Academic literature on the topic 'KCNH6 gene'
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Journal articles on the topic "KCNH6 gene"
Lu, Jing, Han Shen, Qi Li, Feng-Ran Xiong, Ming-Xia Yuan, and Jin-Kui Yang. "Effect of KCNH6 on Hepatic Endoplasmic Reticulum Stress and Glucose Metabolism." Hormone and Metabolic Research 52, no. 09 (August 4, 2020): 669–75. http://dx.doi.org/10.1055/a-1177-6814.
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 textStecyk, Jonathan A. W., Christine S. Couturier, Denis V. Abramochkin, Diarmid Hall, Asia Arrant-Howell, Kerry L. Kubly, Shyanne Lockmann, et al. "Cardiophysiological responses of the air-breathing Alaska blackfish to cold acclimation and chronic hypoxic submergence at 5°C." Journal of Experimental Biology 223, no. 22 (October 5, 2020): jeb225730. http://dx.doi.org/10.1242/jeb.225730.
Full textHeida, 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 textIchise, Eisuke, Tomohiro Chiyonobu, Mitsuru Ishikawa, Yasuyoshi Tanaka, Mami Shibata, Takenori Tozawa, Yoshihiro Taura, et al. "Impaired neuronal activity and differential gene expression in STXBP1 encephalopathy patient iPSC-derived GABAergic neurons." Human Molecular Genetics 30, no. 14 (May 7, 2021): 1337–48. http://dx.doi.org/10.1093/hmg/ddab113.
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 textStengel, Rayk, Eric Rivera-Milla, Nirakar Sahoo, Christina Ebert, Frank Bollig, Stefan H. Heinemann, Roland Schönherr, and Christoph Englert. "Kcnh1 Voltage-gated Potassium Channels Are Essential for Early Zebrafish Development." Journal of Biological Chemistry 287, no. 42 (August 27, 2012): 35565–75. http://dx.doi.org/10.1074/jbc.m112.363978.
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 textDissertations / Theses on the topic "KCNH6 gene"
Liu, Zhao. "USING GENE THERAPY TO PREVENT ATRIAL FIBRILLATION." Case Western Reserve University School of Graduate Studies / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=case1481231548493874.
Full textOzberk, Deniz. "The relationship between single nucleotide polymorphisms in ARRB2, KCNJ6 and BDNF genes and methadone response for pain management in palliative care." Thesis, Griffith University, 2019. http://hdl.handle.net/10072/390006.
Full textThesis (Masters)
Master of Medical Research (MMedRes)
School of Medical Science
Griffith Health
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Jenewein, Tina [Verfasser], Gerhard [Akademischer Betreuer] Thiel, Ralf [Akademischer Betreuer] Galuske, and Silke [Akademischer Betreuer] Kauferstein. "Characterization of sequence variants in the cardiac ion channel genes KCNH2 and SCN5A / Tina Jenewein ; Gerhard Thiel, Ralf Galuske, Silke Kauferstein." Darmstadt : Universitäts- und Landesbibliothek Darmstadt, 2017. http://d-nb.info/1139844121/34.
Full textFORTUNATO, ANGELO. "Identification and characterization of genes involved in the development and progression of colorectal and endometrial cancers." Doctoral thesis, 2012. http://hdl.handle.net/2158/794612.
Full textJenewein, Tina. "Characterization of sequence variants in the cardiac ion channel genes KCNH2 and SCN5A." Phd thesis, 2017. http://tuprints.ulb.tu-darmstadt.de/6793/1/Diss_TinaJenewein_final_2.pdf.
Full textBook chapters on the topic "KCNH6 gene"
Martínez-Barrios, Estefanía, José Cruzalegui, Sergi Cesar, Fredy Chipa, Elena Arbelo, Victoria Fiol, Josep Brugada, Georgia Sarquella-Brugada, and Oscar Campuzano. "Short QT Syndrome: Update on Genetic Basis." In Rare Diseases - Recent Advances [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.106808.
Full textMazzanti, Andrea, Riccardo Maragna, and Silvia G. Priori. "Monogenic and oligogenic cardiovascular diseases: genetics of arrhythmias—long QT syndrome." In ESC CardioMed, 671–76. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0149.
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