Goffin D - Search Results

1

Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses.

Goffin D, Allen M, Zhang L, Amorim M, Wang IT, Reyes AR, Mercado-Berton A, Ong C, Cohen S, Hu L, Blendy JA, Carlson GC, Siegel SJ, Greenberg ME, Zhou Z. Goffin D, et al. Nat Neurosci. 2011 Nov 27;15(2):274-83. doi: 10.1038/nn.2997. Nat Neurosci. 2011. PMID: 22119903 Free PMC article.

2

Loss of CDKL5 disrupts kinome profile and event-related potentials leading to autistic-like phenotypes in mice.

Wang IT, Allen M, Goffin D, Zhu X, Fairless AH, Brodkin ES, Siegel SJ, Marsh ED, Blendy JA, Zhou Z. Wang IT, et al. Among authors: goffin d. Proc Natl Acad Sci U S A. 2012 Dec 26;109(52):21516-21. doi: 10.1073/pnas.1216988110. Epub 2012 Dec 10. Proc Natl Acad Sci U S A. 2012. PMID: 23236174 Free PMC article.

3

Cellular origins of auditory event-related potential deficits in Rett syndrome.

Goffin D, Brodkin ES, Blendy JA, Siegel SJ, Zhou Z. Goffin D, et al. Nat Neurosci. 2014 Jun;17(6):804-6. doi: 10.1038/nn.3710. Epub 2014 Apr 28. Nat Neurosci. 2014. PMID: 24777420 Free PMC article.

4

The neural circuit basis of Rett syndrome.

Goffin D, Zhou ZJ. Goffin D, et al. Front Biol (Beijing). 2012 Oct;7(5):428-435. doi: 10.1007/s11515-012-1248-5. Front Biol (Beijing). 2012. PMID: 24999353 Free PMC article.

5

Loss of MeCP2 function is associated with distinct gene expression changes in the striatum.

Zhao YT, Goffin D, Johnson BS, Zhou Z. Zhao YT, et al. Among authors: goffin d. Neurobiol Dis. 2013 Nov;59:257-66. doi: 10.1016/j.nbd.2013.08.001. Epub 2013 Aug 13. Neurobiol Dis. 2013. PMID: 23948639 Free PMC article.

6

Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome.

Johnson BS, Zhao YT, Fasolino M, Lamonica JM, Kim YJ, Georgakilas G, Wood KH, Bu D, Cui Y, Goffin D, Vahedi G, Kim TH, Zhou Z. Johnson BS, et al. Among authors: goffin d. Nat Med. 2017 Oct;23(10):1203-1214. doi: 10.1038/nm.4406. Epub 2017 Sep 18. Nat Med. 2017. PMID: 28920956 Free PMC article.

7

Elevating expression of MeCP2 T158M rescues DNA binding and Rett syndrome-like phenotypes.

Lamonica JM, Kwon DY, Goffin D, Fenik P, Johnson BS, Cui Y, Guo H, Veasey S, Zhou Z. Lamonica JM, et al. Among authors: goffin d. J Clin Invest. 2017 May 1;127(5):1889-1904. doi: 10.1172/JCI90967. Epub 2017 Apr 10. J Clin Invest. 2017. PMID: 28394263 Free PMC article.

8

Dopamine-dependent tuning of striatal inhibitory synaptogenesis.

Goffin D, Ali AB, Rampersaud N, Harkavyi A, Fuchs C, Whitton PS, Nairn AC, Jovanovic JN. Goffin D, et al. J Neurosci. 2010 Feb 24;30(8):2935-50. doi: 10.1523/JNEUROSCI.4411-09.2010. J Neurosci. 2010. PMID: 20181591 Free PMC article.

9

GABAA receptor activity shapes the formation of inhibitory synapses between developing medium spiny neurons.

Arama J, Abitbol K, Goffin D, Fuchs C, Sihra TS, Thomson AM, Jovanovic JN. Arama J, et al. Among authors: goffin d. Front Cell Neurosci. 2015 Aug 6;9:290. doi: 10.3389/fncel.2015.00290. eCollection 2015. Front Cell Neurosci. 2015. PMID: 26300728 Free PMC article.

10

D1-like dopamine receptors regulate GABAA receptor function to modulate hippocampal neural progenitor cell proliferation.

Goffin D, Aarum J, Schroeder JE, Jovanovic JN, Chuang TT. Goffin D, et al. J Neurochem. 2008 Nov;107(4):964-75. doi: 10.1111/j.1471-4159.2008.05679.x. J Neurochem. 2008. PMID: 19006818 Free article.

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