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Results: 1 to 20 of 163

Similar articles for PubMed (Select 9312006)

1.

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias.

Chouabe C, Neyroud N, Guicheney P, Lazdunski M, Romey G, Barhanin J.

EMBO J. 1997 Sep 1;16(17):5472-9.

2.

Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias.

Mohammad-Panah R, Demolombe S, Neyroud N, Guicheney P, Kyndt F, van den Hoff M, Baró I, Escande D.

Am J Hum Genet. 1999 Apr;64(4):1015-23.

3.

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.

Wollnik B, Schroeder BC, Kubisch C, Esperer HD, Wieacker P, Jentsch TJ.

Hum Mol Genet. 1997 Oct;6(11):1943-9.

4.

Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk.

Chouabe C, Neyroud N, Richard P, Denjoy I, Hainque B, Romey G, Drici MD, Guicheney P, Barhanin J.

Cardiovasc Res. 2000 Mar;45(4):971-80.

5.

A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly.

Schmitt N, Schwarz M, Peretz A, Abitbol I, Attali B, Pongs O.

EMBO J. 2000 Feb 1;19(3):332-40.

6.

Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome.

Neyroud N, Denjoy I, Donger C, Gary F, Villain E, Leenhardt A, Benali K, Schwartz K, Coumel P, Guicheney P.

Eur J Hum Genet. 1998 Mar-Apr;6(2):129-33.

7.

Long QT syndrome: ionic basis and arrhythmia mechanism in long QT syndrome type 1.

Sanguinetti MC.

J Cardiovasc Electrophysiol. 2000 Jun;11(6):710-2.

PMID:
10868746
8.

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.

Neyroud N, Tesson F, Denjoy I, Leibovici M, Donger C, Barhanin J, Fauré S, Gary F, Coumel P, Petit C, Schwartz K, Guicheney P.

Nat Genet. 1997 Feb;15(2):186-9.

PMID:
9020846
9.
10.

Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits.

Franqueza L, Lin M, Shen J, Splawski I, Keating MT, Sanguinetti MC.

J Biol Chem. 1999 Jul 23;274(30):21063-70. Erratum in: J Biol Chem 1999 Aug 27;274(35):25188.

11.

A dominant negative isoform of the long QT syndrome 1 gene product.

Demolombe S, Baró I, Péréon Y, Bliek J, Mohammad-Panah R, Pollard H, Morid S, Mannens M, Wilde A, Barhanin J, Charpentier F, Escande D.

J Biol Chem. 1998 Mar 20;273(12):6837-43.

12.

Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.

Chen Q, Zhang D, Gingell RL, Moss AJ, Napolitano C, Priori SG, Schwartz PJ, Kehoe E, Robinson JL, Schulze-Bahr E, Wang Q, Towbin JA.

Circulation. 1999 Mar 16;99(10):1344-7.

13.

Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.

Sanguinetti MC.

Ann N Y Acad Sci. 1999 Apr 30;868:406-13. Review.

PMID:
10414310
14.

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.

Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, Sørland SJ, Lund O, Malcolm S, Pembrey M, Bhattacharya S, Bitner-Glindzicz M.

Hum Mol Genet. 1997 Nov;6(12):2179-85.

15.

Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome.

Wang Z, Li H, Moss AJ, Robinson J, Zareba W, Knilans T, Bowles NE, Towbin JA.

Mol Genet Metab. 2002 Apr;75(4):308-16.

PMID:
12051962
16.

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.

Sanguinetti MC, Curran ME, Zou A, Shen J, Spector PS, Atkinson DL, Keating MT.

Nature. 1996 Nov 7;384(6604):80-3.

PMID:
8900283
17.

Dominant-negative KvLQT1 mutations underlie the LQT1 form of long QT syndrome.

Shalaby FY, Levesque PC, Yang WP, Little WA, Conder ML, Jenkins-West T, Blanar MA.

Circulation. 1997 Sep 16;96(6):1733-6.

18.

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.

Neyroud N, Richard P, Vignier N, Donger C, Denjoy I, Demay L, Shkolnikova M, Pesce R, Chevalier P, Hainque B, Coumel P, Schwartz K, Guicheney P.

Circ Res. 1999 Feb 19;84(3):290-7.

19.

George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafness.

Splawski I, Timothy KW, Vincent GM, Atkinson DL, Keating MT.

Proc Assoc Am Physicians. 1997 Sep;109(5):504-11.

PMID:
9285950
20.

Involvement of IsK-associated K+ channel in heart rate control of repolarization in a murine engineered model of Jervell and Lange-Nielsen syndrome.

Drici MD, Arrighi I, Chouabe C, Mann JR, Lazdunski M, Romey G, Barhanin J.

Circ Res. 1998 Jul 13;83(1):95-102.

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