Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Lupoli, Sara"'
Autor:
Sorosina, Melissa, Barizzone, Nadia, Clarelli, Ferdinando, Anand, Santosh, Lupoli, Sara, Salvi, Erika, Mangano, Eleonora, Bordoni, Roberta, Roostaei, Tina, Mascia, Elisabetta, Zuccalà, Miriam, Vecchio, Domizia, Cavalla, Paola, Santoro, Silvia, Ferrè, Laura, Zollo, Alen, Barlassina, Cristina, Cusi, Daniele, Martinelli, Vittorio, Comi, Giancarlo, Leone, Maurizio, Filippi, Massimo, Patsopoulos, Nikolaos A, De Jager, Philip L, De Bellis, Gianluca, Esposito, Federica, D'Alfonso, Sandra, Martinelli Boneschi, Filippo, Paolo Ragonese
Publikováno v:
Journal of Neurology. 269:4510-4522
Background Over 200 genetic loci have been associated with multiple sclerosis (MS) explaining ~ 50% of its heritability, suggesting that additional mechanisms may account for the “missing heritability” phenomenon. Objective To analyze a large coh
Akademický článek
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Autor:
Martinelli-Boneschi, Filippo, Giacalone, Giacomo, Magnani, Giuseppe, Biella, Gloria, Coppi, Elisabetta, Santangelo, Roberto, Brambilla, Paola, Esposito, Federica, Lupoli, Sara, Clerici, Francesca, Benussi, Luisa, Ghidoni, Roberta, Galimberti, Daniela, Squitti, Rosanna, Confaloni, Annamaria, Bruno, Giuseppe, Pichler, Sabrina, Mayhaus, Manuel, Riemenschneider, Matthias, Mariani, Claudio, Comi, Giancarlo, Scarpini, Elio, Binetti, Giuliano, Forloni, Gianluigi, Franceschi, Massimo, Albani, Diego
Publikováno v:
In Neurobiology of Aging June 2013 34(6):1711-1711
Autor:
Sanna, Serena, Barizzone, Nadia, Zara, Ilenia, Sorosina, Melissa, Lupoli, Sara, Porcu, Eleonora, Pitzalis, Maristella, Zoledziewska, Magdalena, Esposito, Federica, Leone, Maurizio, Mulas, Antonella, Cocco, Eleonora, Ferrigno, Paola, Guerini, Franca R., Brambilla, Paola, Farina, Gabriele, Murru, Raffaele, Deidda, Francesca, Sanna, Sonia, Loi, Alessia, Barlassina, Cristina, Vecchio, Domizia, Zauli, Andrea, Clarelli, Ferdinando, Braga, Daniele, Poddie, Fausto, Cantello, Roberto, Martinelli, Vittorio, Comi, Giancarlo, Frau, Jessica, Lorefice, Lorena, Pugliatti, Maura, Rosati, Giulio, Progemus, Salvetti, Marco, Melis, Maurizio, Marrosu, Maria G., Cusi, Daniele, Cucca, Francesco, Martinelli Boneschi, Filippo, D'Alfonso, Sandra
Publikováno v:
Multiple Sclerosis, 21(11), 1385-95. SAGE Publications Inc.
