Terzic A - 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: terzic a. 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: terzic a. 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

Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy.

O'Cochlain DF, Perez-Terzic C, Reyes S, Kane GC, Behfar A, Hodgson DM, Strommen JA, Liu XK, van den Broek W, Wansink DG, Wieringa B, Terzic A. O'Cochlain DF, et al. Among authors: terzic a. Hum Mol Genet. 2004 Oct 15;13(20):2505-18. doi: 10.1093/hmg/ddh266. Epub 2004 Aug 18. Hum Mol Genet. 2004. PMID: 15317754

4

ATP-sensitive K+ channel knockout compromises the metabolic benefit of exercise training, resulting in cardiac deficits.

Kane GC, Behfar A, Yamada S, Perez-Terzic C, O'Cochlain F, Reyes S, Dzeja PP, Miki T, Seino S, Terzic A. Kane GC, et al. Among authors: terzic a. Diabetes. 2004 Dec;53 Suppl 3:S169-75. doi: 10.2337/diabetes.53.suppl_3.s169. Diabetes. 2004. PMID: 15561907

5

Cardiac KATP channels in health and disease.

Kane GC, Liu XK, Yamada S, Olson TM, Terzic A. Kane GC, et al. Among authors: terzic a. 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.

6

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. Among authors: terzic a. 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

7

KCNJ11 gene knockout of the Kir6.2 KATP channel causes maladaptive remodeling and heart failure in hypertension.

Kane GC, Behfar A, Dyer RB, O'Cochlain DF, Liu XK, Hodgson DM, Reyes S, Miki T, Seino S, Terzic A. Kane GC, et al. Among authors: terzic a. Hum Mol Genet. 2006 Aug 1;15(15):2285-97. doi: 10.1093/hmg/ddl154. Epub 2006 Jun 16. Hum Mol Genet. 2006. PMID: 16782803

8

Gene knockout of the KCNJ8-encoded Kir6.1 K(ATP) channel imparts fatal susceptibility to endotoxemia.

Kane GC, Lam CF, O'Cochlain F, Hodgson DM, Reyes S, Liu XK, Miki T, Seino S, Katusic ZS, Terzic A. Kane GC, et al. Among authors: terzic a. FASEB J. 2006 Nov;20(13):2271-80. doi: 10.1096/fj.06-6349com. FASEB J. 2006. PMID: 17077304

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: terzic a. 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. Among authors: terzic a. 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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