Janus kinase inhibition in complement component 1 deficiency-Reference-Cited by-同舟云学术

Janus kinase inhibition in complement component 1 deficiency

Published:2020-12 Issue:6 Volume:146 Page:1439-1442.e5
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Wolf Christine,Brück Normi,Koss Sarah,Griep Constanze,Kirschfink Michael,Palm-Beden Katharina,Fang Mingyan,Röber Nadja,Winkler Stefan,Berner Reinhard,Latz Eike,Günther Claudia,Lee-Kirsch Min Ae

Funder

Deutsche Forschungsgemeinschaft

Shenzhen Municipal Government of China

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference17 articles.

1. Early components of the complement classical activation pathway in human systemic autoimmune diseases;Lintner;Front Immunol,2016

2. Brief report: Deficiency of complement 1r subcomponent in early-onset systemic lupus erythematosus: the role of disease-modifying alleles in a monogenic disease;Demirkaya;Arthritis Rheumatol (Hoboken, NJ),2017

3. A case of systemic lupus erythematosus with C1q deficiency, increased serum interferon-α levels and high serum interferogenic activity;Bolin;Rheumatology (Oxford),2019

4. Human lupus autoantibody-DNA complexes activate DCs through cooperation of CD32 and TLR9;Means;J Clin Invest,2005

5. Familial chilblain lupus due to a gain-of-function mutation in STING;König;Ann Rheum Dis,2017

Cited by 18 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. Monogenic lupus – from gene to targeted therapy;Molecular and Cellular Pediatrics;2024-09-12

2. Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System Inflammation;Journal of Clinical Immunology;2024-08-28

3. UNC93B1 variants underlie TLR7-dependent autoimmunity;Science Immunology;2024-02-23

4. Absence of Type I Interferon Autoantibodies or Significant Interferon Signature Alterations in Adults With Post–COVID-19 Syndrome;Open Forum Infectious Diseases;2023-12-19

5. Hemophagocytic lymphohistiocytosis–like hyperinflammation due to a de novo mutation in DPP9;Journal of Allergy and Clinical Immunology;2023-11