Sfoglia per Autore
Molecular Genetics Of The T(15;17) Of Acute Promyelocytic Leukemia
1994 M., Alcalay; M., Fagioli; Grignani, Francesco; Pf, Ferrucci; L., Tomassoni; Rogaia, Daniela; Liberatore, Concetta; M., Ruthardt; Mencarelli, Amedea; Grignani, Fausto; Pg, Pelicci
Pathogenetic Relevance Of The Acute Promyelocytic Leukemia-Specific PML/RARa Fusion Protein
1994 Grignani, Francesco; M., Fagioli; M., Alcalay; Pf, Ferrucci; L., Tomassoni; Rogaia, Daniela; Liberatore, Concetta; M., Ruthardt; Mencarelli, Amedea; Grignani, Fausto; P. G., Pelicci
Molecular Pathogenesis of Acute Promyelocytic Leukaemia.
1994 Grignani, Francesco; M., Fagioli; M., Alcalay; L., Tomassoni; Rogaia, Daniela; Grignani, Fausto; Pg, Pelicci
The acute promyelocytic leukemia-specific PML/RAR alpha fusion protein reduces the frequency of commitment to apoptosis upon growth factor deprivation of GM-CSF-dependent myeloid cells.
1995 Rogaia, Daniela; Grignani, Francesco; Grignani, Fausto; Nicoletti, Ildo; Pelicci, Pier Giuseppe
Acute promyelocytic leukemia cells resistant to retinoic acid show further perturbation of the RARa signal transduction system.
1995 S., Dermime; Grignani, Francesco; Rogaia, Daniela; Liberatore, Concetta; E., Marchesi; C., GAMBACORTI PASSERINI
Effects on differentiation by the promyelocytic leukemia PML/RARa protein depend on the fusion of the PML protein-dimerization and RARa DNA binding domains.
1996 Grignani, Francesco; Testa, U; Rogaia, Daniela; Ferrucci, PIER FRANCESCO; Samoggia, P; Pinto, A; Aldinucci, D; Gelmetti, Vania; Fagioli, Marta; Alcalay, M; Grignani, Fausto; Nicoletti, Ildo; Peschle, C; Pelicci, Pier Giuseppe
The localization of the HRX proteinto specific nuclear subomains is altered by fusion with its eps15 translocation partner
1997 Rogaia, Daniela; Grignani, Francesco; R., Carbone; D., Riganelli; F., Lococo; T., Nakamura; Cm, Croce; PP DI, Fiore; Pg, Pelicci
Terminal megakaryocytic differentiationof TF-1 cells is induced by phorbol esters and thrombopoietin and is blocked by expression of PML/RARa fusion protein.
1998 U., Testa; Grignani, Francesco; Hj, Hassan; Rogaia, Daniela; R., Masciulli; V., Gelmetti; R., Guerriero; G., Macioce; Liberatore, Concetta; T., Barberi; G., Mariani; Pg, Pelicci; C., Peschle
Formation of PML/RAR alpha high molecular weight nuclear complexes through the PML coiled-coil region is essential for the PML/RAR alpha-mediated retinoic acid response
1999 Grignani, Francesco; Gelmetti, V.; Fanelli, M; Rogaia, Daniela; De Matteis, S; Ferrara, Ff; Bonci, D; Grignani, Fausto; Nervi, C; Pelicci, P. G.
Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q).
2010 Prontera, Paolo; Buldrini, B.; Aiello, V.; Rogaia, Daniela; Mencarelli, Amedea; Gruppioni, R.; Bonfatti, A.; Beltrami, N.; Donti, Emilio; Sensi, A.
Deletion 2p15-16.1 syndrome: Case Report and Review
2011 Prontera, Paolo; L., Bernardini; G., Stangoni; A., Capalbo; Rogaia, Daniela; Romani, Rita; C., Ardisia; B., Dallapiccola; Donti, Emilio
Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locus.
2011 Prontera, Paolo; Rogaia, Daniela; Sobacchi, C.; Tavares, V. L.; Mazzotta, Giovanni; Passos Bueno, M. R.; Donti, Emilio
Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia.
2011 Prontera, Paolo; Stangoni, G.; Ardisia, C.; Rogaia, Daniela; Mencarelli, Amedea; Donti, Emilio
Nablus mask-like facial syndrome: deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotype.
