Journal articles on the topic 'KCNH2 gene'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the top 50 journal articles for your research on the topic 'KCNH2 gene.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.
Heida, Annejet, Lisette J. M. E. van der Does, Ahmed A. Y. Ragab, and Natasja M. S. de Groot. "A Rare Case of the Digenic Inheritance of Long QT Syndrome Type 2 and Type 6." Case Reports in Medicine 2019 (June 20, 2019): 1–4. http://dx.doi.org/10.1155/2019/1384139.
Full textLarsen, Lars Allan, Paal Skytt Andersen, Jørgen Kanters, Ida Hastrup Svendsen, Joes Ramsøe Jacobsen, Jens Vuust, Göran Wettrell, Lisbeth Tranebjærg, Jørn Bathen, and Michael Christiansen. "Screening for Mutations and Polymorphisms in the Genes KCNH2 and KCNE2 Encoding the Cardiac HERG/MiRP1 Ion Channel: Implications for Acquired and Congenital Long Q-T Syndrome." Clinical Chemistry 47, no. 8 (August 1, 2001): 1390–95. http://dx.doi.org/10.1093/clinchem/47.8.1390.
Full textМаксимов, В. Н., Д. Е. Иванощук, П. С. Орлов, А. А. Иванова, С. К. Малютина, С. В. Максимова, И. А. Родина, О. В. Хамович, and В. П. Новосёлов. "The first results of gene panel sequencing in sudden cardiac death in young men." Nauchno-prakticheskii zhurnal «Medicinskaia genetika», no. 5(214) (May 29, 2020): 36–38. http://dx.doi.org/10.25557/2073-7998.2020.05.36-38.
Full textOrlov, P. S., D. E. Ivanoshchuk, A. M. Nesterets, A. A. Kuznetsov, A. A. Ivanova, S. K. Maliutina, D. V. Denisova, E. V. Striukova, V. N. Maksimov, and S. V. Maksimova. "The results of next-generation sequencing in men with borderline QT interval prolongation (pilot study)." Complex Issues of Cardiovascular Diseases 11, no. 2 (April 28, 2022): 98–106. http://dx.doi.org/10.17802/2306-1278-2022-11-2-98-106.
Full textZou, Anruo, Zhixin Lin, Margaret Humble, Christopher D. Creech, P. Kay Wagoner, Douglas Krafte, Timothy J. Jegla, and Alan D. Wickenden. "Distribution and functional properties of human KCNH8 (Elk1) potassium channels." American Journal of Physiology-Cell Physiology 285, no. 6 (December 2003): C1356—C1366. http://dx.doi.org/10.1152/ajpcell.00179.2003.
Full textCaballero, Ricardo, Raquel G. Utrilla, Irene Amorós, Marcos Matamoros, Marta Pérez-Hernández, David Tinaquero, Silvia Alfayate, et al. "Tbx20 controls the expression of the KCNH2 gene and of hERG channels." Proceedings of the National Academy of Sciences 114, no. 3 (January 3, 2017): E416—E425. http://dx.doi.org/10.1073/pnas.1612383114.
Full textFarrelly, A. M., S. Ro, B. P. Callaghan, M. A. Khoyi, N. Fleming, B. Horowitz, K. M. Sanders, and K. D. Keef. "Expression and function of KCNH2 (HERG) in the human jejunum." American Journal of Physiology-Gastrointestinal and Liver Physiology 284, no. 6 (June 1, 2003): G883—G895. http://dx.doi.org/10.1152/ajpgi.00394.2002.
Full textСивцев, А. А., Л. И. Свинцова, И. В. Плотникова, И. Ж. Жалсанова, А. Е. Постригань, Л. И. Минайчева, О. Ю. Джаффарова, and Н. А. Скрябин. "Analysis of mutations spectrum in the KCNQ1, KCNH2 and SCN5A genes in patients with long QT syndrome using massively parallel sequencing." Nauchno-prakticheskii zhurnal «Medicinskaia genetika», no. 5(214) (May 29, 2020): 20–22. http://dx.doi.org/10.25557/2073-7998.2020.05.20-22.
