Viral and host factors determine innate immune responses in airway epithelial cells from children with wheeze and atopy von Spann, Kirsten M, Baturcam, Engin, Schagen, Johanna, Jones, Carmen, Straub, Claire P, Preston, F Maxine, Chen, Linping, Phipps, Simon, Sly, Peter D, Fantino, Emmanuelle

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siRNA against the G gene of human metapneumovirus von Preston, Faith Maxine, Straub, Claire P, Ramirez, Ruben, Mahalingam, Suresh, Spann, Kirsten M

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Mutation of the elongin C binding domain of human respiratory syncytial virus non-structural protein 1 (NS1) results in degradation of NS1 and attenuation of the virus von Straub, Claire P, Lau, Wei-Har, Preston, Faith M, Headlam, Madeleine J, Gorman, Jeffery J, Collins, Peter L, Spann, Kirsten M

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Mutation of the elongin C binding domain of human respiratory syncytial virus non-structural protein 1 von Straub, Claire P, Lau, Wei-Har, Preston, Faith M, Headlam, Madeleine J, Gorman, Jeffery J, Collins, Peter L, Spann, Kirsten M

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Genetic deficiency of indoleamine 2,3-dioxygenase promotes gut microbiota-mediated metabolic health von Laurans, Ludivine, Venteclef, Nicolas, Haddad, Yacine, Chajadine, Mouna, Alzaid, Fawaz, Metghalchi, Sarvenaz, Sovran, Bruno, Denis, Raphael G. P., Dairou, Julien, Cardellini, Marina, Moreno-Navarrete, Jose-Maria, Straub, Marjolene, Jegou, Sarah, McQuitty, Claire, Viel, Thomas, Esposito, Bruno, Tavitian, Bertrand, Callebert, Jacques, Luquet, Serge H., Federici, Massimo, Fernandez-Real, José Manuel, Burcelin, Remy, Launay, Jean-Marie, Tedgui, Alain, Mallat, Ziad, Sokol, Harry, Taleb, Soraya

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Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study von Nicholas, Jennifer, Grossman, Murray, McMillan, Corey T, Massimo, Lauren, Van Deerlin, Vivianna M, Warren, Jason D, Fox, Nick C, Bocchetta, Martina, Boeve, Bradley F, Knopman, David S, Rademakers, Rosa, van Swieten, John C, Meeter, Lieke H, Dopper, Elise GP, Snowden, Julie S, Saxon, Jennifer, Pickering-Brown, Stuart, Le Ber, Isabelle, Brice, Alexis, Caroppo, Paola, Ghidoni, Roberta, Pievani, Michela, Binetti, Giuliano, Dickerson, Bradford C, Lucente, Diane, Graff, Caroline, Ghoshal, Nupur, Galimberti, Daniela, Scarpini, Elio, Mackenzie, Ian R, Hsiung, Ging-Yuek R, Sengdy, Pheth, Boxer, Adam L, Taylor, Joanne B, Synofzik, Matthis, Wilke, Carlo, Sulzer, Patricia, Kwok, John, Lladó, Albert, Borrego-Ecija, Sergi, Santana, Isabel, Almeida, Maria Rosário, Tábuas-Pereira, Miguel, Moreno, Fermin, Barandiaran, Myriam, Indakoetxea, Begoña, Levin, Johannes, Danek, Adrian, Rowe, James B, Anderl-Straub, Sarah, Masellis, Mario, Black, Sandra E, Lautrette, Geraldine, Vandenberghe, Rik, Rogalski, Emily J, Weintraub, Sandra, Gerhard, Alexander, Onyike, Chiadi U, Papageorgiou, Sokratis G, Bras, Jose, Rohrer, Jonathan D, Heller, Carolin, Convery, Rhian S, Shafei, Rachelle M, Jones, David T, Baker, Matt, Gavrilova, Ralitza, Domoto-Reilly, Kimiko, Poos, Jackie M, Van der Ende, Emma L, Panman, Jessica L, Seelaar, Harro, Fostinelli, Silvia, Chiang, Huei-Hsin, Arighi, Andrea, Fenoglio, Chiara, Heuer, Hilary, Miller, Bruce, Karydas, Anna, Fong, Jamie, João Leitão, Maria, Santiago, Beatriz, Ferreira, Carlos, De Arriba, Maria, Tainta, Mikel, Zulaica, Miren, Ferreira, Catarina, Semler, Elisa, Ludolph, Albert, Miltenberger, Gabriel, Rogaeva, Ekaterina, Bruffaerts, Rose, Vandenbulcke, Mathieu, Mesulam, M Marsel, Bigio, Eileen, Kroupis, Christos, Stefanis, Leonidas, Shoesmith, Christien, Robertson, Erik, Geschwind, Daniel

