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ab15090 has been referenced in 19 publications.

  • Meng X  et al. Genetic Deficiency of Mtdh Gene in Mice Causes Male Infertility via Impaired Spermatogenesis and Alterations in the Expression of Small Non-coding RNAs. J Biol Chem 290:11853-64 (2015). IHC ; Mouse . PubMed: 25787082
  • Ishiguro K  et al. Meiosis-specific cohesin mediates homolog recognition in mouse spermatocytes. Genes Dev 28:594-607 (2014). ICC/IF ; Mouse . PubMed: 24589552
  • Llano E  et al. STAG3 is a strong candidate gene for male infertility. Hum Mol Genet 23:3421-31 (2014). Mouse . PubMed: 24608227
  • Broering TJ  et al. BRCA1 establishes DNA damage signaling and pericentric heterochromatin of the X chromosome in male meiosis. J Cell Biol 205:663-75 (2014). PubMed: 24914237
  • Winters T  et al. Meiotic cohesin STAG3 is required for chromosome axis formation and sister chromatid cohesion. EMBO J 33:1256-70 (2014). PubMed: 24797474
  • Nilsen A  et al. ALKBH4 Depletion in Mice Leads to Spermatogenic Defects. PLoS One 9:e105113 (2014). IHC-P ; Mouse . PubMed: 25153837
  • Zhou J  et al. A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice. Biol Reprod 88:159 (2013). PubMed: 23677977
  • Horn HF  et al. A mammalian KASH domain protein coupling meiotic chromosomes to the cytoskeleton. J Cell Biol 202:1023-39 (2013). PubMed: 24062341
  • Luo M  et al. MEIOB exhibits single-stranded DNA-binding and exonuclease activities and is essential for meiotic recombination. Nat Commun 4:2788 (2013). PubMed: 24240703
  • Fukuda T  et al. Phosphorylation of chromosome core components may serve as axis marks for the status of chromosomal events during mammalian meiosis. PLoS Genet 8:e1002485 (2012). WB ; Mouse . PubMed: 22346761
  • Llano E  et al. Meiotic cohesin complexes are essential for the formation of the axial element in mice. J Cell Biol 197:877-85 (2012). PubMed: 22711701
  • Nicholas CR  et al. Intact fetal ovarian cord formation promotes mouse oocyte survival and development. BMC Dev Biol 10:2 (2010). IHC-P ; Mouse . PubMed: 20064216
  • Fukuda T  et al. A novel mammalian HORMA domain-containing protein, HORMAD1, preferentially associates with unsynapsed meiotic chromosomes. Exp Cell Res 316:158-71 (2010). PubMed: 19686734
  • Wu S  et al. Loss of YY1 impacts the heterochromatic state and meiotic double-strand breaks during mouse spermatogenesis. Mol Cell Biol 29:6245-56 (2009). ICC/IF ; Mouse . PubMed: 19786570
  • Ryu KY  et al. The mouse polyubiquitin gene Ubb is essential for meiotic progression. Mol Cell Biol 28:1136-46 (2008). ICC/IF ; Mouse . PubMed: 18070917
  • Mahadevaiah SK  et al. Extensive meiotic asynapsis in mice antagonises meiotic silencing of unsynapsed chromatin and consequently disrupts meiotic sex chromosome inactivation. J Cell Biol 182:263-76 (2008). ICC/IF ; Mouse . PubMed: 18663141
  • Ollinger R  et al. Deletion of the pluripotency-associated Tex19.1 gene causes activation of endogenous retroviruses and defective spermatogenesis in mice. PLoS Genet 4:e1000199 (2008). ICC/IF ; Mouse . PubMed: 18802469
  • Ward JO  et al. Mutation in mouse hei10, an e3 ubiquitin ligase, disrupts meiotic crossing over. PLoS Genet 3:e139 (2007). ICC/IF ; Mouse . PubMed: 17784788
  • Dann CT  et al. Heritable and stable gene knockdown in rats. Proc Natl Acad Sci U S A 103:11246-51 (2006). PubMed: 16844779