Searching journal content for articles similar to Barbosa-Morais et al. 16 (1): 66.

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  1. ...driver of differential expression compared to age (887 genes compared to 206 genes at FDR < 0.01). For proteins, age is a stronger driver compared to sex (2084 genes compared to 408 genes at FDR < 0.01). Thus the number of proteins showing significant change with age is greater that the number...
  2. ..., such as indels and splice-site polymorphs, and associating them with the coding potential of exonic loci. By systematically annotating exonic loci through EUIDs, ENACT allows inference of their multifaceted roles within gene isoforms and a detailed understanding of how exonic diversity impacts protein variations...
  3. ..., “spliceosome”; 14 genes, “RNA degradation”), and protein processing (53 genes, “Ribosome”; 10 genes, “proteasome”). We also found that some signaling pathways, such as mTOR and FoxO, were significantly enriched. Inactivation of TOR in both Drosophila and mammalian cells has shown that TOR controls both cell...
  4. ...application for quantifying differential isoform usage but also to functionally annotate such isoforms, using the module IsoAnnot (de la Fuente et al. 2020). IsoAnnot maps protein features (e.g., Pfam domains) across isoforms of a gene, and determines how splicing leads to partial or full removal of protein...
  5. ...conservation. CIRs are closer to the 5′-end, whereas LIRs are closer to the 3′-end of transcripts. EIciRNA-generating genes are more actively transcribed and associated with epigenetic marks of gene activation. Computational analyses and -wide CRISPR screening revealed that SRSF1 binds to CIRs and inhibits...
  6. ...by the splicing process, where splice sites, conserved sequence elements at the exon/intron boundaries, are recognized by the spliceosome.The vast majority (>99%) of all introns are excised by the major or U2-type spliceosome, associated with a multitude of accessory proteins (Wahl et al. 2009), and most...
  7. ...Genome-wide identification and characterization of transcription start sites and promoters in the tunicate Ciona intestinalis Rui Yokomori 1 , Kotaro Shimai 2 , Koki Nishitsuji 3 , Yutaka Suzuki 1 , Takehiro G. Kusakabe 2 , 4...
  8. ...and transcriptionally active transposons in A. thaliana is illustrated by our comprehensive analysis of the cotranscriptional and translational features of Ty1/Copia elements, a family of young and active retroelements in plant s, and how such features impact their biology. Genome-wide transcript profiling revealed...
  9. ...in Supplemental Fig. S9) in all the samples (Fig. 2A). A comparison of the identified differentially expressed genes (DEGs) (Supplemental Table S1) with the genes undergoing differential AS (DAS) (Supplemental Table S2), which were obtained with the Pacific Biosciences (PacBio) RSH platforms, revealed that more...
  10. ...Genome-wide mapping of alternative splicing in Arabidopsis thaliana Sergei A. Filichkin 1 , Henry D. Priest 1 , Scott A. Givan 1 , Rongkun Shen 1 , 3 , Douglas W. Bryant 1 , 2 , Samuel E. Fox 1 , Weng-Keen Wong 2...
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