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Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis von Mohassel, Payam, Donkervoort, Sandra, Lone, Museer A., Nalls, Matthew, Gable, Kenneth, Gupta, Sita D., Foley, A. Reghan, Hu, Ying, Saute, Jonas Alex Morales, Moreira, Ana Lucila, Kok, Fernando, Introna, Alessandro, Logroscino, Giancarlo, Grunseich, Christopher, Nickolls, Alec R., Pourshafie, Naemeh, Neuhaus, Sarah B., Saade, Dimah, Gangfuß, Andrea, Kölbel, Heike, Piccus, Zoe, Le Pichon, Claire E., Fiorillo, Chiara, Ly, Cindy V., Töpf, Ana, Brady, Lauren, Specht, Sabine, Zidell, Aliza, Pedro, Helio, Mittelmann, Eric, Thomas, Florian P., Chao, Katherine R., Konersman, Chamindra G., Cho, Megan T., Brandt, Tracy, Straub, Volker, Connolly, Anne M., Schara, Ulrike, Roos, Andreas, Tarnopolsky, Mark, Höke, Ahmet, Brown, Robert H., Lee, Chia-Hsueh, Hornemann, Thorsten, Dunn, Teresa M., Bönnemann, Carsten G.

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A comparison of the bone and growth phenotype of mdx, mdx: Cmah(-/-) and mdx:Utrn(+/-) murine models with the C57BL/10 wild-type mouse von Wood, Claire L., Suchacki, Karla J., van't Hof, Rob, Cawthorn, Will P., Dillon, Scott, Straub, Volker, Wong, Sze Choong, Ahmed, Syed F., Farquharson, Colin

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Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Ea... von Ferreiro, Ana, Quijano-Roy, Susana, Pichereau, Claire, Moghadaszadeh, Behzad, Goemans, Nathalie, Bönnemann, Carsten, Jungbluth, Heinz, Straub, Volker, Villanova, Marcello, Leroy, Jean-Paul, Romero, Norma B., Martin, Jean-Jacques, Muntoni, Francesco, Voit, Thomas, Estournet, Brigitte, Richard, Pascale, Fardeau, Michel, Guicheney, Pascale

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B cells orchestrate tolerance to the neuromyelitis optica autoantigen AQP4 von Afzali, Ali Maisam, Nirschl, Lucy, Sie, Christopher, Pfaller, Monika, Ulianov, Oleksii, Hassler, Tobias, Federle, Christine, Petrozziello, Elisabetta, Kalluri, Sudhakar Reddy, Chen, Hsin Hsiang, Tyystjärvi, Sofia, Muschaweckh, Andreas, Lammens, Katja, Delbridge, Claire, Büttner, Andreas, Steiger, Katja, Seyhan, Gönül, Ottersen, Ole Petter, Öllinger, Rupert, Rad, Roland, Jarosch, Sebastian, Straub, Adrian, Mühlbauer, Anton, Grassmann, Simon, Hemmer, Bernhard, Böttcher, Jan P., Wagner, Ingrid, Kreutzfeldt, Mario, Merkler, Doron, Pardàs, Irene Bonafonte, Schmidt Supprian, Marc, Buchholz, Veit R., Heink, Sylvia, Busch, Dirk H., Klein, Ludger, Korn, Thomas

