Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Claudio Forcato"'
Autor:
Anna Doffini, Claudio Forcato, Chiara Mangano, Debora Lattuada, Roberta Aversa, Chiara Maranta, Emilia Giovannone, Genny Buson, Chiara Bolognesi, Rebecca Maiocchi, Martina Dori, Liyana Jamal, Raidah Ahmad, George S.H. Yeo, Tai Wai Yeo, Silvia Saragozza, Rosamaria Silipigni, Marta Serafini, Andrea Biondi, Sofia Perego, Patrizia Vergani, Enrico Ferrazzi, Paola Ricciardi-Castagnoli, Thomas Musci, Francesca Romana Grati
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100672- (2023)
Externí odkaz:
https://doaj.org/article/39475ffc993a46449e9ae1a5b2d26534
Autor:
Marianne Oulhen, Patrycja Pawlikowska, Tala Tayoun, Marianna Garonzi, Genny Buson, Claudio Forcato, Nicolò Manaresi, Agathe Aberlenc, Laura Mezquita, Yann Lecluse, Pernelle Lavaud, Charles Naltet, David Planchard, Benjamin Besse, Françoise Farace
Publikováno v:
npj Precision Oncology, Vol 5, Iss 1, Pp 1-11 (2021)
Abstract Gatekeeper mutations are identified in only 50% of the cases at resistance to Anaplastic Lymphoma Kinase (ALK)-tyrosine kinase inhibitors (TKIs). Circulating tumor cells (CTCs) are relevant tools to identify additional resistance mechanisms
Externí odkaz:
https://doaj.org/article/17945349780b47ecb1ff35beb8ce4404
Autor:
Federica Isidori, Deborah Malvi, Silvia Fittipaldi, Claudio Forcato, Isotta Bozzarelli, Claudia Sala, Giovanni Raulli, Antonia D’Errico, Michelangelo Fiorentino, Marco Seri, Kausilia K. Krishnadath, Elena Bonora, Sandro Mattioli, EAC-BAGH group
Publikováno v:
BMC Cancer, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background We report on a female patient who underwent primary radical resection for a stage 2B Her-2-positive Barrett’s-type esophageal adenocarcinoma (EAC). Despite Her-2 targeted therapy, her disease recurred and required repeated metas
Externí odkaz:
https://doaj.org/article/3a7df160cd0b498f8280c02362db206e
Autor:
Loris Bertoldi, Claudio Forcato, Nicola Vitulo, Giovanni Birolo, Fabio De Pascale, Erika Feltrin, Riccardo Schiavon, Franca Anglani, Susanna Negrisolo, Alessandra Zanetti, Francesca D’Avanzo, Rosella Tomanin, Georgine Faulkner, Alessandro Vezzi, Giorgio Valle
Publikováno v:
BMC Bioinformatics, Vol 18, Iss 1, Pp 1-11 (2017)
Abstract Background Whole genome and exome sequencing are contributing to the extraordinary progress in the study of human genetic variants. In this fast developing field, appropriate and easily accessible tools are required to facilitate data analys
Externí odkaz:
https://doaj.org/article/ebb3745f6f204781b412817f9f8b45b3
Autor:
Alberto Ferrarini, Claudio Forcato, Genny Buson, Paola Tononi, Valentina Del Monaco, Mario Terracciano, Chiara Bolognesi, Francesca Fontana, Gianni Medoro, Rui Neves, Birte Möhlendick, Karim Rihawi, Andrea Ardizzoni, Semini Sumanasuriya, Penny Flohr, Maryou Lambros, Johann de Bono, Nikolas H Stoecklein, Nicolò Manaresi
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0193689 (2018)
Chromosomal instability and associated chromosomal aberrations are hallmarks of cancer and play a critical role in disease progression and development of resistance to drugs. Single-cell genome analysis has gained interest in latest years as a source
Externí odkaz:
https://doaj.org/article/8c6ff371798a4662bf53ba6d47d85225
