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Items: 1 to 20 of 129


Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis.

Dhindsa RS, Bradrick SS, Yao X, Heinzen EL, Petrovski S, Krueger BJ, Johnson MR, Frankel WN, Petrou S, Boumil RM, Goldstein DB.

Neurol Genet. 2015 Apr 17;1(1):e4. doi: 10.1212/01.NXG.0000464295.65736.da. eCollection 2015 Jun.


Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy.

Asinof SK, Sukoff Rizzo SJ, Buckley AR, Beyer BJ, Letts VA, Frankel WN, Boumil RM.

PLoS Genet. 2015 Jun 30;11(6):e1005347. doi: 10.1371/journal.pgen.1005347. eCollection 2015 Jun.


DBA/2J genetic background exacerbates spontaneous lethal seizures but lessens amyloid deposition in a mouse model of Alzheimer's disease.

Jackson HM, Onos KD, Pepper KW, Graham LC, Akeson EC, Byers C, Reinholdt LG, Frankel WN, Howell GR.

PLoS One. 2015 May 1;10(5):e0125897. doi: 10.1371/journal.pone.0125897. eCollection 2015.


SWDreader: a wavelet-based algorithm using spectral phase to characterize spike-wave morphological variation in genetic models of absence epilepsy.

Richard CD, Tanenbaum A, Audit B, Arneodo A, Khalil A, Frankel WN.

J Neurosci Methods. 2015 Mar 15;242:127-40. doi: 10.1016/j.jneumeth.2014.12.016. Epub 2014 Dec 27.


A genetic interaction network model of a complex neurological disease.

Tyler AL, McGarr TC, Beyer BJ, Frankel WN, Carter GW.

Genes Brain Behav. 2014 Nov;13(8):831-40. doi: 10.1111/gbb.12178. Epub 2014 Oct 27.


Unraveling genetic modifiers in the gria4 mouse model of absence epilepsy.

Frankel WN, Mahaffey CL, McGarr TC, Beyer BJ, Letts VA.

PLoS Genet. 2014 Jul 10;10(7):e1004454. doi: 10.1371/journal.pgen.1004454. eCollection 2014 Jul.


Antiepileptic activity of preferential inhibitors of persistent sodium current.

Anderson LL, Thompson CH, Hawkins NA, Nath RD, Petersohn AA, Rajamani S, Bush WS, Frankel WN, Vanoye CG, Kearney JA, George AL Jr.

Epilepsia. 2014 Aug;55(8):1274-83. doi: 10.1111/epi.12657. Epub 2014 May 23.


Hidden in plain sight: spike-wave discharges in mouse inbred strains.

Letts VA, Beyer BJ, Frankel WN.

Genes Brain Behav. 2014 Jul;13(6):519-26. doi: 10.1111/gbb.12142. Epub 2014 Jun 16.


Physiological and genetic analysis of multiple sodium channel variants in a model of genetic absence epilepsy.

Oliva MK, McGarr TC, Beyer BJ, Gazina E, Kaplan DI, Cordeiro L, Thomas E, Dib-Hajj SD, Waxman SG, Frankel WN, Petrou S.

Neurobiol Dis. 2014 Jul;67:180-90. doi: 10.1016/j.nbd.2014.03.007. Epub 2014 Mar 19.


Loss of MeCP2 from forebrain excitatory neurons leads to cortical hyperexcitation and seizures.

Zhang W, Peterson M, Beyer B, Frankel WN, Zhang ZW.

J Neurosci. 2014 Feb 12;34(7):2754-63. doi: 10.1523/JNEUROSCI.4900-12.2014.


Modes and regulation of endocytic membrane retrieval in mouse auditory hair cells.

Neef J, Jung S, Wong AB, Reuter K, Pangrsic T, Chakrabarti R, Kügler S, Lenz C, Nouvian R, Boumil RM, Frankel WN, Wichmann C, Moser T.

J Neurosci. 2014 Jan 15;34(3):705-16. doi: 10.1523/JNEUROSCI.3313-13.2014.


Elevated Id2 expression results in precocious neural stem cell depletion and abnormal brain development.

Park HJ, Hong M, Bronson RT, Israel MA, Frankel WN, Yun K.

Stem Cells. 2013 May;31(5):1010-21. doi: 10.1002/stem.1351.


CELF4 regulates translation and local abundance of a vast set of mRNAs, including genes associated with regulation of synaptic function.

Wagnon JL, Briese M, Sun W, Mahaffey CL, Curk T, Rot G, Ule J, Frankel WN.

PLoS Genet. 2012;8(11):e1003067. doi: 10.1371/journal.pgen.1003067. Epub 2012 Nov 29.


Aberrant sodium channel activity in the complex seizure disorder of Celf4 mutant mice.

Sun W, Wagnon JL, Mahaffey CL, Briese M, Ule J, Frankel WN.

J Physiol. 2013 Jan 1;591(1):241-55. doi: 10.1113/jphysiol.2012.240168. Epub 2012 Oct 22.


The genomic landscape shaped by selection on transposable elements across 18 mouse strains.

Nellåker C, Keane TM, Yalcin B, Wong K, Agam A, Belgard TG, Flint J, Adams DJ, Frankel WN, Ponting CP.

Genome Biol. 2012 Jun 15;13(6):R45. doi: 10.1186/gb-2012-13-6-r45.


A new mode of corticothalamic transmission revealed in the Gria4(-/-) model of absence epilepsy.

Paz JT, Bryant AS, Peng K, Fenno L, Yizhar O, Frankel WN, Deisseroth K, Huguenard JR.

Nat Neurosci. 2011 Aug 21;14(9):1167-73. doi: 10.1038/nn.2896.


Etiology of a genetically complex seizure disorder in Celf4 mutant mice.

Wagnon JL, Mahaffey CL, Sun W, Yang Y, Chao HT, Frankel WN.

Genes Brain Behav. 2011 Oct;10(7):765-77. doi: 10.1111/j.1601-183X.2011.00717.x. Epub 2011 Aug 3.


A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice.

Tokuda S, Mahaffey CL, Monks B, Faulkner CR, Birnbaum MJ, Danzer SC, Frankel WN.

Hum Mol Genet. 2011 Mar 1;20(5):988-99. doi: 10.1093/hmg/ddq544. Epub 2010 Dec 15.


Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.

Hawkins NA, Martin MS, Frankel WN, Kearney JA, Escayg A.

Neurobiol Dis. 2011 Mar;41(3):655-60. doi: 10.1016/j.nbd.2010.11.016. Epub 2010 Dec 13.


A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice.

Boumil RM, Letts VA, Roberts MC, Lenz C, Mahaffey CL, Zhang ZW, Moser T, Frankel WN.

PLoS Genet. 2010 Aug 5;6(8). pii: e1001046. doi: 10.1371/journal.pgen.1001046.

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