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Functional and structural analysis of cytokine-selective IL6ST defects that cause recessive hyper-IgE syndrome.
Chen, Yin-Huai; Zastrow, Diane B; Metcalfe, Riley D; Gartner, Lisa; Krause, Freia; Morton, Craig J; Marwaha, Shruti; Fresard, Laure; Huang, Yong; Zhao, Chunli; McCormack, Colleen; Bick, David; Worthey, Elizabeth A; Eng, Christine M; Gold, Jessica; Montgomery, Stephen B; Fisher, Paul G; Ashley, Euan A; Wheeler, Matthew T; Parker, Michael W; Shanmugasundaram, Veerabahu; Putoczki, Tracy L; Schmidt-Arras, Dirk; Laurence, Arian; Bernstein, Jonathan A; Griffin, Michael D W; Uhlig, Holm H.
Affiliation
  • Chen YH; Translational Gastroenterology Unit, University of Oxford, Oxford, United Kingdom.
  • Zastrow DB; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif.
  • Metcalfe RD; Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Australia.
  • Gartner L; Translational Gastroenterology Unit, University of Oxford, Oxford, United Kingdom.
  • Krause F; Christian-Albrechts-University Kiel, Institute of Biochemistry, Kiel, Germany.
  • Morton CJ; Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Australia.
  • Marwaha S; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif.
  • Fresard L; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif; Department of Pathology, Stanford School of Medicine, Stanford, Calif.
  • Huang Y; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif.
  • Zhao C; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif.
  • McCormack C; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif.
  • Bick D; Hudson Alpha Institute for Biotechnology, Huntsville, Ala.
  • Worthey EA; Hudson Alpha Institute for Biotechnology, Huntsville, Ala.
  • Eng CM; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif; Baylor College of Medicine, Houston, Tex.
  • Gold J; Department of Pediatrics, Stanford University School of Medicine, Stanford, Calif.
  • Undiagnosed Diseases Network; National Institutes of Health Undiagnosed Diseases Network, Common Fund, Office of the Director and the National Human Genome Research Institute, National Institutes of Health, Bethesda, Md.
  • Montgomery SB; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif; Department of Pathology, Stanford School of Medicine, Stanford, Calif; Department of Genetics, Stanford University School of Medicine, Stanford, Calif.
  • Fisher PG; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif; Department of Neurology, Stanford University School of Medicine, Stanford University, Stanford, Calif.
  • Ashley EA; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif; Department of Genetics, Stanford University School of Medicine, Stanford, Calif.
  • Wheeler MT; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif; Department of Medicine, Stanford School of Medicine, Stanford, Calif.
  • Parker MW; Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Australia; St Vincent's Institute of Medical Research, Melbourne, Australia.
  • Shanmugasundaram V; Bristol-Myers Squibb, Cambridge, Mass.
  • Putoczki TL; Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia; Department of Medical Biology, The University of Melbourne, Melbourne, Australia.
  • Schmidt-Arras D; Christian-Albrechts-University Kiel, Institute of Biochemistry, Kiel, Germany.
  • Laurence A; Translational Gastroenterology Unit, University of Oxford, Oxford, United Kingdom. Electronic address: arian.laurence@ndm.ox.ac.uk.
  • Bernstein JA; Center for Undiagnosed Diseases, Stanford University, Stanford, Calif; Department of Pediatrics, Stanford University School of Medicine, Stanford, Calif.
  • Griffin MDW; Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Australia.
  • Uhlig HH; Translational Gastroenterology Unit, University of Oxford, Oxford, United Kingdom; Department of Paediatrics, University of Oxford, Oxford, United Kingdom; Oxford National Institute for Health Research Biomedical Research Centre, Oxford, United Kingdom.
J Allergy Clin Immunol ; 148(2): 585-598, 2021 08.
Article in En | MEDLINE | ID: mdl-33771552
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / Cytokine Receptor gp130 / Molecular Dynamics Simulation / Job Syndrome Type of study: Clinical_trials / Prognostic_studies Limits: Child / Humans / Male Language: En Journal: J Allergy Clin Immunol Year: 2021 Type: Article Affiliation country: United kingdom
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / Cytokine Receptor gp130 / Molecular Dynamics Simulation / Job Syndrome Type of study: Clinical_trials / Prognostic_studies Limits: Child / Humans / Male Language: En Journal: J Allergy Clin Immunol Year: 2021 Type: Article Affiliation country: United kingdom