Cox GA - 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. Cell. 1997 Oct 3;91(1):139-48. doi: 10.1016/s0092-8674(01)80016-7. Cell. 1997. PMID: 9335342 Free article.

2

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

3

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

4

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

5

The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titin.

Garvey SM, Rajan C, Lerner AP, Frankel WN, Cox GA. Garvey SM, et al. Among authors: cox ga. Genomics. 2002 Feb;79(2):146-9. doi: 10.1006/geno.2002.6685. Genomics. 2002. PMID: 11829483

6

A rostrocaudal muscular dystrophy caused by a defect in choline kinase beta, the first enzyme in phosphatidylcholine biosynthesis.

Sher RB, Aoyama C, Huebsch KA, Ji S, Kerner J, Yang Y, Frankel WN, Hoppel CL, Wood PA, Vance DE, Cox GA. Sher RB, et al. Among authors: cox ga. J Biol Chem. 2006 Feb 24;281(8):4938-48. doi: 10.1074/jbc.M512578200. Epub 2005 Dec 21. J Biol Chem. 2006. PMID: 16371353 Free article.

7

Gait analysis detects early changes in transgenic SOD1(G93A) mice.

Wooley CM, Sher RB, Kale A, Frankel WN, Cox GA, Seburn KL. Wooley CM, et al. Among authors: cox ga. Muscle Nerve. 2005 Jul;32(1):43-50. doi: 10.1002/mus.20228. Muscle Nerve. 2005. PMID: 15880561 Free PMC article.

8

Effect of genetic background on the dystrophic phenotype in mdx mice.

Coley WD, Bogdanik L, Vila MC, Yu Q, Van Der Meulen JH, Rayavarapu S, Novak JS, Nearing M, Quinn JL, Saunders A, Dolan C, Andrews W, Lammert C, Austin A, Partridge TA, Cox GA, Lutz C, Nagaraju K. Coley WD, et al. Among authors: cox ga. Hum Mol Genet. 2016 Jan 1;25(1):130-45. doi: 10.1093/hmg/ddv460. Epub 2015 Nov 12. Hum Mol Genet. 2016. PMID: 26566673 Free PMC article.

9

From ER to Eph receptors: new roles for VAP fragments.

Ackerman SL, Cox GA. Ackerman SL, et al. Among authors: cox ga. Cell. 2008 Jun 13;133(6):949-51. doi: 10.1016/j.cell.2008.05.028. Cell. 2008. PMID: 18555770 Free article.

10

Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes.

Morelli KH, Seburn KL, Schroeder DG, Spaulding EL, Dionne LA, Cox GA, Burgess RW. Morelli KH, et al. Among authors: cox ga. Cell Rep. 2017 Mar 28;18(13):3178-3191. doi: 10.1016/j.celrep.2017.03.009. Cell Rep. 2017. PMID: 28355569 Free PMC article.

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