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Etiology of a genetically complex seizure disorder in Celf4 mutant mice.
Wagnon JL, Mahaffey CL, Sun W, Yang Y, Chao HT, Frankel WN. Wagnon JL, et al. Among authors: frankel wn. Genes Brain Behav. 2011 Oct;10(7):765-77. doi: 10.1111/j.1601-183X.2011.00717.x. Epub 2011 Aug 3. Genes Brain Behav. 2011. PMID: 21745337 Free PMC article.
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: frankel wn. Nat Genet. 1998 Aug;19(4):340-7. doi: 10.1038/1228. Nat Genet. 1998. PMID: 9697694
Szt2, a novel gene for seizure threshold in mice.
Frankel WN, Yang Y, Mahaffey CL, Beyer BJ, O'Brien TP. Frankel WN, et al. 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.
Genetic complexity of absence seizures in substrains of C3H mice.
Tokuda S, Beyer BJ, Frankel WN. Tokuda S, et al. Among authors: frankel wn. Genes Brain Behav. 2009 Apr;8(3):283-9. doi: 10.1111/j.1601-183X.2008.00472.x. Epub 2009 Dec 17. Genes Brain Behav. 2009. PMID: 19170754 Free PMC article.
Mouse models for the Wolf-Hirschhorn deletion syndrome.
Näf D, Wilson LA, Bergstrom RA, Smith RS, Goodwin NC, Verkerk A, van Ommen GJ, Ackerman SL, Frankel WN, Schimenti JC. Näf D, et al. Among authors: frankel wn. Hum Mol Genet. 2001 Jan 15;10(2):91-8. doi: 10.1093/hmg/10.2.91. Hum Mol Genet. 2001. PMID: 11152656
155 results