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Nutrition and neurodevelopment in children: focus on NUTRIMENTHE project von Anjos, Tania, Altmäe, Signe, Emmett, Pauline, Tiemeier, Henning, Closa-Monasterolo, Ricardo, Luque, Verónica, Wiseman, Sheila, Pérez-García, Miguel, Lattka, Eva, Demmelmair, Hans, Egan, Bernadette, Straub, Niels, Szajewska, Hania, Evans, Jayne, Horton, Claire, Paus, Tomas, Isaacs, Elizabeth, van Klinken, Jan Willem, Koletzko, Berthold, Campoy, Cristina

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Mapping the differences in care for 5,000 Spinal Muscular Atrophy patients, a survey of 24 national registries in North America, Australasia and Europe von Bladen, Catherine L., Thompson, Rachel, Jackson, Jacqueline M., Garland, Connie, Wegel, Claire, Ambrosini, Anna, Pisano, Paolo, Walter, Maggie C., Schreiber, Olivia, Lusakowska, Anna, Jedrzejowska, Maria, Kostera-Pruszczyk, Anna, van der Pol, Ludo, Wadman, Renske I., Gredal, Ole, Karaduman, Ayse, Topaloglu, Haluk, Yilmaz, Oznur, Matyushenko, Vitaliy, Rasic, Vedrana Milic, Kosac, Ana, Karcagi, Veronika, Garami, Marta, Herczegfalvi, Agnes, Monges, Soledad, Moresco, Angelica, Chertkoff, Lilien, Chamova, Teodora, Guergueltcheva, Velina, Butoianu, Niculina, Craiu, Dana, Korngut, Lawrence, Campbell, Craig, Haberlova, Jana, Strenkova, Jana, Alejandro, Moises, Jimenez, Alatorre, Ortiz, Genaro Gabriel, Enriquez, Gracia Viviana Gonzalez, Rodrigues, Miriam, Roxburgh, Richard, Dawkins, Hugh, Youngs, Leanne, Lahdetie, Jaana, Angelkova, Natalija, Saugier-Veber, Pascal, Cuisset, Jean-Marie, Bloetzer, Clemens, Jeannet, Pierre-Yves, Klein, Andrea, Nascimento, Andres, Tizzano, Eduardo, Salgado, David, Mercuri, Eugenio, Sejersen, Thomas, Kirschner, Jan, Rafferty, Karen, Straub, Volker, Bushby, Kate, Verschuuren, Jan, Beroud, Christophe, Lochmüller, Hanns

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B cells orchestrate tolerance to the neuromyelitis optica autoantigen AQP4 von Afzali, Ali Maisam, Nirschl, Lucy, Sie, Christopher, Pfaller, Monika, Ulianov, Oleksii, Hassler, Tobias, Federle, Christine, Petrozziello, Elisabetta, Kalluri, Sudhakar Reddy, Chen, Hsin Hsiang, Tyystjaervi, Sofia, Muschaweckh, Andreas, Lammens, Katja, Delbridge, Claire, Buettner, Andreas, Steiger, Katja, Seyhan, Gonul, Ottersen, Ole Petter, Ollinger, Rupert, Rad, Roland, Jarosch, Sebastian, Straub, Adrian, Muehlbauer, Anton, Grassmann, Simon, Hemmer, Bernhard, Boettcher, Jan P, Wagner, Ingrid, Kreutzfeldt, Mario, Merkler, Doron, Pardas, Irene Bonafonte, Supprian, Marc Schmidt, Buchholz, Veit R, Heink, Sylvia, Busch, Dirk H, Klein, Ludger, Korn, Thomas

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Genetic deficiency of indoleamine 2,3-dioxygenase promotes gut microbiota-mediated metabolic health von Laurans, Ludivine, Venteclef, Nicolas, Haddad, Yacine, Chajadine, Mouna, Alzaid, Fawaz, Metghalchi, Sarvenaz, Sovran, Bruno, Denis, Raphael GP, Dairou, Julien, Cardellini, Marina, Moreno-Navarrete, Jose-Maria, Straub, Marjolene, Jegou, Sarah, McQuitty, Claire, Viel, Thomas, Esposito, Bruno, Tavitian, Bertrand, Callebert, Jacques, Luquet, Serge H, Federici, Massimo, Fernandez-Real, José Manuel, Burcelin, Remy, Launay, Jean-Marie, Tedgui, Alain, Mallat, Ziad, Sokol, Harry, Taleb, Soraya

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