, Santini D, Ceccarelli C, Gasparre G. Guerra F, et al. Among authors: ceccarelli c. Gynecol Oncol. 2011 Aug;122(2):457-8. doi: 10.1016/j.ygyno.2011.04.036. Epub 2011 May 18. Gynecol Oncol. 2011. PMID: 21592547

9

A mutation threshold distinguishes the antitumorigenic effects of the mitochondrial gene MTND1, an oncojanus function.

Gasparre G, Kurelac I, Capristo M, Iommarini L, Ghelli A, Ceccarelli C, Nicoletti G, Nanni P, De Giovanni C, Scotlandi K, Betts CM, Carelli V, Lollini PL, Romeo G, Rugolo M, Porcelli AM. Gasparre G, et al. Among authors: ceccarelli c. Cancer Res. 2011 Oct 1;71(19):6220-9. doi: 10.1158/0008-5472.CAN-11-1042. Epub 2011 Aug 18. Cancer Res. 2011. PMID: 21852384

10

Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion.

Pradella LM, Zuntini R, Magini P, Ceccarelli C, Neri I, Cerasoli S, Graziano C, Gasparre G, Turchetti D. Pradella LM, et al. Among authors: ceccarelli c. J Med Genet. 2011 Nov;48(11):779-82. doi: 10.1136/jmedgenet-2011-100152. Epub 2011 Sep 16. J Med Genet. 2011. PMID: 21926107

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