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Items: 1 to 20 of 61

1.
2.

Modelling the long QT syndrome with induced pluripotent stem cells.

Itzhaki I, Maizels L, Huber I, Zwi-Dantsis L, Caspi O, Winterstern A, Feldman O, Gepstein A, Arbel G, Hammerman H, Boulos M, Gepstein L.

Nature. 2011 Mar 10;471(7337):225-9. doi: 10.1038/nature09747. Epub 2011 Jan 16.

PMID:
21240260
3.

Zebrafish behavioral profiling links drugs to biological targets and rest/wake regulation.

Rihel J, Prober DA, Arvanites A, Lam K, Zimmerman S, Jang S, Haggarty SJ, Kokel D, Rubin LL, Peterson RT, Schier AF.

Science. 2010 Jan 15;327(5963):348-51. doi: 10.1126/science.1183090.

4.

A primate-specific, brain isoform of KCNH2 affects cortical physiology, cognition, neuronal repolarization and risk of schizophrenia.

Huffaker SJ, Chen J, Nicodemus KK, Sambataro F, Yang F, Mattay V, Lipska BK, Hyde TM, Song J, Rujescu D, Giegling I, Mayilyan K, Proust MJ, Soghoyan A, Caforio G, Callicott JH, Bertolino A, Meyer-Lindenberg A, Chang J, Ji Y, Egan MF, Goldberg TE, Kleinman JE, Lu B, Weinberger DR.

Nat Med. 2009 May;15(5):509-18. doi: 10.1038/nm.1962. Epub 2009 May 3.

5.

Identification of the gene causing long QT syndrome in an Israeli family.

Tenenbaum M, Lavi S, Magal N, Halpern GJ, Bolocan I, Boulos M, Kapeliovich M, Shohat M, Hammerman H.

Isr Med Assoc J. 2008 Nov;10(11):809-11.

6.

Fever-induced QTc prolongation and ventricular arrhythmias in individuals with type 2 congenital long QT syndrome.

Amin AS, Herfst LJ, Delisle BP, Klemens CA, Rook MB, Bezzina CR, Underkofler HA, Holzem KM, Ruijter JM, Tan HL, January CT, Wilde AA.

J Clin Invest. 2008 Jul;118(7):2552-61. doi: 10.1172/JCI35337.

7.

MicroRNA miR-133 represses HERG K+ channel expression contributing to QT prolongation in diabetic hearts.

Xiao J, Luo X, Lin H, Zhang Y, Lu Y, Wang N, Zhang Y, Yang B, Wang Z.

J Biol Chem. 2007 Apr 27;282(17):12363-7. Epub 2007 Mar 7. Retraction in: J Biol Chem. 2011 Aug 12;286(32):28656.

8.

Female predominance and transmission distortion in the long-QT syndrome.

Imboden M, Swan H, Denjoy I, Van Langen IM, Latinen-Forsblom PJ, Napolitano C, Fressart V, Breithardt G, Berthet M, Priori S, Hainque B, Wilde AA, Schulze-Bahr E, Feingold J, Guicheney P.

N Engl J Med. 2006 Dec 28;355(26):2744-51.

9.

Molecular ablation of ventricular tachycardia after myocardial infarction.

Sasano T, McDonald AD, Kikuchi K, Donahue JK.

Nat Med. 2006 Nov;12(11):1256-8. Epub 2006 Oct 29.

10.

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.

11.

Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome.

Millat G, Chevalier P, Restier-Miron L, Da Costa A, Bouvagnet P, Kugener B, Fayol L, Gonzàlez Armengod C, Oddou B, Chanavat V, Froidefond E, Perraudin R, Rousson R, Rodriguez-Lafrasse C.

Clin Genet. 2006 Sep;70(3):214-27.

PMID:
16922724
12.

Mechanisms of pharmacological rescue of trafficking-defective hERG mutant channels in human long QT syndrome.

Gong Q, Jones MA, Zhou Z.

J Biol Chem. 2006 Feb 17;281(7):4069-74. Epub 2005 Dec 16.

13.

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population.

Gouas L, Nicaud V, Berthet M, Forhan A, Tiret L, Balkau B, Guicheney P; D.E.S.I.R. Study Group.

Eur J Hum Genet. 2005 Nov;13(11):1213-22.

14.

Genetics of acquired long QT syndrome.

Roden DM, Viswanathan PC.

J Clin Invest. 2005 Aug;115(8):2025-32. Review.

15.

Short QT syndrome.

Schimpf R, Wolpert C, Gaita F, Giustetto C, Borggrefe M.

Cardiovasc Res. 2005 Aug 15;67(3):357-66. Review.

16.

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.

Tester DJ, Will ML, Haglund CM, Ackerman MJ.

Heart Rhythm. 2005 May;2(5):507-17.

PMID:
15840476
17.

Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.

Hong K, Bjerregaard P, Gussak I, Brugada R.

J Cardiovasc Electrophysiol. 2005 Apr;16(4):394-6.

PMID:
15828882
18.

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.

Priori SG, Pandit SV, Rivolta I, Berenfeld O, Ronchetti E, Dhamoon A, Napolitano C, Anumonwo J, di Barletta MR, Gudapakkam S, Bosi G, Stramba-Badiale M, Jalife J.

Circ Res. 2005 Apr 15;96(7):800-7. Epub 2005 Mar 10.

19.

Degradation of trafficking-defective long QT syndrome type II mutant channels by the ubiquitin-proteasome pathway.

Gong Q, Keeney DR, Molinari M, Zhou Z.

J Biol Chem. 2005 May 13;280(19):19419-25. Epub 2005 Mar 10.

20.

In vivo identification of genes that modify ether-a-go-go-related gene activity in Caenorhabditis elegans may also affect human cardiac arrhythmia.

Petersen CI, McFarland TR, Stepanovic SZ, Yang P, Reiner DJ, Hayashi K, George AL, Roden DM, Thomas JH, Balser JR.

Proc Natl Acad Sci U S A. 2004 Aug 10;101(32):11773-8. Epub 2004 Jul 27.

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