Zobrazeno 1 - 10
of 45
pro vyhledávání: '"C Lo Cunsolo"'
Autor:
Massimo Carella, C. Lo Cunsolo, Clelia Tiziana Storlazzi, Doron Tolomeo, Giovanni Martinelli, Pietro D'Addabbo, Gemma Macchia, Tommaso Mazza, P. Iuzzolino, Emanuela Ottaviani, Alberto L'Abbate, Orazio Palumbo, M.F. Miccoli, Vito Racanelli, Angelo Lonoce
Publikováno v:
Cancer genetics. 237
Acute myeloid leukemia with myelodysplasia-related changes (AML-MRC) is a heterogeneous hematological disorder defined by morphological, genetic, and clinical features. Patients with AML-MRC often show cytogenetic changes, which are associated with p
Autor:
P. Iuzzolino, Angelo Lonoce, Francesco Albano, Giorgina Specchia, Luciana Impera, Clelia Tiziana Storlazzi, Claudio Doglioni, Ettore Macrì, C. Lo Cunsolo, M. C. Guastadisegni, S. Funes, Mariano Rocchi, Ioannis Panagopoulos
Publikováno v:
Leukemia. 21:2221-2225
Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma
Autor:
F. Laveder, Luciana Impera, Clelia Tiziana Storlazzi, C. Lo Cunsolo, Mariano Rocchi, Ioannis Panagopoulos, S. Funes, Francesco Albano, P. Iuzzolino
Publikováno v:
Oncogene. 27(47)
Follicular lymphoma is the second most frequent type of non-Hodgkin's lymphoma in adults. The basic molecular defect consists of the t(14;18)(q32;q21) translocation, juxtaposing the B-cell lymphoma protein 2 gene BCL2 to the immunoglobulin heavy chai
Publikováno v:
British Journal of Cancer
Rapid tumour progression in neuroblastoma is associated with MYCN amplification, deletion of the short arm of chromosome 1 and gain of 17q. However, patients with advanced disease without MYCN amplification and/or 1p deletion have a very poor outcome
Autor:
M, Romani, P, Scaruffi, I, Casciano, K, Mazzocco, C, Lo Cunsolo, A, Cavazzana, C, Gambini, L, Boni, B, De Bernardi, G P, Tonini
Publikováno v:
International journal of cancer. 84(4)
The tp73 gene, a tp53 homologue, has been sub-regionally mapped at 1p36.3, a chromosomal region frequently deleted in neuroblastoma. Due to its chromosomal localization and to the mono-allelic expression observed in some neuroblastoma cell lines, it
Autor:
B. De Bernardi, M Dagnino, Paola Scaruffi, Massimo Conte, Claudia Milanaccio, Roberto Cusano, G. P. Tonini, C Lo Cunsolo, Achille Iolascon, Katia Mazzocco
Loss of heterozygosity (LOH) and deletion of chromosome 1p are very often found in sporadic neuroblastoma. Nevertheless, very few data are available concerning 1p LOH in familial neuroblastoma. Families with recurrent neuroblastoma are rare and analy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::173e0fcdaf58bc07f08477963e9d929e
http://hdl.handle.net/11588/482933
http://hdl.handle.net/11588/482933
Autor:
G P Tonini, L Boni, A Pession, D Rogers, A Iolascon, G Basso, L Cordero di Montezemolo, F Casale, P Perri, K Mazzocco, P Scaruffi, C Lo Cunsolo, N Marchese, C Milanaccio, M Conte, P Bruzzi, B De Bernardi
Publikováno v:
Scopus-Elsevier
PURPOSE To evaluate the prognostic role of MYCN oncogene amplification in children with neuroblastoma. PATIENTS AND METHODS Of 694 children (age, 0 to 15 years) with previously untreated neuroblastoma, 295 (42%) were evaluated at diagnosis for MYCN g
Akademický článek
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Publikováno v:
Scopus-Elsevier
We report the refined chromosomal localization of the putative tumor suppressor gene TP73 (alias p73) within the genomic region between the anonymous loci D1Z2 and D1S47. The region measures less than 6 Mb and covers a genetic distance of 16 cM. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2353d7dd41782cd27c7770435439fb79
http://www.scopus.com/inward/record.url?eid=2-s2.0-0032407952&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0032407952&partnerID=MN8TOARS