Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Shoaib Faizi"'
Autor:
Kyle E. Simpson, Ravichandra Venkateshappa, Zhao Kai Pang, Shoaib Faizi, Glen F. Tibbits, Tom W. Claydon
Publikováno v:
Frontiers in Physiology, Vol 11 (2021)
Long-QT Syndrome (LQTS) is a cardiac electrical disorder, distinguished by irregular heart rates and sudden death. Accounting for ∼40% of cases, LQTS Type 2 (LQTS2), is caused by defects in the Kv11.1 (hERG) potassium channel that is critical for c
Externí odkaz:
https://doaj.org/article/b450a30b75aa4511bf75650755a958cf
Autor:
Thomas W. Claydon, Glen F. Tibbits, Eric Lin, Diana Hunter, Yen May Cheng, Damon Poburko, Raj Johal, Mandy Yip, Ravichandra Venkateshappa, Shoaib Faizi, Kyle E. Simpson
Publikováno v:
Journal of visualized experiments : JoVE. (187)
Clustered regularly interspaced short palindromic repeats (CRISPR) in animal models enable precise genetic manipulation for the study of physiological phenomena. Zebrafish have been used as an effective genetic model to study numerous questions relat
Autor:
Zhao Kai Pang, Shoaib Faizi, Glen F. Tibbits, Tom W. Claydon, Ravichandra Venkateshappa, Kyle E. Simpson
Publikováno v:
Frontiers in Physiology, Vol 11 (2021)
Frontiers in Physiology
Frontiers in Physiology
Long-QT Syndrome (LQTS) is a cardiac electrical disorder, distinguished by irregular heart rates and sudden death. Accounting for ∼40% of cases, LQTS Type 2 (LQTS2), is caused by defects in the Kv11.1 (hERG) potassium channel that is critical for c
Autor:
Yu Patrick, Shi, ZhaoKai, Pang, Ravichandra, Venkateshappa, Marvin, Gunawan, Jacob, Kemp, Elson, Truong, Cherlene, Chang, Eric, Lin, Sanam, Shafaattalab, Shoaib, Faizi, Kaveh, Rayani, Glen F, Tibbits, Victoria E, Claydon, Thomas W, Claydon
Publikováno v:
American journal of physiology. Heart and circulatory physiology. 319(2)
Human ether-à-go-go related gene (hERG) K
Autor:
Shi, Yu, Zhaokai Pang, Ravichandra Venkateshappa, Gunawan, Marvin, Kemp, Jacob, Elson Truong, Cherlene Chang, Lin, Eric, Shafaattalab, Sanam, Shoaib Faizi, Rayani, Kaveh, Tibbits, Glen F, Claydon, Victoria E., Claydon, Thomas
hERG K+ channels are important in cardiac repolarization and their dysfunction causes prolongation of the ventricular action potential, Long QT Syndrome, and arrhythmia. As such, approaches to augment hERG channel function, such as activator compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54c7fad16cca30e4ca3025e1e2123c19
Autor:
Shi, Yu, Zhaokai Pang, Ravichandra Venkateshappa, Gunawan, Marvin, Kemp, Jacob, Elson Truong, Cherlene Chang, Lin, Eric, Shafaattalab, Sanam, Shoaib Faizi, Rayani, Kaveh, Tibbits, Glen F, Claydon, Thomas
hERG K+ channels are important in cardiac repolarization and their dysfunction causes prolongation of the ventricular action potential, Long QT Syndrome, and arrhythmia. As such, approaches to augment hERG channel function, such as activator compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66b18f707fbb5419269a6f7c9baadbd4
Autor:
Shi, Yu, Zhaokai Pang, Ravichandra Venkateshappa, Gunawan, Marvin, Kemp, Jacob, Elson Truong, Cherlene Chang, Lin, Eric, Shafaattalab, Sanam, Shoaib Faizi, Rayani, Kaveh, Tibbits, Glen F, Claydon, Victoria E., Claydon, Thomas
hERG K+ channels are important in cardiac repolarization and their dysfunction causes prolongation of the ventricular action potential, Long QT Syndrome, and arrhythmia. As such, approaches to augment hERG channel function, such as activator compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09dcbabaf8daa916e93d20c0236bcb12