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
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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
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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
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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).
IHC-P, WB
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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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