Yoo JW - Search Results

1

Kv1.1 potassium channel deficiency reveals brain-driven cardiac dysfunction as a candidate mechanism for sudden unexplained death in epilepsy.

Glasscock E, Yoo JW, Chen TT, Klassen TL, Noebels JL. Glasscock E, et al. Among authors: yoo jw. J Neurosci. 2010 Apr 14;30(15):5167-75. doi: 10.1523/JNEUROSCI.5591-09.2010. J Neurosci. 2010. PMID: 20392939 Free PMC article.

2

Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.

Goldman AM, Glasscock E, Yoo J, Chen TT, Klassen TL, Noebels JL. Goldman AM, et al. Sci Transl Med. 2009 Oct 14;1(2):2ra6. doi: 10.1126/scitranslmed.3000289. Sci Transl Med. 2009. PMID: 20368164 Free PMC article.

3

Masking epilepsy by combining two epilepsy genes.

Glasscock E, Qian J, Yoo JW, Noebels JL. Glasscock E, et al. Among authors: yoo jw. Nat Neurosci. 2007 Dec;10(12):1554-8. doi: 10.1038/nn1999. Epub 2007 Nov 4. Nat Neurosci. 2007. PMID: 17982453

4

Genetic enhancement of thalamocortical network activity by elevating alpha 1g-mediated low-voltage-activated calcium current induces pure absence epilepsy.

Ernst WL, Zhang Y, Yoo JW, Ernst SJ, Noebels JL. Ernst WL, et al. Among authors: yoo jw. J Neurosci. 2009 Feb 11;29(6):1615-25. doi: 10.1523/JNEUROSCI.2081-08.2009. J Neurosci. 2009. PMID: 19211869 Free PMC article.

5

A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment.

Price MG, Yoo JW, Burgess DL, Deng F, Hrachovy RA, Frost JD Jr, Noebels JL. Price MG, et al. Among authors: yoo jw. J Neurosci. 2009 Jul 8;29(27):8752-63. doi: 10.1523/JNEUROSCI.0915-09.2009. J Neurosci. 2009. PMID: 19587282 Free PMC article.

6

Knockout of Zn transporters Zip-1 and Zip-3 attenuates seizure-induced CA1 neurodegeneration.

Qian J, Xu K, Yoo J, Chen TT, Andrews G, Noebels JL. Qian J, et al. J Neurosci. 2011 Jan 5;31(1):97-104. doi: 10.1523/JNEUROSCI.5162-10.2011. J Neurosci. 2011. PMID: 21209194 Free PMC article.

7

MeCP2 is critical within HoxB1-derived tissues of mice for normal lifespan.

Ward CS, Arvide EM, Huang TW, Yoo J, Noebels JL, Neul JL. Ward CS, et al. J Neurosci. 2011 Jul 13;31(28):10359-70. doi: 10.1523/JNEUROSCI.0057-11.2011. J Neurosci. 2011. PMID: 21753013 Free PMC article.

8

Genetic suppression of transgenic APP rescues Hypersynchronous network activity in a mouse model of Alzeimer's disease.

Born HA, Kim JY, Savjani RR, Das P, Dabaghian YA, Guo Q, Yoo JW, Schuler DR, Cirrito JR, Zheng H, Golde TE, Noebels JL, Jankowsky JL. Born HA, et al. Among authors: yoo jw. J Neurosci. 2014 Mar 12;34(11):3826-40. doi: 10.1523/JNEUROSCI.5171-13.2014. J Neurosci. 2014. PMID: 24623762 Free PMC article.

9

Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.

Bi W, Yan J, Shi X, Yuva-Paylor LA, Antalffy BA, Goldman A, Yoo JW, Noebels JL, Armstrong DL, Paylor R, Lupski JR. Bi W, et al. Among authors: yoo jw. Hum Mol Genet. 2007 Aug 1;16(15):1802-13. doi: 10.1093/hmg/ddm128. Epub 2007 May 21. Hum Mol Genet. 2007. PMID: 17517686

10

Delayed postnatal loss of P/Q-type calcium channels recapitulates the absence epilepsy, dyskinesia, and ataxia phenotypes of genomic Cacna1a mutations.

Mark MD, Maejima T, Kuckelsberg D, Yoo JW, Hyde RA, Shah V, Gutierrez D, Moreno RL, Kruse W, Noebels JL, Herlitze S. Mark MD, et al. Among authors: yoo jw. J Neurosci. 2011 Mar 16;31(11):4311-26. doi: 10.1523/JNEUROSCI.5342-10.2011. J Neurosci. 2011. PMID: 21411672 Free PMC article.

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