Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy von Béziat, Vivien, Rapaport, Franck, Hu, Jiafen, Titeux, Matthias, Bonnet des Claustres, Mathilde, Bourgey, Mathieu, Griffin, Heather, Bandet, Élise, Ma, Cindy S., Sherkat, Roya, Rokni-Zadeh, Hassan, Louis, David M., Changi-Ashtiani, Majid, Delmonte, Ottavia M., Fukushima, Toshiaki, Habib, Tanwir, Guennoun, Andrea, Khan, Taushif, Bender, Noemi, Rahman, Mahbuba, About, Frédégonde, Yang, Rui, Rao, Geetha, Rouzaud, Claire, Li, Jingwei, Shearer, Debra, Balogh, Karla, Al Ali, Fatima, Ata, Manar, Dabiri, Soroosh, Momenilandi, Mana, Nammour, Justine, Alyanakian, Marie-Alexandra, Leruez-Ville, Marianne, Guenat, David, Materna, Marie, Marcot, Léa, Vladikine, Natasha, Soret, Christine, Vahidnezhad, Hassan, Youssefian, Leila, Saeidian, Amir Hossein, Uitto, Jouni, Catherinot, Émilie, Navabi, Shadi Sadat, Zarhrate, Mohammed, Woodley, David T., Jeljeli, Mohamed, Abraham, Thomas, Belkaya, Serkan, Lorenzo, Lazaro, Rosain, Jérémie, Bayat, Mousa, Lanternier, Fanny, Lortholary, Olivier, Zakavi, Faramarz, Gros, Philippe, Orth, Gérard, Abel, Laurent, Prétet, Jean-Luc, Fraitag, Sylvie, Jouanguy, Emmanuelle, Davis, Mark M., Tangye, Stuart G., Notarangelo, Luigi D., Marr, Nico, Waterboer, Tim, Langlais, David, Doorbar, John, Hovnanian, Alain, Christensen, Neil, Bossuyt, Xavier, Shahrooei, Mohammad, Casanova, Jean-Laurent

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Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency von Lévy, Romain, Gothe, Florian, Momenilandi, Mana, Magg, Thomas, Materna, Marie, Peters, Philipp, Raedler, Johannes, Philippot, Quentin, Rack-Hoch, Anita Lena, Langlais, David, Bourgey, Mathieu, Lanz, Anna-Lisa, Ogishi, Masato, Rosain, Jérémie, Martin, Emmanuel, Latour, Sylvain, Vladikine, Natasha, Distefano, Marco, Khan, Taushif, Rapaport, Franck, Schulz, Marian S, Holzer, Ursula, Fasth, Anders, Sogkas, Georgios, Speckmann, Carsten, Troilo, Arianna, Bigley, Venetia, Roppelt, Anna, Dinur-Schejter, Yael, Toker, Ori, Bronken Martinsen, Karen Helene, Sherkat, Roya, Somekh, Ido, Somech, Raz, Shouval, Dror S, Kühl, Jörn-Sven, Ip, Winnie, McDermott, Elizabeth M, Cliffe, Lucy, Ozen, Ahmet, Baris, Safa, Rangarajan, Hemalatha G, Jouanguy, Emmanuelle, Puel, Anne, Bustamante, Jacinta, Alyanakian, Marie-Alexandra, Fusaro, Mathieu, Wang, Yi, Kong, Xiao-Fei, Cobat, Aurélie, Boutboul, David, Castelle, Martin, Aguilar, Claire, Hermine, Olivier, Cheminant, Morgane, Suarez, Felipe, Yildiran, Alisan, Bousfiha, Aziz, Al-Mousa, Hamoud, Alsohime, Fahad, Cagdas, Deniz, Abraham, Roshini S, Knutsen, Alan P, Fevang, Borre, Bhattad, Sagar, Kiykim, Ayca, Erman, Baran, Arikoglu, Tugba, Unal, Ekrem, Kumar, Ashish, Geier, Christoph B, Baumann, Ulrich, Neven, Bénédicte, Rohlfs, Meino, Walz, Christoph, Abel, Laurent, Malissen, Bernard, Marr, Nico, Klein, Christoph, Casanova, Jean-Laurent, Hauck, Fabian, Béziat, Vivien

