Olson TM - Search Results

1

Pharmacological Modulation of Calcium Homeostasis in Familial Dilated Cardiomyopathy: An In Vitro Analysis From an RBM20 Patient-Derived iPSC Model.

Wyles SP, Hrstka SC, Reyes S, Terzic A, Olson TM, Nelson TJ. Wyles SP, et al. Among authors: olson tm. Clin Transl Sci. 2016 Jun;9(3):158-67. doi: 10.1111/cts.12393. Epub 2016 Apr 22. Clin Transl Sci. 2016. PMID: 27105042 Free PMC article.

2

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.

3

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.

4

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

5

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.

6

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.

7

K(ATP) channel polymorphism is associated with left ventricular size in hypertensive individuals: a large-scale community-based study.

Reyes S, Terzic A, Mahoney DW, Redfield MM, Rodeheffer RJ, Olson TM. Reyes S, et al. Among authors: olson tm. Hum Genet. 2008 Jul;123(6):665-7. doi: 10.1007/s00439-008-0519-3. Epub 2008 May 27. Hum Genet. 2008. PMID: 18504616 Free PMC article.

8

Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology.

Menon SC, Michels VV, Pellikka PA, Ballew JD, Karst ML, Herron KJ, Nelson SM, Rodeheffer RJ, Olson TM. Menon SC, et al. Among authors: olson tm. Clin Genet. 2008 Nov;74(5):445-54. doi: 10.1111/j.1399-0004.2008.01062.x. Epub 2008 Jul 21. Clin Genet. 2008. PMID: 18651846 Free PMC article.

9

KATP channel Kir6.2 E23K variant overrepresented in human heart failure is associated with impaired exercise stress response.

Reyes S, Park S, Johnson BD, Terzic A, Olson TM. Reyes S, et al. Among authors: olson tm. Hum Genet. 2009 Dec;126(6):779-89. doi: 10.1007/s00439-009-0731-9. Hum Genet. 2009. PMID: 19685080 Free PMC article.

10

Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy.

Brauch KM, Karst ML, Herron KJ, de Andrade M, Pellikka PA, Rodeheffer RJ, Michels VV, Olson TM. Brauch KM, et al. Among authors: olson tm. J Am Coll Cardiol. 2009 Sep 1;54(10):930-41. doi: 10.1016/j.jacc.2009.05.038. J Am Coll Cardiol. 2009. PMID: 19712804 Free PMC article.

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