2012 Allanson, J; Smith, A; Hare, H; Albrecht, B; Bijlsma, E; Dallapiccola, B; Donti, Emilio; Fitzpatrick, D; Isidor, B; Lachlan, K; Le Caignec, C; Prontera, Paolo; Raas Rothschild, A; Rogaia, Daniela; van Bon, B; Aradhya, S; Crocker, Sf; Jarinova, O; McGowan Jordan, J; Boycott, K; Bulman, D; Fagerberg, C. R.
Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression?
2013 Prontera, Paolo; A., Bartocci; V., Ottaviani; I., Isidori; Rogaia, Daniela; C., Ardisia; G., Guercini; Mencarelli, Amedea; Donti, Emilio
Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly.
2014 Prontera, Paolo; Ottaviani, V; Toccaceli, D; Rogaia, Daniela; Ardisia, C; Romani, Rita; Stangoni, G; Pierini, A; Donti, Emilio
Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism
2017 Cinque, Luigia; Sparaneo, Angelo; Penta, Laura; Mencarelli, Amedea; Rogaia, Daniela; Esposito, Susanna; Fabrizio, Federico Pio; Baorda, Filomena; Verrotti, Alberto; Falorni, Alberto; Stangoni, Gabriela; Hendy, Geoffrey N.; Guarnieri, Vito; Prontera, Paolo
Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New "c.[5867T > A]+[=]"; "p.[Leu1956Gln]+[=]" NSD1 Missense Mutation and Complex Skin Hamartoma
2018 Mencarelli, A; Prontera, P; Mencarelli, A; Rogaia, D; Stangoni, G; Cecconi, M; Esposito, S.
Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene
2019 Prontera, P; Rogaia, D; Sallicandro, E; Mencarelli, A; Imperatore, V; Squeo, Gm; Merla, G; Elisei, S; Moretti-Ferreira, D; Esposito, S; Stangoni, G.
Lethal and non-lethal GLIS1 related malformation syndromes
2019 Prontera, P; Le Caignec, C; Philippe, J; Martin-Coignard, D; Gunn, Cs; Lindenbaum, P; Bokobza, C; Redon, R; Sallicandro, E; Mencarelli, A; Rogaia, D; Gradassi, C; Schippa, M; Romani, R; Ardisia, C; Merla, G; Troiani, S; Stangoni, G; Davis, Ee
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Molecular Genetics Of The T(15;17) Of Acute Promyelocytic Leukemia | 1994 | M., Alcalay; M., Fagioli; Grignani, Francesco; Pf, Ferrucci; L., Tomassoni; Rogaia, Daniela; Liberatore, Concetta; M., Ruthardt; Mencarelli, Amedea; Grignani, Fausto; Pg, Pelicci | |
| Pathogenetic Relevance Of The Acute Promyelocytic Leukemia-Specific PML/RARa Fusion Protein | 1994 | Grignani, Francesco; M., Fagioli; M., Alcalay; Pf, Ferrucci; L., Tomassoni; Rogaia, Daniela; Liberatore, Concetta; M., Ruthardt; Mencarelli, Amedea; Grignani, Fausto; P. G., Pelicci | |
| Molecular Pathogenesis of Acute Promyelocytic Leukaemia. | 1994 | Grignani, Francesco; M., Fagioli; M., Alcalay; L., Tomassoni; Rogaia, Daniela; Grignani, Fausto; Pg, Pelicci | |
| The acute promyelocytic leukemia-specific PML/RAR alpha fusion protein reduces the frequency of commitment to apoptosis upon growth factor deprivation of GM-CSF-dependent myeloid cells. | 1995 | Rogaia, Daniela; Grignani, Francesco; Grignani, Fausto; Nicoletti, Ildo; Pelicci, Pier Giuseppe | |
| Acute promyelocytic leukemia cells resistant to retinoic acid show further perturbation of the RARa signal transduction system. | 1995 | S., Dermime; Grignani, Francesco; Rogaia, Daniela; Liberatore, Concetta; E., Marchesi; C., GAMBACORTI PASSERINI | |
| Effects on differentiation by the promyelocytic leukemia PML/RARa protein depend on the fusion of the PML protein-dimerization and RARa DNA binding domains. | 1996 | Grignani, Francesco; Testa, U; Rogaia, Daniela; Ferrucci, PIER FRANCESCO; Samoggia, P; Pinto, A; Aldinucci, D; Gelmetti, Vania; Fagioli, Marta; Alcalay, M; Grignani, Fausto; Nicoletti, Ildo; Peschle, C; Pelicci, Pier Giuseppe | |
