Meisler MH - Search Results

1

De novo exon duplication in a new allele of mouse Glra1 (spasmodic).

Holland KD, Fleming MT, Cheek S, Moran JL, Beier DR, Meisler MH. Holland KD, et al. Among authors: meisler mh. Genetics. 2006 Dec;174(4):2245-7. doi: 10.1534/genetics.106.065532. Epub 2006 Oct 8. Genetics. 2006. PMID: 17028313 Free PMC article.

2

Insertional mutation on mouse chromosome 18 with vestibular and craniofacial abnormalities.

Ting CN, Kohrman D, Burgess DL, Boyle A, Altschuler RA, Gholizadeh G, Samuelson LC, Jang W, Meisler MH. Ting CN, et al. Among authors: meisler mh. Genetics. 1994 Jan;136(1):247-54. doi: 10.1093/genetics/136.1.247. Genetics. 1994. PMID: 7511123 Free PMC article.

3

Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'.

Burgess DL, Kohrman DC, Galt J, Plummer NW, Jones JM, Spear B, Meisler MH. Burgess DL, et al. Among authors: meisler mh. Nat Genet. 1995 Aug;10(4):461-5. doi: 10.1038/ng0895-461. Nat Genet. 1995. PMID: 7670495

4

Mouse Brca1: localization sequence analysis and identification of evolutionarily conserved domains.

Abel KJ, Xu J, Yin GY, Lyons RH, Meisler MH, Weber BL. Abel KJ, et al. Among authors: meisler mh. Hum Mol Genet. 1995 Dec;4(12):2265-73. doi: 10.1093/hmg/4.12.2265. Hum Mol Genet. 1995. PMID: 8634697

5

Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron.

Kohrman DC, Harris JB, Meisler MH. Kohrman DC, et al. Among authors: meisler mh. J Biol Chem. 1996 Jul 19;271(29):17576-81. doi: 10.1074/jbc.271.29.17576. J Biol Chem. 1996. PMID: 8663325 Free article.

6

Gene symbol: COL11A1. Disease: Marshall syndrome.

Meisler MH, Griffith AJ, Warman M, Tiller G, Sprunger LK. Meisler MH, et al. Hum Genet. 1998 Apr;102(4):498. doi: 10.1007/s004390050731. Hum Genet. 1998. PMID: 9600252 Free article. 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: meisler mh. 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. Among authors: meisler mh. 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

Sequence interpretation. Functional annotation of mouse genome sequences.

Nadeau JH, Balling R, Barsh G, Beier D, Brown SD, Bucan M, Camper S, Carlson G, Copeland N, Eppig J, Fletcher C, Frankel WN, Ganten D, Goldowitz D, Goodnow C, Guenet JL, Hicks G, Hrabe de Angelis M, Jackson I, Jacob HJ, Jenkins N, Johnson D, Justice M, Kay S, Kingsley D, Lehrach H, Magnuson T, Meisler M, Poustka A, Rinchik EM, Rossant J, Russell LB, Schimenti J, Shiroishi T, Skarnes WC, Soriano P, Stanford W, Takahashi JS, Wurst W, Zimmer A; International Mouse Mutagenesis Consortium. Nadeau JH, et al. Science. 2001 Feb 16;291(5507):1251-5. doi: 10.1126/science.1058244. Science. 2001. PMID: 11233449 No abstract available.

10

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. Among authors: meisler mh. 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.

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