182 related articles for article (PubMed ID: 8661019)
21. [Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block].
Lupoglazoff JM; Denjoy I; Cheav T; Berthet M; Extramiana F; Cauchemez B; Villain E; Leenhardt A; Guicheney P
Arch Mal Coeur Vaiss; 2002 May; 95(5):440-6. PubMed ID: 12085742
[TBL] [Abstract][Full Text] [Related]
22. Genetic polymorphisms and haplotypes of the human cardiac sodium channel alpha subunit gene (SCN5A) in Japanese and their association with arrhythmia.
Maekawa K; Saito Y; Ozawa S; Adachi-Akahane S; Kawamoto M; Komamura K; Shimizu W; Ueno K; Kamakura S; Kamatani N; Kitakaze M; Sawada J
Ann Hum Genet; 2005 Jul; 69(Pt 4):413-28. PubMed ID: 15996170
[TBL] [Abstract][Full Text] [Related]
23. Human periplakin: genomic organization in a clonally unstable region of chromosome 16p with an abundance of repetitive sequence elements.
Aho S; Rothenberger K; Tan EM; Ryoo YW; Cho BH; McLean WH; Uitto J
Genomics; 1999 Mar; 56(2):160-8. PubMed ID: 10051401
[TBL] [Abstract][Full Text] [Related]
24. Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp.
Fisher SE; Ciccodicola A; Tanaka K; Curci A; Desicato S; D'urso M; Craig IW
Genomics; 1997 Oct; 45(2):340-7. PubMed ID: 9344658
[TBL] [Abstract][Full Text] [Related]
25. Isolation and molecular characterization of the porcine stearoyl-CoA desaturase gene.
Ren J; Knorr C; Huang L; Brenig B
Gene; 2004 Sep; 340(1):19-30. PubMed ID: 15556291
[TBL] [Abstract][Full Text] [Related]
26. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
Wang Q; Curran ME; Splawski I; Burn TC; Millholland JM; VanRaay TJ; Shen J; Timothy KW; Vincent GM; de Jager T; Schwartz PJ; Toubin JA; Moss AJ; Atkinson DL; Landes GM; Connors TD; Keating MT
Nat Genet; 1996 Jan; 12(1):17-23. PubMed ID: 8528244
[TBL] [Abstract][Full Text] [Related]
27. High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia.
Hofman-Bang J; Behr ER; Hedley P; Tfelt-Hansen J; Kanters JK; Haunsøe S; McKenna WJ; Christiansen M
Clin Genet; 2006 Jun; 69(6):504-11. PubMed ID: 16712702
[TBL] [Abstract][Full Text] [Related]
28. The gene for human protein Z is localized to chromosome 13 at band q34 and is coded by eight regular exons and one alternative exon.
Fujimaki K; Yamazaki T; Taniwaki M; Ichinose A
Biochemistry; 1998 May; 37(19):6838-46. PubMed ID: 9578570
[TBL] [Abstract][Full Text] [Related]
29. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
Lee PL; Gelbart T; West C; Halloran C; Beutler E
Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
[TBL] [Abstract][Full Text] [Related]
30. Human CFTR gene sequences in regions flanking exon 10: a simple repeat sequence polymorphism in intron 9.
Xu Z; Gruenert DC
Biochem Biophys Res Commun; 1996 Feb; 219(1):140-5. PubMed ID: 8619797
[TBL] [Abstract][Full Text] [Related]
31. Differential evolution of voltage-gated sodium channels in tetrapods and teleost fishes.
Widmark J; Sundström G; Ocampo Daza D; Larhammar D
Mol Biol Evol; 2011 Jan; 28(1):859-71. PubMed ID: 20924084
[TBL] [Abstract][Full Text] [Related]
32. Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A.
Plummer NW; Galt J; Jones JM; Burgess DL; Sprunger LK; Kohrman DC; Meisler MH
Genomics; 1998 Dec; 54(2):287-96. PubMed ID: 9828131
[TBL] [Abstract][Full Text] [Related]
33. [Molecular genetics of the long QT syndrome: clinical aspects].
Sepp R; Csanády M
Orv Hetil; 1999 Nov; 140(47):2633-8. PubMed ID: 10613047
[TBL] [Abstract][Full Text] [Related]
34. Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations.
Remme CA; Wilde AA; Bezzina CR
Trends Cardiovasc Med; 2008 Apr; 18(3):78-87. PubMed ID: 18436145
[TBL] [Abstract][Full Text] [Related]
35. Novel mutations in domain I of SCN5A cause Brugada syndrome.
Vatta M; Dumaine R; Antzelevitch C; Brugada R; Li H; Bowles NE; Nademanee K; Brugada J; Brugada P; Towbin JA
Mol Genet Metab; 2002 Apr; 75(4):317-24. PubMed ID: 12051963
[TBL] [Abstract][Full Text] [Related]
36. Exon-intron structure of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4).
Steinlein O; Weiland S; Stoodt J; Propping P
Genomics; 1996 Mar; 32(2):289-94. PubMed ID: 8833159
[TBL] [Abstract][Full Text] [Related]
37. An autopsy case of sudden unexpected nocturnal death syndrome with R1193Q polymorphism in the SCN5A gene.
Matsusue A; Kashiwagi M; Hara K; Waters B; Sugimura T; Kubo S
Leg Med (Tokyo); 2012 Nov; 14(6):317-9. PubMed ID: 22682427
[TBL] [Abstract][Full Text] [Related]
38. Non-SCN5A related Brugada syndromes: verification of normal splicing and trafficking of SCN5A without exonic mutations.
Nakano Y; Tashiro S; Kinoshita E; Kinoshita-Kikuta E; Takenaka S; Miyoshi M; Ogi H; Sakoda E; Oda N; Suenari K; Tonouchi Y; Okimoto T; Hirai Y; Miura F; Yamaoka K; Koike T; Chayama K
Ann Hum Genet; 2007 Jan; 71(Pt 1):8-17. PubMed ID: 17227473
[TBL] [Abstract][Full Text] [Related]
39. Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing.
Ackerman MJ; Splawski I; Makielski JC; Tester DJ; Will ML; Timothy KW; Keating MT; Jones G; Chadha M; Burrow CR; Stephens JC; Xu C; Judson R; Curran ME
Heart Rhythm; 2004 Nov; 1(5):600-7. PubMed ID: 15851227
[TBL] [Abstract][Full Text] [Related]
40. New SCN5A mutation in a SUDEP victim with idiopathic epilepsy.
Aurlien D; Leren TP; Taubøll E; Gjerstad L
Seizure; 2009 Mar; 18(2):158-60. PubMed ID: 18752973
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
