Jones JM - Search Results

1

Prominent role of forebrain excitatory neurons in SCN8A encephalopathy.

Bunton-Stasyshyn RKA, Wagnon JL, Wengert ER, Barker BS, Faulkner A, Wagley PK, Bhatia K, Jones JM, Maniaci MR, Parent JM, Goodkin HP, Patel MK, Meisler MH. Bunton-Stasyshyn RKA, et al. Among authors: jones jm. Brain. 2019 Feb 1;142(2):362-375. doi: 10.1093/brain/awy324. Brain. 2019. PMID: 30601941 Free PMC article.

2

Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.

Sharkey LM, Jones JM, Hedera P, Meisler MH. Sharkey LM, et al. Among authors: jones jm. Parkinsonism Relat Disord. 2009 May;15(4):321-3. doi: 10.1016/j.parkreldis.2008.06.010. Epub 2008 Aug 20. Parkinsonism Relat Disord. 2009. PMID: 18718804 Free PMC article.

3

Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism.

Liu Y, Lopez-Santiago LF, Yuan Y, Jones JM, Zhang H, O'Malley HA, Patino GA, O'Brien JE, Rusconi R, Gupta A, Thompson RC, Natowicz MR, Meisler MH, Isom LL, Parent JM. Liu Y, et al. Among authors: jones jm. Ann Neurol. 2013 Jul;74(1):128-39. doi: 10.1002/ana.23897. Epub 2013 Jul 2. Ann Neurol. 2013. PMID: 23821540 Free PMC article.

4

Modeling human epilepsy by TALEN targeting of mouse sodium channel Scn8a.

Jones JM, Meisler MH. Jones JM, et al. Genesis. 2014 Feb;52(2):141-8. doi: 10.1002/dvg.22731. Epub 2013 Dec 12. Genesis. 2014. PMID: 24288358 Free PMC article.

5

Convulsive seizures and SUDEP in a mouse model of SCN8A epileptic encephalopathy.

Wagnon JL, Korn MJ, Parent R, Tarpey TA, Jones JM, Hammer MF, Murphy GG, Parent JM, Meisler MH. Wagnon JL, et al. Among authors: jones jm. Hum Mol Genet. 2015 Jan 15;24(2):506-15. doi: 10.1093/hmg/ddu470. Epub 2014 Sep 16. Hum Mol Genet. 2015. PMID: 25227913 Free PMC article.

6

Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome.

Auerbach DS, Jones J, Clawson BC, Offord J, Lenk GM, Ogiwara I, Yamakawa K, Meisler MH, Parent JM, Isom LL. Auerbach DS, et al. Among authors: jones j. PLoS One. 2013 Oct 14;8(10):e77843. doi: 10.1371/journal.pone.0077843. eCollection 2013. PLoS One. 2013. PMID: 24155976 Free PMC article.

7

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: jones jm. Hum Mol Genet. 2002 Oct 15;11(22):2765-75. doi: 10.1093/hmg/11.22.2765. Hum Mol Genet. 2002. PMID: 12374766

8

The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular trafficking.

Sharkey LM, Cheng X, Drews V, Buchner DA, Jones JM, Justice MJ, Waxman SG, Dib-Hajj SD, Meisler MH. Sharkey LM, et al. Among authors: jones jm. J Neurosci. 2009 Mar 4;29(9):2733-41. doi: 10.1523/JNEUROSCI.6026-08.2009. J Neurosci. 2009. PMID: 19261867 Free PMC article.

9

Novel SCN1A mutation in a proband with malignant migrating partial seizures of infancy.

Freilich ER, Jones JM, Gaillard WD, Conry JA, Tsuchida TN, Reyes C, Dib-Hajj S, Waxman SG, Meisler MH, Pearl PL. Freilich ER, et al. Among authors: jones jm. Arch Neurol. 2011 May;68(5):665-71. doi: 10.1001/archneurol.2011.98. Arch Neurol. 2011. PMID: 21555645 Free PMC article.

10

Rbfox proteins regulate alternative splicing of neuronal sodium channel SCN8A.

O'Brien JE, Drews VL, Jones JM, Dugas JC, Barres BA, Meisler MH. O'Brien JE, et al. Among authors: jones jm. Mol Cell Neurosci. 2012 Feb;49(2):120-6. doi: 10.1016/j.mcn.2011.10.005. Epub 2011 Oct 21. Mol Cell Neurosci. 2012. PMID: 22044765 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

890 results

Search Page