Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Marco Peronaci"'
Autor:
Rocco Piazza, Vera Magistroni, Sara Redaelli, Mario Mauri, Luca Massimino, Alessandro Sessa, Marco Peronaci, Maciej Lalowski, Rabah Soliymani, Caterina Mezzatesta, Alessandra Pirola, Federica Banfi, Alicia Rubio, Delphine Rea, Fabio Stagno, Emilio Usala, Bruno Martino, Leonardo Campiotti, Michele Merli, Francesco Passamonti, Francesco Onida, Alessandro Morotti, Francesca Pavesi, Marco Bregni, Vania Broccoli, Marc Baumann, Carlo Gambacorti-Passerini
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-13 (2018)
SETBP1 variants occur as somatic mutations in several malignancies and as de novo germline mutations in developmental disorders. Here the authors provide evidence that SETBP1 binds to gDNA in AT-rich promoter regions to promote target gene upregulati
Externí odkaz:
https://doaj.org/article/ba93d3f63f634212b28426582bbfc01b
Autor:
Jun-Hung Cho, Bhaumik Patel, Santosh Bonala, Sasikanth Manne, Yan Zhou, Surya K. Vadrevu, Jalpa Patel, Marco Peronaci, Shanawaz Ghouse, Elizabeth P. Henske, Fabrice Roegiers, Krinio Giannikou, David J. Kwiatkowski, Hossein Mansouri, Maciej M. Markiewski, Brandon White, Magdalena Karbowniczek
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-16 (2017)
Tuberous sclerosis complex (TSC) is a rare genetic condition causing tumours with differentiation abnormalities; however the molecular mechanisms causing these defects are unclear. Here the authors show that Notch cooperates with Rheb to block cell d
Externí odkaz:
https://doaj.org/article/c032945d8d7b42608e09e9eacf6389a4
Autor:
Alessandro Sessa, Luca Massimino, Marc Baumann, Fabio Stagno, Sara Redaelli, Francesco Onida, Francesco Passamonti, Emilio Usala, Delphine Rea, Leonardo Campiotti, Alicia Rubio, Alessandra Pirola, Vera Magistroni, Bruno Martino, Michele Merli, Vania Broccoli, Mario Mauri, Maciej Lalowski, Marco Peronaci, Marco Bregni, Rabah Soliymani, Alessandro Morotti, Rocco Piazza, Carlo Gambacorti-Passerini, Federica Banfi, Francesca Pavesi, Caterina Mezzatesta
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-13 (2018)
Nature Communications
Nature Communications
SETBP1 variants occur as somatic mutations in several hematological malignancies such as atypical chronic myeloid leukemia and as de novo germline mutations in the Schinzel–Giedion syndrome. Here we show that SETBP1 binds to gDNA in AT-rich promote
Autor:
Marco Peronaci, Luca Mologni, Alessandra Pirola, Carlo Gambacorti-Passerini, Monica Ceccon, Sara Redaelli, Roberta Rigolio, Laura Antolini
Publikováno v:
Oncotarget
ALK-positive Anaplastic Large Cell Lymphoma (ALCL) represents a subset of Non-Hodgkin Lymphoma whose treatment benefited from crizotinib development, a dual ALK/MET inhibitor. Crizotinib blocks ALK-triggered pathways such as PI3K/AKT/ mTOR, indispens
Autor:
Yan Zhou, Krinio Giannikou, Santosh Bonala, Marco Peronaci, Maciej M. Markiewski, Sasikanth Manne, Brandon White, Hossein Mansouri, Shanawaz M. Ghouse, Jun-Hung Cho, David J. Kwiatkowski, Fabrice Roegiers, Jalpa Patel, Magdalena Karbowniczek, Bhaumik Patel, Surya Kumari Vadrevu, Elizabeth P. Henske
Publikováno v:
Nature Communications
Nature Communications, Vol 8, Iss 1, Pp 1-16 (2017)
Nature Communications, Vol 8, Iss 1, Pp 1-16 (2017)
