Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Donglin Bai

Showing results (31-40 of 67) with videos related to

Pageof 7
Sort By:
The Biochemical Journal|May 16, 2024
Genetically engineered human embryonic kidney cells as a novel vehicle for dual patch clamp study of human gap junction channelsHonghong Chen, Yi X Li, Robert S Wong, et al.
International Journal of Molecular Sciences|January 11, 2022
Interrogation of Carboxy-Terminus Localized <i>GJA1</i> Variants Associated with Erythrokeratodermia Variabilis et ProgressivaSergiu A Lucaciu, Qing Shao, Rhett Figliuzzi, et al.
Communications Biology|June 11, 2026
Quantifying electrostatic control of docking and binding energetics in functional Cx36 gap junctionsRobert S Wong, Zhiyuan Song, Yu T Zheng, et al.
Journal of Molecular and Cellular Cardiology|April 24, 2020
The amino terminal domain plays an important role in transjunctional voltage-dependent gating kinetics of Cx45 gap junctionsArtur Santos-Miranda, Honghong Chen, Robert C Chen, et al.
The Journal of Biological Chemistry|April 12, 2011
Asparagine 175 of connexin32 is a critical residue for docking and forming functional heterotypic gap junction channels with connexin26So Nakagawa, Xiang-Qun Gong, Shoji Maeda, et al.
Cardiovascular Research|August 19, 2009
Sodium-hydrogen exchange inhibition attenuates glycoside-induced hypertrophy in rat ventricular myocytesXiaohong Tracey Gan, Xiang-Qun Gong, Jenny Xue, et al.
Journal of Cell Science|April 23, 2013
Autosomal recessive GJA1 (Cx43) gene mutations cause oculodentodigital dysplasia by distinct mechanismsTao Huang, Qing Shao, Andrew MacDonald, et al.
The Biochemical Journal|October 6, 2018
Variants with increased negative electrostatic potential in the Cx50 gap junction pore increased unitary channel conductance and magnesium modulationMary Grace Tejada, Swathy Sudhakar, Nicholas K Kim, et al.
American Journal of Physiology. Cell Physiology|December 25, 2023
Human Cx50 Isoleucine177 prevents heterotypic docking and formation of functional gap junction channels with Cx43Robert S Wong, Honghong Chen, Yi X Li, et al.
Molecular Biology of the Cell|July 20, 2012
Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasiaQing Shao, Qin Liu, Robert Lorentz, et al.
Pageof 7

Showing results (31-40 of 67) with videos related to

Sort By:
Pageof 7
The Biochemical Journal|May 16, 2024
Genetically engineered human embryonic kidney cells as a novel vehicle for dual patch clamp study of human gap junction channelsHonghong Chen, Yi X Li, Robert S Wong, et al.
International Journal of Molecular Sciences|January 11, 2022
Interrogation of Carboxy-Terminus Localized <i>GJA1</i> Variants Associated with Erythrokeratodermia Variabilis et ProgressivaSergiu A Lucaciu, Qing Shao, Rhett Figliuzzi, et al.
Communications Biology|June 11, 2026
Quantifying electrostatic control of docking and binding energetics in functional Cx36 gap junctionsRobert S Wong, Zhiyuan Song, Yu T Zheng, et al.
Journal of Molecular and Cellular Cardiology|April 24, 2020
The amino terminal domain plays an important role in transjunctional voltage-dependent gating kinetics of Cx45 gap junctionsArtur Santos-Miranda, Honghong Chen, Robert C Chen, et al.
The Journal of Biological Chemistry|April 12, 2011
Asparagine 175 of connexin32 is a critical residue for docking and forming functional heterotypic gap junction channels with connexin26So Nakagawa, Xiang-Qun Gong, Shoji Maeda, et al.
Cardiovascular Research|August 19, 2009
Sodium-hydrogen exchange inhibition attenuates glycoside-induced hypertrophy in rat ventricular myocytesXiaohong Tracey Gan, Xiang-Qun Gong, Jenny Xue, et al.
Journal of Cell Science|April 23, 2013
Autosomal recessive GJA1 (Cx43) gene mutations cause oculodentodigital dysplasia by distinct mechanismsTao Huang, Qing Shao, Andrew MacDonald, et al.
The Biochemical Journal|October 6, 2018
Variants with increased negative electrostatic potential in the Cx50 gap junction pore increased unitary channel conductance and magnesium modulationMary Grace Tejada, Swathy Sudhakar, Nicholas K Kim, et al.
American Journal of Physiology. Cell Physiology|December 25, 2023
Human Cx50 Isoleucine177 prevents heterotypic docking and formation of functional gap junction channels with Cx43Robert S Wong, Honghong Chen, Yi X Li, et al.
Molecular Biology of the Cell|July 20, 2012
Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasiaQing Shao, Qin Liu, Robert Lorentz, et al.
Pageof 7