Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Martina, Moretti"'
Autor:
Tiziana Pierini, Carlotta Nardelli, Anair Graciela Lema Fernandez, Valentina Pierini, Fabrizia Pellanera, Valeria Nofrini, Paolo Gorello, Martina Moretti, Silvia Arniani, Giovanni Roti, Paolo Giovenali, Marco Lupattelli, Giulio Metro, Carmen Molica, Corrado Castrioto, Rodolfo Corinaldesi, Maria Elena Laurenti, Stefano Ascani, Cristina Mecucci, Roberta La Starza
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-10 (2020)
Abstract The catalytic activity of human Telomerase Reverse Transcriptase (TERT) compensates for the loss of telomere length, eroded during each cell cycle, to ensure a correct division of stem and germinal cells. In human tumors, ectopic TERT reacti
Externí odkaz:
https://doaj.org/article/0a3c7a582305424985af628c58b06709
Autor:
Anna Ferrari, Silvia Arniani, Barbara Crescenzi, Stefano Ascani, Leonardo Flenghi, Valentina Pierini, Martina Moretti, Donatella Beacci, Silvia Romoli, Valentina Bardelli, Daniele Calistri, Giovanni Martinelli, Cristina Mecucci, Roberta La Starza
Publikováno v:
Leukemia & Lymphoma. 63:1356-1362
Autor:
Magda Zanelli, Maurizio Zizzo, Francesca Sanguedolce, Maria Elena Laurenti, Angelo Genua, Martina Moretti, Giovanni Martino, Alessandra Soriano, Stefano Ascani
Publikováno v:
Pathologica
Autor:
Silvia Arniani, Valentina Pierini, Fabrizia Pellanera, Caterina Matteucci, Danika Di Giacomo, Valentina Bardelli, Martina Quintini, Elena Mavridou, Anair Graciela Lema Fernandez, Carlotta Nardelli, Martina Moretti, Paolo Gorello, Barbara Crescenzi, Silvia Romoli, Donatella Beacci, Marco Cerrano, Nicola Fracchiolla, Simona Sica, Fabio Forghieri, Fabio Giglio, Michela Dargenio, Loredana Elia, Roberta La Starza, Cristina Mecucci
Publikováno v:
Leukemia. 36(11)
Chromothripsis is a mitotic catastrophe that arises from multiple double strand breaks and incorrect re-joining of one or a few chromosomes. We report on incidence, distribution, and features of chromothriptic events in T-cell acute lymphoblastic leu
Autor:
Jan Cools, Martina Moretti, Peter Vandenberghe, Paolo Gorello, Giovanni Roti, Renato Bassan, Giovanna De Santis, Rocco Piazza, Nicoletta Testoni, Fabrizia Pellanera, Roberta La Starza, Jean-Pierre Bourquin, Cristina Mecucci, Kim De Keersmaecker, Zeynep Kalender Atak, Christine J. Harrison, Valentina Pierini, Beat Bornhauser, Danika Di Giacomo, Caterina Matteucci, Silvia Arniani, Stein Aerts
Acute leukemias (ALs) of ambiguous lineage are a heterogeneous group of high-risk leukemias characterized by coexpression of myeloid and lymphoid markers. In this study, we identified a distinct subgroup of immature acute leukemias characterized by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7f4076a9858b583e4bfae0624e9e774
http://hdl.handle.net/10281/345360
http://hdl.handle.net/10281/345360
Autor:
Martina Moretti, Valentina Bardelli, Claire Schwab, Tim Pieters, Loredana Ruggeri, Clelia Tiziana Storlazzi, Doron Tolomeo, Danika Di Giacomo, Tiziana Pierini, Maurizio Caniglia, Pieter Van Vlierberghe, Fabrizia Pellanera, Roberta La Starza, Antonella Vitale, Christine J. Harrison, Silvia Arniani, Sabina Chiaretti, Loredana Elia, Valentina Pierini, Paolo Gorello, Elena Mastrodicasa, Giovanni Roti, Cristina Mecucci, André Pedro Pinto De Almeida
Publikováno v:
GENES CHROMOSOMES & CANCER
We investigated MYB rearrangements (MYB-R) and the levels of MYB expression, in 331 pediatric and adult patients with T-cell acute lymphoblastic leukemia (T-ALL). MYB-R were detected in 17 cases and consisted of MYB tandem duplication (tdup) (= 14) o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3536a9e43c1829c97aea554332843e07
http://hdl.handle.net/11391/1492534
http://hdl.handle.net/11391/1492534
Autor:
Luisa M. R. Napolitano, Martina Moretti, Silvia Ravera, Viviana Chiappetta, Giuseppe Cortone, Nicoletta Zini, Barbara Crescenzi, Flavio Faletra, Roberta Bottega, Enrico Cappelli, Francesca M. Pisani, Michela Faleschini, Anna Savoia, Silvia Onesti, Silvia Arniani, Job de Lange, Cristina Mecucci, Fabio Sirchia, Barbara Medagli
Publikováno v:
Journal of cellular physiology
236 (2021): 5664–5675. doi:10.1002/jcp.30265
info:cnr-pdr/source/autori:Bottega, Roberta; Ravera, Silvia; Napolitano, Luisa M. R.; Chiappetta, Viviana; Zini, Nicoletta; Crescenzi, Barbara; Arniani, Silvia; Faleschini, Michela; Cortone, Giuseppe; Faletra, Flavio; Medagli, Barbara; Sirchia, Fabio; Moretti, Martina; de Lange, Job; Cappelli, Enrico; Mecucci, Cristina; Onesti, Silvia; Pisani, Francesca M.; Savoia, Anna/titolo:Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: a comparison with Fanconi anemia./doi:10.1002%2Fjcp.30265/rivista:Journal of cellular physiology (Print)/anno:2021/pagina_da:5664/pagina_a:5675/intervallo_pagine:5664–5675/volume:236
Journal of Cellular Physiology, 236(8), 5664-5675. Wiley-Liss Inc.
