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Items: 4

1.

Activity-dependent aberrations in gene expression and alternative splicing in a mouse model of Rett syndrome.

Osenberg S, Karten A, Sun J, Li J, Charkowick S, Felice CA, Kritzer M, Nguyen MVC, Yu P, Ballas N.

Proc Natl Acad Sci U S A. 2018 Jun 5;115(23):E5363-E5372. doi: 10.1073/pnas.1722546115. Epub 2018 May 16.

2.

Acute and crucial requirement for MeCP2 function upon transition from early to late adult stages of brain maturation.

Du F, Nguyen MV, Karten A, Felice CA, Mandel G, Ballas N.

Hum Mol Genet. 2016 May 1;25(9):1690-702. doi: 10.1093/hmg/ddw038. Epub 2016 Feb 16.

3.

Oligodendrocyte lineage cells contribute unique features to Rett syndrome neuropathology.

Nguyen MV, Felice CA, Du F, Covey MV, Robinson JK, Mandel G, Ballas N.

J Neurosci. 2013 Nov 27;33(48):18764-74. doi: 10.1523/JNEUROSCI.2657-13.2013.

4.

MeCP2 is critical for maintaining mature neuronal networks and global brain anatomy during late stages of postnatal brain development and in the mature adult brain.

Nguyen MV, Du F, Felice CA, Shan X, Nigam A, Mandel G, Robinson JK, Ballas N.

J Neurosci. 2012 Jul 18;32(29):10021-34. doi: 10.1523/JNEUROSCI.1316-12.2012.

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