11 results for author:"Kearney J.A." in Literature citations
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| Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibility. Jorge B.S., Campbell C.M., Miller A.R., Rutter E.D., Gurnett C.A., Vanoye C.G., George A.L. Jr., Kearney J.A. Proc. Natl. Acad. Sci. U.S.A. 108:5443-5448(2011) · Mapped (2) |
| Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus. Hawkins N.A., Martin M.S., Frankel W.N., Kearney J.A., Escayg A. Neurobiol. Dis. 41:655-660(2011) · Mapped (59) |
| Impaired motor function in mice with cell-specific knockout of sodium channel Scn8a (NaV1.6) in cerebellar purkinje neurons and granule cells. Levin S.I., Khaliq Z.M., Aman T.K., Grieco T.M., Kearney J.A., Raman I.M., Meisler M.H. J. Neurophysiol. 96:785-793(2006) · Mapped (8) |
| Analysis of gene expression differences between utrophin/dystrophin-deficient vs mdx skeletal muscles reveals a specific upregulation of slow muscle genes in limb muscles. Baker P.E., Kearney J.A., Gong B., Merriam A.P., Kuhn D.E., Porter J.D., Rafael-Fortney J.A. Neurogenetics 7:81-91(2006) · Mapped (21) |
| Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2. Kearney J.A., Yang Y., Beyer B., Bergren S.K., Claes L., Dejonghe P., Frankel W.N. Hum. Mol. Genet. 15:1043-1048(2006) · Mapped (30) |
| Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy. Kearney J.A., Wiste A.K., Stephani U., Trudeau M.M., Siegel A., Ramachandrannair R., Elterman R.D., Muhle H., Reinsdorf J., Shields W.D. et al. Pediatr. Neurol. 34:116-120(2006) · UniProtKB (1) |
| Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a. Bergren S.K., Chen S., Galecki A., Kearney J.A. Mamm. Genome 16:683-690(2005) · Mapped (8) |
| A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction. Spampanato J., Kearney J.A., de Haan G., McEwen D.P., Escayg A., Aradi I., MacDonald B.T., Levin S.I., Soltesz I., Benna P. et al. J. Neurosci. 24:10022-10034(2004) · UniProtKB (1) · Mapped (6) |
| Sodium channels SCN1A, SCN2A and SCN3A in familial autism. Weiss L.A., Escayg A., Kearney J.A., Trudeau M., MacDonald B.T., Mori M., Reichert J., Buxbaum J.D., Meisler M.H. Mol. Psychiatry 8:186-194(2003) · UniProtKB (3) · Mapped (13) |
| Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6). Kearney J.A., Buchner D.A., De Haan G., Adamska M., Levin S.I., Furay A.R., Albin R.L., Jones J.M., Montal M., Stevens M.J. et al. Hum. Mol. Genet. 11:2765-2775(2002) · Mapped (8) |
| Calcium channel beta4 (CACNB4): human ortholog of the mouse epilepsy gene lethargic. Escayg A., Jones J.M., Kearney J.A., Hitchcock P.F., Meisler M.H. |