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Items: 5

1.

The G-rich Repeats in FMR1 and C9orf72 Loci Are Hotspots for Local Unpairing of DNA.

Abu Diab M, Mor-Shaked H, Cohen E, Cohen-Hadad Y, Ram O, Epsztejn-Litman S, Eiges R.

Genetics. 2018 Dec;210(4):1239-1252. doi: 10.1534/genetics.118.301672. Epub 2018 Nov 5.

PMID:
30396881
2.

Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome.

Mor-Shaked H, Eiges R.

Front Mol Neurosci. 2018 Feb 6;11:31. doi: 10.3389/fnmol.2018.00031. eCollection 2018. Review.

3.

Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells.

Mor-Shaked H, Eiges R.

Genes (Basel). 2016 Sep 28;7(10). pii: E77. Review.

4.

Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cells.

Yanovsky-Dagan S, Mor-Shaked H, Eiges R.

World J Stem Cells. 2015 Jun 26;7(5):823-38. doi: 10.4252/wjsc.v7.i5.823. Review.

5.

FMR1 epigenetic silencing commonly occurs in undifferentiated fragile X-affected embryonic stem cells.

Avitzour M, Mor-Shaked H, Yanovsky-Dagan S, Aharoni S, Altarescu G, Renbaum P, Eldar-Geva T, Schonberger O, Levy-Lahad E, Epsztejn-Litman S, Eiges R.

Stem Cell Reports. 2014 Nov 11;3(5):699-706. doi: 10.1016/j.stemcr.2014.09.001. Epub 2014 Oct 3.

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