Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Paola Temperani"'
Autor:
Giandomenico Russo, Maria Grazia Narducci, Domenica Taruscio, Giuseppe Alfonso Lombardo, Alessandro Monopoli, Paola Temperani, Maria Cristina Picchio, Enrico Scala, Marina Frontani, Paola Torreri, Federica Censi, Armando Magrelli, Francesca Sampogna, Mauro Helmer Citterich, Paolo Fadda, Diego Arcelli, Cristina Cristofoletti, Elisabetta Caprini
Supplementary Table 4 from Identification of Key Regions and Genes Important in the Pathogenesis of Sézary Syndrome by Combining Genomic and Expression Microarrays
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::859dfadc674a90d9e898a45b4b58aa7a
https://doi.org/10.1158/0008-5472.22383428.v1
https://doi.org/10.1158/0008-5472.22383428.v1
Autor:
Giandomenico Russo, Maria Grazia Narducci, Domenica Taruscio, Giuseppe Alfonso Lombardo, Alessandro Monopoli, Paola Temperani, Maria Cristina Picchio, Enrico Scala, Marina Frontani, Paola Torreri, Federica Censi, Armando Magrelli, Francesca Sampogna, Mauro Helmer Citterich, Paolo Fadda, Diego Arcelli, Cristina Cristofoletti, Elisabetta Caprini
Genome Data Link from Identification of Key Regions and Genes Important in the Pathogenesis of Sézary Syndrome by Combining Genomic and Expression Microarrays
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dad601e85f1843d2b5d4132c3621ef3
https://doi.org/10.1158/0008-5472.22383446.v1
https://doi.org/10.1158/0008-5472.22383446.v1
Autor:
Giandomenico Russo, Maria Grazia Narducci, Domenica Taruscio, Giuseppe Alfonso Lombardo, Alessandro Monopoli, Paola Temperani, Maria Cristina Picchio, Enrico Scala, Marina Frontani, Paola Torreri, Federica Censi, Armando Magrelli, Francesca Sampogna, Mauro Helmer Citterich, Paolo Fadda, Diego Arcelli, Cristina Cristofoletti, Elisabetta Caprini
Supplementary Table 1 from Identification of Key Regions and Genes Important in the Pathogenesis of Sézary Syndrome by Combining Genomic and Expression Microarrays
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2def7c1682ffe14cfb8280060c456ed0
https://doi.org/10.1158/0008-5472.22383437
https://doi.org/10.1158/0008-5472.22383437
Autor:
Giandomenico Russo, Maria Grazia Narducci, Domenica Taruscio, Giuseppe Alfonso Lombardo, Alessandro Monopoli, Paola Temperani, Maria Cristina Picchio, Enrico Scala, Marina Frontani, Paola Torreri, Federica Censi, Armando Magrelli, Francesca Sampogna, Mauro Helmer Citterich, Paolo Fadda, Diego Arcelli, Cristina Cristofoletti, Elisabetta Caprini
Supplementary Figure 2 from Identification of Key Regions and Genes Important in the Pathogenesis of Sézary Syndrome by Combining Genomic and Expression Microarrays
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::746e965baa1ff282e501a003a587a49c
https://doi.org/10.1158/0008-5472.22383440.v1
https://doi.org/10.1158/0008-5472.22383440.v1
Autor:
Giandomenico Russo, Maria Grazia Narducci, Domenica Taruscio, Giuseppe Alfonso Lombardo, Alessandro Monopoli, Paola Temperani, Maria Cristina Picchio, Enrico Scala, Marina Frontani, Paola Torreri, Federica Censi, Armando Magrelli, Francesca Sampogna, Mauro Helmer Citterich, Paolo Fadda, Diego Arcelli, Cristina Cristofoletti, Elisabetta Caprini
In this study, we used single nucleotide polymorphism and comparative genomic hybridization array to study DNA copy number changes and loss of heterozygosity for 28 patients affected by Sézary syndrome (SS), a rare form of cutaneous T-cell lymphoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abb6c0d3696df8e31fe563003aeb4358
https://doi.org/10.1158/0008-5472.c.6500537
https://doi.org/10.1158/0008-5472.c.6500537
Autor:
Giandomenico Russo, Maria Grazia Narducci, Domenica Taruscio, Giuseppe Alfonso Lombardo, Alessandro Monopoli, Paola Temperani, Maria Cristina Picchio, Enrico Scala, Marina Frontani, Paola Torreri, Federica Censi, Armando Magrelli, Francesca Sampogna, Mauro Helmer Citterich, Paolo Fadda, Diego Arcelli, Cristina Cristofoletti, Elisabetta Caprini
Supplementary Table 3 from Identification of Key Regions and Genes Important in the Pathogenesis of Sézary Syndrome by Combining Genomic and Expression Microarrays
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::085cba53df6685e35a7c15af840a7bae
https://doi.org/10.1158/0008-5472.22383431.v1
https://doi.org/10.1158/0008-5472.22383431.v1
Autor:
Giandomenico Russo, Maria Grazia Narducci, Domenica Taruscio, Giuseppe Alfonso Lombardo, Alessandro Monopoli, Paola Temperani, Maria Cristina Picchio, Enrico Scala, Marina Frontani, Paola Torreri, Federica Censi, Armando Magrelli, Francesca Sampogna, Mauro Helmer Citterich, Paolo Fadda, Diego Arcelli, Cristina Cristofoletti, Elisabetta Caprini
Supplementary Table 2 from Identification of Key Regions and Genes Important in the Pathogenesis of Sézary Syndrome by Combining Genomic and Expression Microarrays
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dd23196079fb4165f0b98db20ec5c98
https://doi.org/10.1158/0008-5472.22383434.v1
https://doi.org/10.1158/0008-5472.22383434.v1
Autor:
Monica Morselli, Giuseppe Torelli, Francesca Giacobbi, Mario Luppi, Paola Temperani, Franco Narni, Leonardo Potenza, Amedea Donelli, Annalisa Imovilli, Angela Ferrari, Giovanni Riva
Publikováno v:
American Journal of Hematology. 81:45-50
Isolated extramedullary relapse (IEMR) is a pattern of acute myeloid leukemia (AML) relapse post-allogeneic bone marrow transplantation (alloBMT). Less is known about IEMR post-autologous BMT (autoBMT) and about factors associated with IEMR. We repor
Autor:
Paola Vaccari, Mario Luppi, Paola Temperani, Franco Narni, Giuseppe Longo, Giuseppe Torelli, Giovanni Emilia, Amedea Donelli, Francesca Giacobbi
Publikováno v:
Cancer Genetics and Cytogenetics. 101:35-38
A woman with t(15;17) and PMLIRARa positive acute promyelocytic leukemia (APL-M3v) achieved a complete remission (CR) with cytogenetic and molecular conversion, after one-month ATRA plus idarubicin treatment. During CR, less than one-month after cons
Publikováno v:
Cancer Genetics and Cytogenetics. 83:121-126
Following retrospective screening of our karyotype data from 414 consecutive non-childhood, neoplastic, and preneoplastic hematologic diseases, we have isolated 11 cases with alterations involving one or two chromosome termini, including: a) nonclona