Infections by Transovarially Transmitted DMelSV in Drosophila Have No Impact on Ovarian Transposable Element Transcripts but Increase Their Amounts in the Soma von Roy, Marlène, Viginier, Barbara, Mayeux, Camille A, Ratinier, Maxime, Fablet, Marie

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Quels sont les apports des analyses conjointes archéoentomologiques et archéobotaniques dans les contextes arctiques ? von Mayeux, Camille, Alix, Claire, Petit, Christophe, Elliott, Michelle

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Formation processes of archaeobotanical assemblages of an early Thule Iñupiaq dwelling at Cape Espenberg, northwest Alaska von Mayeux, Camille, Alix, Claire, Mason, Owen, Bigelow, Nancy, Petit, Christophe

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Contrôle des éléments transposables et réponse aux infections virales chez Drosophila von Mayeux, Camille

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Quels sont les apports des analyses conjointes archéoentomologiques et archéobotaniques dans les contextes arctiques ? von Mayeux, Camille, Alix, Claire, Petit, Christophe, Elliott, Michelle

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À table von Bacoup, Paul, Bonoron, Alexandrine, Caurette, Natacha, Chantran, Aurélie, Laguardia, Marie, Laurent, Anne-Sophie, Le Bailly, Matthieu, Mancina, Pauline, Marty, Astrid, Mayeux, Camille, Mazauric, Rémi, Valamoti, Soultana-Maria, Viaut, Charles, Wall, Euan, Webb, Russell

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Les plantes dans l’alimentation thuléenne von Mayeux, Camille

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Erythropoietin downregulates red blood cell clearance, increasing transfusion efficacy in severely anemic recipients von Casimir, Madeleine, Colard, Martin, Dussiot, Michael, Roussel, Camille, Martinez, Anaïs, Peyssonnaux, Carole, Mayeux, Patrick, Benghiat, Samantha, Manceau, Sandra, Francois, Anne, Marin, Nathalie, Pène, Frédéric, Buffet, Pierre A., Hermine, Olivier, Amireault, Pascal

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Rare genetic variation in fibronectin 1 (FN1) protects against APOEε4 in Alzheimer’s disease von Bhattarai, Prabesh, Gunasekaran, Tamil Iniyan, Belloy, Michael E., Reyes-Dumeyer, Dolly, Jülich, Dörthe, Tayran, Hüseyin, Yilmaz, Elanur, Flaherty, Delaney, Turgutalp, Bengisu, Sukumar, Gauthaman, Alba, Camille, McGrath, Elisa Martinez, Hupalo, Daniel N., Bacikova, Dagmar, Le Guen, Yann, Lantigua, Rafael, Medrano, Martin, Rivera, Diones, Recio, Patricia, Nuriel, Tal, Ertekin-Taner, Nilüfer, Teich, Andrew F., Dickson, Dennis W., Holley, Scott, Greicius, Michael, Dalgard, Clifton L., Zody, Michael, Mayeux, Richard, Kizil, Caghan, Vardarajan, Badri N.

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Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function: A Meta-analysis of Community-Based Cohorts von Zhang, Yuankai, Liu, Xue, Wiggins, Kerri L., Kurniansyah, Nuzulul, Guo, Xiuqing, Rodrigue, Amanda L, Zhao, Wei, Yanek, Lisa R, Ratliff, Scott M., Pitsillides, Achilleas, Aguirre Patiño, Juan Sebastian, Sofer, Tamar, Arking, Dan E., Austin, Thomas R., Beiser, Alexa S., Blangero, John, Boerwinkle, Eric, Bressler, Jan, Curran, Joanne E., Hou, Lifang, Hughes, Timothy M., Kardia, Sharon L, Launer, Lenore, Levy, Daniel, Mosley, Tom H., Nasrallah, Ilya M., Rich, Stephen S., Rotter, Jerome I., Seshadri, Sudha, Tarraf, Wassim, González, Kevin A., Ramachandran, Vasan, Yaffe, Kristine, Nyquist, Paul A, Psaty, Bruce M, DeCarli, Charles S., Smith, Jennifer A, Glahn, David C, González, Hector M, Bis, Joshua C, Fornage, Myriam, Heckbert, Susan R., Fitzpatrick, Annette L., Liu, Chunyu, Satizabal, Claudia L.

