Meisler MH - Search Results

1

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: meisler mh. Hum Mol Genet. 1999 Mar;8(3):471-9. doi: 10.1093/hmg/8.3.471. Hum Mol Genet. 1999. PMID: 9949206

2

Localization of insulin-2 (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7.

Jones JM, Meisler MH, Seldin MF, Lee BK, Eicher EM. Jones JM, et al. Among authors: meisler mh. Genomics. 1992 Sep;14(1):197-9. doi: 10.1016/s0888-7543(05)80308-8. Genomics. 1992. PMID: 1358794 Free article.

3

Mouse chromosome 3.

Meisler MH, Todd JA, Rodrigues N, Wakeland EK, Seldin MF. Meisler MH, et al. Mamm Genome. 1992;3 Spec No:S44-54. doi: 10.1007/BF00648421. Mamm Genome. 1992. PMID: 1498442 Free article. Review. No abstract available.

4

Mouse chromosome 3.

Meisler MH, Seldin MF. Meisler MH, et al. Mamm Genome. 1991;1 Spec No:S42-50. doi: 10.1007/BF00656485. Mamm Genome. 1991. PMID: 1799809 Free article. Review. No abstract available.

5

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.

6

Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15.

Kohrman DC, Plummer NW, Schuster T, Jones JM, Jang W, Burgess DL, Galt J, Spear BT, Meisler MH. Kohrman DC, et al. Among authors: meisler mh. Genomics. 1995 Mar 20;26(2):171-7. doi: 10.1016/0888-7543(95)80198-u. Genomics. 1995. PMID: 7601440

7

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

8

Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus.

Keller SA, Jones JM, Boyle A, Barrow LL, Killen PD, Green DG, Kapousta NV, Hitchcock PF, Swank RT, Meisler MH. Keller SA, et al. Among authors: meisler mh. Genomics. 1994 Sep 15;23(2):309-20. doi: 10.1006/geno.1994.1506. Genomics. 1994. PMID: 7835879 Free article.

9

SCNN1, an epithelial cell sodium channel gene in the conserved linkage group on mouse chromosome 6 and human chromosome 12.

Meisler MH, Barrow LL, Canessa CM, Rossier BC. Meisler MH, et al. Genomics. 1994 Nov 1;24(1):185-6. doi: 10.1006/geno.1994.1599. Genomics. 1994. PMID: 7896277 Free article.

10

Molecular characterization of a novel human gene, SEC13R, related to the yeast secretory pathway gene SEC13, and mapping to a conserved linkage group on human chromosome 3p24-p25 and mouse chromosome 6.

Swaroop A, Yang-Feng TL, Liu W, Gieser L, Barrow LL, Chen KC, Agarwal N, Meisler MH, Smith DI. Swaroop A, et al. Among authors: meisler mh. Hum Mol Genet. 1994 Aug;3(8):1281-6. doi: 10.1093/hmg/3.8.1281. Hum Mol Genet. 1994. PMID: 7987303

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