Frankel WN - Search Results

1

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.

2

Genetic epilepsy model derived from common inbred mouse strains.

Frankel WN, Taylor BA, Noebels JL, Lutz CM. Frankel WN, et al. Genetics. 1994 Oct;138(2):481-9. doi: 10.1093/genetics/138.2.481. Genetics. 1994. PMID: 7828829 Free PMC article.

3

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: frankel wn. PLoS Genet. 2007 Jul;3(7):e124. doi: 10.1371/journal.pgen.0030124. PLoS Genet. 2007. PMID: 17677002 Free PMC article.

4

New seizure frequency QTL and the complex genetics of epilepsy in EL mice.

Frankel WN, Valenzuela A, Lutz CM, Johnson EW, Dietrich WF, Coffin JM. Frankel WN, et al. Mamm Genome. 1995 Dec;6(12):830-8. doi: 10.1007/BF00292431. Mamm Genome. 1995. PMID: 8747920

5

Congenic strains reveal effects of the epilepsy quantitative trait locus, El2, separate from other El loci.

Frankel WN, Johnson EW, Lutz CM. Frankel WN, et al. Mamm Genome. 1995 Dec;6(12):839-43. doi: 10.1007/BF00292432. Mamm Genome. 1995. PMID: 8747921

6

Absence epilepsy in tottering mutant mice is associated with calcium channel defects.

Fletcher CF, Lutz CM, O'Sullivan TN, Shaughnessy JD Jr, Hawkes R, Frankel WN, Copeland NG, Jenkins NA. Fletcher CF, et al. Among authors: frankel wn. Cell. 1996 Nov 15;87(4):607-17. doi: 10.1016/s0092-8674(00)81381-1. Cell. 1996. PMID: 8929530 Free article.

7

Neuropeptide Y receptor genes on human chromosome 4q31-q32 map to conserved linkage groups on mouse chromosomes 3 and 8.

Lutz CM, Frankel WN, Richards JE, Thompson DA. Lutz CM, et al. Among authors: frankel wn. Genomics. 1997 May 1;41(3):498-500. doi: 10.1006/geno.1997.4698. Genomics. 1997. PMID: 9169155

8

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.

9

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: frankel wn. Nat Genet. 2000 Oct;26(2):198-202. doi: 10.1038/79923. Nat Genet. 2000. PMID: 11017077

10

Reduced GABAergic Neuron Excitability, Altered Synaptic Connectivity, and Seizures in a KCNT1 Gain-of-Function Mouse Model of Childhood Epilepsy.

Shore AN, Colombo S, Tobin WF, Petri S, Cullen ER, Dominguez S, Bostick CD, Beaumont MA, Williams D, Khodagholy D, Yang M, Lutz CM, Peng Y, Gelinas JN, Goldstein DB, Boland MJ, Frankel WN, Weston MC. Shore AN, et al. Among authors: frankel wn. Cell Rep. 2020 Oct 27;33(4):108303. doi: 10.1016/j.celrep.2020.108303. Cell Rep. 2020. PMID: 33113364 Free PMC article.

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