Background: Recent studies identified > 100 non-HLA (human leukocyte antigen) multiple sclerosis (MS) susceptibility variants in Northern European populations, but their role in Southern Europeans is largely unexplored. Objective: We aimed to investi
Autor:
Justice, Anne E., Winkler, Thomas W., Feitosa, Mary F., Graff, Misa, Fisher, Virginia A., Young, Kristin, Barata, Llilda, Deng, Xuan, Czajkowski, Jacek, Hadley, David, Ngwa, Julius S., Ahluwalia, Tarunveer S., Chu, Audrey Y., Heard-Costa, Nancy L., Lim, Elise, Perez, Jeremiah, Eicher, John D., Kutalik, Zoltán, Xue, Luting, Mahajan, Anubha, Renström, Frida, Wu, Joseph, Qi, Qibin, Ahmad, Shafqat, Alfred, Tamuno, Amin, Najaf, Bielak, Lawrence F., Bonnefond, Amelie, Bragg, Jennifer, Cadby, Gemma, Chittani, Martina, Coggeshall, Scott, Corre, Tanguy, Direk, Nese, Eriksson, Joel, Fischer, Krista, Gorski, Mathias, Harder, Marie Neergaard, Horikoshi, Momoko, Huang, Tao, Huffman, Jennifer E., Jackson, Anne U., Justesen, Johanne Marie, Kanoni, Stavroula, Kinnunen, Leena, Kleber, Marcus E., Komulainen, Pirjo, Kumari, Meena, Lim, Unhee, Luan, Jian'an, Lyytikäinen, Leo-Pekka, Mangino, Massimo, Manichaikul, Ani, Marten, Jonathan, Middelberg, Rita P.S., Müller-Nurasyid, Martina, Navarro, Pau, Pérusse, Louis, Pervjakova, Natalia, Sarti, Cinzia, Smith, Albert Vernon, Smith, Jennifer A., Stančáková, Alena, Strawbridge, Rona J., Stringham, Heather M., Sung, Yun Ju, Tanaka, Toshiko, Teumer, Alexander, Trompet, Stella, Van Der Laan, Sander W., van der Most, Peter J., Van Vliet-Ostaptchouk, Jana V., Vedantam, Sailaja L., Verweij, Niek, Vink, Jacqueline M., Vitart, Veronique, Wu, Ying, Yengo, Loic, Zhang, Weihua, Zhao, Jing Hua, Zimmermann, Martina E., Zubair, Niha, Abecasis, Gonçalo R., Adair, Linda S., Afaq, Saima, Afzal, Uzma, Bakker, Stephan J.L., Bartz, Traci M., Beilby, John, Bergman, Richard N., Bergmann, Sven, Biffar, Reiner, Blangero, John, Boerwinkle, Eric, Bonnycastle, Lori L., Bottinger, Erwin, Braga, Daniele, Buckley, Brendan M., Buyske, Steve, Campbell, Harry, Chambers, John C., Collins, Francis S., Curran, Joanne E., De Borst, Gert J., de Craen, Anton J.M., de Geus, Eco J.C., Dedoussis, George, Delgado, Graciela E., Den Ruijter, Hester M., Eiriksdottir, Gudny, Eriksson, Anna L., Esko, Tonu, Faul, Jessica D., Ford, Ian, Forrester, Terrence, Gertow, Karl, Gigante, Bruna, Glorioso, Nicola, Gong, Jian, Grallert, Harald, Grammer, Tanja B., Grarup, Niels, Haitjema, Saskia, Hallmans, Goran, Hamsten, Anders, Hansen, Torben, Harris, Tamara B., Hartman, Catharina A., Hassinen, Maija, Hastie, Nicholas D., Heath, Andrew C., Hernandez, Dena, Hindorff, Lucia, Hocking, Lynne J., Hollensted, Mette, Holmen, Oddgeir Lingaas, Homuth, Georg, Hottenga, Jouke Jan, Huang, Jie, Hung, Joseph, Hutri-Kähönen, Nina, Ingelsson, Erik, James, Alan L., Jansson, John-Olov, Jarvelin, Marjo-Riitta, Jhun, Min A., Jørgensen, Marit E., Juonala, Markus, Kähönen, Mika, Karlsson, Magnus, Koistinen, Heikki A, Kolcic, Ivana, Kolovou, Genovefa, Kooperberg, Charles, Krämer, Bernhard K., Kuusisto, Johanna, Kvaløy, Kirsti, Lakka, Timo A., Langenberg, Claudia, Launer, Lenore J., Leander, Karin, Lee, Nanette R., Lind, Lars, Lindgren, Cecilia M., Linneberg, Allan, Lobbens, Stephane, Loh, Marie, Lorentzon, Mattias, Luben, Robert, Lubke, Gitta, Ludolph-Donislawski, Anja, Lupoli, Sara, Madden, Pamela A.F., Männikkö, Reija, Marques-Vidal, Pedro, Martin, Nicholas G., McKenzie, Colin A., McKnight, Barbara, Mellström, Dan, Menni, Cristina, Montgomery, Grant