Sfoglia per Autore
G2-phase radiation response in lymphoblastoid cell lines from Nijmegen breakage syndrome
2002-01-01 Antoccia, A; DI MASI, Alessandra; Maraschio, P; Stumm, M; Ricordy, R; Tanzarella, C.
G2-phase radiation response in lymphoblastoid cell lines from Nijmegen breakage syndrome
2002-01-01 Antoccia, Antonio; DI MASI, Alessandra; Maraschio, P; Stumm, M; Ricordy, R; Tanzarella, C.
Genetic heterogeneity for a Nijmegen breakage-like syndrome
2003-01-01 Maraschio, P; Spadoni, E; Tanzarella, C; Antoccia, A; DI MASI, Alessandra; Maghnie, M; Varon, R; Demuth, I; Tiepolo, L; Danesino, C.
Chromosome instability and nibrin protein variants in NBS heterozygotes
2003-01-01 Tanzarella, C; Antoccia, A; Spadoni, E; DI MASI, Alessandra; Pecile, V; Demori, E; Varon, R; Marseglia, Gl; Tiepolo, L; Maraschio, P.
Genetic heterogeneity for a Nijmegen breakage-like syndrome
2003-01-01 P., Maraschio; E., Spadoni; C., Tanzarella; Antoccia, Antonio; DI MASI, Alessandra; M., Maghnie; R., Varon; I., Demuth; L., Tiepolo; AND C., Danesino
"Chromosome Instability and Nibrin Protein Variants in NBS Heterozygotes"
2003-01-01 Tanzarella, C.; Antoccia, Antonio; Spadoni, E; DI MASI, Alessandra; Pecile, V; Demori, E; Varon, R; Tiepolo, L; Maraschio, P.
Genetic heterogeneity among patients with nijmegen breakage syndrome.
2004-01-01 Antoccia, Antonio; DI MASI, Alessandra; Salvatore, M.; Fiorini, C.; Giliani, S.; Plebani, A.; Taruscio, D.; Tanzarella, Caterina
Genetic and cellular analysis of Italian patients with a Nijmegen breakage-like phenotype
2005-01-01 Antoccia, Antonio; DI MASI, Alessandra; Salvatore, M; Berardinelli, Francesco; Silini, A; Plebani, A; Taruscio, D; Tanzarella, Caterina
Gene expression and apoptosis induction in p53-heterozygous irradiated mice
2006-01-01 DI MASI, Alessandra; Antoccia, A; Dimauro, I; ARGENTINO STORINO, A; Mosiello, A; Mango, R; Novelli, G; Tanzarella, C.; Antoccia, Antonio
Mild Nijmegen breakage syndrome phenotype due to alternative splicing
2006-01-01 Varon, R; Dutrannoy, V; Weikert, G; Tanzarella, C; Antoccia, A; Stockl, L; Spadoni, E; Kruger, La; DI MASI, Alessandra; Sperling, K; Digweed, M; Maraschio, P.
Screening of NBS1 mutations in four NBS unrelated families by sequence-specific primer PCR
2006-01-01 DI MASI, Alessandra; Antoccia, A; Spadoni, E; VARON MATEEVA, R; Maraschio, P; Tanzarella, C.
Nbs1 and gamma-H2AX interaction in cell lines with two different mutations in Nbs1 gene
2006-01-01 Viganotti, M.; DI MASI, Alessandra; Antoccia, Antonio; Polticelli, Fabio; Tanzarella, Caterina
Screening of nijmegen breakage syndrome 1 mutations in four unrelated families by polymerase chain reaction using sequence-specific primers
2006-01-01 DI MASI, Alessandra; Antoccia, Antonio; Spadoni, E; VARON MATEEVA, R; Maraschio, P; Tanzarella,
Gene expression and apoptosis induction in p53-heterozygous irradiated mice
2006-01-01 DI MASI, Alessandra; Antoccia, Antonio; Dimauro, I; ARGENTINO STORINO, A; Mosiello, A; Mango, R; Novelli, G; Tanzarella, C.