Bottega, R, Ravera, S, Napolitano, L M R, Chiappetta, V, Zini, N, Crescenzi, B, Arniani, S, Faleschini, M, Cortone, G, Faletra, F, Medagli, B, Sirchia, F, Moretti, M, de Lange, J, Cappelli, E, Mecucci, C, Onesti, S, Pisani, F M & Savoia, A 2021, ' Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells : A comparison with Fanconi anemia ', Journal of Cellular Physiology, vol. 236, no. 8, pp. 5664-5675 . https://doi.org/10.1002/jcp.30265
236 (2021): 5664–5675. doi:10.1002/jcp.30265
info:cnr-pdr/source/autori:Bottega, Roberta; Ravera, Silvia; Napolitano, Luisa M. R.; Chiappetta, Viviana; Zini, Nicoletta; Crescenzi, Barbara; Arniani, Silvia; Faleschini, Michela; Cortone, Giuseppe; Faletra, Flavio; Medagli, Barbara; Sirchia, Fabio; Moretti, Martina; de Lange, Job; Cappelli, Enrico; Mecucci, Cristina; Onesti, Silvia; Pisani, Francesca M.; Savoia, Anna/titolo:Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: a comparison with Fanconi anemia./doi:10.1002%2Fjcp.30265/rivista:Journal of cellular physiology (Print)/anno:2021/pagina_da:5664/pagina_a:5675/intervallo_pagine:5664–5675/volume:236
Journal of Cellular Physiology, 236(8), 5664-5675. Wiley-Liss Inc.
Bottega, R, Ravera, S, Napolitano, L M R, Chiappetta, V, Zini, N, Crescenzi, B, Arniani, S, Faleschini, M, Cortone, G, Faletra, F, Medagli, B, Sirchia, F, Moretti, M, de Lange, J, Cappelli, E, Mecucci, C, Onesti, S, Pisani, F M & Savoia, A 2021, ' Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells : A comparison with Fanconi anemia ', Journal of Cellular Physiology, vol. 236, no. 8, pp. 5664-5675 . https://doi.org/10.1002/jcp.30265
Warsaw breakage syndrome (WABS), is caused by biallelic mutations of DDX11, a gene coding a DNA helicase. We have recently reported two affected sisters, compound heterozygous for a missense (p.Leu836Pro) and a frameshift (p.Lys303Glufs*22) variant.
Autor:
Alessio Gili, Simona Colla, Paolo Gorello, Valeria Nofrini, Danika Di Giacomo, Caterina Matteucci, Lucia Brandimarte, Giovanni Roti, Tamara Iannotti, Carlotta Nardelli, Fabrizia Pellanera, Anair Graciela Lema Fernandez, Valeria Di Battista, Cristina Mecucci, Silvia Arniani, Martina Moretti
Publikováno v:
Leukemia
Autor:
Tiziana Pierini, Pieter Van Vlierberghe, Paolo Gorello, Robin Foà, Giovanni Roti, Anair Graciela Lema Fernandez, Silvia Arniani, Danika Di Giacomo, Claire Schwab, Sabina Chiaretti, Tiziana C. Storlazzi, Valentina Pierini, Martina Moretti, Fabrizia Pellanera, Roberta La Starza, Gabriella Sammarelli, Giuseppe Basso, Antonella Vitale, Christine J. Harrison, Valeria Nofrini, Cristina Mecucci, Caterina Matteucci
Publikováno v:
The Journal of molecular diagnostics : JMD. 22(5)
T-cell acute lymphoblastic leukemia (T-ALL) results from deregulation of a number of genes via multiple genomic mechanisms. We designed a comprehensive fluorescence in situ hybridization (CI-FISH) assay that consists of genomic probes to simultaneous
Autor:
Silvia Arniani, Valentina Pierini, Barbara Crescenzi, Martina Moretti, Fabrizia Pellanera, Martina Quintini, Cristina Mecucci, Stefano Ascani, Chiara Camerini, Valeria Di Battista
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::984c696ff15051e6ebc2e99886800bcf
http://hdl.handle.net/11391/1451716
http://hdl.handle.net/11391/1451716