W., Musk, A. Bill, Narisu, Narisu, Nauck, Matthias, Nolte, Ilja M., Oldehinkel, Albertine J., Olden, Matthias, Ong, Ken K., Padmanabhan, Sandosh, Peyser, Patricia A., Pisinger, Charlotta, Porteous, David J., Raitakari, Olli T., Rankinen, Tuomo, Rao, Dabeeru C., Rasmussen-Torvik, Laura J., Rawal, Rajesh, Rice, Treva, Ridker, Paul M., Rose, Lynda M., Bien, Stephanie A., Rudan, Igor, Sanna, Serena, Sarzynski, Mark A., Sattar, Naveed, Savonen, Kai, Schlessinger, David, Scholtens, Salome, Schurmann, Claudia, Scott, Robert A., Sennblad, Bengt, Siemelink, Marten A., Silbernagel, Günther, Slagboom, P. Eline, Snieder, Harold, Staessen, Jan A., Stott, David J., Swertz, Morris A., Swift, Amy J., Taylor, Kent D., Tayo, Bamidele O., Thorand, Barbara, Thuillier, Dorothee, Tuomilehto, Jaakko, Uitterlinden, André G., Vandenput, Liesbeth, Vohl, Marie-Claude, Völzke, Henry, Vonk, Judith M., Waeber, Gérard, Waldenberger, Melanie, Westendorp, Rudi G.J., Wild, Sarah, Willemsen, Gonneke, Wolffenbuttel, Bruce H.R., Wong, Andrew, Wright, Alan F., Zhao, Wei, Zillikens, M. Carola, Baldassarre, Damiano, Balkau, Beverley, Bandinelli, Stefania, Böger, Carsten A., Boomsma, Dorret I., Bouchard, Claude, Bruinenberg, Marcel, Chasman, Daniel I., Ida Chen, Yii-Der, Chines, Peter S., Cooper, Richard S., Cucca, Francesco, Cusi, Daniele, De Faire, Ulf, Ferrucci, Luigi, Franks, Paul W., Froguel, Philippe, Gordon-Larsen, Penny, Grabe, Hans Jörgen, Gudnason, Vilmundur, Haiman, Christopher A., Hayward, Caroline, Hveem, Kristian, Johnson, Andrew D., Jukema, J. Wouter, Kardia, Sharon L.R., Kivimäki, Mika, Kooner, Jaspal S., Kuh, Diana, Laakso, Markku, Lehtimaki, Terho, Le Marchand, Loic, März, Winfried, McCarthy, Mark I., Metspalu, Andres, Morris, Andrew P., Ohlsson, Claes, Palmer, Lyle J., Pasterkamp, Gerard, Pedersen, Oluf, Peters, Annette, Peters, Ulrike, Polasek, Ozren, Psaty, Bruce M., Qi, Lu, Rauramaa, Rainer, Smith, Blair H., Sørensen, Thorkild I.A., Strauch, Konstantin, Tiemeier, Henning, Tremoli, Elena, Van Der Harst, Pim, Vestergaard, Henrik, Vollenweider, Peter, Wareham, Nicholas J., Weir, David J., Whitfield, John B., Wilson, James F., Tyrrell, Jessica, Frayling, Timothy M., Barroso, Inês, Boehnke, Michael, Deloukas, Panagiotis, Fox, Caroline S., Hirschhorn, Joel N., Hunter, David J., Spector, Tim D., Strachan, David P., van Duijn, Cornelia M., Heid, Iris M., Mohlke, Karen L., Marchini, Jonathan, Loos, Ruth J.F., Kilpeläinen, Tuomas O., Liu, Ching-Ti, Borecki, Ingrid B., North, Kari E., Cupples, L. Adrienne
Externí odkaz:
http://hdl.handle.net/11250/2499974
Autor:
Salvi, Erika, Kuznetsova, Tatiana, Thijs, Lutgarde, Lupoli, Sara, Stolarz-Skrzypek, Katarzyna, D'Avila, Francesca, Tikhonoff, Valerie, De Astis, Silvia, Barcella, Matteo, Seidlerova, Jitka, Benaglio, Paola, Malyutina, Sofia, Frau, Francesca, Velayutham, Dinesh, Benfante, Roberta, Zagato, Laura, Title, Alexandra, Braga, Daniele, Marek, Diana, Kawecka-Jaszcz, Kalina, Casiglia, Edoardo, Filipovsky, Jan, Nikitin, Yuri, Rivolta, Carlo, Manunta, Paolo, Beckmann, Jacques S., Barlassina, Cristina, Cusi, Daniele, Staessen, Jan A., Czarnecka, Danuta, Gąsowski, Jerzy, Grodzicki, Tomasz, Kloch-Badełek, Małgorzata, Olszanecka, Agnieszka, Wizner, Barbara
Publikováno v:
Hypertension, 62(5), 844-852. LIPPINCOTT WILLIAMS & WILKINS
Hypertension; Vol 62
Hypertension
Hypertension; Vol 62
Hypertension
A case–control study revealed association between hypertension and rs3918226 in the endothelial nitric oxide synthase ( eNOS ) gene promoter (minor/major allele, T/C allele). We aimed at substantiating these preliminary findings by target sequencin
