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Items: 1 to 20 of 32


Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome.

Xie N, Gong H, Suhl JA, Chopra P, Wang T, Warren ST.

PLoS One. 2016 Oct 21;11(10):e0165499. doi: 10.1371/journal.pone.0165499. eCollection 2016.


Where Environment Meets Cognition: A Focus on Two Developmental Intellectual Disability Disorders.

Toma ID, Gil LM, Ossowski S, Dierssen M.

Neural Plast. 2016;2016:4235898. doi: 10.1155/2016/4235898. Epub 2016 Jul 28. Review.


Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells.

Tabolacci E, Mancano G, Lanni S, Palumbo F, Goracci M, Ferrè F, Helmer-Citterich M, Neri G.

Epigenetics Chromatin. 2016 Mar 24;9:12. doi: 10.1186/s13072-016-0060-x. eCollection 2016.


Human pluripotent stem cell models of Fragile X syndrome.

Bhattacharyya A, Zhao X.

Mol Cell Neurosci. 2016 Jun;73:43-51. doi: 10.1016/j.mcn.2015.11.011. Epub 2015 Nov 27. Review.


Bromodomain inhibitors regulate the C9ORF72 locus in ALS.

Zeier Z, Esanov R, Belle KC, Volmar CH, Johnstone AL, Halley P, DeRosa BA, Khoury N, van Blitterswijk M, Rademakers R, Albert J, Brothers SP, Wuu J, Dykxhoorn DM, Benatar M, Wahlestedt C.

Exp Neurol. 2015 Sep;271:241-50. doi: 10.1016/j.expneurol.2015.06.017. Epub 2015 Jun 20.


Repeat-mediated epigenetic dysregulation of the FMR1 gene in the fragile X-related disorders.

Usdin K, Kumari D.

Front Genet. 2015 Jun 3;6:192. doi: 10.3389/fgene.2015.00192. eCollection 2015. Review.


Sirtuins in epigenetic regulation.

Jing H, Lin H.

Chem Rev. 2015 Mar 25;115(6):2350-75. doi: 10.1021/cr500457h. Epub 2015 Jan 28. Review. No abstract available.


The promise and perils of HDAC inhibitors in neurodegeneration.

Didonna A, Opal P.

Ann Clin Transl Neurol. 2015 Jan;2(1):79-101. doi: 10.1002/acn3.147. Epub 2014 Dec 3. Review.


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.


Polycomb group complexes are recruited to reactivated FMR1 alleles in Fragile X syndrome in response to FMR1 transcription.

Kumari D, Usdin K.

Hum Mol Genet. 2014 Dec 15;23(24):6575-83. doi: 10.1093/hmg/ddu378. Epub 2014 Jul 23.


Epigenetic-based therapies for Friedreich ataxia.

Sandi C, Sandi M, Anjomani Virmouni S, Al-Mahdawi S, Pook MA.

Front Genet. 2014 Jun 3;5:165. doi: 10.3389/fgene.2014.00165. eCollection 2014. Review.


A quantitative homogeneous assay for fragile X mental retardation 1 protein.

Schutzius G, Bleckmann D, Kapps-Fouthier S, di Giorgio F, Gerhartz B, Weiss A.

J Neurodev Disord. 2013 Apr 2;5(1):8. doi: 10.1186/1866-1955-5-8.


Epigenetics in Friedreich's Ataxia: Challenges and Opportunities for Therapy.

Sandi C, Al-Mahdawi S, Pook MA.

Genet Res Int. 2013;2013:852080. doi: 10.1155/2013/852080. Epub 2013 Feb 19.


Transcription elongation and tissue-specific somatic CAG instability.

Goula AV, Stys A, Chan JP, Trottier Y, Festenstein R, Merienne K.

PLoS Genet. 2012;8(11):e1003051. doi: 10.1371/journal.pgen.1003051. Epub 2012 Nov 29.


Sirtuin activators and inhibitors.

Villalba JM, Alcaín FJ.

Biofactors. 2012 Sep-Oct;38(5):349-59. doi: 10.1002/biof.1032. Epub 2012 Jun 25. Review.


The role of histone acetylation in memory formation and cognitive impairments.

Peixoto L, Abel T.

Neuropsychopharmacology. 2013 Jan;38(1):62-76. doi: 10.1038/npp.2012.86. Epub 2012 Jun 6. Review.


Epigenetics in nucleotide repeat expansion disorders.

He F, Todd PK.

Semin Neurol. 2011 Nov;31(5):470-83. doi: 10.1055/s-0031-1299786. Epub 2012 Jan 21. Review.


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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