Full textO’Hare, Bailey J., C. S. John Kim, Samantha K. Hamrick, Dan Ye, David J. Tester, and Michael J. Ackerman. "Promise and Potential Peril With Lumacaftor for the Trafficking Defective Type 2 Long-QT Syndrome-Causative Variants, p.G604S, p.N633S, and p.R685P, Using Patient-Specific Re-Engineered Cardiomyocytes." Circulation: Genomic and Precision Medicine 13, no. 5 (October 2020): 466–75. http://dx.doi.org/10.1161/circgen.120.002950.
Full textPolyak, Margarita E., Anna Shestak, Dmitriy Podolyak, and Elena Zaklyazminskaya. "Compound heterozygous mutations in KCNJ2 and KCNH2 in a patient with severe Andersen-Tawil syndrome." BMJ Case Reports 13, no. 8 (August 2020): e235703. http://dx.doi.org/10.1136/bcr-2020-235703.
Full textWang, Feng, Yang Liu, Hongtao Liao, Yumei Xue, Xianzhang Zhan, Xianhong Fang, Yuanhong Liang, et al. "Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population." Cardiology 145, no. 1 (November 21, 2019): 38–45. http://dx.doi.org/10.1159/000502833.
Full textZhai, Yafei, Jinxin Miao, Ying Peng, Guangming Fang, Chuchu Wang, Yaohe Wang, Xiaoyan Zhao, and Jianzeng Dong. "Discovery of Digenic Mutation, KCNH2 c.1898A >C and JUP c.916dupA, in a Chinese Family with Long QT Syndrome via Whole-Exome Sequencing." Cardiovascular Innovations and Applications 4, no. 4 (July 1, 2020): 257–67. http://dx.doi.org/10.15212/cvia.2019.0578.
Full textOno, Makoto, Don E. Burgess, Elizabeth A. Schroder, Claude S. Elayi, Corey L. Anderson, Craig T. January, Bin Sun, Kalyan Immadisetty, Peter M. Kekenes-Huskey, and Brian P. Delisle. "Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients." Biomolecules 10, no. 8 (August 4, 2020): 1144. http://dx.doi.org/10.3390/biom10081144.
Full textBando, Sachiko, Takeshi Soeki, Toshiyuki Niki, Kenya Kusunose, Koji Yamaguchi, Yoshio Taketani, Iwase Takashi, et al. "Congenital Long QT Syndrome with Compound Mutations in KCNH2 Gene." Journal of Arrhythmia 27, Supplement (2011): PJ3_044. http://dx.doi.org/10.4020/jhrs.27.pj3_044.
Full textHayashi, Kenshi, Noboru Fujino, Katsuharu Uchiyama, Hidekazu Ino, Kenji Sakata, Tetsuo Konno, Eiichi Masuta, et al. "Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations." Clinical Science 117, no. 12 (July 1, 2009): 415–24. http://dx.doi.org/10.1042/cs20080528.
Full textBileišienė, Neringa, Jūratė Barysienė, Violeta Mikštienė, Eglė Preikšaitienė, Germanas Marinskis, Monika Keževičiūtė, Algirdas Utkus, and Audrius Aidietis. "Aborted Cardiac Arrest in LQT2 Related to Novel KCNH2 (hERG) Variant Identified in One Lithuanian Family." Medicina 57, no. 7 (July 16, 2021): 721. http://dx.doi.org/10.3390/medicina57070721.
Full textStump, Matthew R., Rachel T. Nguyen, Rachel H. Drgastin, Delaney Search, Qiuming Gong, and Zhengfeng Zhou. "Regulation of Kv11.1 Isoform Expression by Polyadenylate Binding Protein Nuclear 1." International Journal of Molecular Sciences 22, no. 2 (January 16, 2021): 863. http://dx.doi.org/10.3390/ijms22020863.
Full textSilva, Doroteia, Gabriel Miltenberger-Miltenyi, Maria José Correia, and António Nunes Diogo. "Novel mutation in the KCNH2 gene associated with long QT syndrome." Revista Portuguesa de Cardiologia 32, no. 2 (February 2013): 163–64. http://dx.doi.org/10.1016/j.repc.2012.06.012.
Full textSilva, Doroteia, Gabriel Miltenberger-Miltenyi, Maria José Correia, and António Nunes Diogo. "Novel mutation in the KCNH2 gene associated with long QT syndrome." Revista Portuguesa de Cardiologia (English Edition) 32, no. 2 (February 2013): 163–64. http://dx.doi.org/10.1016/j.repce.2013.02.008.
