Di Masi A - Search Results

1

In utero exposure to di-(2-ethylhexyl) phthalate affects liver morphology and metabolism in post-natal CD-1 mice.

Maranghi F, Lorenzetti S, Tassinari R, Moracci G, Tassinari V, Marcoccia D, Di Virgilio A, Eusepi A, Romeo A, Magrelli A, Salvatore M, Tosto F, Viganotti M, Antoccia A, Di Masi A, Azzalin G, Tanzarella C, Macino G, Taruscio D, Mantovani A. Maranghi F, et al. Among authors: di virgilio a, di masi a. Reprod Toxicol. 2010 Jul;29(4):427-32. doi: 10.1016/j.reprotox.2010.03.002. Epub 2010 Mar 20. Reprod Toxicol. 2010. PMID: 20307648

2

Altered microRNA Expression Patterns in Hepatoblastoma Patients.

Magrelli A, Azzalin G, Salvatore M, Viganotti M, Tosto F, Colombo T, Devito R, Di Masi A, Antoccia A, Lorenzetti S, Maranghi F, Mantovani A, Tanzarella C, Macino G, Taruscio D. Magrelli A, et al. Among authors: di masi a. Transl Oncol. 2009 Aug 18;2(3):157-63. doi: 10.1593/tlo.09124. Transl Oncol. 2009. PMID: 19701500 Free PMC article.

3

Characterization of HuH6, Hep3B, HepG2 and HLE liver cancer cell lines by WNT/β - catenin pathway, microRNA expression and protein expression profile.

Di Masi A, Viganotti M, Antoccia A, Magrelli A, Salvatore M, Azzalin G, Tosto F, Lorenzetti S, Maranghi F, Mantovani A, Macino G, Tanzarella C, Taruscio D. Di Masi A, et al. Cell Mol Biol (Noisy-le-grand). 2010 Jun 10;56 Suppl:OL1299-317. Cell Mol Biol (Noisy-le-grand). 2010. PMID: 20937217

4

NBN Gene Polymorphisms and Cancer Susceptibility: A Systemic Review.

Berardinelli F, di Masi A, Antoccia A. Berardinelli F, et al. Among authors: di masi a. Curr Genomics. 2013 Nov;14(7):425-40. doi: 10.2174/13892029113146660012. Curr Genomics. 2013. PMID: 24396275 Free PMC article.

5

Gene expression and apoptosis induction in p53-heterozygous irradiated mice.

di Masi A, Antoccia A, Dimauro I, Argentino-Storino A, Mosiello A, Mango R, Novelli G, Tanzarella C. di Masi A, et al. Mutat Res. 2006 Feb 22;594(1-2):49-62. doi: 10.1016/j.mrfmmm.2005.07.014. Epub 2005 Sep 15. Mutat Res. 2006. PMID: 16169021

6

NBS1 Heterozygosity and Cancer Risk.

di Masi A, Antoccia A. di Masi A, et al. Curr Genomics. 2008 Jun;9(4):275-81. doi: 10.2174/138920208784533610. Curr Genomics. 2008. PMID: 19452044 Free PMC article.

7

Cleavage of the BRCT tandem domains of nibrin by the 657del5 mutation affects the DNA damage response less than the Arg215Trp mutation.

Mendez G, Cilli D, Berardinelli F, Viganotti M, Ascenzi P, Tanzarella C, Antoccia A, di Masi A. Mendez G, et al. Among authors: di masi a. IUBMB Life. 2012 Oct;64(10):853-61. doi: 10.1002/iub.1077. Epub 2012 Sep 3. IUBMB Life. 2012. PMID: 22941933 Free article.

8

The R215W mutation in NBS1 impairs gamma-H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients.

di Masi A, Viganotti M, Polticelli F, Ascenzi P, Tanzarella C, Antoccia A. di Masi A, et al. Biochem Biophys Res Commun. 2008 May 9;369(3):835-40. doi: 10.1016/j.bbrc.2008.02.129. Epub 2008 Mar 6. Biochem Biophys Res Commun. 2008. PMID: 18328813

9

The R527H mutation in LMNA gene causes an increased sensitivity to ionizing radiation.

di Masi A, D'Apice MR, Ricordy R, Tanzarella C, Novelli G. di Masi A, et al. Cell Cycle. 2008 Jul 1;7(13):2030-7. doi: 10.4161/cc.7.13.6149. Epub 2008 Apr 11. Cell Cycle. 2008. PMID: 18604166

10

Screening of Nijmegen breakage syndrome 1 mutations in four unrelated families by polymerase chain reaction using sequence-specific primers.

Di Masi A, Antoccia A, Spadoni E, Varon-Mateeva R, Maraschio P, Tanzarella C. Di Masi A, et al. Genet Test. 2006 Spring;10(1):24-30. doi: 10.1089/gte.2006.10.24. Genet Test. 2006. PMID: 16544999

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