Meisler MH - Search Results

1

SCN8A encephalopathy: Research progress and prospects.

Meisler MH, Helman G, Hammer MF, Fureman BE, Gaillard WD, Goldin AL, Hirose S, Ishii A, Kroner BL, Lossin C, Mefford HC, Parent JM, Patel M, Schreiber J, Stewart R, Whittemore V, Wilcox K, Wagnon JL, Pearl PL, Vanderver A, Scheffer IE. Meisler MH, et al. Epilepsia. 2016 Jul;57(7):1027-35. doi: 10.1111/epi.13422. Epub 2016 Jun 8. Epilepsia. 2016. PMID: 27270488 Free PMC article.

2

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

3

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.

4

A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting.

Kohrman DC, Smith MR, Goldin AL, Harris J, Meisler MH. Kohrman DC, et al. Among authors: meisler mh. J Neurosci. 1996 Oct 1;16(19):5993-9. doi: 10.1523/JNEUROSCI.16-19-05993.1996. J Neurosci. 1996. PMID: 8815882 Free PMC article.

5

Altered subthreshold sodium currents and disrupted firing patterns in Purkinje neurons of Scn8a mutant mice.

Raman IM, Sprunger LK, Meisler MH, Bean BP. Raman IM, et al. Among authors: meisler mh. Neuron. 1997 Oct;19(4):881-91. doi: 10.1016/s0896-6273(00)80969-1. Neuron. 1997. PMID: 9354334 Free article.

6

Functional analysis of the mouse Scn8a sodium channel.

Smith MR, Smith RD, Plummer NW, Meisler MH, Goldin AL. Smith MR, et al. Among authors: meisler mh. J Neurosci. 1998 Aug 15;18(16):6093-102. doi: 10.1523/JNEUROSCI.18-16-06093.1998. J Neurosci. 1998. PMID: 9698304 Free PMC article.

7

Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A.

Plummer NW, Galt J, Jones JM, Burgess DL, Sprunger LK, Kohrman DC, Meisler MH. Plummer NW, et al. Among authors: meisler mh. Genomics. 1998 Dec 1;54(2):287-96. doi: 10.1006/geno.1998.5550. Genomics. 1998. PMID: 9828131

8

A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities.

Kearney JA, Plummer NW, Smith MR, Kapur J, Cummins TR, Waxman SG, Goldin AL, Meisler MH. Kearney JA, et al. Among authors: meisler mh. Neuroscience. 2001;102(2):307-17. doi: 10.1016/s0306-4522(00)00479-6. Neuroscience. 2001. PMID: 11166117

9

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. Neuroscientist. 2001 Apr;7(2):136-45. doi: 10.1177/107385840100700208. Neuroscientist. 2001. PMID: 11496924 Review.

10

Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2.

Spampanato J, Escayg A, Meisler MH, Goldin AL. Spampanato J, et al. Among authors: meisler mh. J Neurosci. 2001 Oct 1;21(19):7481-90. doi: 10.1523/JNEUROSCI.21-19-07481.2001. J Neurosci. 2001. PMID: 11567038 Free PMC article.

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