These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


261 related items for PubMed ID: 22471526

  • 1. Confirmation of an epilepsy modifier locus on mouse chromosome 11 and candidate gene analysis by RNA-Seq.
    Hawkins NA, Kearney JA.
    Genes Brain Behav; 2012 Jun; 11(4):452-60. PubMed ID: 22471526
    [Abstract] [Full Text] [Related]

  • 2. 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; 57(6):e103-7. PubMed ID: 27112236
    [Abstract] [Full Text] [Related]

  • 3. Hlf is a genetic modifier of epilepsy caused by voltage-gated sodium channel mutations.
    Hawkins NA, Kearney JA.
    Epilepsy Res; 2016 Jan; 119():20-3. PubMed ID: 26656780
    [Abstract] [Full Text] [Related]

  • 4. Fine mapping of an epilepsy modifier gene on mouse Chromosome 19.
    Bergren SK, Rutter ED, Kearney JA.
    Mamm Genome; 2009 Jun; 20(6):359-66. PubMed ID: 19513789
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Mapping genetic modifiers of survival in a mouse model of Dravet syndrome.
    Miller AR, Hawkins NA, McCollom CE, Kearney JA.
    Genes Brain Behav; 2014 Feb; 13(2):163-72. PubMed ID: 24152123
    [Abstract] [Full Text] [Related]

  • 11. Fine mapping and candidate gene analysis of a dravet syndrome modifier locus on mouse chromosome 11.
    Kearney JA, Copeland-Hardin LD, Duarte S, Zachwieja NA, Eckart-Frank IK, Hawkins NA.
    Mamm Genome; 2022 Dec; 33(4):565-574. PubMed ID: 35606653
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. 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.
    Neuroscience; 2001 Dec 01; 102(2):307-17. PubMed ID: 11166117
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 14.