HuGE Literature Finder
Records 1-8
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population.
Nature genetics 2017 Apr . Low Siew-Kee, Takahashi Atsushi, Ebana Yusuke, Ozaki Kouichi, Christophersen Ingrid E, Ellinor Patrick T, , Ogishima Soichi, Yamamoto Masayuki, Satoh Mamoru, Sasaki Makoto, Yamaji Taiki, Iwasaki Motoki, Tsugane Shoichiro, Tanaka Keitaro, Naito Mariko, Wakai Kenji, Tanaka Hideo, Furukawa Tetsushi, Kubo Michiaki, Ito Kaoru, Kamatani Yoichiro, Tanaka Toshihi |
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Evaluation of genes encoding for the transient outward current (Ito) identifies the KCND2 gene as a cause of J-wave syndrome associated with sudden cardiac death.
Circulation. Cardiovascular genetics 2014 Dec 7 (6): 782-9. Perrin Mark J, Adler Arnon, Green Sharon, Al-Zoughool Foad, Doroshenko Petro, Orr Nathan, Uppal Shaheen, Healey Jeff S, Birnie David, Sanatani Shubhayan, Gardner Martin, Champagne Jean, Simpson Chris, Ahmad Kamran, van den Berg Maarten P, Chauhan Vijay, Backx Peter H, van Tintelen J Peter, Krahn Andrew D, Gollob Michael |
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Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation.
Heart rhythm : the official journal of the Heart Rhythm Society 2014 Feb 11 (2): 246-51. Olesen Morten S, Andreasen Laura, Jabbari Javad, Refsgaard Lena, Haunsø Stig, Olesen Søren-Peter, Nielsen Jonas B, Schmitt Nicole, Svendsen Jesper |
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A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern.
Heart rhythm : the official journal of the Heart Rhythm Society 2012 Oct 9 (10): 1627-34. Sinner Moritz F, Porthan Kimmo, Noseworthy Peter A, Havulinna Aki S, Tikkanen Jani T, Müller-Nurasyid Martina, Peloso Gina, Ulivi Sheila, Beckmann Britt Maria, Brockhaus A Catharina, Cooper Rebecca R, Gasparini Paolo, Hengstenberg Christian, Hwang Shih-Jen, Iorio Annamaria, Junttila M Juhani, Klopp Norman, Kähönen Mika, Laaksonen Maarit A, Lehtimäki Terho, Lichtner Peter, Lyytikäinen Leo-Pekka, Martens Eimo, Meisinger Christa, Meitinger Thomas, Merchant Faisal M, Nieminen Markku S, Peters Annette, Pietilä Arto, Perz Siegfried, Oikarinen Lasse, Raitakari Olli, Reinhard Wibke, Silander Kaisa, Thorand Barbara, Wichmann H-Erich, Sinagra Gianfranco, Viikari Jorma, O'Donnell Christopher J, Ellinor Patrick T, Huikuri Heikki V, Kääb Stefan, Newton-Cheh Christopher, Salomaa Veik |
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Novel mutations in the KCND3-encoded Kv4.3 K+ channel associated with autopsy-negative sudden unexplained death.
Human mutation 2012 Feb . Giudicessi JR, Ye D, Kritzberger CJ, Nesterenko VV, Tester DJ, Antzelevitch C, Ackerman MJ |
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Transient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2011 Jul 8 (7): 1024-32. Giudicessi John R, Ye Dan, Tester David J, Crotti Lia, Mugione Alessandra, Nesterenko Vladislav V, Albertson Richard M, Antzelevitch Charles, Schwartz Peter J, Ackerman Michael |
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Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndrome.
Clinica chimica acta; international journal of clinical chemistry 2005 Jan 351 (1-2): 95-100. Frank-Hansen Rune, Larsen Lars Allan, Andersen Paal, Jespersgaard Cathrine, Christiansen Micha |
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Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics.
The Canadian journal of cardiology 0 28 (2): 196-200. Holst Anders G, Saber Siamak, Houshmand Massoud, Zaklyazminskaya Elena V, Wang Yinman, Jensen Henrik Kjærulf, Refsgaard Lena, Haunsø Stig, Svendsen Jesper Hastrup, Olesen Morten S, Tfelt-Hansen Jac |
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