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17 results on '"Bianchi, Marika"'

1. Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis

Author

Galli, Jessica, Gavazzi, Francesco, De Simone, Micaela, Giliani, Silvia, Garau, Jessica, Valente, Marialuisa, Vairo, Donatella, Cattalini, Marco, Mortilla, Marzia, Andreoli, (Laura, Badolato, Raffaele, Bianchi, Marika, Carabellese, Nice, Cereda, Cristina, Ferraro, Rosalba, Facchetti, Fabio, Fredi, Micaela, Gualdi, Giulio, Lorenzi, Luisa, Meini, Antonella, Orcesi, Simona, Tincani, Angela, Zanola, Alessandra, Rice, Gillian, and Fazzi, Elisa

Published
2018
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5. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

Author

Crow, Yanick J., Chase, Diana S., Schmidt, Johanna Lowenstein, Szynkiewicz, Marcin, Forte, Gabriella M.A., Gornall, Hannah L., Oojageer, Anthony, Anderson, Beverley, Pizzino, Amy, Helman, Guy, Abdel-Hamid, Mohamed S., Abdel-Salam, Ghada M., Ackroyd, Sam, Aeby, Alec, Agosta, Guillermo, Albin, Catherine, Allon-Shalev, Stavit, Arellano, Montse, Ariaudo, Giada, Aswani, Vijay, Babul-Hirji, Riyana, Baildam, Eileen M., Bahi-Buisson, Nadia, Bailey, Kathryn M., Barnerias, Christine, Barth, Magalie, Battini, Roberta, Beresford, Michael W., Bernard, Geneviève, Bianchi, Marika, de Villemeur, Thierry Billette, Blair, Edward M., Bloom, Miriam, Burlina, Alberto B., Carpanelli, Maria Luisa, Carvalho, Daniel R., Castro-Gago, Manuel, Cavallini, Anna, Cereda, Cristina, Chandler, Kate E., Chitayat, David A., Collins, Abigail E., Corcoles, Concepcion Sierra, Cordeiro, Nuno J.V., Crichiutti, Giovanni, Dabydeen, Lyvia, Dale, Russell C., DArrigo, Stefano, De Goede, Christian G.E.L., De Laet, Corinne, De Waele, Liesbeth M.H., Denzler, Ines, Desguerre, Isabelle, Devriendt, Koenraad, Di Rocco, Maja, Fahey, Michael C., Fazzi, Elisa, Ferrie, Colin D., Figueiredo, António, Gener, Blanca, Goizet, Cyril, Gowrinathan, Nirmala R., Gowrishankar, Kalpana, Hanrahan, Donncha, Isidor, Bertrand, Kara, Bülent, Khan, Nasaim, King, Mary D., Kirk, Edwin P., Kumar, Ram, Lagae, Lieven, Landrieu, Pierre, Lauffer, Heinz, Laugel, Vincent, Piana, Roberta La, Lim, Ming J., Lin, Jean-Pierre S.-M., Linnankivi, Tarja, Mackay, Mark T., Marom, Daphna R., Lourenço, Charles Marques, McKee, Shane A., Moroni, Isabella, Morton, Jenny E.V., Moutard, Marie-Laure, Murray, Kevin, Nabbout, Rima, Nampoothiri, Sheela, Nunez-Enamorado, Noemi, Oades, Patrick J., Olivieri, Ivana, Ostergaard, John R., Pérez-Dueñas, Belén, Prendiville, Julie S., Ramesh, Venkateswaran, Rasmussen, Magnhild, Régal, Luc, Ricci, Federica, Rio, Marlène, Rodriguez, Diana, Roubertie, Agathe, Salvatici, Elisabetta, Segers, Karin A., Sinha, Gyanranjan P., Soler, Doriette, Spiegel, Ronen, Stödberg, Tommy I., Straussberg, Rachel, Swoboda, Kathryn J., Suri, Mohnish, Tacke, Uta, Tan, Tiong Y., te Water Naude, Johann, Teik, Keng Wee, Thomas, Maya Mary, Till, Marianne, Tonduti, Davide, Valente, Enza Maria, Van Coster, Rudy Noel, van der Knaap, Marjo S., Vassallo, Grace, Vijzelaar, Raymon, Vogt, Julie, Wallace, Geoffrey B., Wassmer, Evangeline, Webb, Hannah J., Whitehouse, William P., Whitney, Robyn N., Zaki, Maha S., Zuberi, Sameer M., Livingston, John H., Rozenberg, Flore, Lebon, Pierre, Vanderver, Adeline, Orcesi, Simona, and Rice, Gillian I.

