DE MARCHI, Mario
DE MARCHI, Mario
SCIENZE MEDICHE
A non-redundant ATM-, NBS1-, and p53-dependent apoptotic pathway induced by unrepaired double-strand breaks in human T lymphocytes
2007-01-01 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
2009-01-01 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
2010-01-01 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
2007-01-01 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
2004-01-01 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
2013-01-01 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
2007-01-01 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
2010-01-01 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
2014-01-01 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.
1997-01-01 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
2008-01-01 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.
1975-01-01 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
2006-01-01 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
2014-01-01 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
2004-01-01 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.
2004-01-01 Porcedda P.; Turinetto V.; Lantelme E.; De Marchi M.; Giachino C.
Italy - 1 Regional Report. Population and family analysis
1978-01-01 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
La revisione del recettore in linfociti T umani: aspetti fisiologici e patologici
2006-01-01 Lantelme E.; Porcedda P.; Turinetto V.; Mantovani S.; Amoroso A.; De Marchi M.; Giachino C.
MDM2 309 and TP53 Arg72Pro single nucleotide polymorphisms (SNPs) and clinical outcome in advanced lung cancer patients
2007-01-01 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
2010-01-01 V Disciglio; P Berchialla; D Giachino; M Amenduni; G Livide; M Mencarelli; A Marozza; F Mari; F Ariani; A Renieri; M De Marchi
| 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 | |
| La revisione del recettore in linfociti T umani: aspetti fisiologici e patologici | 2006 | Lantelme E.; Porcedda P.; Turinetto V.; Mantovani S.; Amoroso A.; De Marchi M.; Giachino C. | |
| 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 |