Protein stabilization improves STAT3 function in autosomal dominant hyper-IgE syndrome-Reference-Cited by-同舟云学术

Protein stabilization improves STAT3 function in autosomal dominant hyper-IgE syndrome

Published:2016-12-29 Issue:26 Volume:128 Page:3061-3072
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Bocchini Claire E.¹,Nahmod Karen¹,Katsonis Panagiotis²,Kim Sang³,Kasembeli Moses M.³,Freeman Alexandra⁴,Lichtarge Olivier²,Makedonas George¹,Tweardy David J.³^ORCID

Affiliation:

1. Department of Pediatrics and

2. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX;

3. Division of Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, TX; and

4. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD

Abstract

Publisher's Note: There is an Inside Blood Commentary on this article in this issue.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/128/26/3061/1397623/blood702373.pdf

Reference52 articles.

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

3. Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups;Jiao;Mol Immunol,2008

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

5. Coronary artery abnormalities in Hyper-IgE syndrome;Freeman;J Clin Immunol,2011

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