Kearney JA - Search Results

1

Calcium channel beta 4 (CACNB4): human ortholog of the mouse epilepsy gene lethargic.

Escayg A, Jones JM, Kearney JA, Hitchcock PF, Meisler MH. Escayg A, et al. Among authors: kearney ja. Genomics. 1998 May 15;50(1):14-22. doi: 10.1006/geno.1998.5311. Genomics. 1998. PMID: 9628818

2

Sodium channel mutations in epilepsy and other neurological disorders.

Meisler MH, Kearney JA. Meisler MH, et al. Among authors: kearney ja. J Clin Invest. 2005 Aug;115(8):2010-7. doi: 10.1172/JCI25466. J Clin Invest. 2005. PMID: 16075041 Free PMC article. Review.

3

Identification of epilepsy genes in human and mouse.

Meisler MH, Kearney J, Ottman R, Escayg A. Meisler MH, et al. Annu Rev Genet. 2001;35:567-88. doi: 10.1146/annurev.genet.35.102401.091142. Annu Rev Genet. 2001. PMID: 11700294 Free PMC article. Review.

4

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. Among authors: kearney ja. Novartis Found Symp. 2002;241:72-81; discussion 82-6, 226-32. Novartis Found Symp. 2002. PMID: 11771652 Review.

5

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

6

Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy.

Kearney JA, Wiste AK, Stephani U, Trudeau MM, Siegel A, RamachandranNair R, Elterman RD, Muhle H, Reinsdorf J, Shields WD, Meisler MH, Escayg A. Kearney JA, et al. Pediatr Neurol. 2006 Feb;34(2):116-20. doi: 10.1016/j.pediatrneurol.2005.07.009. Pediatr Neurol. 2006. PMID: 16458823

7

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.

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. Neuroscience. 2001;102(2):307-17. doi: 10.1016/s0306-4522(00)00479-6. Neuroscience. 2001. PMID: 11166117

9

Sodium channels SCN1A, SCN2A and SCN3A in familial autism.

Weiss LA, Escayg A, Kearney JA, Trudeau M, MacDonald BT, Mori M, Reichert J, Buxbaum JD, Meisler MH. Weiss LA, et al. Among authors: kearney ja. Mol Psychiatry. 2003 Feb;8(2):186-94. doi: 10.1038/sj.mp.4001241. Mol Psychiatry. 2003. PMID: 12610651

10

Impaired motor function in mice with cell-specific knockout of sodium channel Scn8a (NaV1.6) in cerebellar purkinje neurons and granule cells.

Levin SI, Khaliq ZM, Aman TK, Grieco TM, Kearney JA, Raman IM, Meisler MH. Levin SI, et al. Among authors: kearney ja. J Neurophysiol. 2006 Aug;96(2):785-93. doi: 10.1152/jn.01193.2005. Epub 2006 May 10. J Neurophysiol. 2006. PMID: 16687615 Free article.

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