Published
2015
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9. Sine causa tetraparesis

Author

Galli, Jessica, primary, Gavazzi, Francesco, additional, De Simone, Micaela, additional, Giliani, Silvia, additional, Garau, Jessica, additional, Valente, Marialuisa, additional, Vairo, Donatella, additional, Cattalini, Marco, additional, Mortilla, Marzia, additional, Andreoli, (Laura, additional, Badolato, Raffaele, additional, Bianchi, Marika, additional, Carabellese, Nice, additional, Cereda, Cristina, additional, Ferraro, Rosalba, additional, Facchetti, Fabio, additional, Fredi, Micaela, additional, Gualdi, Giulio, additional, Lorenzi, Luisa, additional, Meini, Antonella, additional, Orcesi, Simona, additional, Tincani, Angela, additional, Zanola, Alessandra, additional, Rice, Gillian, additional, and Fazzi, Elisa, additional

Published
2018
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11. Characterization of human disease phenotypes associated with mutations inTREX1,RNASEH2A,RNASEH2B,RNASEH2C,SAMHD1,ADAR, andIFIH1

Author

Crow, Yanick J., primary, Chase, Diana S., additional, Lowenstein Schmidt, Johanna, additional, Szynkiewicz, Marcin, additional, Forte, Gabriella M.A., additional, Gornall, Hannah L., additional, Oojageer, Anthony, additional, Anderson, Beverley, additional, Pizzino, Amy, additional, Helman, Guy, additional, Abdel-Hamid, Mohamed S., additional, Abdel-Salam, Ghada M., additional, Ackroyd, Sam, additional, Aeby, Alec, additional, Agosta, Guillermo, additional, Albin, Catherine, additional, Allon-Shalev, Stavit, additional, Arellano, Montse, additional, Ariaudo, Giada, additional, Aswani, Vijay, additional, Babul-Hirji, Riyana, additional, Baildam, Eileen M., additional, Bahi-Buisson, Nadia, additional, Bailey, Kathryn M., additional, Barnerias, Christine, additional, Barth, Magalie, additional, Battini, Roberta, additional, Beresford, Michael W., additional, Bernard, Geneviève, additional, Bianchi, Marika, additional, Billette de Villemeur, Thierry, additional, Blair, Edward M., additional, Bloom, Miriam, additional, Burlina, Alberto B., additional, Luisa Carpanelli, Maria, additional, Carvalho, Daniel R., additional, Castro-Gago, Manuel, additional, Cavallini, Anna, additional, Cereda, Cristina, additional, Chandler, Kate E., additional, Chitayat, David A., additional, Collins, Abigail E., additional, Sierra Corcoles, Concepcion, additional, Cordeiro, Nuno J.V., additional, Crichiutti, Giovanni, additional, Dabydeen, Lyvia, additional, Dale, Russell C., additional, D′Arrigo, Stefano, additional, De Goede, Christian G.E.L., additional, De Laet, Corinne, additional, De Waele, Liesbeth M.H., additional, Denzler, Ines, additional, Desguerre, Isabelle, additional, Devriendt, Koenraad, additional, Di Rocco, Maja, additional, Fahey, Michael C., additional, Fazzi, Elisa, additional, Ferrie, Colin D., additional, Figueiredo, António, additional, Gener, Blanca, additional, Goizet, Cyril, additional, Gowrinathan, Nirmala R., additional, Gowrishankar, Kalpana, additional, Hanrahan, Donncha, additional, Isidor, Bertrand, additional, Kara, Bülent, additional, Khan, Nasaim, additional, King, Mary D., additional, Kirk, Edwin P., additional, Kumar, Ram, additional, Lagae, Lieven, additional, Landrieu, Pierre, additional, Lauffer, Heinz, additional, Laugel, Vincent, additional, Piana, Roberta La, additional, Lim, Ming J., additional, Lin, Jean-Pierre S.