Autor:
D’Avila, Francesca, Meregalli, Mirella, Lupoli, Sara, Barcella, Matteo, Orro, Alessandro, De Santis, Francesca, Sitzia, Clementina, Farini, Andrea, D’Ursi, Pasqualina, Erratico, Silvia, Cristofani, Riccardo, Milanesi, Luciano, Braga, Daniele, Cusi, Daniele, Poletti, Angelo, Barlassina, Cristina, Torrente, Yvan
Publikováno v:
Journal of muscle research and cell motility 37 (2016): 101–115. doi:10.1007/s10974-016-9451-7
info:cnr-pdr/source/autori:D'Avila, Francesca; Meregalli, Mirella; Lupoli, Sara; Barcella, Matteo; Orro, Alessandro; De Santis, Francesca; Sitzia, Clementina; Farini, Andrea; D'Ursi, Pasqualina; Erratico, Silvia; Cristofani, Riccardo; Milanesi, Luciano; Braga, Daniele; Cusi, Daniele; Poletti, Angelo; Barlassina, Cristina; Torrente, Yvan/titolo:Exome sequencing identifies variants in two genes encoding the LIM-proteins NRAP and FHL1 in an Italian patient with BAG3 myofibrillar myopathy/doi:10.1007%2Fs10974-016-9451-7/rivista:Journal of muscle research and cell motility/anno:2016/pagina_da:101/pagina_a:115/intervallo_pagine:101–115/volume:37
info:cnr-pdr/source/autori:D'Avila, Francesca; Meregalli, Mirella; Lupoli, Sara; Barcella, Matteo; Orro, Alessandro; De Santis, Francesca; Sitzia, Clementina; Farini, Andrea; D'Ursi, Pasqualina; Erratico, Silvia; Cristofani, Riccardo; Milanesi, Luciano; Braga, Daniele; Cusi, Daniele; Poletti, Angelo; Barlassina, Cristina; Torrente, Yvan/titolo:Exome sequencing identifies variants in two genes encoding the LIM-proteins NRAP and FHL1 in an Italian patient with BAG3 myofibrillar myopathy/doi:10.1007%2Fs10974-016-9451-7/rivista:Journal of muscle research and cell motility/anno:2016/pagina_da:101/pagina_a:115/intervallo_pagine:101–115/volume:37
Myofibrillar myopathies (MFMs) are genetically heterogeneous dystrophies characterized by the disintegration of Z-disks and myofibrils and are associated with mutations in genes encoding Z-disk or Z-disk-related proteins. The c.626 C > T (p.P209L) mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b1817ba7c2e5c392f149e7e3984dae07
https://publications.cnr.it/doc/361403
https://publications.cnr.it/doc/361403
Autor:
Rizzi, Federica, Conti, Costanza, Dogliotti, Elena, Terranegra, Annalisa, Salvi, Erika, Braga, Daniele, Ricca, Flavia, Lupoli, Sara, Mingione, Alessandra, Pivari, Francesca, Brasacchio, Caterina, Barcella, Matteo, Chittani, Martina, D’Avila, Francesca, Turiel, Maurizio, Lazzaroni, Monica, Soldati, Laura, Cusi, Daniele, Barlassina, Cristina
Publikováno v:
Journal of translational medicine (Online) 14 (2016). doi:10.1186/s12967-016-0941-6
info:cnr-pdr/source/autori:Rizzi, Federica; Conti, Costanza; Dogliotti, Elena; Terranegra, Annalisa; Salvi, Erika; Braga, Daniele; Ricca, Flavia; Lupoli, Sara; Mingione, Alessandra; Pivari, Francesca; Brasacchio, Caterina; Barcella, Matteo; Chittani, Martina; D'Avila, Francesca; Turiel, Maurizio; Lazzaroni, Monica; Soldati, Laura; Cusi, Daniele; Barlassina, Cristina/titolo:Interaction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study/doi:10.1186%2Fs12967-016-0941-6/rivista:Journal of translational medicine (Online)/anno:2016/pagina_da:/pagina_a:/intervallo_pagine:/volume:14
