Single-cell RNA sequencing reveals abnormal transcriptome signature of erythroid progenitors in pure red cell aplasia
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Genetics (clinical),Molecular Biology,Biochemistry
Reference5 articles.
1. Pure red cell aplasia;Means;Blood,2016
2. Human bone marrow assessment by single-cell RNA sequencing, mass cytometry, and flow cytometry;Oetjen;JCI Insight,2018
3. Single-cell profiling of human bone marrow progenitors reveals mechanisms of failing erythropoiesis in Diamond-Blackfan anemia;Iskander;Sci Transl Med,2021
4. Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1;Rio;Blood,2019
5. Decoding the pathogenesis of Diamond-Blackfan anemia using single-cell RNA-seq;Wang;Cell Discov,2022
Cited by 3 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. STK10 mutations block erythropoiesis in acquired pure red cell aplasia via impairing ribosome biogenesis;Annals of Hematology;2024-05-18
2. STK10 mutations block erythropoiesis in acquired pure red cell aplasia via impairing ribosome biogenesis;2024-03-05
3. Acquired pure red cell aplasia: unraveling the immune pathogenesis;Journal of Bio-X Research;2023-12
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