Peissel B - Search Results

1

Characterization of an Italian founder mutation in the RING-finger domain of BRCA1.

Caleca L, Putignano AL, Colombo M, Congregati C, Sarkar M, Magliery TJ, Ripamonti CB, Foglia C, Peissel B, Zaffaroni D, Manoukian S, Tondini C, Barile M, Pensotti V, Bernard L, Papi L, Radice P. Caleca L, et al. Among authors: peissel b. PLoS One. 2014 Feb 6;9(2):e86924. doi: 10.1371/journal.pone.0086924. eCollection 2014. PLoS One. 2014. PMID: 24516540 Free PMC article.

2

Linkage disequilibrium and haplotype mapping of a skin cancer susceptibility locus in outbred mice.

Peissel B, Zaffaroni D, Zanesi N, Zedda I, Manenti G, Rebessi S, Pazzaglia S, Doria G, Covelli V, Dragani TA, Saran A. Peissel B, et al. Mamm Genome. 2000 Nov;11(11):979-81. doi: 10.1007/s003350010184. Mamm Genome. 2000. PMID: 11063253

3

A cancer modifier role for parathyroid hormone-related protein.

Manenti G, Peissel B, Gariboldi M, Falvella FS, Zaffaroni D, Allaria B, Pazzaglia S, Rebessi S, Covelli V, Saran A, Dragani TA. Manenti G, et al. Among authors: peissel b. Oncogene. 2000 Nov 9;19(47):5324-8. doi: 10.1038/sj.onc.1203916. Oncogene. 2000. PMID: 11103933

4

Use of intercross outbred mice and single nucleotide polymorphisms to map skin cancer modifier loci.

Peissel B, Zaffaroni D, Pazzaglia S, Manenti G, Zanesi N, Zedda I, Rebessi S, Covelli V, Dragani TA, Saran A. Peissel B, et al. Mamm Genome. 2001 Apr;12(4):291-4. doi: 10.1007/s003350010274. Mamm Genome. 2001. PMID: 11309660

5

SCCA2-like serpins mediate genetic predisposition to skin tumors.

Gariboldi M, Peissel B, Fabbri A, Saran A, Zaffaroni D, Falvella FS, Spinola M, Tanuma J, Pazzaglia S, Mancuso MT, Maurichi A, Bartoli C, Cataltepe S, Silverman GA, Pilotti S, Hayashizaki Y, Okazaki Y, Dragani TA. Gariboldi M, et al. Among authors: peissel b. Cancer Res. 2003 Apr 15;63(8):1871-5. Cancer Res. 2003. PMID: 12702576

6

The CHEK2 c.1100delC mutation plays an irrelevant role in breast cancer predisposition in Italy.

Caligo MA, Agata S, Aceto G, Crucianelli R, Manoukian S, Peissel B, Scaini MC, Sensi E, Veschi S, Cama A, Radice P, Viel A, D'Andrea E, Montagna M. Caligo MA, et al. Among authors: peissel b. Hum Mutat. 2004 Jul;24(1):100-1. doi: 10.1002/humu.20051. Hum Mutat. 2004. PMID: 15221794 No abstract available.

7

Mutational screening of the RB1 gene in Italian patients with retinoblastoma reveals 11 novel mutations.

Sampieri K, Hadjistilianou T, Mari F, Speciale C, Mencarelli MA, Cetta F, Manoukian S, Peissel B, Giachino D, Pasini B, Acquaviva A, Caporossi A, Frezzotti R, Renieri A, Bruttini M. Sampieri K, et al. Among authors: peissel b. J Hum Genet. 2006;51(3):209-216. doi: 10.1007/s10038-005-0348-3. Epub 2006 Feb 4. J Hum Genet. 2006. PMID: 16463005

8

Incidental carcinomas in prophylactic specimens in BRCA1 and BRCA2 germ-line mutation carriers, with emphasis on fallopian tube lesions: report of 6 cases and review of the literature.

Carcangiu ML, Peissel B, Pasini B, Spatti G, Radice P, Manoukian S. Carcangiu ML, et al. Among authors: peissel b. Am J Surg Pathol. 2006 Oct;30(10):1222-30. doi: 10.1097/01.pas.0000202161.80739.ac. Am J Surg Pathol. 2006. PMID: 17001151

9

Germline mutations of TP53 and BRCA2 genes in breast cancer/sarcoma families.

Manoukian S, Peissel B, Pensotti V, Barile M, Cortesi L, Stacchiotti S, Terenziani M, Barbera F, Pasquini G, Frigerio S, Pierotti MA, Radice P, Della-Torre G. Manoukian S, et al. Among authors: peissel b. Eur J Cancer. 2007 Feb;43(3):601-6. doi: 10.1016/j.ejca.2006.09.024. Epub 2007 Jan 16. Eur J Cancer. 2007. PMID: 17224268

10

Reconstructing the genealogy of a BRCA1 founder mutation by phylogenetic analysis.

Marroni F, Cipollini G, Peissel B, D'Andrea E, Pensabene M, Radice P, Caligo MA, Presciuttini S, Bevilacqua G. Marroni F, et al. Among authors: peissel b. Ann Hum Genet. 2008 May;72(Pt 3):310-8. doi: 10.1111/j.1469-1809.2007.00420.x. Epub 2008 Jan 23. Ann Hum Genet. 2008. PMID: 18215206

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