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humans (62) 62
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Journal Article
Circulation, ISSN 0009-7322, 2007, Volume 115, Issue 4, pp. 432 - 441
Background - Mutations in the ankyrin- B gene ( ANK2) cause type 4 long-QT syndrome and have been described in kindreds with other arrhythmias. The frequency... 
Cell biology | Cytoskeleton | Genetics | Ion channels | Arrhythmia | Calcium | ARRHYTHMIAS | CARDIAC & CARDIOVASCULAR SYSTEMS | calcium | ISOFORM SPECIFICITY | cytoskeleton | ion channels | IMPACT | cell biology | genetics | INOSITOL 1,4,5-TRISPHOSPHATE | arrhythmia | NEONATAL CARDIOMYOCYTES | SUDDEN CARDIAC DEATH | PERIPHERAL VASCULAR DISEASE | LONG-QT-SYNDROME | C-TERMINAL DOMAIN | REGULATORY DOMAIN | HEMATOLOGY | Arrhythmias, Cardiac - chemically induced | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Tachycardia, Ventricular - chemically induced | Arrhythmias, Cardiac - ethnology | Torsades de Pointes - genetics | Long QT Syndrome - chemically induced | Male | Ion Channels - physiology | Genetic Variation | Tachycardia, Ventricular - genetics | Female | African Continental Ancestry Group - genetics | Arrhythmias, Cardiac - genetics | Tachycardia, Ventricular - ethnology | European Continental Ancestry Group - genetics | Myocytes, Cardiac - cytology | Mice, Inbred C57BL | Torsades de Pointes - chemically induced | Genotype | Torsades de Pointes - ethnology | Mexican Americans - genetics | Phenotype | Animals | Long QT Syndrome - ethnology | Myocytes, Cardiac - physiology | Ankyrins - genetics | Long QT Syndrome - genetics | Aged | Cytoskeleton - physiology | Mice | Genetic variation | Heart cells | Physiological aspects | Development and progression | Genetic aspects | Research | Membrane proteins | Index Medicus | Abridged Index Medicus
Journal Article
Circulation: Cardiovascular Genetics, ISSN 1942-325X, 02/2017, Volume 10, Issue 1, pp. e001537 - e001537
BACKGROUND—Long QT syndrome confers susceptibility to ventricular arrhythmia, predisposing to syncope, seizures, and sudden death. While rare globally, long QT... 
genetic variation | heart rate | Wolff-Parkinson-White syndrome | long QT syndrome | arrhythmia | PROTEIN | NODE | MUTATION CAUSES | NEURAL STEM | PHENOTYPE | CARDIAC-ARRHYTHMIA | RECEPTOR | PATHWAY | GENETICS & HEREDITY | DYSFUNCTION | EXCHANGER | Humans | Middle Aged | Arrhythmias, Cardiac - ethnology | Child, Preschool | Male | Structure-Activity Relationship | Ankyrins - chemistry | Genetic Variation | Long QT Syndrome - diagnosis | Transfection | Sodium-Calcium Exchanger - metabolism | Electrocardiography | Adult | Female | Protein Interaction Domains and Motifs | Protein Stability | Child | Arrhythmias, Cardiac - genetics | British Columbia - epidemiology | Arrhythmias, Cardiac - metabolism | Cell Line | Genetic Predisposition to Disease | Rats | Mice, Knockout | Long QT Syndrome - metabolism | Phenotype | Animals | Long QT Syndrome - ethnology | Ankyrins - genetics | Adolescent | Ankyrins - metabolism | Indians, North American - genetics | Long QT Syndrome - genetics | Myocytes, Cardiac - metabolism | Protein Binding | Aged | Arrhythmias, Cardiac - diagnosis | Heart | Arrhythmia | Cardiomyopathy | Cardiomyocytes | Cardiovascular disease | Myocytes | Coronary artery disease | Na+/Ca2+-exchanging ATPase | Genotyping | Syncope | Long QT syndrome | KCNQ1 protein | Potassium channels (voltage-gated) | Ankyrin | Ventricle | Mutation | Localization | Heart diseases | Seizures | Index Medicus | First Nations | membrane binding domain | congenital heart disease | ANK2
Journal Article
Heart Rhythm, ISSN 1547-5271, 04/2017, Volume 14, Issue 4, pp. 572 - 580
Journal Article
Journal Article
Journal Article
by Bihlmeyer, Nathan A and Brody, Jennifer A and Smith, Albert Vernon and Warren, Helen R and Lin, Honghuang and Isaacs, Aaron and Liu, Ching-Ti and Marten, Jonathan and Radmanesh, Farid and Hall, Leanne M and Grarup, Niels and Mei, Hao and Müller-Nurasyid, Martina and Huffman, Jennifer E and Verweij, Niek and Guo, Xiuqing and Yao, Jie and Li-Gao, Ruifang and van den Berg, Marten and Weiss, Stefan and Prins, Bram P and van Setten, Jessica and Haessler, Jeffrey and Lyytikäinen, Leo-Pekka and Li, Man and Alonso, Alvaro and Soliman, Elsayed Z and Bis, Joshua C and Austin, Tom and Chen, Yii-Der Ida and Psaty, Bruce M and Harrris, Tamara B and Launer, Lenore J and Padmanabhan, Sandosh and Dominiczak, Anna and Huang, Paul L and Xie, Zhijun and Ellinor, Patrick T and Kors, Jan A and Campbell, Archie and Murray, Alison D and Nelson, Christopher P and Tobin, Martin D and Bork-Jensen, Jette and Hansen, Torben and Pedersen, Oluf and Linneberg, Allan and Sinner, Moritz F and Peters, Annette and Waldenberger, Melanie and Meitinger, Thomas and Perz, Siegfried and Kolcic, Ivana and Rudan, Igor and de Boer, Rudolf A and van der Meer, Peter and Lin, Henry J and Taylor, Kent D and de Mutsert, Renée and Trompet, Stella and Jukema, J Wouter and Maan, Arie C and Stricker, Bruno H C and Rivadeneira, Fernando and Uitterlinden, André and Völker, Uwe and Homuth, Georg and Völzke, Henry and Felix, Stephan B and Mangino, Massimo and Spector, Timothy D and Bots, Michiel L and Perez, Marco and Raitakari, Olli T and Kähönen, Mika and Mononen, Nina and Gudnason, Vilmundur and Munroe, Patricia B and Lubitz, Steven A and van Duijn, Cornelia M and Newton-Cheh, Christopher H and Hayward, Caroline and Rosand, Jonathan and Samani, Nilesh J and Kanters, Jørgen K and Wilson, James G and Kääb, Stefan and Polasek, Ozren and van der Harst, Pim and Heckbert, Susan R and Rotter, Jerome I and Mook-Kanamori, Dennis O and Eijgelsheim, Mark and Dörr, Marcus and Jamshidi, Yalda and Asselbergs, Folkert W and Kooperberg, Charles and Lehtimäki, Terho and Arking, Dan E and Sotoodehnia, Nona
Circulation. Genomic and precision medicine, ISSN 2574-8300, 01/2018, Volume 11, Issue 1, pp. e001758 - e001758
Journal Article
中国药理学报:英文版, ISSN 1671-4083, 2017, Volume 38, Issue 11, pp. 1580 - 1588
Journal Article
Journal of Electrocardiology, ISSN 0022-0736, 2014, Volume 47, Issue 2, pp. 244 - 250
Journal Article