238 related articles for article (PubMed ID: 17544618)
1. Characterization of 5' untranslated regions of the voltage-gated sodium channels SCN1A, SCN2A, and SCN3A and identification of cis-conserved noncoding sequences.
Martin MS; Tang B; Ta N; Escayg A
Genomics; 2007 Aug; 90(2):225-35. PubMed ID: 17544618
[TBL] [Abstract][Full Text] [Related]
2. Differential expression of exon 5 splice variants of sodium channel alpha subunit mRNAs in the developing mouse brain.
Gazina EV; Richards KL; Mokhtar MB; Thomas EA; Reid CA; Petrou S
Neuroscience; 2010 Mar; 166(1):195-200. PubMed ID: 20006674
[TBL] [Abstract][Full Text] [Related]
3. Interstitial 2q24.3 deletion including SCN2A and SCN3A genes in a patient with autistic features, psychomotor delay, microcephaly and no history of seizures.
Celle ME; Cuoco C; Porta S; Gimelli G; Tassano E
Gene; 2013 Dec; 532(2):294-6. PubMed ID: 24080482
[TBL] [Abstract][Full Text] [Related]
4. Identification of the promoter region and the 5'-untranslated exons of the human voltage-gated sodium channel Nav1.1 gene (SCN1A) and enhancement of gene expression by the 5'-untranslated exons.
Long YS; Zhao QH; Su T; Cai YL; Zeng Y; Shi YW; Yi YH; Chang HH; Liao WP
J Neurosci Res; 2008 Nov; 86(15):3375-81. PubMed ID: 18655196
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. SCN1A, SCN2A and SCN3A gene polymorphisms and responsiveness to antiepileptic drugs: a multicenter cohort study and meta-analysis.
Haerian BS; Baum L; Kwan P; Tan HJ; Raymond AA; Mohamed Z
Pharmacogenomics; 2013 Jul; 14(10):1153-66. PubMed ID: 23859570
[TBL] [Abstract][Full Text] [Related]
7. 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; 16(23):2892-9. PubMed ID: 17881658
[TBL] [Abstract][Full Text] [Related]
8. Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus.
Kasai N; Fukushima K; Ueki Y; Prasad S; Nosakowski J; Sugata K; Sugata A; Nishizaki K; Meyer NC; Smith RJ
Gene; 2001 Feb; 264(1):113-22. PubMed ID: 11245985
[TBL] [Abstract][Full Text] [Related]
9. Heterozygous deletion of SCN2A and SCN3A in a patient with autism spectrum disorder and Tourette syndrome: a case report.
Nickel K; Tebartz van Elst L; Domschke K; Gläser B; Stock F; Endres D; Maier S; Riedel A
BMC Psychiatry; 2018 Aug; 18(1):248. PubMed ID: 30071822
[TBL] [Abstract][Full Text] [Related]
10. Biological concepts in human sodium channel epilepsies and their relevance in clinical practice.
Brunklaus A; Du J; Steckler F; Ghanty II; Johannesen KM; Fenger CD; Schorge S; Baez-Nieto D; Wang HR; Allen A; Pan JQ; Lerche H; Heyne H; Symonds JD; Zuberi SM; Sanders S; Sheidley BR; Craiu D; Olson HE; Weckhuysen S; DeJonge P; Helbig I; Van Esch H; Busa T; Milh M; Isidor B; Depienne C; Poduri A; Campbell AJ; Dimidschstein J; Møller RS; Lal D
Epilepsia; 2020 Mar; 61(3):387-399. PubMed ID: 32090326
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Identifying the promoter region of the human brain sodium channel subtype II gene (SCN2A).
Schade SD; Brown GB
Brain Res Mol Brain Res; 2000 Sep; 81(1-2):187-90. PubMed ID: 11000491
[TBL] [Abstract][Full Text] [Related]
13. Voltage-gated sodium channels in taste bud cells.
Gao N; Lu M; Echeverri F; Laita B; Kalabat D; Williams ME; Hevezi P; Zlotnik A; Moyer BD
BMC Neurosci; 2009 Mar; 10():20. PubMed ID: 19284629
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Na channel gene mutations in epilepsy--the functional consequences.
Yamakawa K
Epilepsy Res; 2006 Aug; 70 Suppl 1():S218-22. PubMed ID: 16806834
[TBL] [Abstract][Full Text] [Related]
16. Multidrug resistance in epilepsy and polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, and SCN3A: correlation among phenotype, genotype, and mRNA expression.
Kwan P; Poon WS; Ng HK; Kang DE; Wong V; Ng PW; Lui CH; Sin NC; Wong KS; Baum L
Pharmacogenet Genomics; 2008 Nov; 18(11):989-98. PubMed ID: 18784617
[TBL] [Abstract][Full Text] [Related]
17. 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; 45(2):149-58. PubMed ID: 14738422
[TBL] [Abstract][Full Text] [Related]
18. Sodium channels SCN1A, SCN2A and SCN3A in familial autism.
Weiss LA; Escayg A; Kearney JA; Trudeau M; MacDonald BT; Mori M; Reichert J; Buxbaum JD; Meisler MH
Mol Psychiatry; 2003 Feb; 8(2):186-94. PubMed ID: 12610651
[TBL] [Abstract][Full Text] [Related]
19. 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(6):1043-8. PubMed ID: 16464983
[TBL] [Abstract][Full Text] [Related]
20. Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A.
Vecchi M; Cassina M; Casarin A; Rigon C; Drigo P; De Palma L; Clementi M
Seizure; 2011 Dec; 20(10):813-6. PubMed ID: 21893419
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
