Sfoglia per Autore
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature
2015-01-01 Valli, Roberto; De Bernardi, Francesca; Frattini, Annalisa; Volpi, Luca; Bignami, Maurizio; Facchetti, Fabio; Pasquali, Francesco; Castelnuovo, PAOLO GIOCONDO MARIA; Maserati, Emanuela
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES
2015-01-01 Maserati, Emanuela; Valli, Roberto; Vinti, Luciana; Frattini, Annalisa; Fabbri, Marco; De Paoli, Elena; Montalbano, Giuseppe; Locatelli, Franco; Pasquali, Francesco
High variability of genomic instability and gene expression profiling in different HeLa clones
2015-01-01 Frattini, Annalisa; Fabbri, Marco; Valli, Roberto; De Paoli, Elena; Montalbano, Giuseppe; Gribaldo, Laura; Pasquali, Francesco; Maserati, Emanuela
Chromosome anomalies as cause of congenital bone marrow failure syndromes
2015-01-01 Valli, Roberto; DE PAOLI, Elena; Montalbano, Giuseppe; Frattini, A; Vinti, L; Pasquali, Francesco; Locatelli, Franco; Maserati, Emanuela
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning
2015-01-01 Pressato, Barbara; Valli, Roberto; Marletta, Cristina; Mare, Lydia; Montalbano, Giuseppe; LO CURTO, Francesco; Pasquali, Francesco; Maserati, Emanuela
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME
2016-01-01 DE PAOLI, Elena; Valli, Roberto; Montalbano, Giuseppe; Frattini, A; Nacci, L; Minelli, A; Di Meglio, A; Leszl, A; Sainati, L; Pasquali, Francesco; Maserati, Emanuela
STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS
2016-01-01 Minelli, Antonell; Nacci, Lucia; Brescia, L; Ramenghi, U; Valli, Roberto; Maserati, Emanuela; Pietrocola, G; Nicolis, E; Locatelli, F; Danesino, C.
EXPRESSION STUDIES IN BONE MARROW OF PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME CARRYING A CHROMOSOME 20 LONG ARMS INTERSTITIAL DELETION
2016-01-01 Valli, Roberto; De Paoli, E.; Montalbano, G.; Minelli, A.; Nacci, L.; Frattini, A.; Pasquali, Francesco; Maserati, Emanuela
Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment?
2016-01-01 Frattini, A; Villa, I; Valli, Roberto; Montalbano, Giuseppe; DE PAOLI, Elena; Bergami, E; Zecca, M; Pasquali, Francesco; Maserati, Emanuela
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients
2016-01-01 Minelli, Antonella; Nacci, Lucia; Valli, Roberto; Pietrocola, Giampiero; Ramenghi, Ugo; Locatelli, Franco; Brescia, Letizia; Nicolis, Elena; Cipolli, Marco; Danesino, Cesare
Expression studies in the bone marrow of patients with Shwachman Diamond Syndrome (SDS) and deletion of the long arm of chromosome 20 encompassing th3 EIF6 gene: relation with benign prognosis.
2017-01-01 Valli, Roberto; Fabbri, M; Frattini, A; Nacci, L; Babini, G; Morini, J; Pasquali, Francesco; Maserati, Emanuela
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome
2017-01-01 Maserati, Emanuela; Valli, Roberto; Nacci, Lucia; Frattini, Annalisa; Grilli, Federico; Pasquali, Francesco
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.
2017-01-01 Valli, Roberto; Maserati, Emanuela
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation
2017-01-01 Nacheva, E; Mokretar, K; Soenmez, A; Pittman, Am; Grace, C; Valli, Roberto; Ejaz, A; Vattathil, S; Maserati, Emanuela; Houlden, H; Taanman, Jw; Schapira, Ah; Proukakis, C.