-M., additional, Linnankivi, Tarja, additional, Mackay, Mark T., additional, Marom, Daphna R., additional, Marques Lourenço, Charles, additional, McKee, Shane A., additional, Moroni, Isabella, additional, Morton, Jenny E.V., additional, Moutard, Marie-Laure, additional, Murray, Kevin, additional, Nabbout, Rima, additional, Nampoothiri, Sheela, additional, Nunez-Enamorado, Noemi, additional, Oades, Patrick J., additional, Olivieri, Ivana, additional, Ostergaard, John R., additional, Pérez-Dueñas, Belén, additional, Prendiville, Julie S., additional, Ramesh, Venkateswaran, additional, Rasmussen, Magnhild, additional, Régal, Luc, additional, Ricci, Federica, additional, Rio, Marlène, additional, Rodriguez, Diana, additional, Roubertie, Agathe, additional, Salvatici, Elisabetta, additional, Segers, Karin A., additional, Sinha, Gyanranjan P., additional, Soler, Doriette, additional, Spiegel, Ronen, additional, Stödberg, Tommy I., additional, Straussberg, Rachel, additional, Swoboda, Kathryn J., additional, Suri, Mohnish, additional, Tacke, Uta, additional, Tan, Tiong Y., additional, te Water Naude, Johann, additional, Wee Teik, Keng, additional, Mary Thomas, Maya, additional, Till, Marianne, additional, Tonduti, Davide, additional, Maria Valente, Enza, additional, Noel Van Coster, Rudy, additional, van der Knaap, Marjo S., additional, Vassallo, Grace, additional, Vijzelaar, Raymon, additional, Vogt, Julie, additional, Wallace, Geoffrey B., additional, Wassmer, Evangeline, additional, Webb, Hannah J., additional, Whitehouse, William P., additional, Whitney, Robyn N., additional, Zaki, Maha S., additional, Zuberi, Sameer M., additional, Livingston, John H., additional, Rozenberg, Flore, additional, Lebon, Pierre, additional, Vanderver, Adeline, additional, Orcesi, Simona, additional, and Rice, Gillian I., additional

Published
2015
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17. G93A SOD1 alters cell cycle in a cellular model of Amyotrophic Lateral Sclerosis

Author

Cova, Emanuela, Ghiroldi, Andrea, Guareschi, Stefania, Mazzini, Giuliano, Gagliardi, Stella, Davin, Annalisa, Bianchi, Marika, Ceroni, Mauro, and Cereda, Cristina

Subjects
*AMYOTROPHIC lateral sclerosis, *CELL cycle regulation, *MOTOR neuron diseases, *GENETIC mutation, *SUPEROXIDE dismutase, *CYCLINS
Abstract

Abstract: Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative multifactorial disease characterized, like other diseases such as Alzheimer''s disease (AD), Parkinson''s disease (PD) or frontotemporal dementia (FTD), by the degeneration of specific neuronal cell populations. Motor neuron loss is distinctive of ALS. However, the causes of onset and progression of motor neuron death are still largely unknown. In about 2% of all cases, mutations in the gene encoding for the Cu/Zn superoxide dismutase (SOD1) are implicated in the disease. Several alterations in the expression or activation of cell cycle proteins have been described in the neurodegenerative diseases and related to cell death. In this work we show that mutant SOD1 can alter cell cycle in a cellular model of ALS. Our findings suggest that modifications in the cell cycle progression could be due to an increased interaction between mutant G93A SOD1 and Bcl-2 through the cyclins regulator p27. As previously described in post mitotic neurons, cell cycle alterations could fatally lead to cell death. [Copyright &y& Elsevier]

Published
2010
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