CELF4 regulates translation and local abundance of a vast set of mRNAs, including genes associated with regulation of synaptic function
Wagnon, Jacy L, Briese, Michael, Sun, Wenzhi, Mahaffey, Connie L, Curk, Tomaž, Rot, Gregor, Ule, Jernej, Frankel, Wayne N
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Published in PLoS genetics (01.11.2012)
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A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice
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Unraveling genetic modifiers in the gria4 mouse model of absence epilepsy
Frankel, Wayne N, Mahaffey, Connie L, McGarr, Tracy C, Beyer, Barbara J, Letts, Verity A
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Complex seizure disorder caused by Brunol4 deficiency in mice
Yang, Yan, Mahaffey, Connie L, Bérubé, Nathalie, Maddatu, Terry P, Cox, Gregory A, Frankel, Wayne N
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Identification of the Mouse Neuromuscular Degeneration Gene and Mapping of a Second Site Suppressor Allele
Cox, Gregory A, Mahaffey, Connie L, Frankel, Wayne N
Published in Neuron (Cambridge, Mass.) (01.12.1998)
Published in Neuron (Cambridge, Mass.) (01.12.1998)
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Aberrant sodium channel activity in the complex seizure disorder of Celf4 mutant mice
Sun, Wenzhi, Wagnon, Jacy L., Mahaffey, Connie L., Briese, Michael, Ule, Jernej, Frankel, Wayne N.
Published in The Journal of physiology (01.01.2013)
Published in The Journal of physiology (01.01.2013)
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Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4
Beyer, Barbara, Deleuze, Charlotte, Letts, Verity A., Mahaffey, Connie L., Boumil, Rebecca M., Lew, Timothy A., Huguenard, John R., Frankel, Wayne N.
Published in Human molecular genetics (15.06.2008)
Published in Human molecular genetics (15.06.2008)
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A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice
TOKUDA, Satoko, MAHAFFEY, Connie L, MONKS, Bobby, FAULKNER, Christian R, BIRNBAUM, Morris J, DANZER, Steve C, FRANKEL, Wayne N
Published in Human molecular genetics (01.03.2011)
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Fierce: a new mouse deletion of Nr2e1; violent behaviour and ocular abnormalities are background-dependent
Young, Kelly A, Berry, Melissa L, Mahaffey, Connie L, Saionz, Jennifer R, Hawes, Norman L, Chang, Bo, Zheng, Qing Yin, Smith, Richard S, Bronson, Roderick T, Nelson, Randy J, Simpson, Elizabeth M
Published in Behavioural brain research (14.05.2002)
Published in Behavioural brain research (14.05.2002)
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The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development
Frankel, Wayne N, Cox, Gregory A, Mahaffey, Connie L, Nystuen, Arne, Letts, Verity A
Published in Nature genetics (01.10.2000)
Published in Nature genetics (01.10.2000)
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Functional characterization of fidgetin, an AAA-family protein mutated in fidget mice
Yang, Yan, Mahaffey, Connie L., Bérubé, Nathalie, Nystuen, Arne, Frankel, Wayne N.
Published in Experimental cell research (10.03.2005)
Published in Experimental cell research (10.03.2005)
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Phenotypic heterogeneity in the stargazin allelic series
Letts, Verity A, Kang, Myoung-Goo, Mahaffey, Connie L, Beyer, Barbara, Tenbrink, Heather, Campbell, Kevin P, Frankel, Wayne N
Published in Mammalian genome (01.08.2003)
Published in Mammalian genome (01.08.2003)
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Unraveling Genetic Modifiers in the Gria4 Mouse Model of Absence Epilepsy: e1004454
Frankel, Wayne N, Mahaffey, Connie L, McGarr, Tracy C, Beyer, Barbara J, Letts, Verity A
Published in PLoS genetics (01.07.2014)
Published in PLoS genetics (01.07.2014)
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The mouse stargazer gene encodes a neuronal Ca2+-channel γ subunit
LETTS, V. A, FELIX, R, BIDDLECOME, G. H, ARIKKATH, J, MAHAFFEY, C. L, VALENZUELA, A, BARTLETT, F. S, MORI, Y, CAMPBELL, K. P, FRANKEL, W. N
Published in Nature genetics (01.08.1998)
Published in Nature genetics (01.08.1998)
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Etiology of a genetically complex seizure disorder in Celf4 mutant mice
Wagnon, J. L., Mahaffey, C. L., Sun, W., Yang, Y., Chao, H.‐T., Frankel, W. N.
Published in Genes, brain and behavior (01.10.2011)
Published in Genes, brain and behavior (01.10.2011)
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Szt2, a novel gene for seizure threshold in mice
Frankel, W. N., Yang, Y., Mahaffey, C. L., Beyer, B. J., O'Brien, T. P.
Published in Genes, brain and behavior (01.07.2009)
Published in Genes, brain and behavior (01.07.2009)
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A Missense Mutation in a Highly Conserved Alternate Exon of Dynamin-1 Causes Epilepsy in Fitful Mice: e1001046
Boumil, Rebecca M, Letts, Verity A, Roberts, Monica C, Lenz, Christine, Mahaffey, Connie L, Zhang, Zhong-wei, Moser, Tobias, Frankel, Wayne N
Published in PLoS genetics (01.08.2010)
Published in PLoS genetics (01.08.2010)
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