Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 24

1.

Molecular aspects of the congenital and acquired Long QT Syndrome: clinical implications.

Saenen JB, Vrints CJ.

J Mol Cell Cardiol. 2008 Apr;44(4):633-46. doi: 10.1016/j.yjmcc.2008.01.006. Epub 2008 Feb 9. Review.

PMID:
18336833
[PubMed - indexed for MEDLINE]
2.

Mutation of an A-kinase-anchoring protein causes long-QT syndrome.

Chen L, Marquardt ML, Tester DJ, Sampson KJ, Ackerman MJ, Kass RS.

Proc Natl Acad Sci U S A. 2007 Dec 26;104(52):20990-5. Epub 2007 Dec 19.

PMID:
18093912
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study.

Aarnoudse AJ, Newton-Cheh C, de Bakker PI, Straus SM, Kors JA, Hofman A, Uitterlinden AG, Witteman JC, Stricker BH.

Circulation. 2007 Jul 3;116(1):10-6. Epub 2007 Jun 18.

PMID:
17576865
[PubMed - indexed for MEDLINE]
Free Article
4.

A common SCN5A variant alters the responsiveness of human sodium channels to class I antiarrhythmic agents.

Shuraih M, Ai T, Vatta M, Sohma Y, Merkle EM, Taylor E, Li Z, Xi Y, Razavi M, Towbin JA, Cheng J.

J Cardiovasc Electrophysiol. 2007 Apr;18(4):434-40. Epub 2007 Jan 10. Erratum in: J Cardiovasc Electrophysiol. 2007 Jun;18(6):690.

PMID:
17331104
[PubMed - indexed for MEDLINE]
5.

Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.

Cronk LB, Ye B, Kaku T, Tester DJ, Vatta M, Makielski JC, Ackerman MJ.

Heart Rhythm. 2007 Feb;4(2):161-6. Epub 2006 Dec 6.

PMID:
17275750
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome.

Vatta M, Ackerman MJ, Ye B, Makielski JC, Ughanze EE, Taylor EW, Tester DJ, Balijepalli RC, Foell JD, Li Z, Kamp TJ, Towbin JA.

Circulation. 2006 Nov 14;114(20):2104-12. Epub 2006 Oct 23.

PMID:
17060380
[PubMed - indexed for MEDLINE]
Free Article
7.

Cardiac sodium channel Nav1.5 is regulated by a multiprotein complex composed of syntrophins and dystrophin.

Gavillet B, Rougier JS, Domenighetti AA, Behar R, Boixel C, Ruchat P, Lehr HA, Pedrazzini T, Abriel H.

Circ Res. 2006 Aug 18;99(4):407-14. Epub 2006 Jul 20.

PMID:
16857961
[PubMed - indexed for MEDLINE]
Free Article
8.

Management of long QT syndrome.

Schwartz PJ.

Nat Clin Pract Cardiovasc Med. 2005 Jul;2(7):346-51. Review.

PMID:
16265560
[PubMed - indexed for MEDLINE]
9.

Molecular basis of arrhythmias.

Shah M, Akar FG, Tomaselli GF.

Circulation. 2005 Oct 18;112(16):2517-29. Review.

PMID:
16230503
[PubMed - indexed for MEDLINE]
Free Article
10.

Molecular etiopathogenesis of limb girdle muscular and congenital muscular dystrophies: boundaries and contiguities.

Guglieri M, Magri F, Comi GP.

Clin Chim Acta. 2005 Nov;361(1-2):54-79. Review.

PMID:
16002060
[PubMed - indexed for MEDLINE]
11.

A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gating.

Wehrens XH, Rossenbacker T, Jongbloed RJ, Gewillig M, Heidbüchel H, Doevendans PA, Vos MA, Wellens HJ, Kass RS.

Hum Mutat. 2003 May;21(5):552.

PMID:
12673799
[PubMed - indexed for MEDLINE]
12.

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death.

Mohler PJ, Schott JJ, Gramolini AO, Dilly KW, Guatimosim S, duBell WH, Song LS, Haurogné K, Kyndt F, Ali ME, Rogers TB, Lederer WJ, Escande D, Le Marec H, Bennett V.

Nature. 2003 Feb 6;421(6923):634-9.

PMID:
12571597
[PubMed - indexed for MEDLINE]
13.

Syntrophin gamma 2 regulates SCN5A gating by a PDZ domain-mediated interaction.

Ou Y, Strege P, Miller SM, Makielski J, Ackerman M, Gibbons SJ, Farrugia G.

J Biol Chem. 2003 Jan 17;278(3):1915-23. Epub 2002 Nov 11.

PMID:
12429735
[PubMed - indexed for MEDLINE]
Free Article
14.

Cardiac arrhythmias: the genetic connection.

Towbin JA.

J Cardiovasc Electrophysiol. 2000 May;11(5):601-2. Review. No abstract available.

PMID:
10826942
[PubMed - indexed for MEDLINE]
15.

Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells.

Piluso G, Mirabella M, Ricci E, Belsito A, Abbondanza C, Servidei S, Puca AA, Tonali P, Puca GA, Nigro V.

J Biol Chem. 2000 May 26;275(21):15851-60.

PMID:
10747910
[PubMed - indexed for MEDLINE]
Free Article
16.

Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins.

Gee SH, Madhavan R, Levinson SR, Caldwell JH, Sealock R, Froehner SC.

J Neurosci. 1998 Jan 1;18(1):128-37.

PMID:
9412493
[PubMed - indexed for MEDLINE]
Free Article
17.

Improved splice site detection in Genie.

Reese MG, Eeckman FH, Kulp D, Haussler D.

J Comput Biol. 1997 Fall;4(3):311-23.

PMID:
9278062
[PubMed - indexed for MEDLINE]
18.

Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome.

Wang DW, Yazawa K, George AL Jr, Bennett PB.

Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13200-5.

PMID:
8917568
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Diagnostic criteria for the long QT syndrome. An update.

Schwartz PJ, Moss AJ, Vincent GM, Crampton RS.

Circulation. 1993 Aug;88(2):782-4. Review. No abstract available.

PMID:
8339437
[PubMed - indexed for MEDLINE]
20.

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24.

Ahn AH, Yoshida M, Anderson MS, Feener CA, Selig S, Hagiwara Y, Ozawa E, Kunkel LM.

Proc Natl Acad Sci U S A. 1994 May 10;91(10):4446-50.

PMID:
8183929
[PubMed - indexed for MEDLINE]
Free PMC Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk