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21.
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Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases. [electronic resource] by
- Maserati, Emanuela
- Aprili, Fiorenza
- Vinante, Fabrizio
- Locatelli, Franco
- Amendola, Giovanni
- Zatterale, Adriana
- Milone, Giuseppe
- Minelli, Antonella
- Bernardi, Franca
- Lo Curto, Francesco
- Pasquali, Francesco
Producer: 20020110
In:
Genes, chromosomes & cancer vol. 33
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22.
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OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas. [electronic resource] by
- Pirrone, Cristina
- Chiaravalli, Anna M
- Marando, Alessandro
- Conti, Andrea
- Rainero, Alessia
- Pistochini, Andrea
- Lo Curto, Francesco
- Pasquali, Francesco
- Castelnuovo, Paolo
- Capella, Carlo
- Porta, Giovanni
Producer: 20170515
In:
European journal of histochemistry : EJH vol. 61
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23.
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Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects. [electronic resource] by
- Maserati, Emanuela
- Minelli, Antonella
- Menna, Giuseppe
- Cecchini, Maria Paola
- Bernardo, Maria Ester
- Rossi, Gabriele
- De Filippi, Paola
- Lo Curto, Francesco
- Danesino, Cesare
- Locatelli, Franco
- Pasquali, Francesco
Producer: 20040305
In:
Cancer genetics and cytogenetics vol. 148
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24.
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Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome. [electronic resource] by
- Nacci, Lucia
- Danesino, Cesare
- Sainati, Laura
- Longoni, Daniela
- Poli, Furio
- Cipolli, Marco
- Perobelli, Sandra
- Nicolis, Elena
- Cannioto, Zemira
- Morini, Jacopo
- Valli, Roberto
- Pasquali, Francesco
- Minelli, Antonella
Producer: 20140618
In:
British journal of haematology vol. 165
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25.
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The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies. [electronic resource] by
- Maserati, Emanuela
- Pressato, Barbara
- Valli, Roberto
- Minelli, Antonella
- Sainati, Laura
- Patitucci, Francesco
- Marletta, Cristina
- Mastronuzzi, Angela
- Poli, Furio
- Lo Curto, Francesco
- Locatelli, Franco
- Danesino, Cesare
- Pasquali, Francesco
Producer: 20090706
In:
British journal of haematology vol. 145
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26.
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The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia. [electronic resource] by
- De Filippi, Paola
- Zecca, Marco
- Novara, Francesca
- Lisini, Daniela
- Maserati, Emanuela
- Pasquali, Francesco
- Rosti, Vittorio
- Carlo-Stella, Carmelo
- Zavras, Niki
- Cagioni, Claudia
- Zuffardi, Orsetta
- Pagliara, Daria
- Danesino, Cesare
- Locatelli, Franco
Producer: 20120917
In:
Pediatric blood & cancer vol. 59
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27.
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Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene. [electronic resource] by
- Nacci, Lucia
- Valli, Roberto
- Maria Pinto, Rita
- Zecca, Marco
- Cipolli, Marco
- Morini, Jacopo
- Cesaro, Simone
- Boveri, Emanuela
- Rosti, Vittorio
- Corti, Paola
- Ambroni, Maura
- Pasquali, Francesco
- Danesino, Cesare
- Maserati, Emanuela
- Minelli, Antonella
Producer: 20170721
In:
Genes, chromosomes & cancer vol. 56
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28.
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Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies. [electronic resource] by
- Maserati, Emanuela
- Minelli, Antonella
- Pressato, Barbara
- Valli, Roberto
- Crescenzi, Barbara
- Stefanelli, Maurizio
- Menna, Giuseppe
- Sainati, Laura
- Poli, Furio
- Panarello, Claudio
- Zecca, Marco
- Curto, Francesco Lo
- Mecucci, Cristina
- Danesino, Cesare
- Pasquali, Francesco
Producer: 20060619
In:
Genes, chromosomes & cancer vol. 45
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29.
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Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas. [electronic resource] by
- Micheloni, Giovanni
- Millefanti, Giorgia
- Conti, Andrea
- Pirrone, Cristina
- Marando, Alessandro
- Rainero, Alessia
- Tararà, Lucia
- Pistochini, Andrea
- Lo Curto, Francesco
- Pasquali, Francesco
- Castelnuovo, Paolo
- Acquati, Francesco
- Grimaldi, Annalisa
- Valli, Roberto
- Porta, Giovanni
Producer: 20200203
In:
Journal of visualized experiments : JoVE no. 144
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30.
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Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498). [electronic resource] by
- Maserati, Emanuela
- Panarello, Claudio
- Morerio, Cristina
- Valli, Roberto
- Pressato, Barbara
- Patitucci, Francesco
- Tassano, Elisa
- Di Cesare-Merlone, Alessandra
- Cugno, Chiara
- Balduini, Carlo L
- Lo Curto, Francesco
- Dufour, Carlo
- Locatelli, Franco
- Pasquali, Francesco
Producer: 20081009
In:
Haematologica vol. 93
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31.
