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Items: 1 to 20 of 105

1.

Association between KCNQ1 genetic variants and QT interval in a Chinese population.

Yu W, Zhang F, Hu W, Zhang R, Wang C, Lu J, Jiang F, Tang S, Peng D, Chen M, Bao Y, Xiang K, Hu C, Jia W.

Diabet Med. 2013 Oct;30(10):1225-9. doi: 10.1111/dme.12237. Epub 2013 Jun 21.

PMID:
23692438
2.

A common variant of NOS1AP is associated with QT interval duration in a Chinese population with Type 2 diabetes.

Lu J, Hu C, Hu W, Zhang R, Wang C, Qin W, Yu W, Xiang K; International Type 2 Diabetes 1q Consortium, Jia W.

Diabet Med. 2010 Sep;27(9):1074-9. doi: 10.1111/j.1464-5491.2010.03072.x.

3.

Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study.

Lehtinen AB, Daniel KR, Shah SA, Nelson MR, Ziegler JT, Freedman BI, Carr JJ, Herrington DM, Langefeld CD, Bowden DW.

Ann Noninvasive Electrocardiol. 2009 Jan;14(1):72-9. doi: 10.1111/j.1542-474X.2008.00276.x.

4.

Association of NOS1AP genetic variants with QT interval duration in families from the Diabetes Heart Study.

Lehtinen AB, Newton-Cheh C, Ziegler JT, Langefeld CD, Freedman BI, Daniel KR, Herrington DM, Bowden DW.

Diabetes. 2008 Apr;57(4):1108-14. doi: 10.2337/db07-1365. Epub 2008 Jan 30.

5.

Gender and age effects on ventricular repolarization abnormality in Japanese general carriers of a G643S common single nucleotide polymorphism for the KCNQ1 gene.

Ozawa T, Ito M, Tamaki S, Yao T, Ashihara T, Kita Y, Okamura T, Ueshima H, Horie M.

Circ J. 2006 Jun;70(6):645-50.

6.

Variant rs2237892 of KCNQ1 Is Potentially Associated with Hypertension and Macrovascular Complications in Type 2 Diabetes Mellitus in A Chinese Han Population.

Zhang W, Wang H, Guan X, Niu Q, Li W.

Genomics Proteomics Bioinformatics. 2015 Dec;13(6):364-70. doi: 10.1016/j.gpb.2015.05.004. Epub 2015 Dec 8.

7.

KCNQ1 haplotypes associate with type 2 diabetes in Malaysian Chinese Subjects.

Saif-Ali R, Ismail IS, Al-Hamodi Z, Al-Mekhlafi HM, Siang LC, Alabsi AM, Muniandy S.

Int J Mol Sci. 2011;12(9):5705-18. doi: 10.3390/ijms12095705. Epub 2011 Sep 5.

8.

Polymorphisms of the KCNQ1 gene are associated with the therapeutic responses of sulfonylureas in Chinese patients with type 2 diabetes.

Li Q, Tang TT, Jiang F, Zhang R, Chen M, Yin J, Bao YQ, Cheng X, Hu C, Jia WP.

Acta Pharmacol Sin. 2017 Jan;38(1):80-89. doi: 10.1038/aps.2016.103. Epub 2016 Oct 3.

9.

KCNQ1 gene polymorphisms are associated with the therapeutic efficacy of repaglinide in Chinese type 2 diabetic patients.

Dai XP, Huang Q, Yin JY, Guo Y, Gong ZC, Lei MX, Jiang TJ, Zhou HH, Liu ZQ.

Clin Exp Pharmacol Physiol. 2012 May;39(5):462-8. doi: 10.1111/j.1440-1681.2012.05701.x.

PMID:
22414228
10.

Relationship between the polymorphisms in KCNQ1 and type 2 diabetes in Chinese Kazakh population.

Cui LJ, Chang XY, Zhu LY, Feng G, Zhou T, Zhang CX, Chong KY, Sun K.