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Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency von Lévy, Romain, Gothe, Florian, Momenilandi, Mana, Magg, Thomas, Materna, Marie, Peters, Philipp, Raedler, Johannes, Philippot, Quentin, Rack-Hoch, Anita Lena, Langlais, David, Bourgey, Mathieu, Lanz, Anna-Lisa, Ogishi, Masato, Rosain, Jérémie, Martin, Emmanuel, Latour, Sylvain, Vladikine, Natasha, Distefano, Marco, Khan, Taushif, Rapaport, Franck, Schulz, Marian, Holzer, Ursula, Fasth, Anders, Sogkas, Georgios, Speckmann, Carsten, Troilo, Arianna, Bigley, Venetia, Roppelt, Anna, Dinur-Schejter, Yael, Toker, Ori, Bronken Martinsen, Karen Helene, Sherkat, Roya, Somekh, Ido, Somech, Raz, Shouval, Dror, Kühl, Jörn-Sven, Ip, Winnie, Mcdermott, Elizabeth, Cliffe, Lucy, Ozen, Ahmet, Baris, Safa, Rangarajan, Hemalatha, Jouanguy, Emmanuelle, Puel, Anne, Bustamante, Jacinta, Alyanakian, Marie-Alexandra, Fusaro, Mathieu, Wang, Yi, Kong, Xiao-Fei, Cobat, Aurélie, Boutboul, David, Castelle, Martin, Aguilar, Claire, Hermine, Olivier, Cheminant, Morgane, Suarez, Felipe, Yildiran, Alisan, Bousfiha, Aziz, Al-Mousa, Hamoud, Alsohime, Fahad, Cagdas, Deniz, Abraham, Roshini, Knutsen, Alan, Fevang, Borre, Bhattad, Sagar, Kiykim, Ayca, Erman, Baran, Arikoglu, Tugba, Unal, Ekrem, Kumar, Ashish, Geier, Christoph, Baumann, Ulrich, Neven, Bénédicte, Calas, Julie, Feuille, Elizabeth, Chan, Angela, Yesil, Gozde, Nammour, Justine, Bandet, Élise, Picard, Capucine, Benhsaien, Ibtihal, Lang, Peter, Atschekzei, Faranaz, Warnatz, Klaus, Hambleton, Sophie, Desai, Mukesh, Karakoc-Aydiner, Elif, Kolukisa, Burcu, Al-Muhsen, Saleh, Alosaimi, Mohammed, Cipe, Funda, Alazami, Anas, Hancioglu, Gonca, Can Meydan, Bilge, Sorte, Hanne, Stray-Pedersen, Asbjørg, Mammayil, Geetha, Tökmeci, Nazan, Shcherbina, Anna, Stepensky, Polina

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Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy von Beziat, Vivien, Rapaport, Franck, Hu, Jiafen, Titeux, Matthias, des Claustres, Mathilde Bonnet, Bourgey, Mathieu, Griffin, Heather, Bandet, Elise, Ma, Cindy S, Sherkat, Roya, Rokni-Zadeh, Hassan, Louis, David M, Changi-Ashtiani, Majid, Delmonte, Ottavia M, Fukushima, Toshiaki, Habib, Tanwir, Guennoun, Andrea, Khan, Taushif, Bender, Noemi, Rahman, Mahbuba, About, Fredegonde, Yang, Rui, Rao, Geetha, Rouzaud, Claire, Li, Jingwei, Shearer, Debra, Balogh, Karla, Al Ali, Fatima, Ata, Manar, Dabiri, Soroosh, Momenilandi, Mana, Nammour, Justine, Alyanakian, Marie-Alexandra, Leruez-Ville, Marianne, Guenat, David, Materna, Marie, Marcot, Lea, Vladikine, Natasha, Soret, Christine, Vahidnezhad, Hassan, Youssefian, Leila, Saeidian, Amir Hossein, Uitto, Jouni, Catherinot, Emilie, Navabi, Shadi Sadat, Zarhrate, Mohammed, Woodley, David T, Jeljeli, Mohamed, Abraham, Thomas, Belkaya, Serkan, Lorenzo, Lazaro, Rosain, Jeremie, Bayat, Mousa, Lanternier, Fanny, Lortholary, Olivier, Zakavi, Faramarz, Gros, Philippe, Orth, Gerard, Abel, Laurent, Pretet, Jean-Luc, Fraitag, Sylvie, Jouanguy, Emmanuelle, Davis, Mark M, Tangye, Stuart G, Notarangelo, Luigi D, Marr, Nico, Waterboer, Tim, Langlais, David, Doorbar, John, Hovnanian, Alain, Christensen, Neil, Bossuyt, Xavier, Shahrooei, Mohammad, Casanova, Jean-Laurent

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Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome von Béziat, Vivien, Tavernier, Simon, Chen, Yin-Huai, Ma, Cindy S, Materna, Marie, Laurence, Arian, Staal, Jens, Aschenbrenner, Dominik, Roels, Lisa, Worley, Lisa, Claes, Kathleen, Gartner, Lisa, Kohn, Lisa A, De Bruyne, Marieke, Schmitz-Abe, Klaus, Charbonnier, Louis-Marie, Keles, Sevgi, Nammour, Justine, Vladikine, Natasha, Maglorius Renkilaraj, Majistor Raj Luxman, Seeleuthner, Yoann, Migaud, Mélanie, Rosain, Jérémie, Jeljeli, Mohamed, Boisson, Bertrand, Van Braeckel, Eva, Rosenfeld, Jill A, Dai, Hongzheng, Burrage, Lindsay C, Murdock, David R, Lambrecht, Bart, Avettand-Fenoel, Véronique, Vogel, Tiphanie P, Esther, Charles R, Haskologlu, Sule, Dogu, Figen, Ciznar, Peter, Boutboul, David, Ouachée-Chardin, Marie, Amourette, Jean, Lebras, Marie-Noëlle, Gauvain, Clément, Tcherakian, Colas, Ikinciogullari, Aydan, Beyaert, Rudi, Abel, Laurent, Milner, Joshua D, Grimbacher, Bodo, Couderc, Louis-Jean, Butte, Manish J, Freeman, Alexandra F, Catherinot, Émilie, Fieschi, Claire, Chatila, Talal A, Tangye, Stuart G, Uhlig, Holm H, Haerynck, Filomeen, Casanova, Jean-Laurent, Puel, Anne, Undiagnosed Diseases Network, [missing]

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