Structural variations are a pervasive feature of human genomes, and there is growing recognition of their role in disease development through their impact on spatial chromatin architecture. This under
we investigated the changes of tRFs in SAMP8 and SAMR1 mouse brains at 7 months of age. A total of 570 tRF transcripts were discovered. Among these transcripts, 8, including 3 upregulated and 5 downre
We established mice lacking of Tsc1 in myeloid cells. RNA sequencing of the total RNA samples which collected from spleen Monocytes/Macrophages of mutant or control mice.
