Searching journal content for articles similar to Kolle et al. 21 (12): 2014.

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  1. ...target expression variation and covariation, but these observations have been limited to a few microRNAs. Here we systematically study microRNA alternative functions in mouse embryonic stem cells (mESCs) by genetically deleting Drosha, leading to global loss of microRNAs. We apply complementary single...
  2. ...and multimodal profiles across time, and extrapolate single-cell profiles in a missing modality. We apply Sunbear to reveal sex-biased transcription during mouse embryonic development and predict dynamic relationships between epigenetic priming and transcription for cells in which multimodal profiles...
  3. ...to comprehensively map GRNs (Badia-i-Mompel et al. 2023). High-throughput RNA sequencing (RNA-seq), which enables -wide analysis of the cellular transcriptome on bulk cells (Ozsolak and Milos 2011), has revolutionized GRN inference by enabling the computational derivation of regulatory networks from gene expression...
  4. ...Gene networks provide a fundamental framework for understanding the molecular mechanisms 13 that govern gene expression. Advances in single-cell RNA sequencing (scRNA-seq) have enabled 14 network inference at cellular resolution; however, most existing approaches rely on predefined 15 clusters or cell...
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  5. ...to analyze the transcriptome, histone modification patterns, and replication timing of germline stem cell (GSC)–like and somatic cyst stem cell (CySC)–like cells. Single-cell RNA sequencing validates previous findings on GSC–CySC intercellular communication and reveals a high expression of chromatin...
  6. ..., we obtained 27 contexts including seven tissue contexts that were not present in GTEx: airway, eye, human embryonic stem cells, induced pluripotent stem cells, multipotent cells, myeloid cells, and PBMCs/T cells (Fig. 1E). The number of samples present in each tissue context following outlier...
  7. ...of microRNA expression analyses is reflected by the existence of thousands of sRNA-seq studies in which matched total RNA-seq data are often unavailable. The lack of paired sequencing experiments limits the analysis of microRNA–gene regulatory networks. Here, we explore whether protein-coding gene...
  8. ...interactions. Here, we use the mouse embryonic stem cell (mESC) model to describe in detail the relationships within the H3K27-H3K36-DNA methylation subnetwork. In particular, we focus on the major epigenetic reorganization caused by deletion of the histone 3 lysine 36 methyltransferase NSD1, which in m...
  9. ...by regulating gene expression, RNA metabolism, and translation. Their dysregulation contributes to the development of human diseases, including cancer. 3-methylcytidine (m3C) primarily occurs in transfer RNA, where it regulates translation, stem cell pluripotency, and mitochondrial function. m3C has also been...
  10. ...(Lewis et al. 2003) but can also result in a variety of genetic diseases (Scotti and Swanson 2016; Zhang et al. 2022; Kurolap et al. 2023). In other cases, the resulting changes in sequence lead to protein products with distinct functions. For example, in human embryonic stem cells, an AS event...
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