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Journal Abstract Search

213 related items for PubMed ID: 21402906

  • 1. Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibility.
    Jorge BS, Campbell CM, Miller AR, Rutter ED, Gurnett CA, Vanoye CG, George AL, Kearney JA.
    Proc Natl Acad Sci U S A; 2011 Mar 29; 108(13):5443-8. PubMed ID: 21402906
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  • 4. Cacna1g is a genetic modifier of epilepsy caused by mutation of voltage-gated sodium channel Scn2a.
    Calhoun JD, Hawkins NA, Zachwieja NJ, Kearney JA.
    Epilepsia; 2016 Jun 29; 57(6):e103-7. PubMed ID: 27112236
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  • 8. Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2.
    Kearney JA, Yang Y, Beyer B, Bergren SK, Claes L, Dejonghe P, Frankel WN.
    Hum Mol Genet; 2006 Mar 15; 15(6):1043-8. PubMed ID: 16464983
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  • 9. Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.
    Hawkins NA, Martin MS, Frankel WN, Kearney JA, Escayg A.
    Neurobiol Dis; 2011 Mar 15; 41(3):655-60. PubMed ID: 21156207
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  • 10. Molecular, Cellular and Functional Changes in the Retinas of Young Adult Mice Lacking the Voltage-Gated K+ Channel Subunits Kv8.2 and K2.1.
    Jiang X, Rashwan R, Voigt V, Nerbonne J, Hunt DM, Carvalho LS.
    Int J Mol Sci; 2021 May 05; 22(9):. PubMed ID: 34063002
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  • 11. The Role of the Voltage-Gated Potassium Channel Proteins Kv8.2 and Kv2.1 in Vision and Retinal Disease: Insights from the Study of Mouse Gene Knock-Out Mutations.
    Hart NS, Mountford JK, Voigt V, Fuller-Carter P, Barth M, Nerbonne JM, Hunt DM, Carvalho LS.
    eNeuro; 2019 May 05; 6(1):. PubMed ID: 30820446
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  • 12. Functional analysis of missense mutations in Kv8.2 causing cone dystrophy with supernormal rod electroretinogram.
    Smith KE, Wilkie SE, Tebbs-Warner JT, Jarvis BJ, Gallasch L, Stocker M, Hunt DM.
    J Biol Chem; 2012 Dec 21; 287(52):43972-83. PubMed ID: 23115240
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  • 14. The retinal clock drives the expression of Kcnv2, a channel essential for visual function and cone survival.
    Hölter P, Kunst S, Wolloscheck T, Kelleher DK, Sticht C, Wolfrum U, Spessert R.
    Invest Ophthalmol Vis Sci; 2012 Oct 05; 53(11):6947-54. PubMed ID: 22969075
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  • 16. Utilising Automated Electrophysiological Platforms in Epilepsy Research.
    Milligan CJ, Pachernegg S.
    Methods Mol Biol; 2021 Oct 05; 2188():133-155. PubMed ID: 33119850
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  • 17. Compound heterozygous KCNV2 variants contribute to cone dystrophy with supernormal rod responses in a Chinese family.
    Liu M, Zhu Y, Huang L, Jiang W, Wu N, Song Y, Lu Y, Ma Y.
    Mol Genet Genomic Med; 2021 Oct 05; 9(10):e1795. PubMed ID: 34535971
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