141 related articles for article (PubMed ID: 27690330)
1. Mapping of a FEB3 homologous febrile seizure locus on mouse chromosome 2 containing candidate genes Scn1a and Scn3a.
Hessel EV; van Lith HA; Wolterink-Donselaar IG; de Wit M; Groot Koerkamp MJ; Holstege FC; Kas MJ; Fernandes C; de Graan PN
Eur J Neurosci; 2016 Dec; 44(11):2950-2957. PubMed ID: 27690330
[TBL] [Abstract][Full Text] [Related]
2. Mapping an X-linked locus that influences heat-induced febrile seizures in mice.
Hessel EV; van Lith HA; Wolterink-Donselaar IG; de Wit M; Hendrickx DA; Kas MJ; de Graan PN
Epilepsia; 2012 Aug; 53(8):1399-410. PubMed ID: 22780306
[TBL] [Abstract][Full Text] [Related]
3. Phenotyping mouse chromosome substitution strains reveal multiple QTLs for febrile seizure susceptibility.
Hessel EV; van Gassen KL; Wolterink-Donselaar IG; Stienen PJ; Fernandes C; Brakkee JH; Kas MJ; de Graan PN
Genes Brain Behav; 2009 Mar; 8(2):248-55. PubMed ID: 19077119
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the sodium channel genes SCN1A, SCN3A, and SCN9A in children with epilepsy with febrile seizures plus(EFS+).
Ma H; Guo Y; Chen Z; Wang L; Tang Z; Zhang J; Miao Q; Zhai Q
Seizure; 2021 May; 88():146-152. PubMed ID: 33895391
[TBL] [Abstract][Full Text] [Related]
5. 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; 12(10):e1006398. PubMed ID: 27768696
[TBL] [Abstract][Full Text] [Related]
6. Characterization of febrile seizures and febrile seizure susceptibility in mouse inbred strains.
van Gassen KL; Hessel EV; Ramakers GM; Notenboom RG; Wolterink-Donselaar IG; Brakkee JH; Godschalk TC; Qiao X; Spruijt BM; van Nieuwenhuizen O; de Graan PN
Genes Brain Behav; 2008 Jul; 7(5):578-86. PubMed ID: 18363854
[TBL] [Abstract][Full Text] [Related]
7. SCN1A rs3812718 polymorphism and susceptibility to epilepsy with febrile seizures: a meta-analysis.
Tang L; Lu X; Tao Y; Zheng J; Zhao P; Li K; Li L
Gene; 2014 Jan; 533(1):26-31. PubMed ID: 24076350
[TBL] [Abstract][Full Text] [Related]
8. GAPDH-mediated posttranscriptional regulations of sodium channel Scn1a and Scn3a genes under seizure and ketogenic diet conditions.
Lin GW; Lu P; Zeng T; Tang HL; Chen YH; Liu SJ; Gao MM; Zhao QH; Yi YH; Long YS
Neuropharmacology; 2017 Feb; 113(Pt A):480-489. PubMed ID: 27816501
[TBL] [Abstract][Full Text] [Related]
9. Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A.
Ito M; Nagafuji H; Okazawa H; Yamakawa K; Sugawara T; Mazaki-Miyazaki E; Hirose S; Fukuma G; Mitsudome A; Wada K; Kaneko S
Epilepsy Res; 2002 Jan; 48(1-2):15-23. PubMed ID: 11823106
[TBL] [Abstract][Full Text] [Related]
10. 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
[TBL] [Abstract][Full Text] [Related]
11. Molecular genetics of febrile seizures.
Iwasaki N; Nakayama J; Hamano K; Matsui A; Arinami T
Epilepsia; 2002; 43 Suppl 9():32-5. PubMed ID: 12383277
[TBL] [Abstract][Full Text] [Related]
12. SCN3A deficiency associated with increased seizure susceptibility.
Lamar T; Vanoye CG; Calhoun J; Wong JC; Dutton SBB; Jorge BS; Velinov M; Escayg A; Kearney JA
Neurobiol Dis; 2017 Jun; 102():38-48. PubMed ID: 28235671
[TBL] [Abstract][Full Text] [Related]
13. 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; 109():34-9. PubMed ID: 25524840
[TBL] [Abstract][Full Text] [Related]
14. Mapping of a chromosome 12 region associated with airway hyperresponsiveness in a recombinant congenic mouse strain and selection of potential candidate genes by expression and sequence variation analyses.
Kanagaratham C; Marino R; Camateros P; Ren J; Houle D; Sladek R; Vidal SM; Radzioch D
PLoS One; 2014; 9(8):e104234. PubMed ID: 25111050
[TBL] [Abstract][Full Text] [Related]
15. Electrophysiological Differences between the Same Pore Region Mutation in SCN1A and SCN3A.
Chen YJ; Shi YW; Xu HQ; Chen ML; Gao MM; Sun WW; Tang B; Zeng Y; Liao WP
Mol Neurobiol; 2015; 51(3):1263-70. PubMed ID: 24990319
[TBL] [Abstract][Full Text] [Related]
16. Mapping a mouse limbic seizure susceptibility locus on chromosome 10.
Winawer MR; Gildersleeve SS; Phillips AG; Rabinowitz D; Palmer AA
Epilepsia; 2011 Nov; 52(11):2076-83. PubMed ID: 21906048
[TBL] [Abstract][Full Text] [Related]
17. 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
[TBL] [Abstract][Full Text] [Related]
18. Confirmation of provisional quantitative trait loci for voluntary alcohol consumption: genetic analysis in chromosome substitution strains and F2 crosses derived from A/J and C57BL/6J progenitors.
Boyle AE; Gill KJ
Pharmacogenet Genomics; 2008 Dec; 18(12):1071-82. PubMed ID: 19008751
[TBL] [Abstract][Full Text] [Related]
19. Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures.
Mantegazza M; Gambardella A; Rusconi R; Schiavon E; Annesi F; Cassulini RR; Labate A; Carrideo S; Chifari R; Canevini MP; Canger R; Franceschetti S; Annesi G; Wanke E; Quattrone A
Proc Natl Acad Sci U S A; 2005 Dec; 102(50):18177-82. PubMed ID: 16326807
[TBL] [Abstract][Full Text] [Related]
20. [Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].
Xu XJ; Zhang YH; Sun HH; Liu XY; Wu HS; Wu XR
Zhonghua Er Ke Za Zhi; 2012 Aug; 50(8):580-6. PubMed ID: 23158734
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
