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Items: 6

1.

A MutSβ-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice?

Zhao XN, Lokanga R, Allette K, Gazy I, Wu D, Usdin K.

PLoS Genet. 2016 Jul 18;12(7):e1006190. doi: 10.1371/journal.pgen.1006190. eCollection 2016 Jul.

2.

Heterozygosity for a hypomorphic Polβ mutation reduces the expansion frequency in a mouse model of the Fragile X-related disorders.

Lokanga RA, Senejani AG, Sweasy JB, Usdin K.

PLoS Genet. 2015 Apr 17;11(4):e1005181. doi: 10.1371/journal.pgen.1005181. eCollection 2015 Apr.

3.

Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders.

Usdin K, Hayward BE, Kumari D, Lokanga RA, Sciascia N, Zhao XN.

Front Genet. 2014 Jul 17;5:226. doi: 10.3389/fgene.2014.00226. eCollection 2014. Review.

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5.

Somatic expansion in mouse and human carriers of fragile X premutation alleles.

Lokanga RA, Entezam A, Kumari D, Yudkin D, Qin M, Smith CB, Usdin K.

Hum Mutat. 2013 Jan;34(1):157-66. doi: 10.1002/humu.22177. Epub 2012 Oct 4.

6.

Chromatin changes in the development and pathology of the Fragile X-associated disorders and Friedreich ataxia.

Kumari D, Lokanga R, Yudkin D, Zhao XN, Usdin K.

Biochim Biophys Acta. 2012 Jul;1819(7):802-10. doi: 10.1016/j.bbagrm.2011.12.009. Epub 2012 Jan 5. Review.

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