Escayg A - Search Results

1

Sodium channels and neurological disease: insights from Scn8a mutations in the mouse.

Meisler MH, Kearney J, Escayg A, MacDonald BT, Sprunger LK. Meisler MH, et al. Among authors: escayg a. Neuroscientist. 2001 Apr;7(2):136-45. doi: 10.1177/107385840100700208. Neuroscientist. 2001. PMID: 11496924 Review.

2

Ion channel mutations in mouse models of inherited neurological disease.

Meisler MH, Sprunger LK, Plummer NW, Escayg A, Jones JM. Meisler MH, et al. Among authors: escayg a. Ann Med. 1997 Dec;29(6):569-74. doi: 10.3109/07853899709007484. Ann Med. 1997. PMID: 9562526 Free article. Review.

3

Calcium channel beta 4 (CACNB4): human ortholog of the mouse epilepsy gene lethargic.

Escayg A, Jones JM, Kearney JA, Hitchcock PF, Meisler MH. Escayg A, et al. Genomics. 1998 May 15;50(1):14-22. doi: 10.1006/geno.1998.5311. Genomics. 1998. PMID: 9628818

4

Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3.

Sprunger LK, Escayg A, Tallaksen-Greene S, Albin RL, Meisler MH. Sprunger LK, et al. Among authors: escayg a. Hum Mol Genet. 1999 Mar;8(3):471-9. doi: 10.1093/hmg/8.3.471. Hum Mol Genet. 1999. PMID: 9949206

5

Coding sequence, genomic organization, and conserved chromosomal localization of the mouse gene Scn11a encoding the sodium channel NaN.

Dib-Hajj SD, Tyrrell L, Escayg A, Wood PM, Meisler MH, Waxman SG. Dib-Hajj SD, et al. Among authors: escayg a. Genomics. 1999 Aug 1;59(3):309-18. doi: 10.1006/geno.1999.5890. Genomics. 1999. PMID: 10444332 Free article.

6

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.

Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, Brice A, LeGuern E, Moulard B, Chaigne D, Buresi C, Malafosse A. Escayg A, et al. Nat Genet. 2000 Apr;24(4):343-5. doi: 10.1038/74159. Nat Genet. 2000. PMID: 10742094 No abstract available.

7

The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5a.

Jones JM, Huang JD, Mermall V, Hamilton BA, Mooseker MS, Escayg A, Copeland NG, Jenkins NA, Meisler MH. Jones JM, et al. Among authors: escayg a. Hum Mol Genet. 2000 Mar 22;9(5):821-8. doi: 10.1093/hmg/9.5.821. Hum Mol Genet. 2000. PMID: 10749990

8

Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.

Escayg A, De Waard M, Lee DD, Bichet D, Wolf P, Mayer T, Johnston J, Baloh R, Sander T, Meisler MH. Escayg A, et al. Am J Hum Genet. 2000 May;66(5):1531-9. doi: 10.1086/302909. Epub 2000 Apr 4. Am J Hum Genet. 2000. PMID: 10762541 Free PMC article.

9

A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.

Escayg A, Heils A, MacDonald BT, Haug K, Sander T, Meisler MH. Escayg A, et al. Am J Hum Genet. 2001 Apr;68(4):866-73. doi: 10.1086/319524. Epub 2001 Mar 14. Am J Hum Genet. 2001. PMID: 11254445 Free PMC article.

10

The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate.

Reid E, Escayg A, Dearlove AM, Meisler MH, Rubinsztein DC. Reid E, et al. Among authors: escayg a. J Med Genet. 2001 Jan;38(1):65-7. doi: 10.1136/jmg.38.1.65. J Med Genet. 2001. PMID: 11334010 Free PMC article. No abstract available.

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