Searching journal content for articles similar to Peng et al. 34 (8): 1235.

Displaying results 1-10 of 6033
For checked items
  1. .../6/7 study by the Gehring group supports a single pathway of decay in human cells, more closely aligned with the initial C. elegans genetics (Boehm et al. 2021). In the work of Boehm et al. (2021), loss of any one of SMG-5/6/7 stabilized a similar set of target mRNAs in human cells. Their work challenges...
  2. ...and identify therapeutic opportunities. Here, we develop a cell type–specific regulatory atlas of the human middle temporal gyrus via leveraging single-nucleus RNA-seq (1,197,032 nuclei) and ATAC-seq (740,875 nuclei) data sets from 84 donors across four stages of AD neuropathological change (ADNC). We observe...
  3. ...substantia nigra samples 82 at four distinct age stages. This approach allowed us to assess cell-type-specific transcriptional 83 and epigenetic changes across aging in an unbiased way at single-cell resolution. 84 85 Results 86 Multiomics atlas of mouse substantia nigra across age 87 To investigate cell...
    OPEN ACCESS ARTICLEACCEPTED MANUSCRIPT
  4. ...), but our long RNA-seq mappings could also be consistent with TR transcription in C. elegans being a byproduct of mRNA transcription.View larger version: In this window In a new window Figure 6. Transcription from a tandem repeat in various tissue types. This shows an alignment of long RNA-seq reads...
  5. ...typically involved bulk analyses of whole embryos with consequent loss of tissue-specific 86 information, and poor detection of signal from minor cell populations. An analysis of HCNEs 87 within CRMs acting in specific germ layers and tissues across disparate vertebrate species is 88 therefore generally...
    ACCEPTED MANUSCRIPT
  6. ..., are highlighted. (D) Gene family expansion and contraction analysis across five Caenorhabditis nematodes. The predicted number of expanded (red) and contracted (green) gene families are indicated for each species as well as the ancestral node. (Cre) C. remanei; (Cbn) C. brenneri; (Cel) C. elegans. (E) Predicted...
  7. ...of nonstop decay [NSD]). However, it is now widely recognized that NMD is also a key post-transcriptional regulatory mechanism for physiologically functional mRNAs (Nasif et al. 2018). Furthermore, other TDD pathways have been discovered that regulate the stability of physiologically functional transcripts...
  8. ...is characterized by both H3K9me3 and H3K27me3 but has open chromatin at the TSS that is equivalent to that of euchromatin states 11 and 12 (Fig. 3B,C). High transcript abundance could be owing to post-transcriptional stabilization of mRNAs produced during larval germline development rather than ongoing...
  9. ...GENE (CZI Cell Science Program et al. 2025), and the Human Cell Atlas (Regev et al. 2017). Similarly, integrating spatial transcriptomics (ST) data sets, which contain both spatial coordinates and gene expression, enables comparative analysis across samples, technologies, and conditions, revealing cellular...
  10. ...studies demonstrate that QuadST effectively controls the type I error, even in misspecified settings, and significantly improves power over existing methods. Applications of QuadST to real data sets reveal biologically significant interaction-changed genes across various cell types.Cells rarely function...
For checked items

Preprint Server