Genet Mol Res. 2016 May 13;15(2). doi: 10.4238/gmr.15027503.

11.

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2.

Kolder ICRM, Tanck MWT, Postema PG, Barc J, Sinner MF, Zumhagen S, Husemann A, Stallmeyer B, Koopmann TT, Hofman N, Pfeufer A, Lichtner P, Meitinger T, Beckmann BM, Myerburg RJ, Bishopric NH, Roden DM, Kääb S, Wilde AAM, Schott JJ, Schulze-Bahr E, Bezzina CR.

Circ Cardiovasc Genet. 2015 Jun;8(3):447-456. doi: 10.1161/CIRCGENETICS.114.000785. Epub 2015 Mar 3.

12.

Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study.

Pfeufer A, Jalilzadeh S, Perz S, Mueller JC, Hinterseer M, Illig T, Akyol M, Huth C, Schöpfer-Wendels A, Kuch B, Steinbeck G, Holle R, Näbauer M, Wichmann HE, Meitinger T, Kääb S.

Circ Res. 2005 Apr 1;96(6):693-701. Epub 2005 Mar 3.

13.

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes in the population of mainland China.

Liu Y, Zhou DZ, Zhang D, Chen Z, Zhao T, Zhang Z, Ning M, Hu X, Yang YF, Zhang ZF, Yu L, He L, Xu H.

Diabetologia. 2009 Jul;52(7):1315-21. doi: 10.1007/s00125-009-1375-y. Epub 2009 May 12.

14.

KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome?

Lahtinen AM, Marjamaa A, Swan H, Kontula K.

BMC Med Genet. 2011 Jan 18;12:11. doi: 10.1186/1471-2350-12-11.

15.

KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population.

Chen Z, Yin Q, Ma G, Qian Q.

Cardiovasc Diabetol. 2010 Aug 11;9:35. doi: 10.1186/1475-2840-9-35.

16.

Genetic variation in KCNQ1 associates with fasting glucose and beta-cell function: a study of 3,734 subjects comprising three ethnicities living in Singapore.

Tan JT, Nurbaya S, Gardner D, Ye S, Tai ES, Ng DP.

Diabetes. 2009 Jun;58(6):1445-9. doi: 10.2337/db08-1138. Epub 2009 Feb 27.

17.

A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.

Ikrar T, Hanawa H, Watanabe H, Okada S, Aizawa Y, Ramadan MM, Komura S, Yamashita F, Chinushi M, Aizawa Y.

J Cardiovasc Electrophysiol. 2008 May;19(5):541-9. doi: 10.1111/j.1540-8167.2007.01076.x. Epub 2008 Feb 4.

PMID:
18266681
18.

Prevalence and risk factors of prolonged QTc interval among Chinese patients with type 2 diabetes.

Li X, Ren H, Xu ZR, Liu YJ, Yang XP, Liu JQ.

Exp Diabetes Res. 2012;2012:234084. doi: 10.1155/2012/234084. Epub 2012 Dec 25.

19.

Common variants in KCNQ1 confer increased risk of type 2 diabetes and contribute to the diabetic epidemic in East Asians: a replication and meta-analysis.

Wang H, Miao K, Zhao J, Liu L, Cui G, Chen C, Wang DW, Ding H.

Ann Hum Genet. 2013 Sep;77(5):380-91. doi: 10.1111/ahg.12029. Epub 2013 Jun 21.

20.

Calcium channel blockers, NOS1AP, and heart-rate-corrected QT prolongation.

van Noord C, Aarnoudse AJ, Eijgelsheim M, Sturkenboom MC, Straus SM, Hofman A, Kors JA, Newton-Cheh C, Witteman JC, Stricker BH.

Pharmacogenet Genomics. 2009 Apr;19(4):260-6. doi: 10.1097/FPC.0b013e328324e556.

PMID:
19247217

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