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  1. ...). One key insight from comparative studies is that the well-characterized genomic organization seen in mice and humans (the long-standing gold standard for MHC genomic research) is actually a derived state, specific to placental mammals. In humans, the MHC spans 4–5 Mb and contains well over 200 genes...
  2. ...(Supplemental Fig. S4), supporting the idea that the Y Chromosome of classical inbred strains originated from Japanese house mice (Japanese fancy mouse) (Bishop et al. 1985; Nagamine et al. 1992; Tucker et al. 1992; Takada et al. 2013).View larger version: In this window In a new window Figure 2. Geographic...
  3. ...that these arrays are embedded in conserved genomic regions, with >90% similarity in the 10-kb flanking regions (Supplemental Fig. S15). However, the PCA showed species-specific clustering of repeats (Fig. 6A), suggesting that the ∼40-kb array was present in the common ancestor but diverged through gene conversion...
  4. ..., Farmington, CT 060329 ∗ equal contribution † corresponding authors10 Running title: Epigenetic variation in nine inbred mouse strains11 Abstract12 The diversity outbred (DO) mice and their inbred founders are widely used models of human disease.13 However, although the genetic diversity of these mice has...
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  5. ...in inbred mouse s (Garretson et al. 2025).The biological mechanisms underlying the elevated rate of dnSNVs in ART-derived mice remain unclear. Known mutational processes often leave distinct genomic signatures, including signatures attributable to oncogenic processes (Alexandrov et al. 2020) and germline...
  6. ..., Sichuan 8 University, Chengdu, Sichuan, 610041, China 9 3. Deep Underground Space Medical Center, West China Hospital, Sichuan University, 10 Chengdu, Chengdu, Sichuan, 610041, China 11 12 # These authors contributed equally 13 * Corresponding author 14 E-mail: danxie@scu.edu.cn (DX), liujifeng777@wchscu...
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  7. ...found to be common but tend to be present in populations at low frequencies, owing to their deleterious effects (Chakraborty et al. 2019). This suggests that they contribute to a genomic architecture of rare alleles with high effect sizes and could reveal new insights concerning the genomic architecture...
  8. ...based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism. PLoS Genet 16: e1008926. doi:10.1371/journal.pgen.1008926 ↵Campbell P, Good JM, Nachman MW. 2013. Meiotic sex chromosome inactivation is disrupted in sterile hybrid male house mice. Genetics 193: 819...
  9. ...contribute to genomic diversification driven by the acquisition of adaptive elements across species.An intriguing possibility for the acquisition of novel, genetically adapted elements is the transfer of organelle DNA (Popadin et al. 2022; Butenko et al. 2024). In many eukaryotic species, organelles...
  10. ...These authors contributed equally to this work. Corresponding author: matthew.webster@imbim.uu.seAbstractMeiotic recombination is a fundamental evolutionary process that facilitates adaptation and the removal of deleterious genetic variation. Social Hymenoptera exhibit some of the highest recombination rates...
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