Mahaffey CL - Search Results

1

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

Letts VA, Felix R, Biddlecome GH, Arikkath J, Mahaffey CL, Valenzuela A, Bartlett FS 2nd, Mori Y, Campbell KP, Frankel WN. Letts VA, et al. Among authors: mahaffey cl. Nat Genet. 1998 Aug;19(4):340-7. doi: 10.1038/1228. Nat Genet. 1998. PMID: 9697694

2

Phenotypic heterogeneity in the stargazin allelic series.

Letts VA, Kang MG, Mahaffey CL, Beyer B, Tenbrink H, Campbell KP, Frankel WN. Letts VA, et al. Among authors: mahaffey cl. Mamm Genome. 2003 Aug;14(8):506-13. doi: 10.1007/s00335-003-2268-x. Mamm Genome. 2003. PMID: 12925883

3

A targeted mutation in Cacng4 exacerbates spike-wave seizures in stargazer (Cacng2) mice.

Letts VA, Mahaffey CL, Beyer B, Frankel WN. Letts VA, et al. Among authors: mahaffey cl. Proc Natl Acad Sci U S A. 2005 Feb 8;102(6):2123-8. doi: 10.1073/pnas.0409527102. Epub 2005 Jan 26. Proc Natl Acad Sci U S A. 2005. PMID: 15677329 Free PMC article.

4

Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele.

Cox GA, Mahaffey CL, Frankel WN. Cox GA, et al. Among authors: mahaffey cl. Neuron. 1998 Dec;21(6):1327-37. doi: 10.1016/s0896-6273(00)80652-2. Neuron. 1998. PMID: 9883726 Free article.

5

The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development.

Cox GA, Mahaffey CL, Nystuen A, Letts VA, Frankel WN. Cox GA, et al. Among authors: mahaffey cl. Nat Genet. 2000 Oct;26(2):198-202. doi: 10.1038/79923. Nat Genet. 2000. PMID: 11017077

6

Complex seizure disorder caused by Brunol4 deficiency in mice.

Yang Y, Mahaffey CL, Bérubé N, Maddatu TP, Cox GA, Frankel WN. Yang Y, et al. Among authors: mahaffey cl. PLoS Genet. 2007 Jul;3(7):e124. doi: 10.1371/journal.pgen.0030124. PLoS Genet. 2007. PMID: 17677002 Free PMC article.

7

Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4.

Beyer B, Deleuze C, Letts VA, Mahaffey CL, Boumil RM, Lew TA, Huguenard JR, Frankel WN. Beyer B, et al. Among authors: mahaffey cl. Hum Mol Genet. 2008 Jun 15;17(12):1738-49. doi: 10.1093/hmg/ddn064. Epub 2008 Mar 3. Hum Mol Genet. 2008. PMID: 18316356 Free PMC article.

8

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. Boumil RM, et al. Among authors: mahaffey cl. PLoS Genet. 2010 Aug 5;6(8):e1001046. doi: 10.1371/journal.pgen.1001046. PLoS Genet. 2010. PMID: 20700442 Free PMC article.

9

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

Frankel WN, Mahaffey CL, McGarr TC, Beyer BJ, Letts VA. Frankel WN, et al. Among authors: mahaffey cl. PLoS Genet. 2014 Jul 10;10(7):e1004454. doi: 10.1371/journal.pgen.1004454. eCollection 2014 Jul. PLoS Genet. 2014. PMID: 25010494 Free PMC article.

10

Szt2, a novel gene for seizure threshold in mice.

Frankel WN, Yang Y, Mahaffey CL, Beyer BJ, O'Brien TP. Frankel WN, et al. Among authors: mahaffey cl. Genes Brain Behav. 2009 Jul;8(5):568-76. doi: 10.1111/j.1601-183X.2009.00509.x. Genes Brain Behav. 2009. PMID: 19624305 Free PMC article.

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