Bagnulo R - Search Results

1

Papillary thyroid carcinoma in Peutz-Jeghers syndrome.

Triggiani V, Guastamacchia E, Renzulli G, Giagulli VA, Tafaro E, Licchelli B, Resta F, Sabbà C, Bagnulo R, Lastella P, Stella A, Resta N. Triggiani V, et al. Among authors: bagnulo r. Thyroid. 2011 Nov;21(11):1273-7. doi: 10.1089/thy.2011.0063. Epub 2011 Aug 30. Thyroid. 2011. PMID: 21877933 Review.

2

A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in Nmd efficiency.

Resta N, Susca FC, Di Giacomo MC, Stella A, Bukvic N, Bagnulo R, Simone C, Guanti G. Resta N, et al. Among authors: bagnulo r. J Cell Physiol. 2006 Oct;209(1):67-73. doi: 10.1002/jcp.20708. J Cell Physiol. 2006. PMID: 16775838

3

A novel cell type-specific role of p38alpha in the control of autophagy and cell death in colorectal cancer cells.

Comes F, Matrone A, Lastella P, Nico B, Susca FC, Bagnulo R, Ingravallo G, Modica S, Lo Sasso G, Moschetta A, Guanti G, Simone C. Comes F, et al. Among authors: bagnulo r. Cell Death Differ. 2007 Apr;14(4):693-702. doi: 10.1038/sj.cdd.4402076. Epub 2006 Dec 8. Cell Death Differ. 2007. PMID: 17159917

4

SCE frequency measurement could be useful in the prenatal diagnosis of Roberts syndrome.

Bukvic N, Resta N, Bukvic D, Susca FC, Bagnulo R, Fanelli M, Guanti G. Bukvic N, et al. Among authors: bagnulo r. Twin Res Hum Genet. 2007 Aug;10(4):655-7. doi: 10.1375/twin.10.4.655. Twin Res Hum Genet. 2007. PMID: 17708708 Free article.

5

Novel splice isoforms of STRADalpha differentially affect LKB1 activity, complex assembly and subcellular localization.

Marignani PA, Scott KD, Bagnulo R, Cannone D, Ferrari E, Stella A, Guanti G, Simone C, Resta N. Marignani PA, et al. Among authors: bagnulo r. Cancer Biol Ther. 2007 Oct;6(10):1627-31. doi: 10.4161/cbt.6.10.4787. Epub 2007 Jul 24. Cancer Biol Ther. 2007. PMID: 17921699

6

Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects.

Resta N, Giorda R, Bagnulo R, Beri S, Della Mina E, Stella A, Piglionica M, Susca FC, Guanti G, Zuffardi O, Ciccone R. Resta N, et al. Among authors: bagnulo r. Hum Genet. 2010 Oct;128(4):373-82. doi: 10.1007/s00439-010-0859-7. Epub 2010 Jul 11. Hum Genet. 2010. PMID: 20623358

7

The association of adrenocortical carcinoma and thyroid cancer in a child with Peutz-Jeghers syndrome.

Yalçin S, Kirli E, Ciftci AO, Karnak I, Resta N, Bagnulo R, Akçören Z, Orhan D, Senocak ME. Yalçin S, et al. Among authors: bagnulo r. J Pediatr Surg. 2011 Mar;46(3):570-3. doi: 10.1016/j.jpedsurg.2011.01.005. J Pediatr Surg. 2011. PMID: 21376213

8

Survey of KRAS, BRAF and PIK3CA mutational status in 209 consecutive Italian colorectal cancer patients.

Bozzao C, Varvara D, Piglionica M, Bagnulo R, Forte G, Patruno M, Russo S, Piscitelli D, Stella A, Resta N. Bozzao C, et al. Among authors: bagnulo r. Int J Biol Markers. 2012 Dec 27;27(4):e366-74. doi: 10.5301/JBM.2012.9765. Int J Biol Markers. 2012. PMID: 23125007 Free article.

9

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: bagnulo r. 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

10

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: bagnulo r. 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

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