Meisler M - Search Results

1

Differential excitatory vs inhibitory SCN expression at single cell level regulates brain sodium channel function in neurodevelopmental disorders.

Du J, Simmons S, Brunklaus A, Adiconis X, Hession CC, Fu Z, Li Y, Shema R, Møller RS, Barak B, Feng G, Meisler M, Sanders S, Lerche H, Campbell AJ, McCarroll S, Levin JZ, Lal D. Du J, et al. Among authors: meisler m. Eur J Paediatr Neurol. 2020 Jan;24:129-133. doi: 10.1016/j.ejpn.2019.12.019. Epub 2019 Dec 28. Eur J Paediatr Neurol. 2020. PMID: 31928904

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

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.

4

Alternative splicing of the sodium channel SCN8A predicts a truncated two-domain protein in fetal brain and non-neuronal cells.

Plummer NW, McBurney MW, Meisler MH. Plummer NW, et al. Among authors: meisler mh. J Biol Chem. 1997 Sep 19;272(38):24008-15. doi: 10.1074/jbc.272.38.24008. J Biol Chem. 1997. PMID: 9295353 Free article.

5

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.

6

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

7

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.

8

Mutations of voltage-gated sodium channels in movement disorders and epilepsy.

Meisler MH, Kearney JA, Sprunger LK, MacDonald BT, Buchner DA, Escayg A. Meisler MH, et al. Novartis Found Symp. 2002;241:72-81; discussion 82-6, 226-32. Novartis Found Symp. 2002. PMID: 11771652 Review.

9

Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6).

Kearney JA, Buchner DA, De Haan G, Adamska M, Levin SI, Furay AR, Albin RL, Jones JM, Montal M, Stevens MJ, Sprunger LK, Meisler MH. Kearney JA, et al. Among authors: meisler mh. Hum Mol Genet. 2002 Oct 15;11(22):2765-75. doi: 10.1093/hmg/11.22.2765. Hum Mol Genet. 2002. PMID: 12374766

10

A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction.

Spampanato J, Kearney JA, de Haan G, McEwen DP, Escayg A, Aradi I, MacDonald BT, Levin SI, Soltesz I, Benna P, Montalenti E, Isom LL, Goldin AL, Meisler MH. Spampanato J, et al. Among authors: meisler mh. J Neurosci. 2004 Nov 3;24(44):10022-34. doi: 10.1523/JNEUROSCI.2034-04.2004. J Neurosci. 2004. PMID: 15525788 Free PMC article.

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