Olson TM - Search Results

1

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation.

Olson TM, Alekseev AE, Liu XK, Park S, Zingman LV, Bienengraeber M, Sattiraju S, Ballew JD, Jahangir A, Terzic A. Olson TM, et al. Hum Mol Genet. 2006 Jul 15;15(14):2185-91. doi: 10.1093/hmg/ddl143. Epub 2006 Jun 13. Hum Mol Genet. 2006. PMID: 16772329

2

Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7.

Olson TM, Michels VV, Lindor NM, Pastores GM, Weber JL, Schaid DJ, Driscoll DJ, Feldt RH, Thibodeau SN. Olson TM, et al. Hum Mol Genet. 1993 Jul;2(7):869-73. doi: 10.1093/hmg/2.7.869. Hum Mol Genet. 1993. PMID: 8364568

3

A 30 kb deletion within the elastin gene results in familial supravalvular aortic stenosis.

Olson TM, Michels VV, Urban Z, Csiszar K, Christiano AM, Driscoll DJ, Feldt RH, Boyd CD, Thibodeau SN. Olson TM, et al. Hum Mol Genet. 1995 Sep;4(9):1677-9. doi: 10.1093/hmg/4.9.1677. Hum Mol Genet. 1995. PMID: 8541862 No abstract available.

4

Familial atrial fibrillation is a genetically heterogeneous disorder.

Darbar D, Herron KJ, Ballew JD, Jahangir A, Gersh BJ, Shen WK, Hammill SC, Packer DL, Olson TM. Darbar D, et al. Among authors: olson tm. J Am Coll Cardiol. 2003 Jun 18;41(12):2185-92. doi: 10.1016/s0735-1097(03)00465-0. J Am Coll Cardiol. 2003. PMID: 12821245 Free article.

5

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating.

Bienengraeber M, Olson TM, Selivanov VA, Kathmann EC, O'Cochlain F, Gao F, Karger AB, Ballew JD, Hodgson DM, Zingman LV, Pang YP, Alekseev AE, Terzic A. Bienengraeber M, et al. Among authors: olson tm. Nat Genet. 2004 Apr;36(4):382-7. doi: 10.1038/ng1329. Epub 2004 Mar 21. Nat Genet. 2004. PMID: 15034580 Free PMC article.

6

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.

Olson TM, Michels VV, Ballew JD, Reyna SP, Karst ML, Herron KJ, Horton SC, Rodeheffer RJ, Anderson JL. Olson TM, et al. JAMA. 2005 Jan 26;293(4):447-54. doi: 10.1001/jama.293.4.447. JAMA. 2005. PMID: 15671429 Free PMC article.

7

Cardiac KATP channels in health and disease.

Kane GC, Liu XK, Yamada S, Olson TM, Terzic A. Kane GC, et al. Among authors: olson tm. J Mol Cell Cardiol. 2005 Jun;38(6):937-43. doi: 10.1016/j.yjmcc.2005.02.026. Epub 2005 Apr 25. J Mol Cell Cardiol. 2005. PMID: 15910878 Free PMC article. Review.

8

A common polymorphism in SCN5A is associated with lone atrial fibrillation.

Chen LY, Ballew JD, Herron KJ, Rodeheffer RJ, Olson TM. Chen LY, et al. Among authors: olson tm. Clin Pharmacol Ther. 2007 Jan;81(1):35-41. doi: 10.1038/sj.clpt.6100016. Clin Pharmacol Ther. 2007. PMID: 17185997 Free PMC article.

9

Aminoglycoside-induced translational read-through in disease: overcoming nonsense mutations by pharmacogenetic therapy.

Zingman LV, Park S, Olson TM, Alekseev AE, Terzic A. Zingman LV, et al. Among authors: olson tm. Clin Pharmacol Ther. 2007 Jan;81(1):99-103. doi: 10.1038/sj.clpt.6100012. Clin Pharmacol Ther. 2007. PMID: 17186006 Review.

10

KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation.

Olson TM, Alekseev AE, Moreau C, Liu XK, Zingman LV, Miki T, Seino S, Asirvatham SJ, Jahangir A, Terzic A. Olson TM, et al. Nat Clin Pract Cardiovasc Med. 2007 Feb;4(2):110-6. doi: 10.1038/ncpcardio0792. Nat Clin Pract Cardiovasc Med. 2007. PMID: 17245405 Free PMC article.

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