| The localization of the HRX proteinto specific nuclear subomains is altered by fusion with its eps15 translocation partner | 1997 | Rogaia, Daniela; Grignani, Francesco; R., Carbone; D., Riganelli; F., Lococo; T., Nakamura; Cm, Croce; PP DI, Fiore; Pg, Pelicci | |
| Terminal megakaryocytic differentiationof TF-1 cells is induced by phorbol esters and thrombopoietin and is blocked by expression of PML/RARa fusion protein. | 1998 | U., Testa; Grignani, Francesco; Hj, Hassan; Rogaia, Daniela; R., Masciulli; V., Gelmetti; R., Guerriero; G., Macioce; Liberatore, Concetta; T., Barberi; G., Mariani; Pg, Pelicci; C., Peschle | |
| Formation of PML/RAR alpha high molecular weight nuclear complexes through the PML coiled-coil region is essential for the PML/RAR alpha-mediated retinoic acid response | 1999 | Grignani, Francesco; Gelmetti, V.; Fanelli, M; Rogaia, Daniela; De Matteis, S; Ferrara, Ff; Bonci, D; Grignani, Fausto; Nervi, C; Pelicci, P. G. | |
| Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q). | 2010 | Prontera, Paolo; Buldrini, B.; Aiello, V.; Rogaia, Daniela; Mencarelli, Amedea; Gruppioni, R.; Bonfatti, A.; Beltrami, N.; Donti, Emilio; Sensi, A. | |
| Deletion 2p15-16.1 syndrome: Case Report and Review | 2011 | Prontera, Paolo; L., Bernardini; G., Stangoni; A., Capalbo; Rogaia, Daniela; Romani, Rita; C., Ardisia; B., Dallapiccola; Donti, Emilio | |
| Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locus. | 2011 | Prontera, Paolo; Rogaia, Daniela; Sobacchi, C.; Tavares, V. L.; Mazzotta, Giovanni; Passos Bueno, M. R.; Donti, Emilio | |
| Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. | 2011 | Prontera, Paolo; Stangoni, G.; Ardisia, C.; Rogaia, Daniela; Mencarelli, Amedea; Donti, Emilio | |
| Nablus mask-like facial syndrome: deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotype. | 2012 | Allanson, J; Smith, A; Hare, H; Albrecht, B; Bijlsma, E; Dallapiccola, B; Donti, Emilio; Fitzpatrick, D; Isidor, B; Lachlan, K; Le Caignec, C; Prontera, Paolo; Raas Rothschild, A; Rogaia, Daniela; van Bon, B; Aradhya, S; Crocker, Sf; Jarinova, O; McGowan Jordan, J; Boycott, K; Bulman, D; Fagerberg, C. R. | |
| Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression? | 2013 | Prontera, Paolo; A., Bartocci; V., Ottaviani; I., Isidori; Rogaia, Daniela; C., Ardisia; G., Guercini; Mencarelli, Amedea; Donti, Emilio | |
| Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly. | 2014 | Prontera, Paolo; Ottaviani, V; Toccaceli, D; Rogaia, Daniela; Ardisia, C; Romani, Rita; Stangoni, G; Pierini, A; Donti, Emilio | |
| Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism | 2017 | Cinque, Luigia; Sparaneo, Angelo; Penta, Laura; Mencarelli, Amedea; Rogaia, Daniela; Esposito, Susanna; Fabrizio, Federico Pio; Baorda, Filomena; Verrotti, Alberto; Falorni, Alberto; Stangoni, Gabriela; Hendy, Geoffrey N.; Guarnieri, Vito; Prontera, Paolo | |
| Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New "c.[5867T > A]+[=]"; "p.[Leu1956Gln]+[=]" NSD1 Missense Mutation and Complex Skin Hamartoma | 2018 | Mencarelli, A; Prontera, P; Mencarelli, A; Rogaia, D; Stangoni, G; Cecconi, M; Esposito, S. | |
| Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene | 2019 | Prontera, P; Rogaia, D; Sallicandro, E; Mencarelli, A; Imperatore, V; Squeo, Gm; Merla, G; Elisei, S; Moretti-Ferreira, D; Esposito, S; Stangoni, G. | |
| Lethal and non-lethal GLIS1 related malformation syndromes | 2019 | Prontera, P; Le Caignec, C; Philippe, J; Martin-Coignard, D; Gunn, Cs; Lindenbaum, P; Bokobza, C; Redon, R; Sallicandro, E; Mencarelli, A; Rogaia, D; Gradassi, C; Schippa, M; Romani, R; Ardisia, C; Merla, G; Troiani, S; Stangoni, G; Davis, Ee |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile