Searching journal content for articles similar to Hashimoto et al. 31 (11): 1983.

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  1. ...and Feschotte 2020). In humans, RTEs are further subdivided into long terminal repeats (LTRs) and non-LTRs, including long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs) (Li et al. 2022). However, LTRs and LINEs facilitate transposition by encoding their own reverse...
  2. ...and potentially impact disease risk. We describe here our investigation into the impact of aging on the epigenetic repression of TEs in normal mammary LEps, the primary suspected cell of origin for luminal breast cancers.ResultsEvolutionarily recent LTR elements function as regulatory elements in mammary LEps...
  3. ..., and stability.Retrotransposons are major contributors to ongoing mutagenesis in mammalian s. The autonomous non-long terminal repeat (non-LTR) retrotransposon Long Interspersed Element 1 (LINE-1 or L1) is actively mobilizing in both humans and mice, and L1 sequences occupy ∼17% of human DNA and ∼18% of mouse...
  4. ...Gen) targeting the L1RS2, L1RS37, AluYRa4, AluYRb4, AluYRc2, AluYRd4, LTR14 (HERVK14), and LTR4 (MacERV1) subfamilies (Supplemental Table S1). The posthybridization library pool was then sequenced with paired-end 2 × 150 mer reads, using two flow cells of an Illumina HiSeq X platform (Macrogen...
  5. ...Mammalian non-LTR retrotransposons: For better or worse, in sickness and in health Victoria P. Belancio , Dale J. Hedges , and Prescott Deininger 1 Tulane Cancer Center and Department of Epidemiology, Tulane University Health Sciences Center, New...
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  6. ....J. ( 2000 ) Statistics with Confidence ( BMJ books , Bristol, UK ) 2d edition . ↵ Batzer, M.A. , Deininger, P.L. ( 2002 ) Alu repeats and human genomic diversity . Nat. Rev. Genet. 35 : 501 – 538 . ↵ Belancio, V.P. , Hedges, D.J. , Deininger, P. ( 2008 ) Mammalian non-LTR retrotransposons: For better...
  7. ...MCAMdata set for human cancers and found that LTRs are also depleted in methylation-prone genes, albeit to a lesser degree than SINE and LINE retrotransposons (Supplemental Fig. S3). However, adding LTR distribution to predict gene predisposition to DNA methylation in human cancer did not significantly improve...
  8. ...; Elsik et al. 2009), including long interspersed elements (LINEs), short interspersed elements (SINEs), and long terminal repeat (LTR) retrotransposons (Deininger and Batzer 2002; Deininger et al. 2003). The activities of LINEs and LTR retrotransposons, which can act as aggressive mutators...
  9. ...; Molto´ et al. 2009). It is known that transposable elements such as ERV1, ERVK, MIR1, LTR10, and MER61 contain binding sites for transcription factors (Wang et al. 2007; Bourque et al. 2008; Kuwabara et al. 2009; Kunarso et al. 2010). Moreover, a B2 SINE retrotransposon has been shown to insulate...
  10. ...; however, increasing evidence suggests that silencing of TEs is often incomplete. The crow family experienced a recent radiation of LTR retrotransposons (LTRs), offering an opportunity to gain insight into the regulatory control of young, potentially still active TEs. We quantified the abundance of TE...
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