An adolescent with marked hyperimmuno-globulinemia E showing minimal change nephrotic syndrome and a STAT3 gene mutation-Reference-Cited by-同舟云学术

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An adolescent with marked hyperimmuno-globulinemia E showing minimal change nephrotic syndrome and a STAT3 gene mutation

Published:2011-04-01 Issue:04 Volume:75 Page:369-373
ISSN:0301-0430
Container-title:Clinical Nephrology
language:en
Short-container-title:CN

Author:

Miyazaki K.,Miyazawa T.,Sugimoto K.,Fujita S.,Yanagida H.,Okada M.,Takemura T.

Publisher

Dustri-Verlgag Dr. Karl Feistle

Subject

Nephrology,General Medicine

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance;Journal of Experimental Medicine;2021-06-17

2. Hyperimmunoglobulin E syndrome associated with nephrotic syndrome–case report;Journal of Dermatology & Cosmetology;2020

3. Co-stimulatory Molecule CD80 (B7.1) in MCNS;Molecular Mechanisms in the Pathogenesis of Idiopathic Nephrotic Syndrome;2016

4. Identification and characterization of distinct IL-17F expression patterns and signaling pathways in chronic lymphocytic leukemia and normal B lymphocytes;Immunologic Research;2015-10-19

5. The Ying and Yang of STAT3 in Human Disease;Journal of Clinical Immunology;2015-08-18

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