Full textBando, Sachiko, Takeshi Soeki, Tomomi Matsuura, Toshiyuki Niki, Takayuki Ise, Koji Yamaguchi, Yoshio Taketani, et al. "Congenital long QT syndrome with compound mutations in the KCNH2 gene." Heart and Vessels 29, no. 4 (September 22, 2013): 554–59. http://dx.doi.org/10.1007/s00380-013-0406-2.
Full textKekenes-Huskey, Peter M., Don E. Burgess, Bin Sun, Daniel C. Bartos, Ezekiel R. Rozmus, Corey L. Anderson, Craig T. January, Lee L. Eckhardt, and Brian P. Delisle. "Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes." International Journal of Molecular Sciences 23, no. 13 (July 2, 2022): 7389. http://dx.doi.org/10.3390/ijms23137389.
Full textParent, Lucie. "A helical segment makes potassium channels go-go." Journal of Biological Chemistry 292, no. 18 (May 5, 2017): 7706–7. http://dx.doi.org/10.1074/jbc.h117.779298.
Full textSun, Yaxun, Xiao-Qing Quan, Samantha Fromme, Robert H. Cox, Ping Zhang, Li Zhang, Donglin Guo, et al. "A novel mutation in the KCNH2 gene associated with short QT syndrome." Journal of Molecular and Cellular Cardiology 50, no. 3 (March 2011): 433–41. http://dx.doi.org/10.1016/j.yjmcc.2010.11.017.
Full textDonner, Birgit C., Christoph Marshall, and Klaus G. Schmidt. "A presumably benign human ether-a-go-go-related gene mutation (R176W) with a malignant primary manifestation of long QT syndrome." Cardiology in the Young 22, no. 3 (November 9, 2011): 360–63. http://dx.doi.org/10.1017/s1047951111001831.
Full textFinley, Melissa R., Yan Li, Fei Hua, James Lillich, Kathy E. Mitchell, Suhasini Ganta, Robert F. Gilmour, and Lisa C. Freeman. "Expression and coassociation of ERG1, KCNQ1, and KCNE1 potassium channel proteins in horse heart." American Journal of Physiology-Heart and Circulatory Physiology 283, no. 1 (July 1, 2002): H126—H138. http://dx.doi.org/10.1152/ajpheart.00622.2001.
Full textZamorano-León, José J., Rosa Yañez, Gabriel Jaime, Pablo Rodriguez-Sierra, Laura Calatrava-Ledrado, Roman R. Alvarez-Granada, Petra Jiménez Mateos-Cáceres, Carlos Macaya, and Antonio J. López-Farré. "KCNH2 Gene Mutation: A Potential Link Between Epilepsy and Long QT-2 Syndrome." Journal of Neurogenetics 26, no. 3-4 (April 19, 2012): 382–86. http://dx.doi.org/10.3109/01677063.2012.674993.
Full textLiu, Zhao, Julie A. Hutt, Barur Rajeshkumar, Yoshihiro Azuma, Kailai L. Duan, and J. Kevin Donahue. "Preclinical efficacy and safety of KCNH2-G628S gene therapy for postoperative atrial fibrillation." Journal of Thoracic and Cardiovascular Surgery 154, no. 5 (November 2017): 1644–51. http://dx.doi.org/10.1016/j.jtcvs.2017.05.052.
Full textSi, Man, Krystle Trosclair, Kathryn A. Hamilton, and Edward Glasscock. "Genetic ablation or pharmacological inhibition of Kv1.1 potassium channel subunits impairs atrial repolarization in mice." American Journal of Physiology-Cell Physiology 316, no. 2 (February 1, 2019): C154—C161. http://dx.doi.org/10.1152/ajpcell.00335.2018.
Full textSinner, Moritz F., Arne Pfeufer, Mahmut Akyol, Britt-Maria Beckmann, Martin Hinterseer, Annette Wacker, Siegfried Perz, et al. "The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)." European Heart Journal 29, no. 7 (January 25, 2008): 907–14. http://dx.doi.org/10.1093/eurheartj/ehm619.
Full textBaye, Jordan, Amanda Massmann, Natasha Petry, Joel Van Heukelom, Kristen De Berg, April Schultz, and Catherine Hajek. "Development and early evaluation of clinical decision support for long QT syndrome population screening." Journal of Translational Genetics and Genomics 6 (2022): 375–87. http://dx.doi.org/10.20517/jtgg.2022.12.
