Tanzarella C - Search Results

1

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. Among authors: tanzarella c. 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

2

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. Among authors: tanzarella c. 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

3

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: tanzarella c. IUBMB Life. 2012 Oct;64(10):853-61. doi: 10.1002/iub.1077. Epub 2012 Sep 3. IUBMB Life. 2012. PMID: 22941933 Free article.

4

Radiation-induced telomere length variations in normal and in Nijmegen Breakage Syndrome cells.

Berardinelli F, Sgura A, Di Masi A, Leone S, Cirrone GA, Romano F, Tanzarella C, Antoccia A. Berardinelli F, et al. Among authors: tanzarella c. Int J Radiat Biol. 2014 Jan;90(1):45-52. doi: 10.3109/09553002.2014.859400. Int J Radiat Biol. 2014. PMID: 24168161

5

Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?

D'Apice MR, Novelli A, di Masi A, Biancolella M, Antoccia A, Gullotta F, Licata N, Minella D, Testa B, Nardone AM, Palmieri G, Calabrese E, Biancone L, Tanzarella C, Frontali M, Sangiuolo F, Novelli G, Pallone F. D'Apice MR, et al. Among authors: tanzarella c. BMC Med Genet. 2015 Apr 2;16:20. doi: 10.1186/s12881-015-0164-3. BMC Med Genet. 2015. PMID: 25927938 Free PMC article.

6

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. Among authors: tanzarella c. 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

7

Chromosomal sensitivity to clastogenic agents and cell cycle perturbations in Nijmegen breakage syndrome lymphoblastoid cell lines.

Antoccia A, Ricordy R, Maraschio P, Prudente S, Tanzarella C. Antoccia A, et al. Among authors: tanzarella c. Int J Radiat Biol. 1997 Jan;71(1):41-9. doi: 10.1080/095530097144409. Int J Radiat Biol. 1997. PMID: 9020962

8

Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell lines.

Antoccia A, Stumm M, Saar K, Ricordy R, Maraschio P, Tanzarella C. Antoccia A, et al. Among authors: tanzarella c. Int J Radiat Biol. 1999 May;75(5):583-91. doi: 10.1080/095530099140221. Int J Radiat Biol. 1999. PMID: 10374940

9

G2-phase radiation response in lymphoblastoid cell lines from Nijmegen breakage syndrome.

Antoccia A, di Masi A, Maraschio P, Stumm M, Ricordy R, Tanzarella C. Antoccia A, et al. Among authors: tanzarella c. Cell Prolif. 2002 Apr;35(2):93-104. doi: 10.1046/j.1365-2184.2002.00234.x. Cell Prolif. 2002. PMID: 11952644 Free PMC article.

10

A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype.

Berardinelli F, di Masi A, Salvatore M, Banerjee S, Myung K, De Villartay JP, Revy P, Plebani A, Soresina A, Taruscio D, Tanzarella C, Antoccia A. Berardinelli F, et al. Among authors: tanzarella c. Eur J Med Genet. 2007 May-Jun;50(3):176-87. doi: 10.1016/j.ejmg.2007.01.006. Epub 2007 Feb 21. Eur J Med Genet. 2007. PMID: 17395558

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