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Page 1
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI.
Carraro M, Minervini G, Giollo M, Bromberg Y, Capriotti E, Casadio R, Dunbrack R, Elefanti L, Fariselli P, Ferrari C, Gough J, Katsonis P, Leonardi E, Lichtarge O, Menin C, Martelli PL, Niroula A, Pal LR, Repo S, Scaini MC, Vihinen M, Wei Q, Xu Q, Yang Y, Yin Y, Zaucha J, Zhao H, Zhou Y, Brenner SE, Moult J, Tosatto SCE. Carraro M, et al. Among authors: menin c. Hum Mutat. 2017 Sep;38(9):1042-1050. doi: 10.1002/humu.23235. Epub 2017 May 16. Hum Mutat. 2017. PMID: 28440912 Free PMC article.
Large genomic deletions inactivate the BRCA2 gene in breast cancer families.
Agata S, Dalla Palma M, Callegaro M, Scaini MC, Menin C, Ghiotto C, Nicoletto O, Zavagno G, Chieco-Bianchi L, D'Andrea E, Montagna M. Agata S, et al. Among authors: menin c. J Med Genet. 2005 Oct;42(10):e64. doi: 10.1136/jmg.2005.032789. J Med Genet. 2005. PMID: 16199546 Free PMC article.
No evidence for linkage with melanoma in Italian melanoma-prone families.
Kerstann KF, Bradford PT, Steighner R, Calista D, Fargnoli MC, Peris K, Scaini MC, Menin C, Ghiorzo P, Bianchi-Scarra' G, Goldstein AM, Landi MT. Kerstann KF, et al. Among authors: menin c. Cancer Epidemiol Biomarkers Prev. 2008 Jul;17(7):1838-40. doi: 10.1158/1055-9965.EPI-08-0264. Cancer Epidemiol Biomarkers Prev. 2008. PMID: 18628440 Free PMC article. No abstract available.
Clinical genetic testing for familial melanoma in Italy: a cooperative study.
Bruno W, Ghiorzo P, Battistuzzi L, Ascierto PA, Barile M, Gargiulo S, Gensini F, Gliori S, Guida M, Lombardo M, Manoukian S, Menin C, Nasti S, Origone P, Pasini B, Pastorino L, Peissel B, Pizzichetta MA, Queirolo P, Rodolfo M, Romanini A, Scaini MC, Testori A, Tibiletti MG, Turchetti D, Leachman SA, Bianchi Scarrà G; IMI, Italian Melanoma Intergroup. Bruno W, et al. Among authors: menin c. J Am Acad Dermatol. 2009 Nov;61(5):775-82. doi: 10.1016/j.jaad.2009.03.039. Epub 2009 Jun 4. J Am Acad Dermatol. 2009. PMID: 19500876
Functional impairment of p16(INK4A) due to CDKN2A p.Gly23Asp missense mutation.
Scaini MC, Rossi E, de Siqueira Torres PL, Zullato D, Callegaro M, Casella C, Quaggio M, Agata S, Malacrida S, Chiarion-Sileni V, Vecchiato A, Alaibac M, Montagna M, Mann GJ, Menin C, D'Andrea E. Scaini MC, et al. Among authors: menin c. Mutat Res. 2009 Dec 1;671(1-2):26-32. doi: 10.1016/j.mrfmmm.2009.08.007. Epub 2009 Aug 25. Mutat Res. 2009. PMID: 19712690
Contribution of susceptibility gene variants to melanoma risk in families from the Veneto region of Italy.
Menin C, Vecchiato A, Scaini MC, Elefanti L, Funari G, De Salvo GL, Quaggio M, Tognazzo S, Agata S, Dalla Santa S, Montagna M, Alaibac M, Chiarion-Sileni V, D'Andrea E. Menin C, et al. Pigment Cell Melanoma Res. 2011 Aug;24(4):728-30. doi: 10.1111/j.1755-148X.2011.00876.x. Epub 2011 Jul 7. Pigment Cell Melanoma Res. 2011. PMID: 21672182 No abstract available.
Survivin expression impacts prognostically on NSCLC but not SCLC.
Rosato A, Menin C, Boldrin D, Dalla Santa S, Bonaldi L, Scaini MC, Del Bianco P, Zardo D, Fassan M, Cappellesso R, Fassina A. Rosato A, et al. Among authors: menin c. Lung Cancer. 2013 Feb;79(2):180-6. doi: 10.1016/j.lungcan.2012.11.004. Epub 2012 Dec 4. Lung Cancer. 2013. PMID: 23218791
91 results