A Single-Base Deletion in the Thrombopoietin (TPO) Gene Causes Familial Essential Thrombocythemia Through a Mechanism of More Efficient Translation of TPO mRNA

Author:

Ghilardi Nico1,Skoda Radek C.1

Affiliation:

1. Biozentrum; University of Basel; Basel, Switzerland

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Cited by 66 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. Relative impact of THPO mutation causing hereditary thrombocythemia;Experimental Hematology;2024-06

2. Hereditary thrombocythemia due to splicing donor site mutation of THPO in a Japanese family;Annals of Hematology;2023-11-14

3. Thrombocytosis in children and adolescents—classification, diagnostic approach, and clinical management;Annals of Hematology;2021-03-12

4. Reprogramming translation for gene therapy;Progress in Molecular Biology and Translational Science;2021

5. Platelet Disorders;Benign Hematologic Disorders in Children;2020-08-19

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