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene
2017-01-01 Nacci, Lucia; Valli, Roberto; Pinto, Rita Maria; Zecca, Marco; Cipolli, Marco; Morini, Jacopo; Cesaro, Simone; Boveri, Emanuela; Rosti, Vittorio; Corti, Paola; Ambroni, Maura; Pasquali, Francesco; Danesino, Cesare; Maserati, Emanuela; Minelli, Antonella
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis
2017-01-01 Valli, Roberto; Annalisa, Frattini; Antonella, Minelli
Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis
2018-01-01 Pasquali, Francesco; Valli, Roberto; Giovanna, D'Amico; Annalisa, Frattini; Montalbano, Giuseppe; Marta, Galbiati; Gianni, Cazzaniga; Danesino, Cesare; Maserati, Emanuela
Whole exome sequencing discloses heterozygous variants in the DNAJC21 and EFL1 genes but not in SRP54 in 6 out of 16 patients with Shwachman-Diamond Syndrome carrying biallelic SBDS mutations
2018-01-01 Morini, Jacopo; Nacci, Lucia; Babini, Gabriele; Cesaro, Simone; Valli, Roberto; Ottolenghi, Andrea; Nicolis, Elena; Pintani, Emily; Maserati, Emanuela; Cipolli, Marco; Danesino, Cesare; Scotti, Claudia; Minelli, Antonella
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML
2018-01-01 Rainero, Alessia; Angaroni, Fabrizio; Conti, Andrea; Pirrone, Cristina; Micheloni, Giovanni; Tararà, Lucia; Millefanti, Giorgia; Maserati, Emanuela; Valli, Roberto; Spinelli, Orietta; Buklijas, Ksenija; Michelato, Anna; Casalone, Rosario; Barlassina, Cristina; Barcella, Matteo; Sirchia, Silvia; Piscitelli, Eleonora; Caccia, Massimo; Porta, Giovanni
NOVEL RECURRENT CHROMOSOMAL CHANGES AND GENE EXPRESSION RELATED TO CHROMOSOME ANOMALIES
2018-01-01 Valli, Roberto
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature | 1-gen-2015 | Valli, Roberto; De Bernardi, Francesca; Frattini, Annalisa; Volpi, Luca; Bignami, Maurizio; Facchetti, Fabio; Pasquali, Francesco; Castelnuovo, PAOLO GIOCONDO MARIA; Maserati, Emanuela | |
| BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES | 1-gen-2015 | Maserati, Emanuela; Valli, Roberto; Vinti, Luciana; Frattini, Annalisa; Fabbri, Marco; De Paoli, Elena; Montalbano, Giuseppe; Locatelli, Franco; Pasquali, Francesco | |
| High variability of genomic instability and gene expression profiling in different HeLa clones | 1-gen-2015 | Frattini, Annalisa; Fabbri, Marco; Valli, Roberto; De Paoli, Elena; Montalbano, Giuseppe; Gribaldo, Laura; Pasquali, Francesco; Maserati, Emanuela | |
| Chromosome anomalies as cause of congenital bone marrow failure syndromes | 1-gen-2015 | Valli, Roberto; DE PAOLI, Elena; Montalbano, Giuseppe; Frattini, A; Vinti, L; Pasquali, Francesco; Locatelli, Franco; Maserati, Emanuela | |
| Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning | 1-gen-2015 | Pressato, Barbara; Valli, Roberto; Marletta, Cristina; Mare, Lydia; Montalbano, Giuseppe; LO CURTO, Francesco; Pasquali, Francesco; Maserati, Emanuela | |
| UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME | 1-gen-2016 | DE PAOLI, Elena; Valli, Roberto; Montalbano, Giuseppe; Frattini, A; Nacci, L; Minelli, A; Di Meglio, A; Leszl, A; Sainati, L; Pasquali, Francesco; Maserati, Emanuela | |
| STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS | 1-gen-2016 | Minelli, Antonell; Nacci, Lucia; Brescia, L; Ramenghi, U; Valli, Roberto; Maserati, Emanuela; Pietrocola, G; Nicolis, E; Locatelli, F; Danesino, C. | |
