Searching journal content for articles similar to Song et al. 9 (6): 581.

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  1. ...gene receptor clusters found within this region (Giglio et al. 2001). Individuals affected by 8p syndrome present with a variety of clinical phenotypes, including agenesis of the corpus callosum, epilepsy, and other neurodevelopmental delays (Vibert et al. 2022).Over the past several decades...
  2. ...SCs surround the stem-cell niche, called the hub (Fas3; blue cell cluster). Individual spermatogonial (SG) cysts are identified by the spectrosome/fusome (Hts) and the extracellular adhesion protein, armadillo (Arm), both blue in the confocal image. Scale bar = 10 µm. (B) A schematic and single z...
  3. ...of large, recent, and interspersed segmental duplications (SDs) (Marques-Bonet et al. 2009). These duplications are not evenly distributed along chromosomes but are clustered at some loci, especially pericentromeric and subtelomeric regions (Bailey et al. 2001; Giannuzzi et al. 2014). SD clusters exhibit...
  4. ..., our data do not support that there is a second region between 15 and 21 Mb, where X and Y do not recombine (“stratum 2”), as has been postulated previously (Wright et al. 2019), nor that there is an even more proximal nonrecombining region (“MSNR1”), as inferred from meiotic mapping (Tripathi et al...
  5. ...crossovers that form physical linkages (chiasmata) to stabilize the chromosomes. Such chiasmata must then be maintained over decades-long meiotic arrest, until meiosis resumes at ovulation. Abnormal number and/or location of crossovers may predispose oocytes to gains or losses of whole chromosomes...
  6. ..., DMC1 and RAD51, which bind ssDNA to form nucleoprotein filaments (Fig. 1A; Crickard and Greene 2018). Dmc1 is expressed only in meiotic cells and is essential for DSB repair and chromosomal synapsis during meiosis in mammals (Pittman et al. 1998; Yoshida et al. 1998). In contrast, RAD51 is expressed...
  7. ...previously noted (Vara et al. 2019).As a caveat to our prediction of threefold shorter A-compartment loops, we note that the physical size of the meiotic loops appears relatively consistent overall along chromosomal axes. Although physical loop size differences can be observed near telomeres...
  8. ...:10.1038/nbt.2727 ↵Cabrero J, López-León MD, Teruel M, Camacho JPM. 2009. Chromosome mapping of H3 and H4 histone gene clusters in 35 species of acridid grasshoppers. Chromosome Res 17: 397–404. doi:10.1007/s10577-009-9030-5 ↵Cantalapiedra CP, Hernández-Plaza A, Letunic I, Bork P, Huerta-Cepas J. 2021...
  9. ...isolated repetitive regions of the and identified those containing at least one YY1 motif for phylogenetic analysis. This phylogenetic analysis revealed that most of these unannotated repetitive regions from autosomal sequences do not cluster by chromosome. In contrast, sequences derived from the X...
  10. ...of an ancestral MAGED cluster and the emergence of two testis-specific ampliconic gene families in mouse: Btbd35 and Ott-like. Thus, one ancestral amplicon gave rise to two unlinked mouse amplicons that each became populated by novel protein-coding genes. The other end of the mouse lineage-specific inversion...
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