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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 channels
Honghong 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 Progressiva
Sergiu 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 junctions
Robert 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 junctions
Artur 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 connexin26
So Nakagawa, Xiang-Qun Gong, Shoji Maeda, et al.
Cardiovascular Research
|
August 19, 2009
Sodium-hydrogen exchange inhibition attenuates glycoside-induced hypertrophy in rat ventricular myocytes
Xiaohong 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 mechanisms
Tao 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 modulation
Mary 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 Cx43
Robert 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 dysplasia
Qing Shao, Qin Liu, Robert Lorentz, et al.
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Search research articles
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Showing results (31-40 of 67) with videos related to
Sort By:
Page
of 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 channels
Honghong 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 Progressiva
Sergiu 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 junctions
Robert 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 junctions
Artur 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 connexin26
So Nakagawa, Xiang-Qun Gong, Shoji Maeda, et al.
Cardiovascular Research
|
August 19, 2009
Sodium-hydrogen exchange inhibition attenuates glycoside-induced hypertrophy in rat ventricular myocytes
Xiaohong 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 mechanisms
Tao 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 modulation
Mary 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 Cx43
Robert 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 dysplasia
Qing Shao, Qin Liu, Robert Lorentz, et al.
Page
of 7