Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Wong, King Yuen"'
Autor:
Zhang, Jingyan, Singh, Daniel P., Ko, Christopher Y., Nikolaienko, Roman, Wong King Yuen, Siobhan M., Schwarz, Jacob A., Treinen, Levy M., Tung, Ching-Chieh, Rožman, Kaja, Svensson, Bengt, Aldrich, Courtney C., Zima, Aleksey V., Thomas, David D., Bers, Donald M., Launikonis, Bradley S., Van Petegem, Filip, Cornea, Razvan L.
Publikováno v:
In Journal of Biological Chemistry January 2022 298(1)
Autor:
Yingjie Liu, Jinhong Wei, Siobhan M Wong King Yuen, Bo Sun, Yijun Tang, Ruiwu Wang, Filip Van Petegem, S R Wayne Chen
Publikováno v:
PLoS ONE, Vol 12, Iss 9, p e0184177 (2017)
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is one of the most lethal inherited cardiac arrhythmias mostly linked to cardiac ryanodine receptor (RyR2) mutations with high disease penetrance. Interestingly, a novel RyR2 mutation G357S
Externí odkaz:
https://doaj.org/article/2b266e6817b440359e39318485ece239
Autor:
Razvan L. Cornea, Ching-Chieh Tung, Daniel P. Singh, Filip Van Petegem, Donald M. Bers, Bengt Svensson, Kaja Rožman, Levy M. Treinen, Siobhan M. Wong King Yuen, Courtney C. Aldrich, Bradley S. Launikonis, Jingyan Zhang, David D. Thomas, Aleksey V. Zima, Jacob A. Schwarz, Christopher Y. Ko, Roman Nikolaienko
Publikováno v:
The Journal of biological chemistry, vol 298, iss 1
The Journal of Biological Chemistry
The Journal of Biological Chemistry
The N-terminal region (NTR) of ryanodine receptor (RyR) channels is critical for the regulation of Ca2+ release during excitation–contraction (EC) coupling in muscle. The NTR hosts numerous mutations linked to skeletal (RyR1) and cardiac (RyR2) myo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62e651b16da8560235f301c406f3eb42
https://escholarship.org/uc/item/1sw1d750
https://escholarship.org/uc/item/1sw1d750
Autor:
Zhichao Xiao, Wenting Guo, Siobhan M Wong King Yuen, Ruiwu Wang, Lin Zhang, Filip Van Petegem, S R Wayne Chen
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0139058 (2015)
The N-terminal domain of the cardiac ryanodine receptor (RyR2) harbors a large number of naturally occurring mutations that are associated with stress-induced ventricular tachyarrhythmia and sudden death. Nearly all these disease-associated N-termina
Externí odkaz:
https://doaj.org/article/b4cd488b227b4b93a6f51d4031d421a0
Autor:
Wong, King Yuen, Spetsakis, Minas E.
Publikováno v:
In Computer Vision and Image Understanding 2006 101(1):45-64
The full abstract for this thesis is available in the body of the thesis, and will be available when the embargo expires.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44fb97a5ef641454802037549fe1b37c
Autor:
Wong King Yuen, Siobhan M., Campiglio, Marta, Ching-Chieh Tung, Flucher, Bernhard E., Van Petegem, Filip
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 11/7/2017, Vol. 114 Issue 45, pE9520-E9528, 9p
Autor:
Ching-Chieh Tung, Filip Van Petegem, Marta Campiglio, Siobhan M. Wong King Yuen, Bernhard E. Flucher
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Significance Skeletal muscle contraction is a tightly orchestrated event that starts with the depolarization of the T-tubular membrane. At the center is a functional and mechanical coupling between two membrane proteins: L-type voltage-gated calcium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c662f4245f96bd6f68c60fd91b3d1c3e
https://pubmed.ncbi.nlm.nih.gov/29078335
https://pubmed.ncbi.nlm.nih.gov/29078335
Autor:
Jinhong Wei, S. R. Wayne Chen, Bo Sun, Ruiwu Wang, Filip Van Petegem, Yingjie Liu, Yijun Tang, Siobhan M. Wong King Yuen
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 9, p e0184177 (2017)
PLoS ONE, Vol 12, Iss 9, p e0184177 (2017)
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is one of the most lethal inherited cardiac arrhythmias mostly linked to cardiac ryanodine receptor (RyR2) mutations with high disease penetrance. Interestingly, a novel RyR2 mutation G357S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b3fc5d30435afe72014e632e72e7cc7
http://europepmc.org/articles/PMC5621672
http://europepmc.org/articles/PMC5621672
Autor:
Liu, Yingjie, Wei, Jinhong, Wong King Yuen, Siobhan M., Sun, Bo, Tang, Yijun, Wang, Ruiwu, Van Petegem, Filip, Chen, S. R. Wayne
Publikováno v:
PLoS ONE; 9/29/2017, Vol. 12 Issue 9, p1-18, 18p