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Journal Abstract Search

219 related items for PubMed ID: 16245025

  • 1. Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a.
    Bergren SK, Chen S, Galecki A, Kearney JA.
    Mamm Genome; 2005 Sep; 16(9):683-90. PubMed ID: 16245025
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  • 4. 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; 41(3):655-60. PubMed ID: 21156207
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  • 5. 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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  • 8. Fine Mapping of a Dravet Syndrome Modifier Locus on Mouse Chromosome 5 and Candidate Gene Analysis by RNA-Seq.
    Hawkins NA, Zachwieja NJ, Miller AR, Anderson LL, Kearney JA.
    PLoS Genet; 2016 Oct 15; 12(10):e1006398. PubMed ID: 27768696
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  • 10. CaMKII modulates sodium current in neurons from epileptic Scn2a mutant mice.
    Thompson CH, Hawkins NA, Kearney JA, George AL.
    Proc Natl Acad Sci U S A; 2017 Feb 14; 114(7):1696-1701. PubMed ID: 28137877
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  • 11. The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy.
    Martin MS, Tang B, Papale LA, Yu FH, Catterall WA, Escayg A.
    Hum Mol Genet; 2007 Dec 01; 16(23):2892-9. PubMed ID: 17881658
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  • 12. Na channel gene mutations in epilepsy--the functional consequences.
    Yamakawa K.
    Epilepsy Res; 2006 Aug 01; 70 Suppl 1():S218-22. PubMed ID: 16806834
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  • 13. Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures.
    Rhodes TH, Vanoye CG, Ohmori I, Ogiwara I, Yamakawa K, George AL.
    J Physiol; 2005 Dec 01; 569(Pt 2):433-45. PubMed ID: 16210358
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  • 16. Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.
    Bonanni P, Malcarne M, Moro F, Veggiotti P, Buti D, Ferrari AR, Parrini E, Mei D, Volzone A, Zara F, Heron SE, Bordo L, Marini C, Guerrini R.
    Epilepsia; 2004 Feb 01; 45(2):149-58. PubMed ID: 14738422
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  • 17. Gabra2 is a genetic modifier of Scn8a encephalopathy in the mouse.
    Yu W, Hill SF, Xenakis JG, Pardo-Manuel de Villena F, Wagnon JL, Meisler MH.
    Epilepsia; 2020 Dec 01; 61(12):2847-2856. PubMed ID: 33140451
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  • 18. SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.
    Liao Y, Anttonen AK, Liukkonen E, Gaily E, Maljevic S, Schubert S, Bellan-Koch A, Petrou S, Ahonen VE, Lerche H, Lehesjoki AE.
    Neurology; 2010 Oct 19; 75(16):1454-8. PubMed ID: 20956790
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  • 19. Epilepsy and sodium channel gene mutations: gain or loss of function?
    Yamakawa K.
    Neuroreport; 2005 Jan 19; 16(1):1-3. PubMed ID: 15618878
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