| EXPRESSION STUDIES IN BONE MARROW OF PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME CARRYING A CHROMOSOME 20 LONG ARMS INTERSTITIAL DELETION | 1-gen-2016 | Valli, Roberto; De Paoli, E.; Montalbano, G.; Minelli, A.; Nacci, L.; Frattini, A.; Pasquali, Francesco; Maserati, Emanuela | |
| Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment? | 1-gen-2016 | Frattini, A; Villa, I; Valli, Roberto; Montalbano, Giuseppe; DE PAOLI, Elena; Bergami, E; Zecca, M; Pasquali, Francesco; Maserati, Emanuela | |
| Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients | 1-gen-2016 | Minelli, Antonella; Nacci, Lucia; Valli, Roberto; Pietrocola, Giampiero; Ramenghi, Ugo; Locatelli, Franco; Brescia, Letizia; Nicolis, Elena; Cipolli, Marco; Danesino, Cesare | |
| Expression studies in the bone marrow of patients with Shwachman Diamond Syndrome (SDS) and deletion of the long arm of chromosome 20 encompassing th3 EIF6 gene: relation with benign prognosis. | 1-gen-2017 | Valli, Roberto; Fabbri, M; Frattini, A; Nacci, L; Babini, G; Morini, J; Pasquali, Francesco; Maserati, Emanuela | |
| Novel recurrent chromosome anomalies in Shwachman Diamond syndrome | 1-gen-2017 | Maserati, Emanuela; Valli, Roberto; Nacci, Lucia; Frattini, Annalisa; Grilli, Federico; Pasquali, Francesco | |
| Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome. | 1-gen-2017 | Valli, Roberto; Maserati, Emanuela | |
| DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation | 1-gen-2017 | Nacheva, E; Mokretar, K; Soenmez, A; Pittman, Am; Grace, C; Valli, Roberto; Ejaz, A; Vattathil, S; Maserati, Emanuela; Houlden, H; Taanman, Jw; Schapira, Ah; Proukakis, C. | |
| Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene | 1-gen-2017 | Nacci, Lucia; Valli, Roberto; Pinto, Rita Maria; Zecca, Marco; Cipolli, Marco; Morini, Jacopo; Cesaro, Simone; Boveri, Emanuela; Rosti, Vittorio; Corti, Paola; Ambroni, Maura; Pasquali, Francesco; Danesino, Cesare; Maserati, Emanuela; Minelli, Antonella | |
| Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis | 1-gen-2017 | Valli, Roberto; Annalisa, Frattini; Antonella, Minelli | |
| Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis | 1-gen-2018 | Pasquali, Francesco; Valli, Roberto; Giovanna, D'Amico; Annalisa, Frattini; Montalbano, Giuseppe; Marta, Galbiati; Gianni, Cazzaniga; Danesino, Cesare; Maserati, Emanuela | |
| Whole exome sequencing discloses heterozygous variants in the DNAJC21 and EFL1 genes but not in SRP54 in 6 out of 16 patients with Shwachman-Diamond Syndrome carrying biallelic SBDS mutations | 1-gen-2018 | Morini, Jacopo; Nacci, Lucia; Babini, Gabriele; Cesaro, Simone; Valli, Roberto; Ottolenghi, Andrea; Nicolis, Elena; Pintani, Emily; Maserati, Emanuela; Cipolli, Marco; Danesino, Cesare; Scotti, Claudia; Minelli, Antonella | |
| gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML | 1-gen-2018 | Rainero, Alessia; Angaroni, Fabrizio; Conti, Andrea; Pirrone, Cristina; Micheloni, Giovanni; Tararà, Lucia; Millefanti, Giorgia; Maserati, Emanuela; Valli, Roberto; Spinelli, Orietta; Buklijas, Ksenija; Michelato, Anna; Casalone, Rosario; Barlassina, Cristina; Barcella, Matteo; Sirchia, Silvia; Piscitelli, Eleonora; Caccia, Massimo; Porta, Giovanni | |
| NOVEL RECURRENT CHROMOSOMAL CHANGES AND GENE EXPRESSION RELATED TO CHROMOSOME ANOMALIES | 1-gen-2018 | Valli, Roberto |
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