Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Elena Lualdi"'
Autor:
Gabriella Sozzi, Silvana Pilotti, Manuel R. Teixeira, Lisa Galli, Federica Facchinetti, Elena Lualdi, Piergiorgio Modena
Supplementary Figure B from SMARCB1/INI1 Tumor Suppressor Gene Is Frequently Inactivated in Epithelioid Sarcomas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d1947e97d4a82f0b70e0369b107cee8
https://doi.org/10.1158/0008-5472.22363697
https://doi.org/10.1158/0008-5472.22363697
Autor:
Gabriella Sozzi, Silvana Pilotti, Manuel R. Teixeira, Lisa Galli, Federica Facchinetti, Elena Lualdi, Piergiorgio Modena
Epithelioid sarcoma is a rare soft tissue neoplasm of uncertain lineage that usually arises in the distal extremities of adults, presents a high rate of recurrences and metastases and frequently poses diagnostic dilemmas. The recently reported large-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1187fc734bee37074a0da6fc4295464d
https://doi.org/10.1158/0008-5472.c.6493844
https://doi.org/10.1158/0008-5472.c.6493844
Autor:
Gabriella Sozzi, Silvana Pilotti, Manuel R. Teixeira, Lisa Galli, Federica Facchinetti, Elena Lualdi, Piergiorgio Modena
Figure Legends from SMARCB1/INI1 Tumor Suppressor Gene Is Frequently Inactivated in Epithelioid Sarcomas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03562f6653b12f2d661f33901d54dd80
https://doi.org/10.1158/0008-5472.22363703
https://doi.org/10.1158/0008-5472.22363703
Autor:
Paolo Radice, Daniela Perotti, Monica Terenziani, Elena Lualdi, Filippo Spreafico, Paola Scarfone, Franca Fossati-Bellani, Giovanna De Vecchi, Eulalia Galea, Paola Collini, Michele Sardella, Gabriella Sozzi
Publikováno v:
American Journal of Medical Genetics Part A. :85-88
Autor:
Blanca Suarez-Merino, Wenli Gu, Cemile Jakupoglu, Oliver Brüstle, Ortrud K. Steinlein, Jian Wang, Elena Lualdi, Gaetano Finocchiaro, Rosa Mola, Tiziana Piepoli, Rolf Bjerkvig, Lucia M. Vicentini, Dorota Goplen, Carolina Frassoni, Maria Grazia Cattaneo, Francesca Inverardi, Barbara Ortino, Pietro Luigi Poliani
Publikováno v:
Neuro-Oncology. 8:96-108
Disruptions of LGI1 in glioblastoma (GBM) cell lines and LGI1 mutations in families with autosomal dominant epilepsy imply a role for LGI1 in glial cells as well as in neurons. Although we and others could not find LGI1 mutations in malignant gliomas
Autor:
Paola Collini, Filippo Spreafico, Paolo Radice, Daniela Perotti, Elena Lualdi, Giovanna De Vecchi, Franca Fossati-Bellani, M. Adele Testi, Gabriella Sozzi, Monica Terenziani
Publikováno v:
Journal of Pediatric Hematology/Oncology. 27:521-525
Summary: The concomitant occurrence of Wilms tumor (WT) was observed in two monozygotic twin sisters without evidence of congenital malformations. Twin 1 was diagnosed with a stage I WT at 11 months of age, whereas twin 2 developed a bilateral (stage
Autor:
Federica Facchinetti, Gianpaolo Dagrada, Maria Debiec-Rychter, Piergiorgio Modena, Elena Lualdi, Gabriella Sozzi, Manuel R. Teixeira, Silvana Pilotti, Florence Pedeutour
Publikováno v:
Genes, Chromosomes and Cancer. 41:283-290
Proximal-type epithelioid sarcoma is a recently described soft-tissue tumor that is distinguished from conventional-type epithelioid sarcoma by a far more aggressive clinical course, frequent location in the proximal anatomic regions, and variable rh
Autor:
Paolo Radice, Piergiorgio Modena, Monica Terenziani, Filippo Spreafico, Elena Lualdi, P. Mondini, Franca Fossati-Bellani, Paola Collini, Fernando Ravagnani, Giovanna De Vecchi, Maria Adele Testi, Francesca Di Renzo, Daniela Perotti, Gabriella Sozzi
Publikováno v:
Human Mutation. 24:400-407
Wilms tumor (WT) is a kidney malignancy of childhood characterized by highly heterogeneous genetic alterations. We previously reported the molecular and cytogenetic characterization of a WT (Case 30) carrying an interstitial deletion in chromosome 7p
Publikováno v:
Biochemical and Biophysical Research Communications. 270:673-675
The lack of expression of the putative tumor suppressor gene DMBT1 has been described in gliomas, lung carcinomas, and other malignancies. To investigate the mechanisms regulating DMBT1 expression we have screened a human genomic library with a 5′
Autor:
Federica Facchinetti, Simone Minardi, Elena Lualdi, Flavio Giordano, Gaetano Finocchiaro, Felice Giangaspero, Marco Forni, Joris A. Veltman, Irene M. Janssen, Maura Massimino, Piergiorgio Modena, Eric F.P.M. Schoenmakers, Lorenzo Genitori, James F. Reid, Riccardo Riccardi, Gabriella Sozzi
Publikováno v:
Journal of Clinical Oncology, 24, 33, pp. 5223-33
Journal of Clinical Oncology, 24, 5223-33
Journal of Clinical Oncology, 24, 5223-33
Purpose To delineate clinically relevant molecular signatures of intracranial ependymoma. Materials and Methods We analyzed 24 primary intracranial ependymomas. For genomic profiling, microarray-based comparative genomic hybridization (CGH) was used
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e22c3e489b442ac0f4fe39c94ff410a7
http://hdl.handle.net/11573/93136
http://hdl.handle.net/11573/93136