Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Antonietta Palmieri"'
Post-translational inhibition of YAP oncogene expression by 4-hydroxynonenal in bladder cancer cells
Autor:
Margherita Grattarola, Arianna Carolina Rosa, Alessandra Compagnone, Rosa Maria Pascale, Antonella Roetto, Chiara Dianzani, Chiara Ullio, Roberta Cavalli, Martina Daga, Marie Angele Cucci, Stefania Pizzimenti, Monica Argenziano, Antonietta Palmieri, Giuseppina Barrera, Maria Maddalena Simile
The transcriptional regulator YAP plays an important role in cancer progression and is negatively controlled by the Hippo pathway. YAP is frequently overexpressed in human cancers, including bladder cancer. Interestingly, YAP expression and activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c862ccff65527ad3dba660aa53413509
http://hdl.handle.net/2318/1718896
http://hdl.handle.net/2318/1718896
Autor:
Alessandra Compagnone, Martina Daga, Antonietta Palmieri, Chiara Ullio, Chiara Dianzani, Luigi Cangemi, Eric Ciamporcero, Roberto Pili, Antonella Roetto, Giuseppina Barrera, Stefania Pizzimenti
Redox adaptation plays an important role in cancer cells drug resistance. The antioxidant response is principally mediated by the transcription factor Nrf2, that induces the transcriptional activation of several genes involved in GSH synthesis, chemo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ed1445589b9451f2eebd2233a42cd29
http://hdl.handle.net/2318/1656160
http://hdl.handle.net/2318/1656160
Autor:
Francesca Tullio, Ludovica Ferbo, Antonella Roetto, Marco De Gobbi, Pasquale Pagliaro, Claudia Penna, Martina Boero, Rosa Maria Pellegrino, Antonietta Palmieri, Giuseppe Saglio
Publikováno v:
BioFactors. 41:360-371
Transferrin receptor 2 (Tfr2) is an iron-modulator transcribed in two isoforms, Tfr2α and Tfr2β. The latter is expressed in the heart. We obtained two mouse models with silencing of Tfr2β: one with a normal systemic iron amount (SIA), i.e., Tfr2-K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e40a2e683ef04e765214da51db869e8
https://doi.org/10.1002/biof.1237
https://doi.org/10.1002/biof.1237
Autor:
Antonella Roetto, Francesco Arcioni, Olivia Minelli, Laura Ceccuzzi, Antonietta Palmieri, Maurizio Caniglia, Cristina Mecucci, Mauro Marchesi, Ylenia Barbanera, Marina Onorato, Paolo Gorello, Antonella Angius, Cecilia Adami, Antonio Piga
Publikováno v:
Hemoglobin. 40(6)
The aim of this study was to describe the mutational spectrum of hemoglobinopathies during the period 1988-2015 in Umbria, Central Italy, which has never been considered endemic for these conditions. Twenty-four different β-globin gene mutations wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c182e7baed8c4f8fc5bffbbb6528e17
https://pubmed.ncbi.nlm.nih.gov/28361595
https://pubmed.ncbi.nlm.nih.gov/28361595
Publikováno v:
British journal of haematology
176 (2017): 491–495.
info:cnr-pdr/source/autori:Augusta Di Savino Valentina Gaidano Antonietta Palmieri Francesca Crasto Alessandro Volpengo Roberta Lorenzatti Patrizia Scaravaglio Alessandro Manello Paolo Nicoli Enrico Gottardi Giuseppe Saglio Daniela Cilloni Marco De Gobbi/titolo:Clinical significance ofTFR2andEPORexpression in bone marrow cells in myelodysplastic syndromes/doi:/rivista:British journal of haematology (Print)/anno:2017/pagina_da:491/pagina_a:495/intervallo_pagine:491–495/volume:176
176 (2017): 491–495.
info:cnr-pdr/source/autori:Augusta Di Savino Valentina Gaidano Antonietta Palmieri Francesca Crasto Alessandro Volpengo Roberta Lorenzatti Patrizia Scaravaglio Alessandro Manello Paolo Nicoli Enrico Gottardi Giuseppe Saglio Daniela Cilloni Marco De Gobbi/titolo:Clinical significance ofTFR2andEPORexpression in bone marrow cells in myelodysplastic syndromes/doi:/rivista:British journal of haematology (Print)/anno:2017/pagina_da:491/pagina_a:495/intervallo_pagine:491–495/volume:176
The experiments were conceived, designed and performed by Augusta Di Savino, Antonietta Palmieri, Marco De Gobbi. RNA extraction from patients' bone marrow samples was performed by Alessandro Volpengo, Francesca Crasto, Roberta Lorenzatti and Enrico
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::1860e89601c18b2a774b96c741048a0b
http://www.cnr.it/prodotto/i/368982
http://www.cnr.it/prodotto/i/368982
Autor:
Ludovica Ferbo, Antonella Roetto, Rosa Maria Pellegrino, Martina Boero, Fulvio Riondato, Giuseppe Saglio, Barbara Miniscalco, Luca Osella, Paolo Pollicino, Antonietta Palmieri
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2017 (2017)
BioMed Research International, Vol 2017 (2017)
Type 3 haemochromatosis (HFE3) is a rare genetic iron overload disease which ultimately lead to compromised organs functioning. HFE3 is caused by mutations in transferrin receptor 2 (TFR2) gene that codes for two main isoforms (Tfr2αand Tfr2β). Tfr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9d7109779dec647cf641cce4ca009f3
http://hdl.handle.net/2318/1640442
http://hdl.handle.net/2318/1640442
Autor:
Paolo Nicoli, Giuseppe Saglio, Francesca Crasto, Roberta Lorenzatti, Valentina Gaidano, Alessandro Volpengo, Alessandro Manello, Antonietta Palmieri, Augusta Di Savino, Patrizia Scaravaglio, Daniela Cilloni, Enrico Gottardi, Marco De Gobbi
Publikováno v:
British journal of haematology. 176(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e08cf8abddcab7d0659ffe81b7cdd779
https://pubmed.ncbi.nlm.nih.gov/26914246
https://pubmed.ncbi.nlm.nih.gov/26914246
Autor:
Ana Margarida Lopes, José Barbot, Domenico Giuseppe D'Ascola, Gabriella Zecchina, Francesca Carnuccio, Graça Porto, Giuseppe Saglio, Rosa Maria Pellegrino, Antonella Roetto, Maria Coutinho, J. E. B. P. Pinto, Mónica Costa, Antonietta Palmieri, Emília Costa
Publikováno v:
British Journal of Haematology. 158:668-672
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e024b53f0e8ad9df1bf44f279c8ac0e4
https://doi.org/10.1111/j.1365-2141.2012.09198.x
https://doi.org/10.1111/j.1365-2141.2012.09198.x