Linking C5 Deficiency to an Exonic Splicing Enhancer Mutation-Reference-Cited by-同舟云学术

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Linking C5 Deficiency to an Exonic Splicing Enhancer Mutation

Published:2005-03-18 Issue:7 Volume:174 Page:4172-4177
ISSN:0022-1767
Container-title:The Journal of Immunology
language:en
Short-container-title:J Immunol

Author:

Pfarr Nicole,Prawitt Dirk,Kirschfink Michael,Schroff Claudia,Knuf Markus,Habermehl Pirmin,Mannhardt Wilma,Zepp Fred,Fairbrother William,Loos Michael,Burge Christopher B.,Pohlenz Joachim

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

Reference27 articles.

1. Complement

2. Complement

3. C5A Anaphylatoxin and Its Seven Transmembrane-Segment Receptor

4. Ember, J. A., M. A. Jagels, T. E. Hugli. 1998. Characterization of complement anaphylatoxins and their biological responses. J. E. Volonakis, and M. M. Frank, eds. The Human Complement System 241. Marcel Dekker, New York.

Cited by 36 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. The efficacy and safety of eculizumab in patients and the role of C5 polymorphisms;Drug Discovery Today;2024-09

2. Molecular aspects of hereditary complement component C5 deficiency in humans;Polish Annals of Medicine;2024-07-15

3. Evidence in disease and non-disease contexts that nonsense mutations cause altered splicing via motif disruption;Nucleic Acids Research;2021-09-01

4. Genetic analysis of four consanguineous multiplex families with inflammatory bowel disease;Gastroenterology Report;2021-07-13

5. Human genetics of meningococcal infections;Human Genetics;2020-02-17

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