Publishing research using ab70270? Please let us know so that we can cite the reference in this datasheet.

ab70270 has been referenced in 7 publications.

  • Zhou Y  et al. CGG-repeat dynamics and FMR1 gene silencing in fragile X syndrome stem cells and stem cell-derived neurons. Mol Autism 7:42 (2016). WB ; Human . PubMed: 27713816
  • Zhao XN  et al. A MutSß-Dependent Contribution of MutSa to Repeat Expansions in Fragile X Premutation Mice? PLoS Genet 12:e1006190 (2016). WB ; Mouse . PubMed: 27427765
  • Liu S  et al. Okazaki fragment maturation involves a-segment error editing by the mammalian FEN1/MutSa functional complex. EMBO J 34:1829-43 (2015). PubMed: 25921062
  • Adihe Lokanga R  et al. X inactivation plays a major role in the gender bias in somatic expansion in a mouse model of the fragile X-related disorders: implications for the mechanism of repeat expansion. Hum Mol Genet N/A:N/A (2014). WB ; Mouse . PubMed: 24858908
  • Lokanga RA  et al. Somatic expansion in mouse and human carriers of fragile X premutation alleles. Hum Mutat 34:157-66 (2013). PubMed: 22887750
  • Kovalenko M  et al. Msh2 acts in medium-spiny striatal neurons as an enhancer of CAG instability and mutant huntingtin phenotypes in Huntington's disease knock-in mice. PLoS One 7:e44273 (2012). WB, IHC-P ; Mouse . PubMed: 22970194
  • Ghosh S  et al. Nonhematopoietic Nrf2 dominantly impedes adult progression of sickle cell anemia in mice. JCI Insight 1:N/A (0). PubMed: 27158670

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