A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling “Nijmegen breakage syndrome” phenotype
2007-01-01 Berardinelli, F; DI MASI, Alessandra; Salvatore, M; Banerjee, S; Myung, K; DE VILLARTAY J., P; Revy, P; Plebani, A; Soresina, A; Taruscio, D; Tanzarella, C; Antoccia, A.
Role of the interaction between NBS1 and gamma-H2AX in the DNA double strand break response
2007-01-01 DI MASI, Alessandra; Antoccia, Antonio; Viganotti, Mara; Polticelli, Fabio; Tanzarella, Caterina
Study of the role of specific mutations in NBS1 gene for the comprehension of the DNA-damage response
2007-01-01 DI MASI, Alessandra; Antoccia, Antonio; Tanzarella, Caterina; Viganotti, Mara; Polticelli, Fabio
A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling “Nijmegen breakage syndrome” phenotype
2007-01-01 Berardinelli, F; DI MASI, Alessandra; Salvatore, M; Banerjee, S; Myung, K; DE VILLARTAY, Jp; Revy, P; Plebani, A; Soresina, A; Taruscio, D; Tanzarella, C; Antoccia, Antonio
Cytogenetics and molecular markers of exposure to low- and high-LET radiation in lymphoblastoid cell lines
2008-01-01 Berardinelli, Francesco; Langone, Francesca; Sgura, Antonella; DI MASI, Alessandra; Cirrone, Pablo; DI ROSA, Francesco; Cuttone, Gacomo; Tanzarella, Caterina; Antoccia, Antonio
The R215W mutation in NBS1 impairs γ-H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients
2008-01-01 DI MASI, Alessandra; Viganotti, M; Polticelli, Fabio; Ascenzi, Paolo; Tanzarella, C; Antoccia, A.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| G2-phase radiation response in lymphoblastoid cell lines from Nijmegen breakage syndrome | 1-gen-2002 | Antoccia, A; DI MASI, Alessandra; Maraschio, P; Stumm, M; Ricordy, R; Tanzarella, C. | |
| G2-phase radiation response in lymphoblastoid cell lines from Nijmegen breakage syndrome | 1-gen-2002 | Antoccia, Antonio; DI MASI, Alessandra; Maraschio, P; Stumm, M; Ricordy, R; Tanzarella, C. | |
| Genetic heterogeneity for a Nijmegen breakage-like syndrome | 1-gen-2003 | Maraschio, P; Spadoni, E; Tanzarella, C; Antoccia, A; DI MASI, Alessandra; Maghnie, M; Varon, R; Demuth, I; Tiepolo, L; Danesino, C. | |
| Chromosome instability and nibrin protein variants in NBS heterozygotes | 1-gen-2003 | Tanzarella, C; Antoccia, A; Spadoni, E; DI MASI, Alessandra; Pecile, V; Demori, E; Varon, R; Marseglia, Gl; Tiepolo, L; Maraschio, P. | |
| Genetic heterogeneity for a Nijmegen breakage-like syndrome | 1-gen-2003 | P., Maraschio; E., Spadoni; C., Tanzarella; Antoccia, Antonio; DI MASI, Alessandra; M., Maghnie; R., Varon; I., Demuth; L., Tiepolo; AND C., Danesino | |
| "Chromosome Instability and Nibrin Protein Variants in NBS Heterozygotes" | 1-gen-2003 | Tanzarella, C.; Antoccia, Antonio; Spadoni, E; DI MASI, Alessandra; Pecile, V; Demori, E; Varon, R; Tiepolo, L; Maraschio, P. | |
| Genetic heterogeneity among patients with nijmegen breakage syndrome. | 1-gen-2004 | Antoccia, Antonio; DI MASI, Alessandra; Salvatore, M.; Fiorini, C.; Giliani, S.; Plebani, A.; Taruscio, D.; Tanzarella, Caterina | |
