Search research articles
Contact Us
Filters
Showing results (41-50 of 55) with videos related to
Page
of 6
Sort By:
Biorxiv : the Preprint Server for Biology
|
August 2, 2024
Endothelial TRPV4/Cx43 Signaling Complex Regulates Vasomotor Tone in Resistance Arteries
Pía C Burboa, Pablo S Gaete, Ping Shu, et al.
The Journal of General Physiology
|
December 12, 2018
The connexin26 human mutation N14K disrupts cytosolic intersubunit interactions and promotes channel opening
Juan M Valdez Capuccino, Payal Chatterjee, Isaac E García, et al.
The Journal of General Physiology
|
May 16, 2023
Remodeled connexin 43 hemichannels alter cardiac excitability and promote arrhythmias
Mauricio A Lillo, Manuel Muñoz, Paula Rhana, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 5, 2002
Metabolic inhibition induces opening of unapposed connexin 43 gap junction hemichannels and reduces gap junctional communication in cortical astrocytes in culture
Jorge E Contreras, Helmut A Sánchez, Eliseo A Eugenin, et al.
Neuromuscular Disorders : NMD
|
February 26, 2018
Normalization of connexin 43 protein levels prevents cellular and functional signs of dystrophic cardiomyopathy in mice
J Patrick Gonzalez, Jayalakshmi Ramachandran, Eric Himelman, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
May 21, 2017
<i>S</i>-nitrosylation of VASP at cysteine 64 mediates the inflammation-stimulated increase in microvascular permeability
Patricia Zamorano, Natalie Marín, Francisco Córdova, et al.
The Journal of General Physiology
|
April 13, 2018
The syndromic deafness mutation G12R impairs fast and slow gating in Cx26 hemichannels
Isaac E García, Felipe Villanelo, Gustavo F Contreras, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
October 7, 2022
A microtubule-connexin-43 regulatory link suppresses arrhythmias and cardiac fibrosis in Duchenne muscular dystrophy mice
Eric Himelman, Julie Nouet, Mauricio A Lillo, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 8, 2024
Large-pore connexin hemichannels function like molecule transporters independent of ion conduction
Pablo S Gaete, Deepak Kumar, Cynthia I Fernandez, et al.
The Journal of Investigative Dermatology
|
January 28, 2015
Keratitis-ichthyosis-deafness syndrome-associated Cx26 mutants produce nonfunctional gap junctions but hyperactive hemichannels when co-expressed with wild type Cx43
Isaac E García, Jaime Maripillán, Oscar Jara, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 55) with videos related to
Sort By:
Page
of 6
Biorxiv : the Preprint Server for Biology
|
August 2, 2024
Endothelial TRPV4/Cx43 Signaling Complex Regulates Vasomotor Tone in Resistance Arteries
Pía C Burboa, Pablo S Gaete, Ping Shu, et al.
The Journal of General Physiology
|
December 12, 2018
The connexin26 human mutation N14K disrupts cytosolic intersubunit interactions and promotes channel opening
Juan M Valdez Capuccino, Payal Chatterjee, Isaac E García, et al.
The Journal of General Physiology
|
May 16, 2023
Remodeled connexin 43 hemichannels alter cardiac excitability and promote arrhythmias
Mauricio A Lillo, Manuel Muñoz, Paula Rhana, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 5, 2002
Metabolic inhibition induces opening of unapposed connexin 43 gap junction hemichannels and reduces gap junctional communication in cortical astrocytes in culture
Jorge E Contreras, Helmut A Sánchez, Eliseo A Eugenin, et al.
Neuromuscular Disorders : NMD
|
February 26, 2018
Normalization of connexin 43 protein levels prevents cellular and functional signs of dystrophic cardiomyopathy in mice
J Patrick Gonzalez, Jayalakshmi Ramachandran, Eric Himelman, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
May 21, 2017
<i>S</i>-nitrosylation of VASP at cysteine 64 mediates the inflammation-stimulated increase in microvascular permeability
Patricia Zamorano, Natalie Marín, Francisco Córdova, et al.
The Journal of General Physiology
|
April 13, 2018
The syndromic deafness mutation G12R impairs fast and slow gating in Cx26 hemichannels
Isaac E García, Felipe Villanelo, Gustavo F Contreras, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
October 7, 2022
A microtubule-connexin-43 regulatory link suppresses arrhythmias and cardiac fibrosis in Duchenne muscular dystrophy mice
Eric Himelman, Julie Nouet, Mauricio A Lillo, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 8, 2024
Large-pore connexin hemichannels function like molecule transporters independent of ion conduction
Pablo S Gaete, Deepak Kumar, Cynthia I Fernandez, et al.
The Journal of Investigative Dermatology
|
January 28, 2015
Keratitis-ichthyosis-deafness syndrome-associated Cx26 mutants produce nonfunctional gap junctions but hyperactive hemichannels when co-expressed with wild type Cx43
Isaac E García, Jaime Maripillán, Oscar Jara, et al.
Page
of 6