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Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability. [electronic resource] by
- Valli, Roberto
- Minelli, Antonella
- Galbiati, Marta
- D'Amico, Giovanna
- Frattini, Annalisa
- Montalbano, Giuseppe
- Khan, Abdul W
- Porta, Giovanni
- Millefanti, Giorgia
- Olivieri, Carla
- Cipolli, Marco
- Cesaro, Simone
- Pasquali, Francesco
- Danesino, Cesare
- Cazzaniga, Gianni
- Maserati, Emanuela
Producer: 20200320
In:
British journal of haematology vol. 184
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32.
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Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies. [electronic resource] by
- Minelli, Antonella
- Maserati, Emanuela
- Rossi, Gabriele
- Bernardo, Maria Ester
- De Stefano, Piero
- Cecchini, Maria Paola
- Valli, Roberto
- Albano, Veronica
- Pierani, Paolo
- Leszl, Anna
- Sainati, Laura
- Lo Curto, Francesco
- Danesino, Cesare
- Locatelli, Franco
- Pasquali, Francesco
Producer: 20040727
In:
Genes, chromosomes & cancer vol. 40
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33.
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A Prospective Study of Hematologic Complications and Long-Term Survival of Italian Patients Affected by Shwachman-Diamond Syndrome. [electronic resource] by
- Cesaro, Simone
- Pegoraro, Anna
- Sainati, Laura
- Lucidi, Vincenzina
- Montemitro, Enza
- Corti, Paola
- Ramenghi, Ugo
- Nasi, Cristina
- Menna, Giuseppe
- Zecca, Marco
- Danesino, Cesare
- Nicolis, Elena
- Pasquali, Francesco
- Perobelli, Sandra
- Tridello, Gloria
- Farruggia, Piero
- Cipolli, Marco
Producer: 20200910
In:
The Journal of pediatrics vol. 219
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34.
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Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes. [electronic resource] by
- Marletta, Cristina
- Valli, Roberto
- Pressato, Barbara
- Mare, Lydia
- Montalbano, Giuseppe
- Menna, Giuseppe
- Loffredo, Giuseppe
- Bernardo, Maria Ester
- Vinti, Luciana
- Ferrari, Simona
- Di Cesare-Merlone, Alessandra
- Zecca, Marco
- Lo Curto, Francesco
- Locatelli, Franco
- Pasquali, Francesco
- Maserati, Emanuela
Producer: 20121231
In:
Molecular cytogenetics vol. 5
Availability: No items available.
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35.
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Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia. [electronic resource] by
- Pagani, Ilaria S
- Spinelli, Orietta
- Mattarucchi, Elia
- Pirrone, Cristina
- Pigni, Diana
- Amelotti, Elisabetta
- Lilliu, Silvia
- Boroni, Chiara
- Intermesoli, Tamara
- Giussani, Ursula
- Caimi, Luigi
- Bolda, Federica
- Baffelli, Renata
- Candi, Eleonora
- Pasquali, Francesco
- Lo Curto, Francesco
- Lanfranchi, Arnalda
- Porta, Fulvio
- Rambaldi, Alessandro
- Porta, Giovanni
Producer: 20150116
In:
Oncoscience vol. 1
Availability: No items available.
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36.
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Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype. [electronic resource] by
- Khan, Abdul Waheed
- Minelli, Antonella
- Frattini, Annalisa
- Montalbano, Giuseppe
- Bogni, Alessia
- Fabbri, Marco
- Porta, Giovanni
- Acquati, Francesco
- Pinto, Rita Maria
- Bergami, Elena
- Mura, Rossella
- Pegoraro, Anna
- Cesaro, Simone
- Cipolli, Marco
- Zecca, Marco
- Danesino, Cesare
- Locatelli, Franco
- Maserati, Emanuela
- Pasquali, Francesco
- Valli, Roberto
Publication details: Molecular cytogenetics 2020
In:
Molecular cytogenetics vol. 13
Availability: No items available.
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37.
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The mammary gland and the homeobox gene Otx1. [electronic resource] by
- Pagani, Ilaria S
- Terrinoni, Alessandro
- Marenghi, Laura
- Zucchi, Ileana
- Chiaravalli, Anna M
- Serra, Valeria
- Rovera, Francesca
- Sirchia, Silvia
- Dionigi, Gianlorenzo
- Miozzo, Monica
- Mozzo, Monica
- Frattini, Annalisa
- Ferrari, Alberta
- Capella, Carlo
- Pasquali, Francesco
- Lo Curto, Francesco
- Curto, Francesco L
- Albertini, Alberto
- Melino, Gerry
- Porta, Giovanni
Producer: 20110217
In:
The breast journal vol. 16 Suppl 1
Availability: No items available.
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