info:cnr-pdr/source/autori:Rizzi, Federica; Conti, Costanza; Dogliotti, Elena; Terranegra, Annalisa; Salvi, Erika; Braga, Daniele; Ricca, Flavia; Lupoli, Sara; Mingione, Alessandra; Pivari, Francesca; Brasacchio, Caterina; Barcella, Matteo; Chittani, Martina; D'Avila, Francesca; Turiel, Maurizio; Lazzaroni, Monica; Soldati, Laura; Cusi, Daniele; Barlassina, Cristina/titolo:Interaction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study/doi:10.1186%2Fs12967-016-0941-6/rivista:Journal of translational medicine (Online)/anno:2016/pagina_da:/pagina_a:/intervallo_pagine:/volume:14
Background: Paraoxonase 1 (PON1) gene polymorphisms and polyphenols intake have been reported independently associated to lipid profile and susceptibility to atherosclerosis and cardiovascular disease. However, the interaction between these factors r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4e62c1de0492dde6812594c0c0d65708
http://www.cnr.it/prodotto/i/369935
http://www.cnr.it/prodotto/i/369935
Autor:
Martinelli Boneschi, Filippo, Clerici, Francesca, Benussi, Luisa, Ghidoni, Roberta, Galimberti, Daniela, Squitti, Rosanna Confaloni, Annamaria, Bruno, Giuseppe, Pichler, Sabrina, Mayhaus, Manuel, Riemenschneider, Matthias, Giacalone, Giacomo, Mariani, Claudio, Scarpini, Elio, Binetti, Giuliano, Forloni, Gianluigi, Franceschi, Massimo, Albani, Diego, Magnani, Giuseppe, Biella, Gloria, Coppi, Elisabetta, Santangelo, Roberto, Brambilla, Paola, Esposito, Federica, Lupoli, Sara, COMI , GIANCARLO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10495::fa5d396db066a24b07d107ea0172a408
Autor:
Yu, Dongmei, Mathews, Carol A, Scharf, Jeremiah M, Neale, Benjamin M, Davis, Lea K, Gamazon, Eric R, Derks, Eske M, Evans, Patrick, Edlund, Christopher K, Crane, Jacquelyn, Fagerness, Jesen A, Osiecki, Lisa, Gallagher, Patience, Gerber, Gloria, Haddad, Stephen, Illmann, Cornelia, McGrath, Lauren M, Mayerfeld, Catherine, Arepalli, Sampath, Barlassina, Cristina, Barr, Cathy L, Bellodi, Laura, Benarroch, Fortu, Berrió, Gabriel Bedoya, Bienvenu, O Joseph, Black, Donald W, Bloch, Michael H, Brentani, Helena, Bruun, Ruth D, Budman, Cathy L, Camarena, Beatriz, Campbell, Desmond D, Cappi, Carolina, Silgado, Julio C Cardona, Cavallini, Maria C, Chavira, Denise A, Chouinard, Sylvain, Cook, Edwin H, Cookson, MR, Coric, Vladimir, Cullen, Bernadette, Cusi, Daniele, Delorme, Richard, Denys, Damiaan, Dion, Yves, Eapen, Valsama, Egberts, Karin, Falkai, Peter, Fernandez, Thomas, Fournier, Eduardo, Garrido, Helena, Geller, Daniel, Gilbert, Donald L, Girard, Simon L, Grabe, Hans J, Grados, Marco A, Greenberg, Benjamin D, Gross-Tsur, Varda, Grünblatt, Edna, Hardy, John, Heiman, Gary A, Hemmings, Sian MJ, Herrera, Luis D, Hezel, Dianne M, Hoekstra, Pieter J, Jankovic, Joseph, Kennedy, James L, King, Robert A, Konkashbaev, Anuar I, Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F, Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L, Lupoli, Sara, Macciardi, Fabio, Maier, Wolfgang, Manunta, Paolo, Marconi, Maurizio, McCracken, James T, Mesa Restrepo, Sandra C, Moessner, Rainald, Moorjani, Priya, Morgan, Jubel, Muller, Heike, Murphy, Dennis L, Naarden, Allan L, Nurmi, Erika, Ochoa, William Cornejo, Ophoff, Roel A, Pakstis, Andrew J, Pato, Michele T, Pato, Carlos N, Piacentini, John, Pittenger, Christopher, Pollak, Yehuda
Publikováno v:
The American journal of psychiatry, vol 172, iss 1
ObjectiveObsessive-compulsive disorder (OCD) and Tourette's syndrome are highly heritable neurodevelopmental disorders that are thought to share genetic risk factors. However, the identification of definitive susceptibility genes for these etiologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::6623fd4c901c542a622c177fc3803b59
https://escholarship.org/uc/item/3zn1b380
https://escholarship.org/uc/item/3zn1b380