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	61.	Strain Echocardiography and LQTS Subtypes: Mechanical Alterations in an Electrical Disorder. [electronic resource] by Jahangir, Arshad Jain, Renuka Producer: 20160201 In: JACC. Cardiovascular imaging vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Generation and characterization of twelve human induced pluripotent stem cell (iPSC) lines from four familial long QT syndrome type 1 (LQT1) patients carrying KCNQ1 c.1201dupC mutation. [electronic resource] by Ge, Ning Liu, Min Ding, Yicheng Krawczyk, Janusz McInerney, Veronica Galvin, Joseph Shen, Sanbing Prendiville, Terence O'Brien, Timothy Producer: 20200626 In: Stem cell research vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	[Long QT--a polymorphic syndrome]. [electronic resource] by Swan, H Producer: 20020115 In: Duodecim; laaketieteellinen aikakauskirja vol. 114 Availability: No items available. Save to lists Add to cart (remove)
	64.	Autonomic control of heart rate and QT interval variability influences arrhythmic risk in long QT syndrome type 1. [electronic resource] by Porta, Alberto Girardengo, Giulia Bari, Vlasta George, Alfred L Brink, Paul A Goosen, Althea Crotti, Lia Schwartz, Peter J Producer: 20150413 In: Journal of the American College of Cardiology vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation. [electronic resource] by Bartos, Daniel C Giudicessi, John R Tester, David J Ackerman, Michael J Ohno, Seiko Horie, Minoru Gollob, Michael H Burgess, Don E Delisle, Brian P Producer: 20141104 In: Heart rhythm vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Prevalence and potential genetic determinants of sensorineural deafness in KCNQ1 homozygosity and compound heterozygosity. [electronic resource] by Giudicessi, John R Ackerman, Michael J Producer: 20131022 In: Circulation. Cardiovascular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Recurrent Torsades with Refractory QT Prolongation in a 54-Year-Old Man. [electronic resource] by Guess, Joel Hubel, Kinsley Wiggins, Amanda Madigan, Cory G Bunin, Jessica Producer: 20190326 In: The American journal of case reports vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel. [electronic resource] by Ye, Dan Tester, David J Zhou, Wei Papagiannis, John Ackerman, Michael J Producer: 20201002 In: Heart rhythm vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Abnormal KCNQ1 trafficking influences disease pathogenesis in hereditary long QT syndromes (LQT1). [electronic resource] by Wilson, Andrew J Quinn, Kathryn V Graves, Fiona M Bitner-Glindzicz, Maria Tinker, Andrew Producer: 20060113 In: Cardiovascular research vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutation. [electronic resource] by Mura, Manuela Lee, Yee-Ki Pisano, Federica Ginevrino, Monia Boni, Marina Calabrò, Federica Crotti, Lia Valente, Enza Maria Schwartz, Peter J Tse, Hung-Fat Gnecchi, Massimiliano Producer: 20200311 In: Stem cell research vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Complex aberrant splicing in the induced pluripotent stem cell-derived cardiomyocytes from a patient with long QT syndrome carrying KCNQ1-A344Aspl mutation. [electronic resource] by Wuriyanghai, Yimin Makiyama, Takeru Sasaki, Kenichi Kamakura, Tsukasa Yamamoto, Yuta Hayano, Mamoru Harita, Takeshi Nishiuchi, Suguru Chen, Jiarong Kohjitani, Hirohiko Hirose, Sayako Yokoi, Fumika Gao, Jingshan Chonabayashi, Kazuhisa Watanabe, Ken Ohno, Seiko Yoshida, Yoshinori Kimura, Takeshi Horie, Minoru Producer: 20190325 In: Heart rhythm vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	The homozygous KCNQ1 gene mutation associated with recessive Romano-Ward syndrome. [electronic resource] by Novotny, Tomas Kadlecova, Jitka Janousek, Jan Gaillyova, Renata Bittnerova, Alexandra Florianova, Alena Sisakova, Martina Toman, Ondrej Chroust, Karel Papousek, Ivo Spinar, Jindrich Producer: 20070104 In: Pacing and clinical electrophysiology : PACE vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Sudden cardiac death, founder populations, and mushrooms: what is the link with gold mines and modifier genes? [electronic resource] by Schwartz, Peter J Producer: 20110809 In: Heart rhythm vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	Mutation location effect on severity of phenotype during exercise testing in type 1 long-QT syndrome: impact of transmembrane and C-loop location. [electronic resource] by Laksman, Zachary W M Hamilton, Robert M Chockalingam, Priya Ballantyne, Emily Stephenson, Elizabeth A Gross, Gil J Gula, Lorne J Klein, George J Wilde, Arthur A M Krahn, Andrew D Producer: 20140423 In: Journal of cardiovascular electrophysiology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	75.	Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome. [electronic resource] by Shimizu, Wataru Noda, Takashi Takaki, Hiroshi Kurita, Takashi Nagaya, Noritoshi Satomi, Kazuhiro Suyama, Kazuhiro Aihara, Naohiko Kamakura, Shiro Sunagawa, Kenji Echigo, Shigeyuki Nakamura, Kazufumi Ohe, Tohru Towbin, Jeffrey A Napolitano, Carlo Priori, Silvia G Producer: 20030312 In: Journal of the American College of Cardiology vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation. [electronic resource] by Bartos, Daniel C Duchatelet, Sabine Burgess, Don E Klug, Didier Denjoy, Isabelle Peat, Rachel Lupoglazoff, Jean-Marc Fressart, Véronique Berthet, Myriam Ackerman, Michael J January, Craig T Guicheney, Pascale Delisle, Brian P Producer: 20110524 In: Heart rhythm vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	Complex excitation dynamics underlie polymorphic ventricular tachycardia in a transgenic rabbit model of long QT syndrome type 1. [electronic resource] by Kim, Tae Yun Kunitomo, Yukiko Pfeiffer, Zachary Patel, Divyang Hwang, Jungmin Harrison, Kathryn Patel, Brijesh Jeng, Paul Ziv, Ohad Lu, Yichun Peng, Xuwen Qu, Zhilin Koren, Gideon Choi, Bum-Rak Producer: 20150928 In: Heart rhythm vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	78.	T-Wave Morphology Analysis in Congenital Long QT Syndrome Discriminates Patients From Healthy Individuals. [electronic resource] by Porta-Sánchez, Andreu Spillane, David R Harris, Louise Xue, Joel Dorsey, Pat Care, Melanie Chauhan, Vijay Gollob, Michael H Spears, Danna A Producer: 20190723 In: JACC. Clinical electrophysiology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	79.	Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner. [electronic resource] by Amin, Ahmad S Giudicessi, John R Tijsen, Anke J Spanjaart, Anne M Reckman, Yolan J Klemens, Christine A Tanck, Michael W Kapplinger, Jamie D Hofman, Nynke Sinner, Moritz F Müller, Martina Wijnen, Wino J Tan, Hanno L Bezzina, Connie R Creemers, Esther E Wilde, Arthur A M Ackerman, Michael J Pinto, Yigal M Producer: 20120521 In: European heart journal vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	80.	High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation. [electronic resource] by Burgess, Don E Bartos, Daniel C Reloj, Allison R Campbell, Kenneth S Johnson, Jonathan N Tester, David J Ackerman, Michael J Fressart, Véronique Denjoy, Isabelle Guicheney, Pascale Moss, Arthur J Ohno, Seiko Horie, Minoru Delisle, Brian P Producer: 20130221 In: Biochemistry vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 153 results.