Searching journal content for articles similar to Soldevila et al. 16 (2): 231.

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  1. ..., such as Neanderthals and Denisovans, into the s of modern humans due to historical gene flow events is known as archaic introgression. As new methods and data sets uncover a more complex intermingling between our ancestors and archaic humans than previously thought, the relevance of archaic introgression has only...
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  2. ...(via CATH, see Methods; note “paralog” refers to genes present in the human not to copies arising from duplication events such as WGD). Filtering steps removed FIEs identified in genes without significant expression in TRACERx lung tumors (LUAD, 3/80 genes; LUSC, 4/41 genes) or where the FunVar score...
  3. ...characterization, as well as expression of these paralogs across iPSCs and fetal brain Iso-Seq libraries, normalized to median haplotype paralog copy number.Using this phylogenetic group classification of cluster 1 and 2 members, we revisited expression of the TBC1D3 gene family in humans, taking advantage...
  4. ...impacts and evolutionary patterns over time remain elusive in humans owing to the technical and ethical complexities of functional studies. Integrating gene age dating with Mendelian disease phenotyping, we reveal a gradual rise in disease gene proportion as gene age increases. Logistic regression...
  5. ...-associated genes as input for a network proximity analysis. This approach evaluates the network relationship between AD-associated genes and drug targets within the human PPI network. We subsequently identified enriched drug candidates by performing GSEA integrating drug–gene signatures from the CMap database...
  6. ...samples highlighted 69 the utility of such analyses, identifying extensive changes not only in gene expression but also 70 4 in the connections between genes and chromatin regions in glia populations during aging and 71 PD(Adams et al. 2024). However, human samples often suffer from the inherent genetic...
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  7. ...between genetic variants and environmental stressors is key to understanding the mechanisms underlying neurological diseases. In this study, we use human brain organoids to explore how varying oxygen levels expose context-dependent gene regulatory effects. By subjecting a genetically diverse panel of 21...
  8. ...expression can be quantified directly from transcript fragments present in sRNA-seq experiments. We analyze studies containing matched total RNA and small RNA from four human tissues and recover transcript fragments from the sRNA-seq data sets. We find that the expression levels of protein-coding gene...
  9. ...environmental and strain comparisons and were the only mouth-form genes to be differentially expressed in the combined analysis. Human homologs of these enzymes modify a variety of molecules, including hormones, glycosaminoglycans, cerebrosides, and catecholamines (Chapman et al. 2004; Hanson et al. 2004...
  10. ...are largely unknown. Here, we profile -wide changes to gene expression and chromatin structure in cardiomyocytes derived from human pluripotent stem cells. We identify and characterize a gene regulatory element essential for regulating MYH6 expression, which encodes human fetal myosin. Using chromatin...
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