L718P mutation in the membrane-proximal cytoplasmic tail of 3 promotes abnormal IIb 3 clustering and lipid microdomain coalescence, and associates with a thrombasthenia-like phenotype
Author:
Publisher
Ferrata Storti Foundation (Haematologica)
Subject
Hematology
Cited by 35 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. Twins With an Identical Novel Mutation in ITGB3: A Case Report of Glanzmann Thrombasthenia–like Syndrome;Annals of Laboratory Medicine;2023-12-28
2. Genetics of inherited thrombocytopenias;Blood;2022-06-02
3. Knock-in mice bearing constitutively active αIIb(R990W) mutation develop macrothrombocytopenia with severe platelet dysfunction;Japanese Journal of Thrombosis and Hemostasis;2022
4. Profiling the Genetic and Molecular Characteristics of Glanzmann Thrombasthenia: Can It Guide Current and Future Therapies?;Journal of Blood Medicine;2021-07
5. Glanzmann Thrombasthenia: Perspectives from Clinical Practice on Accurate Diagnosis and Optimal Treatment Strategies;Journal of Blood Medicine;2021-06
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