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Page 1
Unsuitability of lymphoblastoid cell lines as surrogate of cryopreserved isolated lymphocytes for the analysis of DNA double-strand break repair activity.
Zijno A, Porcedda P, Saini F, Allione A, Garofalo B, Marcon F, Guarrera S, Turinetto V, Minieri V, Funaro A, Crebelli R, Giachino C, Matullo G. Zijno A, et al. Among authors: porcedda p. Mutat Res. 2010 Feb 3;684(1-2):98-105. doi: 10.1016/j.mrfmmm.2009.12.008. Epub 2009 Dec 24. Mutat Res. 2010. PMID: 20035771
A novel defect in mitochondrial p53 accumulation following DNA damage confers apoptosis resistance in Ataxia Telangiectasia and Nijmegen Breakage Syndrome T-cells.
Turinetto V, Porcedda P, Minieri V, Orlando L, Lantelme E, Accomasso L, Amoroso A, De Marchi M, Zannini L, Delia D, Giachino C. Turinetto V, et al. Among authors: porcedda p. DNA Repair (Amst). 2010 Nov 10;9(11):1200-8. doi: 10.1016/j.dnarep.2010.09.003. Epub 2010 Oct 14. DNA Repair (Amst). 2010. PMID: 20947454 Free article.
Involvement of MRE11A and XPA gene polymorphisms in the modulation of DNA double-strand break repair activity: a genotype-phenotype correlation study.
Ricceri F, Porcedda P, Allione A, Turinetto V, Polidoro S, Guarrera S, Rosa F, Voglino F, Pezzotti A, Minieri V, Accomasso L, Cibrario Rocchietti E, Orlando L, Giachino C, Matullo G. Ricceri F, et al. Among authors: porcedda p. DNA Repair (Amst). 2011 Oct 10;10(10):1044-50. doi: 10.1016/j.dnarep.2011.08.003. Epub 2011 Aug 30. DNA Repair (Amst). 2011. PMID: 21880556
COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome.
Longo I, Porcedda P, Mari F, Giachino D, Meloni I, Deplano C, Brusco A, Bosio M, Massella L, Lavoratti G, Roccatello D, Frascá G, Mazzucco G, Muda AO, Conti M, Fasciolo F, Arrondel C, Heidet L, Renieri A, De Marchi M. Longo I, et al. Among authors: porcedda p. Kidney Int. 2002 Jun;61(6):1947-56. doi: 10.1046/j.1523-1755.2002.00379.x. Kidney Int. 2002. PMID: 12028435 Free article.
19 results