PubMed (OMIM) for id: 327586

Year	Number of Results
1971	1
1972	1
1976	1
1979	1
1993	1
1994	2
1997	1
1998	1
1999	1
2001	3
2002	8
2003	1
2005	1
2024	0

1

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. Priori SG, et al. Circ Res. 2005 Apr 15;96(7):800-7. doi: 10.1161/01.RES.0000162101.76263.8c. Epub 2005 Mar 10. Circ Res. 2005. PMID: 15761194

2

PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome.

Donaldson MR, Jensen JL, Tristani-Firouzi M, Tawil R, Bendahhou S, Suarez WA, Cobo AM, Poza JJ, Behr E, Wagstaff J, Szepetowski P, Pereira S, Mozaffar T, Escolar DM, Fu YH, Ptácek LJ. Donaldson MR, et al. Neurology. 2003 Jun 10;60(11):1811-6. doi: 10.1212/01.wnl.0000072261.14060.47. Neurology. 2003. PMID: 12796536

3

Biological pacemaker created by gene transfer.

Miake J, Marbán E, Nuss HB. Miake J, et al. Nature. 2002 Sep 12;419(6903):132-3. doi: 10.1038/419132b. Nature. 2002. PMID: 12226654

4

Amiodarone and acetazolamide for the treatment of genetically confirmed severe Andersen syndrome.

Junker J, Haverkamp W, Schulze-Bahr E, Eckardt L, Paulus W, Kiefer R. Junker J, et al. Neurology. 2002 Aug 13;59(3):466. doi: 10.1212/wnl.59.3.466. Neurology. 2002. PMID: 12177393 No abstract available.

5

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. Tristani-Firouzi M, et al. J Clin Invest. 2002 Aug;110(3):381-8. doi: 10.1172/JCI15183. J Clin Invest. 2002. PMID: 12163457 Free PMC article.

6

KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes.

Andelfinger G, Tapper AR, Welch RC, Vanoye CG, George AL Jr, Benson DW. Andelfinger G, et al. Am J Hum Genet. 2002 Sep;71(3):663-8. doi: 10.1086/342360. Epub 2002 Jul 29. Am J Hum Genet. 2002. PMID: 12148092 Free PMC article.

7

Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies.

Lopes CM, Zhang H, Rohacs T, Jin T, Yang J, Logothetis DE. Lopes CM, et al. Neuron. 2002 Jun 13;34(6):933-44. doi: 10.1016/s0896-6273(02)00725-0. Neuron. 2002. PMID: 12086641 Free article.

8

Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome.

Preisig-Müller R, Schlichthörl G, Goerge T, Heinen S, Brüggemann A, Rajan S, Derst C, Veh RW, Daut J. Preisig-Müller R, et al. Proc Natl Acad Sci U S A. 2002 May 28;99(11):7774-9. doi: 10.1073/pnas.102609499. Proc Natl Acad Sci U S A. 2002. PMID: 12032359 Free PMC article.

9

Sex, hormones, and repolarization.

Pham TV, Rosen MR. Pham TV, et al. Cardiovasc Res. 2002 Feb 15;53(3):740-51. doi: 10.1016/s0008-6363(01)00429-1. Cardiovasc Res. 2002. PMID: 11861044 Review.

10

Gender differences in arrhythmias.

Wolbrette D, Naccarelli G, Curtis A, Lehmann M, Kadish A. Wolbrette D, et al. Clin Cardiol. 2002 Feb;25(2):49-56. doi: 10.1002/clc.4950250203. Clin Cardiol. 2002. PMID: 11841151 Free PMC article. Review.

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