Full textHocker, James D., Olivier B. Poirion, Fugui Zhu, Justin Buchanan, Kai Zhang, Joshua Chiou, Tsui-Min Wang, et al. "Cardiac cell type–specific gene regulatory programs and disease risk association." Science Advances 7, no. 20 (May 2021): eabf1444. http://dx.doi.org/10.1126/sciadv.abf1444.
Full textArmaganijan, L. "Mutação L955V no exon 12 do gene KCNH2 em paciente com síndrome do QT longo." Revista Iberoamericana de Arritmología 4 (2013): 16–20. http://dx.doi.org/10.5031/v4i1.ria10209.
Full textStoldere, Diāna, and Elīna Cimbolineca. "Surgical Approach in Congenital Long QT Interval Syndrome Patients." Acta Chirurgica Latviensis 18, no. 1 (November 18, 2020): 63–69. http://dx.doi.org/10.2478/chilat-2020-0016.
Full textTerrenoire, Cecile, Kai Wang, Kelvin W. Chan Tung, Wendy K. Chung, Robert H. Pass, Jonathan T. Lu, Jyh-Chang Jean, et al. "Induced pluripotent stem cells used to reveal drug actions in a long QT syndrome family with complex genetics." Journal of General Physiology 141, no. 1 (December 31, 2012): 61–72. http://dx.doi.org/10.1085/jgp.201210899.
Full textGuardiola-Ripoll, Maria, Carmen Almodóvar-Payá, Alba Lubeiro, Raymond Salvador, Pilar Salgado-Pineda, Jesús J. Gomar, Amalia Guerrero-Pedraza, et al. "New insights of the role of the KCNH2 gene in schizophrenia: An fMRI case-control study." European Neuropsychopharmacology 60 (July 2022): 38–47. http://dx.doi.org/10.1016/j.euroneuro.2022.04.012.
Full textYoshikane, Yukako, Masao Yoshinaga, Kunihiro Hamamoto, and Shinichi Hirose. "A case of long QT syndrome with triple gene abnormalities: Digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1." Heart Rhythm 10, no. 4 (April 2013): 600–603. http://dx.doi.org/10.1016/j.hrthm.2012.12.008.
Full textPedersen, Philip Juul, Kirsten Brolin Thomsen, Emma Rie Olander, Frank Hauser, Maria de los Angeles Tejada, Kristian Lundgaard Poulsen, Soren Grubb, Rikke Buhl, Kirstine Calloe, and Dan Arne Klaerke. "Molecular Cloning and Functional Expression of the Equine K+ Channel KV11.1 (Ether à Go-Go-Related/KCNH2 Gene) and the Regulatory Subunit KCNE2 from Equine Myocardium." PLOS ONE 10, no. 9 (September 16, 2015): e0138320. http://dx.doi.org/10.1371/journal.pone.0138320.
Full textAL-Eitan, Laith, Islam Al-Dalalah, Afrah Elshammari, Wael Khreisat, and Ayah Almasri. "The Impact of Potassium Channel Gene Polymorphisms on Antiepileptic Drug Responsiveness in Arab Patients with Epilepsy." Journal of Personalized Medicine 8, no. 4 (November 14, 2018): 37. http://dx.doi.org/10.3390/jpm8040037.
Full textOvali, M. A., and M. Uzun. "The effects of melatonin administration on KCNQ and KCNH2 gene expressions and QTc interval in pinealectomised rats." Cellular and Molecular Biology 63, no. 3 (March 31, 2016): 45. http://dx.doi.org/10.14715/cmb/2017.63.3.9.
Full textEddy, Carey-Anne, Judith M. MacCormick, Seo-Kyung Chung, Jackie R. Crawford, Donald R. Love, Mark I. Rees, Jonathan R. Skinner, and Andrew N. Shelling. "Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome." Heart Rhythm 5, no. 9 (September 2008): 1275–81. http://dx.doi.org/10.1016/j.hrthm.2008.05.033.
Full textAnson, Blake D., Michael J. Ackerman, David J. Tester, Melissa L. Will, Brian P. Delisle, Corey L. Anderson, and Craig T. January. "Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels." American Journal of Physiology-Heart and Circulatory Physiology 286, no. 6 (June 2004): H2434—H2441. http://dx.doi.org/10.1152/ajpheart.00891.2003.
