137 related articles for article (PubMed ID: 11896454)
1. Characterisation of the human voltage-gated potassium channel gene, KCNA7, a candidate gene for inherited cardiac disorders, and its exclusion as cause of progressive familial heart block I (PFHBI).
Bardien-Kruger S; Wulff H; Arieff Z; Brink P; Chandy KG; Corfield V
Eur J Hum Genet; 2002 Jan; 10(1):36-43. PubMed ID: 11896454
[TBL] [Abstract][Full Text] [Related]
2. Initial isolation and analysis of the human Kv1.7 (KCNA7) gene, a member of the voltage-gated potassium channel gene family.
Kashuba VI; Kvasha SM; Protopopov AI; Gizatullin RZ; Rynditch AV; Wahlestedt C; Wasserman WW; Zabarovsky ER
Gene; 2001 May; 268(1-2):115-22. PubMed ID: 11368907
[TBL] [Abstract][Full Text] [Related]
3. Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA).
Isbrandt D; Leicher T; Waldschütz R; Zhu X; Luhmann U; Michel U; Sauter K; Pongs O
Genomics; 2000 Mar; 64(2):144-54. PubMed ID: 10729221
[TBL] [Abstract][Full Text] [Related]
4. Cloning and developmental expression of Shaker potassium channels in the cochlea of the chicken.
Duzhyy DE; Sakai Y; Sokolowski BH
Brain Res Mol Brain Res; 2004 Feb; 121(1-2):70-85. PubMed ID: 14969738
[TBL] [Abstract][Full Text] [Related]
5. Genomic organization, chromosomal localization, tissue distribution, and biophysical characterization of a novel mammalian Shaker-related voltage-gated potassium channel, Kv1.7.
Kalman K; Nguyen A; Tseng-Crank J; Dukes ID; Chandy G; Hustad CM; Copeland NG; Jenkins NA; Mohrenweiser H; Brandriff B; Cahalan M; Gutman GA; Chandy KG
J Biol Chem; 1998 Mar; 273(10):5851-7. PubMed ID: 9488722
[TBL] [Abstract][Full Text] [Related]
6. Accessory Kvbeta1 subunits differentially modulate the functional expression of voltage-gated K+ channels in mouse ventricular myocytes.
Aimond F; Kwak SP; Rhodes KJ; Nerbonne JM
Circ Res; 2005 Mar; 96(4):451-8. PubMed ID: 15662035
[TBL] [Abstract][Full Text] [Related]
7. Genomic localization of the human gene for KCNA10, a cGMP-activated K channel.
Orias M; Bray-Ward P; Curran ME; Keating MT; Desir GV
Genomics; 1997 May; 42(1):33-7. PubMed ID: 9177773
[TBL] [Abstract][Full Text] [Related]
8. The KVLQT1 gene is not a common target for mutations in patients with various heart pathologies.
Moric E; Herbert E; Mazurek U; Samelska J; Cholewa K; Trusz-Gluza M; Wilczok T
J Appl Genet; 2002; 43(2):245-54. PubMed ID: 12080180
[TBL] [Abstract][Full Text] [Related]
9. Characterization of the outer pore region of the apamin-sensitive Ca2+-activated K+ channel rSK2.
Jäger H; Grissmer S
Toxicon; 2004 Jun; 43(8):951-60. PubMed ID: 15208028
[TBL] [Abstract][Full Text] [Related]
10. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Ion channel proteins in mouse and human vestibular tissue.
Hotchkiss K; Harvey M; Pacheco M; Sokolowski B
Otolaryngol Head Neck Surg; 2005 Jun; 132(6):916-23. PubMed ID: 15944564
[TBL] [Abstract][Full Text] [Related]
13. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
14. A truncated splice variant of KCNQ1 cloned from rat heart.
Yamada Y; Chen X; Kobayashi T; Kamada Y; Nagashima M; Tsutsuura M; Seki S; Yamakage M; Namiki A; Tohse N
Biochem Biophys Res Commun; 2002 Jun; 294(2):199-204. PubMed ID: 12051693
[TBL] [Abstract][Full Text] [Related]
15. Localization of two potassium channel beta subunit genes, KCNA1B and KCNA2B.
Schultz D; Litt M; Smith L; Thayer M; McCormack K
Genomics; 1996 Feb; 31(3):389-91. PubMed ID: 8838324
[TBL] [Abstract][Full Text] [Related]
16. Voltage-gated potassium channel genes are clustered in paralogous regions of the mouse genome.
Lock LF; Gilbert DJ; Street VA; Migeon MB; Jenkins NA; Copeland NG; Tempel BL
Genomics; 1994 Apr; 20(3):354-62. PubMed ID: 8034307
[TBL] [Abstract][Full Text] [Related]
17. Expression of Shaker-type voltage-gated potassium channel genes in the guinea-pig.
Manabe I; Tsuboi M; Ahmmed GU; Sasaki N; Ohtahara A; Yamamoto Y; Hiroe K; Yoshida A; Hisatome I; Shigemasa C
Res Commun Mol Pathol Pharmacol; 1998 Jan; 99(1):33-40. PubMed ID: 9523353
[TBL] [Abstract][Full Text] [Related]
18. Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome.
Yamaguchi M; Shimizu M; Ino H; Terai H; Hayashi K; Mabuchi H; Hoshi N; Higashida H
Clin Sci (Lond); 2003 Apr; 104(4):377-82. PubMed ID: 12653681
[TBL] [Abstract][Full Text] [Related]
19. The Kv2.2 alpha subunit contributes to delayed rectifier K(+) currents in myocytes from rabbit corpus cavernosum.
Malysz J; Farrugia G; Ou Y; Szurszewski JH; Nehra A; Gibbons SJ
J Androl; 2002; 23(6):899-910. PubMed ID: 12399537
[TBL] [Abstract][Full Text] [Related]
20. Complete loss of the cytoplasmic carboxyl terminus of the KCNQ2 potassium channel: a novel mutation in a large Czech pedigree with benign neonatal convulsions or other epileptic phenotypes.
Pereira S; Roll P; Krizova J; Genton P; Brazdil M; Kuba R; Cau P; Rektor I; Szepetowski P
Epilepsia; 2004 Apr; 45(4):384-90. PubMed ID: 15030501
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]