DE MARCHI, Mario

DE MARCHI, Mario  

SCIENZE MEDICHE  

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Risultati 1 - 20 di 39 (tempo di esecuzione: 0.031 secondi).
Titolo Data di pubblicazione Autore(i) File
A non-redundant ATM-, NBS1-, and p53-dependent apoptotic pathway induced by unrepaired double-strand breaks in human T lymphocytes 2007 Turinetto V; Porcedda P; Lantelme E; De Marchi M; Amoroso A; Giachino C
A novel defect in mitochondrial p53 accumulation following DNA damage confers apoptosis resistance in Ataxia Telangiectasia and Nijmegen Breakage Syndrome T cells 2009 V Turinetto; P Porcedda; E Lantelme; L Orlando; L Accomasso; V Minieri; M De Marchi; A Amoroso; D Delia; C Giachino
A novel defect in mitochondrial p53 accumulation following DNA damage confers apoptosis resistance in Ataxia Telangiectasia and Nijmegen Breakage Syndrome T-cells 2010 Turinetto, Valentina; Porcedda, P; Orlando, Luca; Lantelme, Erica Maria; Accomasso, Lisa; Minieri, Valentina; Amoroso, Antonio; DE MARCHI, Mario; Delia, D; Giachino, Claudia
A rapid flow cytometry test based on histone H2AX phosphorylation for the sensitive and specific diagnosis of Ataxia Telangiectasia 2007 Giachino C; Turinetto V; Cavalieri S; Lantelme E; Orlando L; Ricardi U; De Marchi M; Amoroso A; Gregori D; Porcedda P
Activation of human mature T lymphocytes through TCR engagement in the presence of IL-7 can induce receptor revision 2004 Lantelme E.; Mantovani S.; Turinetto V.; Porcedda P.; De Marchi M.; Giachino C.
Analysis of BclI, N363S and ER22/23EK polymorphism of the glucocorticoid receptor gene in a large series of patients with adrenal incidentaloma 2013 G. Reimondo; M. Coletta; D. Giachino; I. Chiodini; D. Kastelan; V. Morelli; S. Cannavi; A. Cuccurullo; P. Beck-Peccoz; M. De Marchi; M. Terzolo
Analysis of TP53 Arg72Pro and MDM2 SNP309 T>G polymorphisms as modifier factors in hereditary retinoblastoma 2007 K. Sampieri; F. Ariani; D. Giachino; G. Mandrile; M. De Marchi; M. Bruttini; M. Mencarelli; F. Mari; T. Hadjistilianou; S. De Francesco; A. Acquaviva; A. Renieri
Apoptosis resistance following DNA damage in Ataxia Telangiectasia and Nijmegen Breakage Syndrome cells is conferred by a novel defect in mitochondrial p53 accumulation 2010 V Turinetto; L Orlando; E Lantelme; L Accomasso; V Minieri; A Amoroso; M De Marchi; D Delia; C Giachino
Bi-allelic MSH6 mutations in a case of early onset multiple primary tumors resembling Lynch and Turcot syndrome 2014 G. C. Casalis Cavalchini; D. Giachino; G. Mandrile; I. Borelli; M. Micheletti; T. Venesio; M. De Marchi; B. Pasini
Characterization of the chymotriptic activity of the 26 S protease from bovine brain. 1997 M. PICCININI; O.TAZARTES; M. CURTO; M. DE MARCHI; M. MOSTERT; R. BRUNO; M.T. RINAUDO
Clinical and genetic study of primary hyperoxaluria in Italy 2008 Robbiano A ; Mandrile G ; Giachino D ; Petrarulo M ; Pirulli D ; Zadro C ; Marangella M ; Amoroso A ; Peruzzi L ; Murer L ; Picca S ; De Marchi M
Collaborative Partecipation to the Sixth International Workshop. II: the LD data. 1975 Carbonara A; Miggiano V; De Marchi M; Trucco M; Galfrè G; Baricordi R; Belvedere MC; Curtoni ES; Savina C; Varetto O; Ceppellini R
Functional analysis of new Blau syndrome-associated CARD15 mutations 2006 M. M. van Duist; M. De Marchi
Heterozygous deletion of KLHL1/ATXN8OS at the SCA8 locus are likely not associated with cerebellar impairment in humans 2014 G. Mandrile; E. Di Gregorio; H. Goel; D. F. Giachino; S. De Mercanti; M. Iudicello; S. Losa; M. Rolando; L. Ranum; M. De Marchi; A. Brusco
Inefficient elimination of DNA double-strand-break containing lymphocytes in Ataxia Telangiectasia and Nijmegen Breakage Syndrome 2004 Porcedda P.; Turinetto V.; Lantelme E.; De Marchi M.; Giachino C.
Inefficient elimination of lymphocytes containing unresolved DNA breaks contributes to the oncogenic risk of patients with chromosome instability syndromes. 2004 Porcedda P.; Turinetto V.; Lantelme E.; De Marchi M.; Giachino C.
Italy - 1 Regional Report. Population and family analysis 1978 Savi M; Neri TM; Mattiuz PL; Baricordi O; Conighi C; Menicucci A; Gandini E; Mazzilli C; Trabace S; Sirchia G; Mercuriali F; Pizzi C; Poli F; Rosso di Sansecondo V; Scalamogna M; Fagiolo U; Pasini C; Laurentaci G; Favoino B; Di Biasi R; Magri D; Castagneto M; Luciani G; Misefari V; Gambelunghe C; Macri M; Gabrielli A; Peyretti F; Reali G; Barbanti M; Carbonara A; Belvedere MC; Borelli I; Curtoni ES; De Marchi M; Diotallevi P; Meo T; Olivetti E; Piazza A; Richiardi P; Trucco M; Wright P
MDM2 309 and TP53 Arg72Pro single nucleotide polymorphisms (SNPs) and clinical outcome in advanced lung cancer patients 2007 S. Novello; G. Mandrile; D. F. Giachino; P. Ghio; G. Selvaggi; D. Gregori; M. De Marchi; G. V. Scagliotti
MDM2 and TP53 are modifier genes of retinoblastoma 2010 V Disciglio; P Berchialla; D Giachino; M Amenduni; G Livide; M Mencarelli; A Marozza; F Mari; F Ariani; A Renieri; M De Marchi
Mutation analysis of the MSH6 gene in 52 MLH1/MSH2-negative, HNPCC suspect Italian patients 2006 P. Pazienza*; M. Barberis*; I. Borelli; S. Regazzoni; D. Giachino; G. Casalis Cavalchini; A. Allavena; M. Micheletti; A. Arrigoni; M. Schena; E. Grosso; T. Venesio; E. David; B. Pasini; N. Migone; M. De Marchi