Full textPark, Jong Keun, Yong-Seog Oh, Jee-hyun Choi, and Sungjoo Kim Yoon. "Single Nucleotide Deletion Mutation of KCNH2 Gene is Responsible for LQT Syndrome in a 3-Generation Korean Family." Journal of Korean Medical Science 28, no. 9 (2013): 1388. http://dx.doi.org/10.3346/jkms.2013.28.9.1388.
Full textTanaka, Yoshihiro, Kenshi Hayashi, Noboru Fujino, Tetsuo Konno, Hayato Tada, Chiaki Nakanishi, Akihiko Hodatsu, et al. "Functional analysis of KCNH2 gene mutations of type 2 long QT syndrome in larval zebrafish using microscopy and electrocardiography." Heart and Vessels 34, no. 1 (July 25, 2018): 159–66. http://dx.doi.org/10.1007/s00380-018-1231-4.
Full textGiustetto, Carla, Chiara Scrocco, Daniela Giachino, Claudio Rapezzi, Barbara Mognetti, and Fiorenzo Gaita. "The lack of effect of sotalol in short QT syndrome patients carrying the T618I mutation in the KCNH2 gene." HeartRhythm Case Reports 1, no. 5 (September 2015): 373–78. http://dx.doi.org/10.1016/j.hrcr.2015.07.001.
Full textVERKERK, A., R. WILDERS, E. SCHULZEBAHR, L. BEEKMAN, Z. BHUIYAN, J. BERTRAND, L. ECKARDT, D. LIN, M. BORGGREFE, and G. BREITHARDT. "Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome." Cardiovascular Research 68, no. 3 (December 1, 2005): 441–53. http://dx.doi.org/10.1016/j.cardiores.2005.06.027.
Full textWojdyła-Hordyńska, Agnieszka, Grzegorz Hordyński, Patrycja Pruszkowska-Skrzep, and Oskar Kowalski. "TRIGGER ABLATION IN LONG QT TYPE 2 PATIENT." In a good rythm 1, no. 46 (March 22, 2018): 28–30. http://dx.doi.org/10.5604/01.3001.0011.6496.
Full textAndrsova, Irena, Tomas Novotny, Jitka Kadlecova, Alexandra Bittnerova, Pavel Vit, Alena Florianova, Martina Sisakova, Renata Gaillyova, Lenka Manouskova, and Jindrich Spinar. "Clinical characteristics of 30 Czech families with long QT syndrome and KCNQ1 and KCNH2 gene mutations: importance of exercise testing." Journal of Electrocardiology 45, no. 6 (November 2012): 746–51. http://dx.doi.org/10.1016/j.jelectrocard.2012.05.004.
Full textZamorano-León, José J., Sergio Alonso-Orgaz, Javier Moreno, Rafael Cinza, Maria J. García-Torrent, Nicasio Pérez-Castellano, Julián Pérez-Villacastín, Carlos Macaya, and Antonio J. López-Farré. "Novel mutation (H402R) in the S1 domain of KCNH2-encoded gene associated with long QT syndrome in a Spanish family." International Journal of Cardiology 142, no. 2 (July 2010): 206–8. http://dx.doi.org/10.1016/j.ijcard.2008.11.166.
Full textLiu, Li, Kenshi Hayashi, Tomoya Kaneda, Hidekazu Ino, Noboru Fujino, Katsuharu Uchiyama, Tetsuo Konno, et al. "A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome." Heart Rhythm 10, no. 1 (January 2013): 61–67. http://dx.doi.org/10.1016/j.hrthm.2012.09.053.
Full textKałużna, Sandra, Mariusz J. Nawrocki, Karol Jopek, Greg Hutchings, Bartłomiej Perek, Marek Jemielity, Bartosz Kempisty, Agnieszka Malińska, Paul Mozdziak, and Michał Nowicki. "In search of markers useful for evaluation of graft patency - molecular analysis of ‘muscle system process’ for internal thoracic artery and saphenous vein conduits." Medical Journal of Cell Biology 8, no. 1 (April 29, 2020): 12–23. http://dx.doi.org/10.2478/acb-2020-0002.
Full text