Viel A - Search Results

1

Lynch syndrome and Muir-Torre phenotype associated with a recurrent variant in the 3'UTR of the MSH6 gene.

Cini G, Carnevali I, Sahnane N, Chiaravalli AM, Dell'Elice A, Maestro R, Pin E, Bestetti I, Radovic S, Armelao F, Viel A, Tibiletti MG. Cini G, et al. Among authors: viel a. Cancer Genet. 2021 Jun;254-255:1-10. doi: 10.1016/j.cancergen.2021.01.005. Epub 2021 Jan 19. Cancer Genet. 2021. PMID: 33516942

2

Phenotypic features and genetic characterization of male breast cancer families: identification of two recurrent BRCA2 mutations in north-east of Italy.

Miolo G, Puppa LD, Santarosa M, De Giacomi C, Veronesi A, Bidoli E, Tibiletti MG, Viel A, Dolcetti R. Miolo G, et al. Among authors: viel a. BMC Cancer. 2006 Jun 9;6:156. doi: 10.1186/1471-2407-6-156. BMC Cancer. 2006. PMID: 16764716 Free PMC article.

3

The role of MYH gene in genetic predisposition to colorectal cancer: another piece of the puzzle.

Avezzù A, Agostini M, Pucciarelli S, Lise M, Urso ED, Mammi I, Maretto I, Enzo MV, Pastrello C, Lise M, Nitti D, Viel A. Avezzù A, et al. Among authors: viel a. Cancer Lett. 2008 Sep 18;268(2):308-13. doi: 10.1016/j.canlet.2008.04.004. Epub 2008 May 20. Cancer Lett. 2008. PMID: 18495334

4

Somatic mosaicism in a patient with Lynch syndrome.

Pastrello C, Fornasarig M, Pin E, Berto E, Pivetta B, Viel A. Pastrello C, et al. Among authors: viel a. Am J Med Genet A. 2009 Feb;149A(2):212-5. doi: 10.1002/ajmg.a.32620. Am J Med Genet A. 2009. PMID: 19133695

5

Premature senescence is a major response to DNA cross-linking agents in BRCA1-defective cells: implication for tailored treatments of BRCA1 mutation carriers.

Santarosa M, Del Col L, Tonin E, Caragnano A, Viel A, Maestro R. Santarosa M, et al. Among authors: viel a. Mol Cancer Ther. 2009 Apr;8(4):844-54. doi: 10.1158/1535-7163.MCT-08-0951. Mol Cancer Ther. 2009. PMID: 19372557

6

Association between hsa-mir-146a genotype and tumor age-of-onset in BRCA1/BRCA2-negative familial breast and ovarian cancer patients.

Pastrello C, Polesel J, Della Puppa L, Viel A, Maestro R. Pastrello C, et al. Among authors: viel a. Carcinogenesis. 2010 Dec;31(12):2124-6. doi: 10.1093/carcin/bgq184. Epub 2010 Sep 1. Carcinogenesis. 2010. PMID: 20810544

7

BRCA1 modulates the expression of hnRNPA2B1 and KHSRP.

Santarosa M, Del Col L, Viel A, Bivi N, D'Ambrosio C, Scaloni A, Tell G, Maestro R. Santarosa M, et al. Among authors: viel a. Cell Cycle. 2010 Dec 1;9(23):4666-73. doi: 10.4161/cc.9.23.14022. Epub 2010 Dec 1. Cell Cycle. 2010. PMID: 21099359 Free PMC article.

8

Integrated analysis of unclassified variants in mismatch repair genes.

Pastrello C, Pin E, Marroni F, Bedin C, Fornasarig M, Tibiletti MG, Oliani C, Ponz de Leon M, Urso ED, Della Puppa L, Agostini M, Viel A. Pastrello C, et al. Among authors: viel a. Genet Med. 2011 Feb;13(2):115-24. doi: 10.1097/GIM.0b013e3182011489. Genet Med. 2011. PMID: 21239990 Free article.

9

MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH-Associated Polyposis.

Pin E, Pastrello C, Tricarico R, Papi L, Quaia M, Fornasarig M, Carnevali I, Oliani C, Fornasin A, Agostini M, Maestro R, Barana D, Aretz S, Genuardi M, Viel A. Pin E, et al. Among authors: viel a. Int J Cancer. 2013 Mar 1;132(5):1060-9. doi: 10.1002/ijc.27761. Epub 2012 Aug 28. Int J Cancer. 2013. PMID: 22865608

10

MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events.

Aretz S, Tricarico R, Papi L, Spier I, Pin E, Horpaopan S, Cordisco EL, Pedroni M, Stienen D, Gentile A, Panza A, Piepoli A, de Leon MP, Friedl W, Viel A, Genuardi M. Aretz S, et al. Among authors: viel a. Eur J Hum Genet. 2014 Jul;22(7):923-9. doi: 10.1038/ejhg.2012.309. Epub 2013 Jan 30. Eur J Hum Genet. 2014. PMID: 23361220 Free PMC article.

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