Autor:
Sara De Iudicibus, Marianna Lucafò, Nicola Vitulo, Stefano Martelossi, Rosanna Zimbello, Fabio De Pascale, Claudio Forcato, Samuele Naviglio, Alessia Di Silvestre, Marco Gerdol, Gabriele Stocco, Giorgio Valle, Alessandro Ventura, Matteo Bramuzzo, Giuliana Decorti
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 5, p 1399 (2018)
The aim of this research was the identification of novel pharmacogenomic biomarkers for better understanding the complex gene regulation mechanisms underpinning glucocorticoid (GC) action in paediatric inflammatory bowel disease (IBD). This goal was
Externí odkaz:
https://doaj.org/article/1e9dd3012c5f4cdebcad80f983f4fde7
Autor:
Nicola Vitulo, Alessandro Albiero, Claudio Forcato, Davide Campagna, Francesca Dal Pero, Paolo Bagnaresi, Moreno Colaiacovo, Primetta Faccioli, Antonella Lamontanara, Hana Šimková, Marie Kubaláková, Gaetano Perrotta, Paolo Facella, Loredana Lopez, Marco Pietrella, Giulio Gianese, Jaroslav Doležel, Giovanni Giuliano, Luigi Cattivelli, Giorgio Valle, A Michele Stanca
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26421 (2011)
Wheat is one of the world's most important crops and is characterized by a large polyploid genome. One way to reduce genome complexity is to isolate single chromosomes using flow cytometry. Low coverage DNA sequencing can provide a snapshot of indivi
Externí odkaz:
https://doaj.org/article/d703daeecdab4b6eb53d4be261d8370d
Autor:
Anna Doffini, Claudio Forcato, Chiara Mangano, Debora Lattuada, Roberta Aversa, Chiara Maranta, Emilia D. Giovannone, Genny Buson, Chiara Bolognesi, Rebecca Maiocchi, Martina Dori, Liyana Jamal, Raidah B. Ahmad, George S. H. Yeo, Tai Wai Yeo, Silvia Saragozza, Rosamaria Silipigni, Marta Serafini, Andrea Biondi, Sofia Perego, Patrizia Vergani, Enrico Ferrazzi, Paola Ricciardi‐Castagnoli, Thomas J. Musci, Francesca Romana Grati
Publikováno v:
Prenatal diagnosisREFERENCES.
Objective: To develop a multi-step workflow for the isolation of circulating extravillous trophoblasts (cEVTs) by describing the key steps enabling a semi-automated process, including a proprietary algorithm for fetal cell origin genetic confirmation
Autor:
Luis Chiriboga, Matija Snuderl, Valerio Conti, Briana Zeck, Javier Hernaez Rodriguez, Adriana Heguy, Maristela L. Onozato, Claudio Forcato, Anna Maria Buccoliero, Hussein Mohamed, Sitharam Ramaswami, Marianna Garonzi, Kaicen Zhu, Jonathan Serrano, Jane A. Skok, Varshini Vasudevaraja, Eveline Teresa Hidalgo, Daniel Friedman, Aristotelis Tsirigos, Arline Faustin, A. John Iafrate, David Zagzag, Renzo Guerrini, Cristiana Pelorosso, James M. Stafford, Orrin Devinsky, Lily M. Tredwin, John G. Golfinos
Publikováno v:
J Neuropathol Exp Neurol
Epilepsy is a heterogenous group of disorders defined by recurrent seizure activity due to abnormal synchronized activity of neurons. A growing number of epilepsy cases are believed to be caused by genetic factors and copy number variants (CNV) contr
Autor:
Claudio Forcato, Nicolò Manaresi, Chiara Bolognesi, Marianna Garonzi, Francesca Fontana, Michael Hummel, Rossana Lanzellotto, Andrea Raspadori, Chiara Mangano, Paola Tononi, Gianni Medoro, Genny Buson, Alberto Ferrarini
Publikováno v:
Blood Cancer Journal, Vol 9, Iss 12, Pp 1-5 (2019)
Blood Cancer Journal
Blood Cancer Journal