Distinct mutations at the same positions of STAT3 cause either loss or gain of function-Reference-Cited by-同舟云学术

Distinct mutations at the same positions of STAT3 cause either loss or gain of function

Published:2016-10 Issue:4 Volume:138 Page:1222-1224.e2
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Chandrasekaran Prabha^ORCID,Zimmerman Ofer,Paulson Michelle,Sampaio Elizabeth P.,Freeman Alexandra F.,Sowerwine Kathryn J.,Hurt Darell,Alcántara-Montiel Julio C.,Hsu Amy P.,Holland Steven M.

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference22 articles.

1. Crystal structure of unphosphorylated STAT3 core fragment;Ren;Biochem Biophys Res Commun,2008

2. STAT3 mutations in the hyper-IgE syndrome;Holland;N Engl J Med,2007

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

4. Somatic STAT3 mutations in large granular lymphocytic leukemia;Koskela;N Engl J Med,2012

5. Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease;Flanagan;Nat Genet,2014

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