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Missense and loss‐of‐function variants at GWAS loci in familial Alzheimer's disease von Gunasekaran, Tamil Iniyan, Reyes‐Dumeyer, Dolly, Faber, Kelley M., Goate, Alison, Boeve, Brad, Cruchaga, Carlos, Pericak‐Vance, Margaret, Haines, Jonathan L., Rosenberg, Roger, Tsuang, Debby, Mejia, Diones Rivera, Medrano, Martin, Lantigua, Rafael A., Sweet, Robert A., Bennett, David A., Wilson, Robert S., Alba, Camille, Dalgard, Clifton, Foroud, Tatiana, Vardarajan, Badri N., Mayeux, Richard

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Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease von Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen, Sims, Rebecca, Ahmad, Shahzad, Amin, Najaf, Norsworthy, Penny, Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Amouyel, Philippe, Beecham, Gary, Berr, Claudine, Bis, Joshua, Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J. Nicholas, Daniele, Antonio, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Denning, Nicola, Destefano, Anita, Farrer, Lindsay, Fernández, Maria Victoria, Fox, Nick, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan, Holmes, Clive, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris, Kraaij, Robert, Lathrop, Marc, Lemstra, Afina, Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel, Marshall, Rachel, Martin, Eden, Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel, Morgan, Kevin, Myers, Richard, Nacmias, Benedetta, Naj, Adam, Napolioni, Valerio, Pasquier, Florence, Pastor, Pau, Pericak-Vance, Margaret, Raybould, Rachel, Redon, Richard, Reinders, Marcel, Richard, Anne-Claire, Riedel-Heller, Steffi, Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie, Saad, Salha, Sanchez-Juan, Pascual, Schellenberg, Gerard, Scheltens, Philip, Schott, Jonathan, Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik, Sorbi, Sandro, van Spaendonk, Resie, Spalletta, Gianfranco, Tesi, Niccolo’, Tijms, Betty, Uitterlinden, André, van der Lee, Sven, Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimon, Jordi, van Swieten, John, Greicius, Michael, Yokoyama, Jennifer, Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo

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Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation von Bis, Joshua, Jian, Xueqiu, Kunkle, Brian, Chen, Yuning, Hamilton-Nelson, Kara, Bush, William, Salerno, William, Lancour, Daniel, Ma, Yiyi, Renton, Alan, Marcora, Edoardo, Farrell, John, Zhao, Yi, Qu, Liming, Ahmad, Shahzad, Amin, Najaf, Amouyel, Philippe, Beecham, Gary, Below, Jennifer, Campion, Dominique, Cantwell, Laura, Charbonnier, Camille, Chung, Jaeyoon, Crane, Paul, Cruchaga, Carlos, Cupples, L. Adrienne, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Fulton, Lucinda, Gabriel, Stacey, Genin, Emmanuelle, Gibbs, Richard, Goate, Alison, Grenier-Boley, Benjamin, Gupta, Namrata, Haines, Jonathan, Havulinna, Aki, Helisalmi, Seppo, Hiltunen, Mikko, Howrigan, Daniel, Ikram, M. Arfan, Kaprio, Jaakko, Konrad, Jan, Kuzma, Amanda, Lander, Eric, Lathrop, Mark, Lehtimäki, Terho, Lin, Honghuang, Mattila, Kari, Mayeux, Richard, Muzny, Donna, Nasser, Waleed, Neale, Benjamin, Nho, Kwangsik, Nicolas, Gaël, Patel, Devanshi, Pericak-Vance, Margaret, Perola, Markus, Psaty, Bruce, Quenez, Olivier, Rajabli, Farid, Redon, Richard, Reitz, Christiane, Remes, Anne, Salomaa, Veikko, Sarnowski, Chloe, Schmidt, Helena, Schmidt, Michael, Schmidt, Reinhold, Soininen, Hilkka, Thornton, Timothy, Tosto, Giuseppe, Tzourio, Christophe, van der Lee, Sven, van Duijn, Cornelia, Valladares, Otto, Vardarajan, Badri, Wang, Li-San, Wang, Weixin, Wijsman, Ellen, Wilson, Richard, Witten, Daniela, Worley, Kim, Zhang, Xiaoling, Bellenguez, Celine, Lambert, Jean-Charles, Kurki, Mitja, Palotie, Aarno, Daly, Mark, Boerwinkle, Eric, Lunetta, Kathryn, Destefano, Anita, Dupuis, Josée, Martin, Eden, Schellenberg, Gerard, Seshadri, Sudha, Naj, Adam, Fornage, Myriam, Farrer, Lindsay

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Erythropoietin induces the tyrosine phosphorylation of its own receptor in human erythropoietin-responsive cells von Dusanter-Fourt, I, Casadevall, N, Lacombe, C, Muller, O, Billat, C, Fischer, S, Mayeux, P

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Structure of the murine erythropoietin receptor complex. Characterization of the erythropoietin cross-linked proteins von MAYEUX, P, LACOMBE, C, CASADEVALL, N, CHRETIEN, S, DUSANTER, I, GISSELBRECHT, S

