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1 Ergebnisse
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Dominant-negative mutations in human IL6ST underlie hyper-I..:
Béziat, Vivien
;
Tavernier, Simon J
;
Chen, Yin-Huai
...
qt8bn1d5qg. , 2020
Link:
https://escholarship.org/uc/item/8bn1d5qg
RT Journal T1
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt8bn1d5qg&Exemplar=1&LAN=DE A1 Béziat, Vivien A1 Tavernier, Simon J A1 Chen, Yin-Huai A1 S., Cindy A1 Materna, Marie A1 Laurence, Arian A1 Staal, Jens A1 Aschenbrenner, Dominik A1 Roels, Lisa A1 Worley, Lisa A1 Claes, Kathleen A1 Gartner, Lisa A1 Kohn, Lisa A A1 De Bruyne, Marieke A1 Schmitz-Abe, Klaus A1 Charbonnier, Louis-Marie A1 Keles, Sevgi A1 Nammour, Justine A1 Vladikine, Natasha A1 Renkilaraj, Majistor Raj Luxman Maglorius A1 Seeleuthner, Yoann A1 Migaud, Mélanie A1 Rosain, Jérémie A1 Jeljeli, Mohamed A1 Boisson, Bertrand A1 Van Braeckel, Eva A1 Rosenfeld, Jill A A1 Dai, Hongzheng A1 Burrage, Lindsay C A1 Murdock, David R A1 Lambrecht, Bart N A1 Avettand-Fenoel, Véronique A1 Vogel, Tiphanie P A1 Network, Undiagnosed Diseases A1 Esther, Charles R A1 Haskologlu, Sule A1 Dogu, Figen A1 Ciznar, Peter A1 Boutboul, David A1 Ouachée-Chardin, Marie A1 Amourette, Jean A1 Lebras, Marie-Noëlle A1 Gauvain, Clément A1 Tcherakian, Colas A1 Ikinciogullari, Aydan A1 Beyaert, Rudi A1 Abel, Laurent A1 Milner, Joshua D A1 Grimbacher, Bodo A1 Couderc, Louis-Jean A1 Butte, Manish J A1 Freeman, Alexandra F A1 Catherinot, Émilie A1 Fieschi, Claire A1 Chatila, Talal A A1 Tangye, Stuart G A1 Uhlig, Holm H A1 Haerynck, Filomeen A1 Casanova, Jean-Laurent A1 Puel, Anne PB eScholarship, University of California YR 2020 K1 Biomedical and Clinical Sciences K1 Health Sciences K1 Clinical Research K1 Rare Diseases K1 Genetics K1 Aetiology K1 2.1 Biological and endogenous factors K1 Adolescent K1 Alleles K1 C-Reactive Protein K1 Cell Membrane K1 Cells K1 Cultured K1 Child K1 Cytokine Receptor gp130 K1 Cytokines K1 Female K1 Fibroblasts K1 Genes K1 Dominant K1 Population K1 HEK293 Cells K1 Humans K1 Job Syndrome K1 Kinetics K1 Loss of Function Mutation K1 Male K1 Middle Aged K1 Models K1 Biological K1 Mutation K1 Pedigree K1 Phenotype K1 Th2 Cells K1 Up-Regulation K1 Young Adult K1 Undiagnosed Diseases Network K1 Medical and Health Sciences K1 Immunology JF qt8bn1d5qg LK http://dx.doi.org/https://escholarship.org/uc/item/8bn1d5qg DO https://escholarship.org/uc/item/8bn1d5qg SF ELIB - SuUB Bremen
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