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185 related items for PubMed ID: 38862622

  • 1. Fine mapping and candidate gene analysis of Dravet syndrome modifier loci on mouse chromosomes 7 and 8.
    Hawkins NA, Speakes N, Kearney JA.
    Mamm Genome; 2024 Sep; 35(3):334-345. PubMed ID: 38862622
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  • 2. Fine Mapping and Candidate Gene Analysis of Dravet Syndrome Modifier Loci on Mouse Chromosomes 7 and 8.
    Hawkins NA, Speakes N, Kearney JA.
    bioRxiv; 2024 Apr 18. PubMed ID: 38659879
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  • 3. 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 18; 12(10):e1006398. PubMed ID: 27768696
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  • 4. 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 18; 13(2):163-72. PubMed ID: 24152123
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  • 5. 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 18; 33(4):565-574. PubMed ID: 35606653
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  • 10. Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndrome.
    Calhoun JD, Hawkins NA, Zachwieja NJ, Kearney JA.
    Epilepsia; 2017 Aug 18; 58(8):e111-e115. PubMed ID: 28556246
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  • 11. Gabra2 is a genetic modifier of Dravet syndrome in mice.
    Hawkins NA, Nomura T, Duarte S, Barse L, Williams RW, Homanics GE, Mulligan MK, Contractor A, Kearney JA.
    Mamm Genome; 2021 Oct 18; 32(5):350-363. PubMed ID: 34086081
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  • 12. Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
    Lim BC, Hwang H, Kim H, Chae JH, Choi J, Kim KJ, Hwang YS, Yum MS, Ko TS.
    Epilepsy Res; 2015 Jan 18; 109():34-9. PubMed ID: 25524840
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  • 13. Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.
    Rubinstein M, Westenbroek RE, Yu FH, Jones CJ, Scheuer T, Catterall WA.
    Neurobiol Dis; 2015 Jan 18; 73():106-17. PubMed ID: 25281316
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  • 14. Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice.
    Mistry AM, Thompson CH, Miller AR, Vanoye CG, George AL, Kearney JA.
    Neurobiol Dis; 2014 May 18; 65():1-11. PubMed ID: 24434335
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  • 16. A novel rat model of Dravet syndrome recapitulates clinical hallmarks.
    Li M, Yang L, Qian W, Ray S, Lu Z, Liu T, Zou YY, Naumann RK, Wang H.
    Neurobiol Dis; 2023 Aug 18; 184():106193. PubMed ID: 37295561
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  • 17. Temporal manipulation of the Scn1a gene reveals its essential role in adult brain function.
    Di Berardino C, Mainardi M, Brusco S, Benvenuto E, Broccoli V, Colasante G.
    Brain; 2024 Apr 04; 147(4):1216-1230. PubMed ID: 37812819
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  • 18. Proteomic signature of the Dravet syndrome in the genetic Scn1a-A1783V mouse model.
    Miljanovic N, Hauck SM, van Dijk RM, Di Liberto V, Rezaei A, Potschka H.
    Neurobiol Dis; 2021 Sep 04; 157():105423. PubMed ID: 34144125
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  • 19. Scn1a gene reactivation after symptom onset rescues pathological phenotypes in a mouse model of Dravet syndrome.
    Valassina N, Brusco S, Salamone A, Serra L, Luoni M, Giannelli S, Bido S, Massimino L, Ungaro F, Mazzara PG, D'Adamo P, Lignani G, Broccoli V, Colasante G.
    Nat Commun; 2022 Jan 10; 13(1):161. PubMed ID: 35013317
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  • 20. 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 10; 11(4):452-60. PubMed ID: 22471526
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