Frankel WN - Search Results

1

A null mutation in inositol polyphosphate 4-phosphatase type I causes selective neuronal loss in weeble mutant mice.

Nystuen A, Legare ME, Shultz LD, Frankel WN. Nystuen A, et al. Among authors: frankel wn. Neuron. 2001 Oct 25;32(2):203-12. doi: 10.1016/s0896-6273(01)00468-8. Neuron. 2001. PMID: 11683991 Free article.

2

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.

3

Mouse strain backgrounds: more than black and white.

Frankel WN. Frankel WN. Neuron. 1998 Feb;20(2):183. doi: 10.1016/s0896-6273(00)80447-x. Neuron. 1998. PMID: 9491980 Free article. No abstract available.

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: frankel wn. Neuron. 1998 Dec;21(6):1327-37. doi: 10.1016/s0896-6273(00)80652-2. Neuron. 1998. PMID: 9883726 Free article.

5

Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice.

Cox GA, Lutz CM, Yang CL, Biemesderfer D, Bronson RT, Fu A, Aronson PS, Noebels JL, Frankel WN. Cox GA, et al. Among authors: frankel wn. Cell. 1997 Oct 3;91(1):139-48. doi: 10.1016/s0092-8674(01)80016-7. Cell. 1997. PMID: 9335342 Free article.

6

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

7

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.

8

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.

9

Mouse mutagenesis is 'in'. Sharing experience and resources in large-scale functional genomics: mutagenesis of the mouse genome, Georgia Genetics Symposium II, Athens, Georgia, 6-9 September 2000.

Frankel WN. Frankel WN. Trends Genet. 2000 Dec;16(12):540. doi: 10.1016/s0168-9525(00)02148-x. Trends Genet. 2000. PMID: 11188368 No abstract available.

10

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

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