Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Diego Arcelli"'
Autor:
Antonella Bresin, Gianluca Ragone, Cristina Cristofoletti, Diego Arcelli, Cristian Bassi, Elisabetta Caprini, Maria Teresa Fiorenza, Mauro Helmer Citterich, Giandomenico Russo, Maria Grazia Narducci
Publikováno v:
PLoS ONE, Vol 13, Iss 10, p e0204775 (2018)
T Cell Leukemia/Lymphoma 1A is expressed during B-cell differentiation and, when over-expressed, acts as an oncogene in mouse (Tcl1a) and human (TCL1A) B-cell chronic lymphocytic leukemia (B-CLL) and T-cell prolymphocytic leukemia (T-PLL). Furthermor
Externí odkaz:
https://doaj.org/article/00780a3a5c14415eb26b3ce7a07dc273
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:
Cristina Lapucci, Daniela Prandstraller, Silvia Berto, Antonella Perolo, Antonio Farina, Nicola Rizzo, Elena Contro, Diego Arcelli, Lara Stefani
Publikováno v:
Molecular Diagnosis & Therapy. 21:653-661
Objective: Maternal plasma is a source of circulating placental nucleic acids. This study was designed to detect aberrantly expressed placental mRNA genes circulating in the maternal plasma of pregnancies affected with fetal conotruncal anomalies (CN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e75f78ab6816992d6e8af46e077590f
https://doi.org/10.1007/s40291-017-0295-7
https://doi.org/10.1007/s40291-017-0295-7
Autor:
Grazia Graziani, Diego Arcelli, Annalisa Susanna Dorio, Lucio Tentori, Giulia d'Amati, Federica Ruffini, Stefania D'Atri, Pedro Miguel Lacal
Publikováno v:
Oncology Reports. 30:2887-2896
The molecular mechanisms responsible for the elevated metastatic potential of malignant melanoma are still not fully understood. In order to shed light on the molecules involved in the acquisition by melanoma of a highly aggressive phenotype, we comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ccd194dd2899953149e70e2fea4afbf
https://doi.org/10.3892/or.2013.2791
https://doi.org/10.3892/or.2013.2791