A novel homozygous Y140X mutation of ISG15 causes diverse type I interferonopathies in sibling patients with cutaneous lesions or recurrent parenchymal pneumonia-Reference-Cited by-同舟云学术

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A novel homozygous Y140X mutation of ISG15 causes diverse type I interferonopathies in sibling patients with cutaneous lesions or recurrent parenchymal pneumonia

Published:2023-12 Issue: Volume:257 Page:109844
ISSN:1521-6616
Container-title:Clinical Immunology
language:en
Short-container-title:Clinical Immunology

Author:

Xu Qiling,Li Wenyan,Zhao Qian,Zhao Lu,Lv Ge,Sun Gan,Gao Yelei,Ding Yuan,Zhang Zhiyong,Zhou Lina,Chen Yongwen,Tang Xuemei,Zhu Jin,Zhao Xiaodong,An Yunfei

Funder

Chongqing Municipal Education Commission

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference31 articles.

1. ISG15 in antiviral immunity and beyond;Perng;Nat. Rev. Microbiol.,2018

2. Interferon induces a 15-kilodalton protein exhibiting marked homology to ubiquitin;Haas;J. Biol. Chem.,1987

3. Precursor Processing of Pro-ISG15/UCRP, an Interferon-β-induced Ubiquitin-like Protein;Potter;J. Biol. Chem.,1999

4. ISG15 Arg151 and the ISG15-conjugating enzyme UbE1L are important for innate immune control of Sindbis virus;Giannakopoulos;J. Virol.,2009

5. Structural basis of the specificity of USP18 toward ISG15;Basters;Nat. Struct. Mol. Biol.,2017

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