| Genetic and cellular analysis of Italian patients with a Nijmegen breakage-like phenotype | 1-gen-2005 | Antoccia, Antonio; DI MASI, Alessandra; Salvatore, M; Berardinelli, Francesco; Silini, A; Plebani, A; Taruscio, D; Tanzarella, Caterina | |
| Gene expression and apoptosis induction in p53-heterozygous irradiated mice | 1-gen-2006 | DI MASI, Alessandra; Antoccia, A; Dimauro, I; ARGENTINO STORINO, A; Mosiello, A; Mango, R; Novelli, G; Tanzarella, C.; Antoccia, Antonio | |
| Mild Nijmegen breakage syndrome phenotype due to alternative splicing | 1-gen-2006 | Varon, R; Dutrannoy, V; Weikert, G; Tanzarella, C; Antoccia, A; Stockl, L; Spadoni, E; Kruger, La; DI MASI, Alessandra; Sperling, K; Digweed, M; Maraschio, P. | |
| Screening of NBS1 mutations in four NBS unrelated families by sequence-specific primer PCR | 1-gen-2006 | DI MASI, Alessandra; Antoccia, A; Spadoni, E; VARON MATEEVA, R; Maraschio, P; Tanzarella, C. | |
| Nbs1 and gamma-H2AX interaction in cell lines with two different mutations in Nbs1 gene | 1-gen-2006 | Viganotti, M.; DI MASI, Alessandra; Antoccia, Antonio; Polticelli, Fabio; Tanzarella, Caterina | |
| Screening of nijmegen breakage syndrome 1 mutations in four unrelated families by polymerase chain reaction using sequence-specific primers | 1-gen-2006 | DI MASI, Alessandra; Antoccia, Antonio; Spadoni, E; VARON MATEEVA, R; Maraschio, P; Tanzarella, | |
| Gene expression and apoptosis induction in p53-heterozygous irradiated mice | 1-gen-2006 | DI MASI, Alessandra; Antoccia, Antonio; Dimauro, I; ARGENTINO STORINO, A; Mosiello, A; Mango, R; Novelli, G; Tanzarella, C. | |
| A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling “Nijmegen breakage syndrome” phenotype | 1-gen-2007 | Berardinelli, F; DI MASI, Alessandra; Salvatore, M; Banerjee, S; Myung, K; DE VILLARTAY J., P; Revy, P; Plebani, A; Soresina, A; Taruscio, D; Tanzarella, C; Antoccia, A. | |
| Role of the interaction between NBS1 and gamma-H2AX in the DNA double strand break response | 1-gen-2007 | DI MASI, Alessandra; Antoccia, Antonio; Viganotti, Mara; Polticelli, Fabio; Tanzarella, Caterina | |
| Study of the role of specific mutations in NBS1 gene for the comprehension of the DNA-damage response | 1-gen-2007 | DI MASI, Alessandra; Antoccia, Antonio; Tanzarella, Caterina; Viganotti, Mara; Polticelli, Fabio | |
| A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling “Nijmegen breakage syndrome” phenotype | 1-gen-2007 | Berardinelli, F; DI MASI, Alessandra; Salvatore, M; Banerjee, S; Myung, K; DE VILLARTAY, Jp; Revy, P; Plebani, A; Soresina, A; Taruscio, D; Tanzarella, C; Antoccia, Antonio | |
| Cytogenetics and molecular markers of exposure to low- and high-LET radiation in lymphoblastoid cell lines | 1-gen-2008 | Berardinelli, Francesco; Langone, Francesca; Sgura, Antonella; DI MASI, Alessandra; Cirrone, Pablo; DI ROSA, Francesco; Cuttone, Gacomo; Tanzarella, Caterina; Antoccia, Antonio | |
| The R215W mutation in NBS1 impairs γ-H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients | 1-gen-2008 | DI MASI, Alessandra; Viganotti, M; Polticelli, Fabio; Ascenzi, Paolo; Tanzarella, C; Antoccia, A. |
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