PubMed (OMIM) for id: 1641146

Year	Number of Results
1970	2
1971	1
1973	1
1974	1
1975	1
1976	2
1977	3
1978	1
1979	1
1980	3
1981	1
1982	3
1986	2
1991	4
1992	1
1993	3
1994	7
1996	5
1997	9
1998	10
1999	11
2000	3
2001	6
2002	4
2003	6
2004	7
2005	1
2024	0

1

KCNQ1-dependent transport in renal and gastrointestinal epithelia.

Vallon V, Grahammer F, Volkl H, Sandu CD, Richter K, Rexhepaj R, Gerlach U, Rong Q, Pfeifer K, Lang F. Vallon V, et al. Proc Natl Acad Sci U S A. 2005 Dec 6;102(49):17864-9. doi: 10.1073/pnas.0505860102. Epub 2005 Nov 28. Proc Natl Acad Sci U S A. 2005. PMID: 16314573 Free PMC article.

2

Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes.

Umlauf D, Goto Y, Cao R, Cerqueira F, Wagschal A, Zhang Y, Feil R. Umlauf D, et al. Nat Genet. 2004 Dec;36(12):1296-300. doi: 10.1038/ng1467. Epub 2004 Oct 31. Nat Genet. 2004. PMID: 15516932

3

Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.

Lewis A, Mitsuya K, Umlauf D, Smith P, Dean W, Walter J, Higgins M, Feil R, Reik W. Lewis A, et al. Nat Genet. 2004 Dec;36(12):1291-5. doi: 10.1038/ng1468. Epub 2004 Oct 31. Nat Genet. 2004. PMID: 15516931

4

Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans.

Casimiro MC, Knollmann BC, Yamoah EN, Nie L, Vary JC Jr, Sirenko SG, Greene AE, Grinberg A, Huang SP, Ebert SN, Pfeifer K. Casimiro MC, et al. Genomics. 2004 Sep;84(3):555-64. doi: 10.1016/j.ygeno.2004.06.007. Genomics. 2004. PMID: 15498462

5

Truncated KCNQ1 mutant, A178fs/105, forms hetero-multimer channel with wild-type causing a dominant-negative suppression due to trafficking defect.

Aizawa Y, Ueda K, Wu LM, Inagaki N, Hayashi T, Takahashi M, Ohta M, Kawano S, Hirano Y, Yasunami M, Aizawa Y, Kimura A, Hiraoka M. Aizawa Y, et al. FEBS Lett. 2004 Sep 10;574(1-3):145-50. doi: 10.1016/j.febslet.2004.08.018. FEBS Lett. 2004. PMID: 15358555 Free article.

6

KCNE1 binds to the KCNQ1 pore to regulate potassium channel activity.

Melman YF, Um SY, Krumerman A, Kagan A, McDonald TV. Melman YF, et al. Neuron. 2004 Jun 24;42(6):927-37. doi: 10.1016/j.neuron.2004.06.001. Neuron. 2004. PMID: 15207237 Free article.

7

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome.

Bellocq C, van Ginneken AC, Bezzina CR, Alders M, Escande D, Mannens MM, Baró I, Wilde AA. Bellocq C, et al. Circulation. 2004 May 25;109(20):2394-7. doi: 10.1161/01.CIR.0000130409.72142.FE. Circulation. 2004. PMID: 15159330

8

Effective long-term control of cardiac events with beta-blockers in a family with a common LQT1 mutation.

Wedekind H, Schwarz M, Hauenschild S, Djonlagic H, Haverkamp W, Breithardt G, Wülfing T, Pongs O, Isbrandt D, Schulze-Bahr E. Wedekind H, et al. Clin Genet. 2004 Mar;65(3):233-41. doi: 10.1111/j.0009-9163.2004.00221.x. Clin Genet. 2004. PMID: 14756674

9

Risk stratification in the long-QT syndrome.

Priori SG, Schwartz PJ, Napolitano C, Bloise R, Ronchetti E, Grillo M, Vicentini A, Spazzolini C, Nastoli J, Bottelli G, Folli R, Cappelletti D. Priori SG, et al. N Engl J Med. 2003 May 8;348(19):1866-74. doi: 10.1056/NEJMoa022147. N Engl J Med. 2003. PMID: 12736279 Free article.

10

The long-QT syndrome--bedside to bench to bedside.

Vincent GM. Vincent GM. N Engl J Med. 2003 May 8;348(19):1837-8. doi: 10.1056/NEJMp030039. N Engl J Med. 2003. PMID: 12736277 No abstract available.

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