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Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease von Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen GJ, Sims, Rebecca, Ahmad, Shahzad, Amin, Najaf, Norsworthy, Penny J, Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Beecham, Gary W, Berr, Claudine, Bis, Joshua C, Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J Nicholas, Daniele, Antonio, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, DeStefano, Anita L, Farrer, Lindsay A, Fernández, Maria Victoria, Fox, Nick C, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan JP, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L, Ikram, M Arfan, Ikram, M Kamran, Jansen, Iris E, Kraaij, Robert, Lathrop, Marc, Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel MAM, Marshall, Rachel, Martin, Eden R, Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel O, Morgan, Kevin, Myers, Richard M, Nacmias, Benedetta, Naj, Adam C, Napolioni, Valerio, Pasquier, Florence, Pericak-Vance, Margaret A, Raybould, Rachel, Redon, Richard, Reinders, Marcel JT, Richard, Anne-Claire, Riedel-Heller, Steffi G, Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S, Saad, Salha, Sanchez-Juan, Pascual, Schellenberg, Gerard D, Scheltens, Philip, Schott, Jonathan M, Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik A, Sorbi, Sandro, van Spaendonk, Resie, Spalletta, Gianfranco, Tesi, Niccolo, Uitterlinden, André G, van der Lee, Sven J, Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimon, Jordi, van Swieten, John C, Greicius, Michael D, Yokoyama, Jennifer S, Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje M, Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean-Charles

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Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease von Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen G. J, Sims, Rebecca, Ahmad, Shahzad, Norsworthy, Penny J, Dols Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Beecham, Gary W, Berr, Claudine, Bis, Joshua C, Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Cochran, J. Nicholas, Daniele, Antonio, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, DeStefano, Anita L, Farrer, Lindsay A, Fernández, Maria Victoria, Fox, Nick C, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan J. P, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris E, Kraaij, Robert, Lathrop, Marc, Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel M. A. M, Marshall, Rachel, Martin, Eden R, Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel O, Morgan, Kevin, Myers, Richard M, Nacmias, Benedetta, Naj, Adam C, Napolioni, Valerio, Pasquier, Florence, Pericak-Vance, Margaret A, Raybould, Rachel, Redon, Richard, Reinders, Marcel J. T, Richard, Anne-Claire, Riedel-Heller, Steffi, Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S, Saad, Salha, Sánchez-Juan, Pascual, Schellenberg, Gerard D, Scheltens, Philip, Schott, Jonathan M, Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik A, Sorbi, Sandro, van Spaendonk, Resie, Spalletta, Gianfranco, Tesi, Niccolo, Tijms, Betty M, Uitterlinden, André G, van der Lee, Sven J, Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimón, Jordi, van Swieten, John C, Greicius, Michael D, Yokoyama, Jennifer S, Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje M, Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean-Charles, Universitat Autònoma de Barcelona

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Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease von Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen G. J, Sims, Rebecca, Ahmad, Shahzad, Norsworthy, Penny J, Dols Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Beecham, Gary W, Berr, Claudine, Bis, Joshua C, Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J. Nicholas, Daniele, Antonio, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, DeStefano, Anita L, Farrer, Lindsay A, Fernández, Maria Victoria, Fox, Nick C, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan J. P, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris E, Kraaij, Robert, Lathrop, Marc, Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel M. A. M, Marshall, Rachel, Martin, Eden R, Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel O, Morgan, Kevin, Myers, Richard M, Nacmias, Benedetta, Naj, Adam C, Napolioni, Valerio, Pasquier, Florence, Pericak-Vance, Margaret A, Raybould, Rachel, Redon, Richard, Reinders, Marcel J. T, Richard, Anne-Claire, Riedel-Heller, Steffi G, Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S, Saad, Salha, Sánchez-Juan, Pascual, Schellenberg, Gerard D, Scheltens, Philip, Schott, Jonathan M, Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik A, Sorbi, Sandro, van Spaendonk, Resie, Spalletta, Gianfranco, Tesi, Niccolo, Uitterlinden, André G, van der Lee, Sven J, Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimón, Jordi, van Swieten, John C, Greicius, Michael D, Yokoyama, Jennifer S, Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje M, Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean-Charles, Universitat Autònoma de Barcelona

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Erythropoietin induces the association of phosphatidylinositol 3′‐kinase with a tyrosine‐phosphorylated protein complex containing the erythropoietin receptor von MAYEUX, Patrick, DUSANTER‐FOURT, Isabelle, MULLER, Odile, MAUDUIT, Philippe, SABBAH, Michèle, DRUKER, Brian, VAINCHENKER, William, FISCHER, Sigmund, LACOMBE, Catherine, GISSELBRECHT, Sylvie

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Diving mask device, has air tank made of flexible material without elastic property, where air tank is communicated with water-tight compartment of mask by free circulation of air... von FRESSER CAMILLE JULIEN MICHEL, MAYEUX DUBERNET DE BOSCQ STEPHANE, MICOULAUD FRANCHI JEAN ARTHUR

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