ABIN1 mutant (Q478H) contribute to progressive myelodysplastic syndromes liked diseases by type I IFNs signaling
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE220301
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To understand the mechanism of MDS in Abin1Q478H/Q478H mice, we performed RNA-seq analysis of bone marrow lineage-negative cells from 5 months Abin1Q478H/Q478H mice and WT control mice to gain a global view of the transcriptome profile regulated by ABIN1(Q478H) mutation. Comparative gene expression profiling analysis of RNA-seq data for bone marrow lineage-negative cells from 5 months Abin1Q478H/Q478H mice and WT control mice
创建时间：
2023-04-26
