Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 64

1.

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.

Splawski I, Timothy KW, Sharpe LM, Decher N, Kumar P, Bloise R, Napolitano C, Schwartz PJ, Joseph RM, Condouris K, Tager-Flusberg H, Priori SG, Sanguinetti MC, Keating MT.

Cell. 2004 Oct 1;119(1):19-31.

2.

Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers.

Priori SG, Napolitano C, Schwartz PJ, Grillo M, Bloise R, Ronchetti E, Moncalvo C, Tulipani C, Veia A, Bottelli G, Nastoli J.

JAMA. 2004 Sep 15;292(11):1341-4.

PMID:
15367556
3.

Calmodulin mediates Ca2+ sensitivity of sodium channels.

Kim J, Ghosh S, Liu H, Tateyama M, Kass RS, Pitt GS.

J Biol Chem. 2004 Oct 22;279(43):45004-12. Epub 2004 Aug 16.

4.

Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome: multicenter study in Japan.

Shimizu W, Horie M, Ohno S, Takenaka K, Yamaguchi M, Shimizu M, Washizuka T, Aizawa Y, Nakamura K, Ohe T, Aiba T, Miyamoto Y, Yoshimasa Y, Towbin JA, Priori SG, Kamakura S.

J Am Coll Cardiol. 2004 Jul 7;44(1):117-25.

5.

A cardiac arrhythmia syndrome caused by loss of ankyrin-B function.

Mohler PJ, Splawski I, Napolitano C, Bottelli G, Sharpe L, Timothy K, Priori SG, Keating MT, Bennett V.

Proc Natl Acad Sci U S A. 2004 Jun 15;101(24):9137-42. Epub 2004 Jun 3.

6.

Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity.

Donaldson MR, Yoon G, Fu YH, Ptacek LJ.

Ann Med. 2004;36 Suppl 1:92-7. Review.

PMID:
15176430
7.

Pharmacological rescue of trafficking defective HERG channels formed by coassembly of wild-type and long QT mutant N470D subunits.

Gong Q, Anderson CL, January CT, Zhou Z.

Am J Physiol Heart Circ Physiol. 2004 Aug;287(2):H652-8. Epub 2004 Apr 8.

8.

LQT4 gene: the "missing" ankyrin.

Yong S, Tian X, Wang Q.

Mol Interv. 2003 May;3(3):131-6. Review.

9.

The Na+ channel inactivation gate is a molecular complex: a novel role of the COOH-terminal domain.

Motoike HK, Liu H, Glaaser IW, Yang AS, Tateyama M, Kass RS.

J Gen Physiol. 2004 Feb;123(2):155-65.

10.

Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome.

Zareba W, Moss AJ, Sheu G, Kaufman ES, Priori S, Vincent GM, Towbin JA, Benhorin J, Schwartz PJ, Napolitano C, Hall WJ, Keating MT, Qi M, Robinson J, Andrews ML; International LQTS Registry, University of Rochester, Rochester, New York.

J Cardiovasc Electrophysiol. 2003 Nov;14(11):1149-53.

PMID:
14678125
11.

Defective potassium channel Kir2.1 trafficking underlies Andersen-Tawil syndrome.

Bendahhou S, Donaldson MR, Plaster NM, Tristani-Firouzi M, Fu YH, Ptácek LJ.

J Biol Chem. 2003 Dec 19;278(51):51779-85. Epub 2003 Oct 1.

12.

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death.

JERVELL A, LANGE-NIELSEN F.

Am Heart J. 1957 Jul;54(1):59-68. No abstract available.

PMID:
13435203
13.

The electrical constants of Purkinje fibres.

WEIDMANN S.

J Physiol. 1952 Nov;118(3):348-60. No abstract available.

14.

Long QT syndrome: novel insights into the mechanisms of cardiac arrhythmias.

Kass RS, Moss AJ.

J Clin Invest. 2003 Sep;112(6):810-5. Review.

15.

Long QT Syndrome.

Moss AJ.

JAMA. 2003 Apr 23-30;289(16):2041-4. Review. No abstract available.

PMID:
12709446
16.

Exercise stress test amplifies genotype-phenotype correlation in the LQT1 and LQT2 forms of the long-QT syndrome.

Takenaka K, Ai T, Shimizu W, Kobori A, Ninomiya T, Otani H, Kubota T, Takaki H, Kamakura S, Horie M.

Circulation. 2003 Feb 18;107(6):838-44.

17.

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
18.

Requirement of subunit expression for cAMP-mediated regulation of a heart potassium channel.

Kurokawa J, Chen L, Kass RS.

Proc Natl Acad Sci U S A. 2003 Feb 18;100(4):2122-7. Epub 2003 Feb 3.

19.

A novel mutation (T65P) in the PAS domain of the human potassium channel HERG results in the long QT syndrome by trafficking deficiency.

Paulussen A, Raes A, Matthijs G, Snyders DJ, Cohen N, Aerssens J.

J Biol Chem. 2002 Dec 13;277(50):48610-6. Epub 2002 Sep 26.

20.

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).

Tristani-Firouzi M, Jensen JL, Donaldson MR, Sansone V, Meola G, Hahn A, Bendahhou S, Kwiecinski H, Fidzianska A, Plaster N, Fu YH, Ptacek LJ, Tawil R.

J Clin Invest. 2002 Aug;110(3):381-8.

Items per page

Supplemental Content

Write to the Help Desk