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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 2
2004 1
2005 1
2006 1
2008 2
2009 1
2010 2
2011 2
2013 2
2016 1
2018 1
2021 0
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17 results
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Page 1
Recent progress in congenital long QT syndrome.
Lu JT, Kass RS. Lu JT, et al. Curr Opin Cardiol. 2010 May;25(3):216-21. doi: 10.1097/HCO.0b013e32833846b3. Curr Opin Cardiol. 2010. PMID: 20224391 Free PMC article. Review.
LMNA cardiomyopathy: cell biology and genetics meet clinical medicine.
Lu JT, Muchir A, Nagy PL, Worman HJ. Lu JT, et al. Dis Model Mech. 2011 Sep;4(5):562-8. doi: 10.1242/dmm.006346. Epub 2011 Aug 2. Dis Model Mech. 2011. PMID: 21810905 Free PMC article. Review.
Post-Translational Modifications and Diastolic Calcium Leak Associated to the Novel RyR2-D3638A Mutation Lead to CPVT in Patient-Specific hiPSC-Derived Cardiomyocytes.
Acimovic I, Refaat MM, Moreau A, Salykin A, Reiken S, Sleiman Y, Souidi M, Přibyl J, Kajava AV, Richard S, Lu JT, Chevalier P, Skládal P, Dvořak P, Rotrekl V, Marks AR, Scheinman MM, Lacampagne A, Meli AC. Acimovic I, et al. Among authors: lu jt. J Clin Med. 2018 Nov 8;7(11):423. doi: 10.3390/jcm7110423. J Clin Med. 2018. PMID: 30413023 Free PMC article.
Gene-engineered models for genetic manipulation and functional analysis of the cardiovascular system in mice.
Chu PH, Lu JT, Chen J. Chu PH, et al. Among authors: lu jt. Chang Gung Med J. 2003 Dec;26(12):868-78. Chang Gung Med J. 2003. PMID: 15008321 Free article. Review.
Calcium-triggered short-coupled polymorphous ventricular tachycardia.
Yeh DD, Lu JT, Kim A, Yeh RW, Scheinman MM. Yeh DD, et al. Among authors: lu jt. Pacing Clin Electrophysiol. 2010 Jan;33(1):117-22. doi: 10.1111/j.1540-8159.2009.02537.x. Pacing Clin Electrophysiol. 2010. PMID: 20444143
A mutation abolishing the ZMPSTE24 cleavage site in prelamin A causes a progeroid disorder.
Wang Y, Lichter-Konecki U, Anyane-Yeboa K, Shaw JE, Lu JT, Östlund C, Shin JY, Clark LN, Gundersen GG, Nagy PL, Worman HJ. Wang Y, et al. Among authors: lu jt. J Cell Sci. 2016 May 15;129(10):1975-80. doi: 10.1242/jcs.187302. Epub 2016 Mar 31. J Cell Sci. 2016. PMID: 27034136 Free PMC article.
Defects in cardiac conduction system lineages and malignant arrhythmias: developmental pathways and disease.
St Amand TR, Lu JT, Chien KR. St Amand TR, et al. Among authors: lu jt. Novartis Found Symp. 2003;250:260-70; discussion 271-5, 276-9. Novartis Found Symp. 2003. PMID: 12956335 Review.
Identification of cardiac-specific myosin light chain kinase.
Chan JY, Takeda M, Briggs LE, Graham ML, Lu JT, Horikoshi N, Weinberg EO, Aoki H, Sato N, Chien KR, Kasahara H. Chan JY, et al. Among authors: lu jt. Circ Res. 2008 Mar 14;102(5):571-80. doi: 10.1161/CIRCRESAHA.107.161687. Epub 2008 Jan 17. Circ Res. 2008. PMID: 18202317 Free PMC article.
Ablation of Nkx2-5 at mid-embryonic stage results in premature lethality and cardiac malformation.
Terada R, Warren S, Lu JT, Chien KR, Wessels A, Kasahara H. Terada R, et al. Among authors: lu jt. Cardiovasc Res. 2011 Jul 15;91(2):289-99. doi: 10.1093/cvr/cvr037. Epub 2011 Feb 1. Cardiovasc Res. 2011. PMID: 21285290 Free PMC article.
An LQTS6 MiRP1 mutation suppresses pacemaker current and is associated with sinus bradycardia.
Nawathe PA, Kryukova Y, Oren RV, Milanesi R, Clancy CE, Lu JT, Moss AJ, Difrancesco D, Robinson RB. Nawathe PA, et al. Among authors: lu jt. J Cardiovasc Electrophysiol. 2013 Sep;24(9):1021-7. doi: 10.1111/jce.12163. Epub 2013 Apr 30. J Cardiovasc Electrophysiol. 2013. PMID: 23631727 Free PMC article.
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