Angelini S - Search Results

1

Micronuclei in humans induced by exposure to low level of ionizing radiation: influence of polymorphisms in DNA repair genes.

Angelini S, Kumar R, Carbone F, Maffei F, Forti GC, Violante FS, Lodi V, Curti S, Hemminki K, Hrelia P. Angelini S, et al. Mutat Res. 2005 Feb 15;570(1):105-17. doi: 10.1016/j.mrfmmm.2004.10.007. Mutat Res. 2005. PMID: 15680408

2

Clinical prognostic value of the SMYD2/3 as new epigenetic biomarkers in solid cancer patients: a systematic review and meta-analysis.

Razmi M, Yazdanpanah A, Etemad-Moghadam S, Alaeddini M, Angelini S, Eini L. Razmi M, et al. Among authors: angelini s. Expert Rev Mol Diagn. 2022 Nov 17:1-15. doi: 10.1080/14737159.2022.2144235. Online ahead of print. Expert Rev Mol Diagn. 2022. PMID: 36346387

3

XPD exon 10 and 23 polymorphisms and DNA repair in human skin in situ.

Hemminki K, Xu G, Angelini S, Snellman E, Jansen CT, Lambert B, Hou SM. Hemminki K, et al. Among authors: angelini s. Carcinogenesis. 2001 Aug;22(8):1185-8. doi: 10.1093/carcin/22.8.1185. Carcinogenesis. 2001. PMID: 11470747

4

The XPD variant alleles are associated with increased aromatic DNA adduct level and lung cancer risk.

Hou SM, Fält S, Angelini S, Yang K, Nyberg F, Lambert B, Hemminki K. Hou SM, et al. Among authors: angelini s. Carcinogenesis. 2002 Apr;23(4):599-603. doi: 10.1093/carcin/23.4.599. Carcinogenesis. 2002. PMID: 11960912

5

Micronuclei frequencies in hospital workers occupationally exposed to low levels of ionizing radiation: influence of smoking status and other factors.

Maffei F, Angelini S, Forti GC, Lodi V, Violante FS, Mattioli S, Hrelia P. Maffei F, et al. Among authors: angelini s. Mutagenesis. 2002 Sep;17(5):405-9. doi: 10.1093/mutage/17.5.405. Mutagenesis. 2002. PMID: 12202628

6

Simultaneous detection of the exon 10 polymorphism and a novel intronic single base insertion polymorphism in the XPD gene using single strand conformation polymorphism.

Kumar R, Angelini S, Hemminki K. Kumar R, et al. Among authors: angelini s. Mutagenesis. 2003 Mar;18(2):207-9. doi: 10.1093/mutage/18.2.207. Mutagenesis. 2003. PMID: 12621078

7

BRAF mutations in metastatic melanoma: a possible association with clinical outcome.

Kumar R, Angelini S, Czene K, Sauroja I, Hahka-Kemppinen M, Pyrhönen S, Hemminki K. Kumar R, et al. Among authors: angelini s. Clin Cancer Res. 2003 Aug 15;9(9):3362-8. Clin Cancer Res. 2003. PMID: 12960123

8

[Biomarkers of effects and susceptibility for risk assessment].

Hrelia P, Maffei F, Angelini S, Cantelli-Forti G. Hrelia P, et al. Among authors: angelini s. G Ital Med Lav Ergon. 2003 Jul-Sep;25(3):342-3. G Ital Med Lav Ergon. 2003. PMID: 14582253 Italian.

9

Activating BRAF and N-Ras mutations in sporadic primary melanomas: an inverse association with allelic loss on chromosome 9.

Kumar R, Angelini S, Hemminki K. Kumar R, et al. Among authors: angelini s. Oncogene. 2003 Dec 18;22(58):9217-24. doi: 10.1038/sj.onc.1206909. Oncogene. 2003. PMID: 14681681

10

BRAF mutations are common somatic events in melanocytic nevi.

Kumar R, Angelini S, Snellman E, Hemminki K. Kumar R, et al. Among authors: angelini s. J Invest Dermatol. 2004 Feb;122(2):342-8. doi: 10.1046/j.0022-202X.2004.22225.x. J Invest Dermatol. 2004. PMID: 15009715 Free article.

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