PMC Articles for MedGen (Select 1824077) - PMC - NCBI

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Items: 10

Select item 88657431.

Identification through action potential clamp of proarrhythmic consequences of the short QT syndrome T618I hERG ‘hotspot’ mutation

Chunyun Du, Henggui Zhang, Stephen C. Harmer, Jules C. Hancox

Biochem Biophys Res Commun. 2022 Mar 12; 596: 49–55. doi: 10.1016/j.bbrc.2022.01.057

PMCID:: PMC8865743

Abstract Article PDF–2.5M

Select item 70183292.

Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population

Azam AMIRIAN, Zahra ZAFARI, Zohreh SHARIFI, Alireza KORDAFSHARI, Morteza KARIMIPOOR, Sirous ZEINALI

Turk J Med Sci. 2019; 49(2): 453–457. Published online 2019 Apr 18. doi: 10.3906/sag-1805-43

PMCID:: PMC7018329

Abstract Article PDF–76K

Select item 69326373.

T‐Wave Morphology in Short QT Syndrome

Olli Anttonen, Juhani Junttila, Carla Giustetto, Fiorenzo Gaita, Eeva Linna, Mari Karsikas, Tapio Seppänen, Juha S. Perkiömäki, Timo H. Mäkikallio, Ramon Brugada, Heikki V. Huikuri

Ann Noninvasive Electrocardiol. 2009 Jul; 14(3): 262–267. Published online 2009 Jul 9. doi: 10.1111/j.1542-474X.2009.00308.x

PMCID:: PMC6932637

Abstract Article PDF–506K

Select item 64055694.

Long‐Term Follow‐Up of Patients With Short QT Syndrome: Clinical Profile and Outcome

Ibrahim El‐Battrawy, Johanna Besler, Volker Liebe, Rainer Schimpf, Erol Tülümen, Boris Rudic, Siegfried Lang, Christian Wolpert, Xiaobo Zhou, Ibrahim Akin, Martin Borggrefe

J Am Heart Assoc. 2018 Dec 4; 7(23): e010073. Published online 2018 Nov 27. doi: 10.1161/JAHA.118.010073

PMCID:: PMC6405569

Abstract Article PDF–1.1M

Select item 59075815.

Modeling Short QT Syndrome Using Human‐Induced Pluripotent Stem Cell–Derived Cardiomyocytes

Ibrahim El‐Battrawy, Huan Lan, Lukas Cyganek, Zhihan Zhao, Xin Li, Fanis Buljubasic, Siegfried Lang, Gökhan Yücel, Katherine Sattler, Wolfram‐Hubertus Zimmermann, Jochen Utikal, Thomas Wieland, Ursula Ravens, Martin Borggrefe, Xiao‐Bo Zhou, Ibrahim Akin

J Am Heart Assoc. 2018 Apr 3; 7(7): e007394. Published online 2018 Mar 24. doi: 10.1161/JAHA.117.007394

PMCID:: PMC5907581

Abstract Article PDF–3.9M

Select item 55595556.

In silico investigation of a KCNQ1 mutation associated with short QT syndrome

Ismail Adeniran, Dominic G. Whittaker, Aziza El Harchi, Jules C. Hancox, Henggui Zhang

Sci Rep. 2017; 7: 8469. Published online 2017 Aug 16. doi: 10.1038/s41598-017-08367-2

PMCID:: PMC5559555

Abstract Article PDF–6.8M

Select item 35304467.

Action Potential Clamp and Pharmacology of the Variant 1 Short QT Syndrome T618I hERG K⁺ Channel

Aziza El Harchi, Dario Melgari, Yi Hong Zhang, Henggui Zhang, Jules C. Hancox

PLoS One. 2012; 7(12): e52451. Published online 2012 Dec 26. doi: 10.1371/journal.pone.0052451

PMCID:: PMC3530446

Abstract Article PDF–1005K

Select item 32405858.

Increased Vulnerability of Human Ventricle to Re-entrant Excitation in hERG-linked Variant 1 Short QT Syndrome

Ismail Adeniran, Mark J. McPate, Harry J. Witchel, Jules C. Hancox, Henggui Zhang

PLoS Comput Biol. 2011 Dec; 7(12): e1002313. Published online 2011 Dec 15. doi: 10.1371/journal.pcbi.1002313

PMCID:: PMC3240585

Abstract Article PDF–1.4M

Select item 23757229.

Kv7.1 (KCNQ1) properties and channelopathies

David Peroz, Nicolas Rodriguez, Frank Choveau, Isabelle Baró, Jean Mérot, Gildas Loussouarn

J Physiol. 2008 Apr 1; 586(Pt 7): 1785–1789. Published online 2007 Dec 20. doi: 10.1113/jphysiol.2007.148254

PMCID:: PMC2375722

Abstract Article PDF–320K

Select item 236142510.

Cellular Basis for Arrhythmogenesis in an Experimental Model of the SQT1 Form of the Short QT Syndrome

Chinmay Patel, Charles Antzelevitch

Heart Rhythm. Author manuscript; available in PMC 2009 Apr 1.

Published in final edited form as: Heart Rhythm. 2008 Apr; 5(4): 585–590. Published online 2008 Jan 29. doi: 10.1016/j.hrthm.2008.01.022

PMCID:: PMC2361425

Abstract Article PDF–579K

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PMC Articles for MedGen (Select 1824077) (10)
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PLB1 phospholipase B1 [Homo sapiens]
Gene ID:151056

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gi|1786488214|gb|MN853781.1|

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