Blendy JA - Search Results

1

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: blendy ja. 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.

2

Loss of signaling through the G protein, Gz, results in abnormal platelet activation and altered responses to psychoactive drugs.

Yang J, Wu J, Kowalska MA, Dalvi A, Prevost N, O'Brien PJ, Manning D, Poncz M, Lucki I, Blendy JA, Brass LF. Yang J, et al. Among authors: blendy ja. Proc Natl Acad Sci U S A. 2000 Aug 29;97(18):9984-9. doi: 10.1073/pnas.180194597. Proc Natl Acad Sci U S A. 2000. PMID: 10954748 Free PMC article.

3

Pharmacogenomic evaluation of the antidepressant citalopram in the mouse tail suspension test.

Crowley JJ, Brodkin ES, Blendy JA, Berrettini WH, Lucki I. Crowley JJ, et al. Among authors: blendy ja. Neuropsychopharmacology. 2006 Nov;31(11):2433-42. doi: 10.1038/sj.npp.1301065. Epub 2006 Mar 22. Neuropsychopharmacology. 2006. PMID: 16554742

4

Mouse model of OPRM1 (A118G) polymorphism has sex-specific effects on drug-mediated behavior.

Mague SD, Isiegas C, Huang P, Liu-Chen LY, Lerman C, Blendy JA. Mague SD, et al. Among authors: blendy ja. Proc Natl Acad Sci U S A. 2009 Jun 30;106(26):10847-52. doi: 10.1073/pnas.0901800106. Epub 2009 Jun 15. Proc Natl Acad Sci U S A. 2009. PMID: 19528658 Free PMC article.

5

Assessment of NMDA receptor NR1 subunit hypofunction in mice as a model for schizophrenia.

Halene TB, Ehrlichman RS, Liang Y, Christian EP, Jonak GJ, Gur TL, Blendy JA, Dow HC, Brodkin ES, Schneider F, Gur RC, Siegel SJ. Halene TB, et al. Among authors: blendy ja. Genes Brain Behav. 2009 Oct;8(7):661-75. doi: 10.1111/j.1601-183X.2009.00504.x. Epub 2009 May 8. Genes Brain Behav. 2009. PMID: 19563516 Free PMC article.

6

Decreased CREB levels suppress epilepsy.

Zhu X, Han X, Blendy JA, Porter BE. Zhu X, et al. Among authors: blendy ja. Neurobiol Dis. 2012 Jan;45(1):253-63. doi: 10.1016/j.nbd.2011.08.009. Epub 2011 Aug 10. Neurobiol Dis. 2012. PMID: 21867753 Free PMC article.

7

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. Among authors: blendy ja. Nat Neurosci. 2011 Nov 27;15(2):274-83. doi: 10.1038/nn.2997. Nat Neurosci. 2011. PMID: 22119903 Free PMC article.

8

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. Among authors: blendy ja. 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.

9

Mouse model of OPRM1 (A118G) polymorphism increases sociability and dominance and confers resilience to social defeat.

Briand LA, Hilario M, Dow HC, Brodkin ES, Blendy JA, Berton O. Briand LA, et al. Among authors: blendy ja. J Neurosci. 2015 Feb 25;35(8):3582-90. doi: 10.1523/JNEUROSCI.4685-14.2015. J Neurosci. 2015. PMID: 25716856 Free PMC article.

10

Tagging methyl-CpG-binding domain proteins reveals different spatiotemporal expression and supports distinct functions.

Wood KH, Johnson BS, Welsh SA, Lee JY, Cui Y, Krizman E, Brodkin ES, Blendy JA, Robinson MB, Bartolomei MS, Zhou Z. Wood KH, et al. Among authors: blendy ja. Epigenomics. 2016 Apr;8(4):455-73. doi: 10.2217/epi-2015-0004. Epub 2016 Apr 12. Epigenomics. 2016. PMID: 27066839 Free PMC article.

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