Normal polymorphic variations and transcription of the decay accelerating factor gene in paroxysmal nocturnal hemoglobinuria cells.-Reference-Cited by-同舟云学术

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Normal polymorphic variations and transcription of the decay accelerating factor gene in paroxysmal nocturnal hemoglobinuria cells.

Published:1988-02-01 Issue:3 Volume:85 Page:880-884
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Stafford H. A.,Tykocinski M. L.,Lublin D. M.,Holers V. M.,Rosse W. F.,Atkinson J. P.,Medof M. E.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Cited by 76 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 complement alternative pathway in paroxysmal nocturnal hemoglobinuria: From a pathogenic mechanism to a therapeutic target;Immunological Reviews;2022-09-15

2. Discovering C3 targeting therapies for paroxysmal nocturnal hemoglobinuria: Achievements and pitfalls;Seminars in Immunology;2022-01

3. How we(’ll) treat paroxysmal nocturnal haemoglobinuria: diving into the future;British Journal of Haematology;2021-08-05

4. Anti-complement Treatment for Paroxysmal Nocturnal Hemoglobinuria: Time for Proximal Complement Inhibition? A Position Paper From the SAAWP of the EBMT;Frontiers in Immunology;2019-06-14

5. DAF in diabetic patients is subject to glycation/inactivation at its active site residues;Molecular Immunology;2018-01

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