Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

Author:

Woellner Cristina,Gertz E. Michael,Schäffer Alejandro A.,Lagos Macarena,Perro Mario,Glocker Erik-Oliver,Pietrogrande Maria C.,Cossu Fausto,Franco José L.,Matamoros Nuria,Pietrucha Barbara,Heropolitańska-Pliszka Edyta,Yeganeh Mehdi,Moin Mostafa,Español Teresa,Ehl Stephan,Gennery Andrew R.,Abinun Mario,Bręborowicz Anna,Niehues Tim,Kilic Sara Sebnem,Junker Anne,Turvey Stuart E.,Plebani Alessandro,Sánchez Berta,Garty Ben-Zion,Pignata Claudio,Cancrini Caterina,Litzman Jiri,Sanal Özden,Baumann Ulrich,Bacchetta Rosa,Hsu Amy P.,Davis Joie N.,Hammarström Lennart,Davies E. Graham,Eren Efrem,Arkwright Peter D.,Moilanen Jukka S.,Viemann Dorothee,Khan Sujoy,Maródi László,Cant Andrew J.,Freeman Alexandra F.,Puck Jennifer M.,Holland Steven M.,Grimbacher Bodo

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference28 articles.

1. Hyper-IgE syndrome with recurrent infections—an autosomal dominant multisystem disorder;Grimbacher;N Engl J Med,1999

2. Job's syndrome: recurrent, “cold”, staphylococcal abscesses;Davis;Lancet,1966

3. Extreme hyperimmunoglobulinemia E and undue susceptibility to infection;Buckley;Pediatrics,1972

4. Genetic linkage of hyper-IgE syndrome to chromosome 4;Grimbacher;Am J Hum Genet,1999

5. Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome;Minegishi;Nature,2007

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