Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy

Autor: 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

Publikováno v: In Cell 8 July 2021 184(14):3812-3828

Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses

Autor: Barbieux, Claire, Bonnet Des Claustres, Mathilde, Fahrner, Matthias, Petrova, Evgeniya, Tsoi, Lam, Gouin, Olivier, Leturcq, Florent, Nicaise-Roland, Pascale, Bole, Christine, Béziat, Vivien, Bourrat, Emmanuelle, Schilling, Oliver, Gudjonsson, Johann, Hovnanian, Alain

Publikováno v: Journal of Allergy and Clinical Immunology
Journal of Allergy and Clinical Immunology, 2021, ⟨10.1016/j.jaci.2021.08.024⟩
Journal of Allergy and Clinical Immunology, Elsevier, 2021, ⟨10.1016/j.jaci.2021.08.024⟩

International audience; Background: Netherton syndrome (NS) is a rare recessive skin disorder caused by loss-of-function mutations in SPINK5 encoding the protease inhibitor LEKTI (lymphoepithelial Kazal-type–related inhibitor). NS patients experien

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::45a772f891d8b291c5ed4aaba2c5a0e7
https://hal.science/hal-03559943/file/06-netherton-syndrome-subtypes-share-IL.pdf

Secukinumab Therapy for Netherton Syndrome.

Autor: Luchsinger, Isabelle, Knöpfel, Nicole, Theiler, Martin, Bonnet des Claustres, Mathilde, Barbieux, Claire, Schwieger-Briel, Agnes, Brunner, Corinne, Donghi, Davide, Buettcher, Michael, Meier-Schiesser, Barbara, Hovnanian, Alain, Weibel, Lisa

Publikováno v: JAMA Dermatology; Aug2020, Vol. 156 Issue 8, p907-911, 5p