Differentiation abnormalities are a hallmark of tuberous sclerosis complex (TSC) manifestations; however, the genesis of these abnormalities remains unclear. Here we report on mechanisms controlling the multi-lineage, early neuronal progenitor and ne
Autor:
Roberta Spinelli, Vera Magistroni, Giuseppe Gaipa, Elena Maria Elli, Emilio Usala, Cristina Panuzzo, Matteo Carrabba, Carla Donadoni, Vincenzo Piazza, Peter J. Campbell, Luca Malcovati, Diletta Fontana, Dong-Wook Kim, Nora Viniou, Elli Papaemmanuil, Leonardo Campiotti, Giuseppe Saglio, Mario Cazzola, Graham R. Bignell, Andrea Parmiani, Heiko Becker, Marco Peronaci, Argiris Symeonidis, Rocco Piazza, Delphine Rea, Alessandra Pirola, Konstantinos Zervakis, Carlo Gambacorti-Passerini, Jacqueline Boultwood, Giovanni Signore, Sara Redaelli, Alessandro Morotti
Despite the recent identification of recurrent SETBP1 mutations in atypical chronic myeloid leukemia (aCML), a complete description of the somatic lesions responsible for the onset of this disorder is still lacking. To find additional somatic abnorma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23a17ce82a93f171bc2598aa31c7d60d
http://hdl.handle.net/10281/66894
http://hdl.handle.net/10281/66894
Autor:
Graham R. Bignell, Luca Malcovati, Giuseppe Gaipa, Marco Peronaci, Alessandra Pirola, Alessandro Morotti, Vera Magistroni, Leonardo Campiotti, Heiko Becker, Konstantinos Zervakis, Giovanni Signore, Emilio Usala, Peter J. Campbell, Argiris Symeonidis, Giuseppe Saglio, Sara Redaelli, Andrea Parmiani, Mario Cazzola, Delphine Rea, Matteo Carrabba, Cristina Panuzzo, Jacqueline Boultwood, Elena Maria Elli, Carla Donadoni, Vincenzo Piazza, Diletta Fontana, Nora-Athina Viniou, Dong-Wook Kim, Roberta Spinelli, Elli Papaemmanuil, Rocco Piazza, Carlo Gambacorti-Passerini
Atypical Chronic Myeloid Leukemia (aCML) is a clonal disorder belonging to the Myeloproliferative/Myelodysplastic (MPN/MDS) group. The molecular lesions responsible for the onset of aCML remained unknown until 2013 when recurrent somatic mutations of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83db76010ba7a56326ad254490351d21
http://hdl.handle.net/11383/2080861
http://hdl.handle.net/11383/2080861
Autor:
Marco Peronaci, Gaetano Donofrio, Mirca Lazzaretti, Ken Patrene, Cristina Mancini, Denise Toscani, Antonino Neri, Luca Agnelli, Martine Amiot, Marina Bolzoni, Judith L. Anderson, Simona Colla, Eugenia Martella, G. David Roodman, Daniela Guasco, Franco Aversa, Nicola Giuliani, Paola Storti, Irma Airoldi
Publikováno v:
Blood. 120:2947-2947
Abstract 2947 It has been previously reported that bone marrow (BM) microenvironment is hypoxic in multiple myeloma (MM) patients and that hypoxia inducible factor (HIF)-1α is overexpressed by MM cells. However, the potential role of HIF-1α as a th
Autor:
Marco Peronaci, Gabriella Sammarelli, Franco Aversa, Denise Toscani, Nicola Giuliani, Paola Storti, Luisa Craviotto, Domenica Ronchetti, Benedetta Dalla Palma, Daniela Guasco, Luca Agnelli, Marina Bolzoni, Sabrina Bonomini, Antonino Neri
Publikováno v:
Blood. 120:1811-1811
Abstract 1811 Symptomatic multiple myeloma (MM), smoldering MM (SMM) and monoclonal gammopathy of uncertain significance (MGUS) are well known different pathological and clinical entities of plasma cell (PC) disorders. Nevertheless molecular studies