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Journal of Cell Science
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April 6, 2018
Mice harbouring an oculodentodigital dysplasia-linked Cx43 G60S mutation have severe hearing loss
Julia M Abitbol, John J Kelly, Kevin J Barr, et al.
Cell Communication & Adhesion
|
March 15, 2006
Rat epidermal keratinocytes as an organotypic model for examining the role of Cx43 and Cx26 in skin differentiation
Amy C Maher, Tamsin Thomas, Jessica L Riley, 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.
Journal of Vascular Research
|
May 20, 2016
Critical Role of Cx40 in Reduced Endothelial Electrical Coupling by Lipopolysaccharide and Hypoxia-Reoxygenation
Mohammad Siddiqui, Scott Swarbreck, Qing Shao, et al.
The Journal of Biological Chemistry
|
April 22, 2017
Induction of cell death and gain-of-function properties of connexin26 mutants predict severity of skin disorders and hearing loss
Eric R Press, Qing Shao, John J Kelly, et al.
Journal of Anatomy
|
January 11, 2016
Global deletion of Panx3 produces multiple phenotypic effects in mouse humeri and femora
Deidre Caskenette, Silvia Penuela, Vanessa Lee, et al.
Frontiers in Cell and Developmental Biology
|
April 18, 2020
<i>GJB2</i> Mutations Linked to Hearing Loss Exhibit Differential Trafficking and Functional Defects as Revealed in Cochlear-Relevant Cells
Rianne Beach, Julia M Abitbol, Brian L Allman, et al.
The Journal of Biological Chemistry
|
August 19, 2007
Connexin levels regulate keratinocyte differentiation in the epidermis
Stéphanie Langlois, Amy C Maher, Janet L Manias, et al.
Cell Death & Disease
|
May 26, 2018
Correction to: Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice
Eric Press, Katanya C Alaga, Kevin Barr, et al.
Cells
|
January 18, 2020
Involvement of the Gap Junction Protein, Connexin43, in the Formation and Function of Invadopodia in the Human U251 Glioblastoma Cell Line
Amandine Chepied, Zeinaba Daoud-Omar, Annie-Claire Meunier-Balandre, et al.
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of 14
Search research articles
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Showing results (71-80 of 136) with videos related to
Sort By:
Page
of 14
Journal of Cell Science
|
April 6, 2018
Mice harbouring an oculodentodigital dysplasia-linked Cx43 G60S mutation have severe hearing loss
Julia M Abitbol, John J Kelly, Kevin J Barr, et al.
Cell Communication & Adhesion
|
March 15, 2006
Rat epidermal keratinocytes as an organotypic model for examining the role of Cx43 and Cx26 in skin differentiation
Amy C Maher, Tamsin Thomas, Jessica L Riley, 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.
Journal of Vascular Research
|
May 20, 2016
Critical Role of Cx40 in Reduced Endothelial Electrical Coupling by Lipopolysaccharide and Hypoxia-Reoxygenation
Mohammad Siddiqui, Scott Swarbreck, Qing Shao, et al.
The Journal of Biological Chemistry
|
April 22, 2017
Induction of cell death and gain-of-function properties of connexin26 mutants predict severity of skin disorders and hearing loss
Eric R Press, Qing Shao, John J Kelly, et al.
Journal of Anatomy
|
January 11, 2016
Global deletion of Panx3 produces multiple phenotypic effects in mouse humeri and femora
Deidre Caskenette, Silvia Penuela, Vanessa Lee, et al.
Frontiers in Cell and Developmental Biology
|
April 18, 2020
<i>GJB2</i> Mutations Linked to Hearing Loss Exhibit Differential Trafficking and Functional Defects as Revealed in Cochlear-Relevant Cells
Rianne Beach, Julia M Abitbol, Brian L Allman, et al.
The Journal of Biological Chemistry
|
August 19, 2007
Connexin levels regulate keratinocyte differentiation in the epidermis
Stéphanie Langlois, Amy C Maher, Janet L Manias, et al.
Cell Death & Disease
|
May 26, 2018
Correction to: Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice
Eric Press, Katanya C Alaga, Kevin Barr, et al.
Cells
|
January 18, 2020
Involvement of the Gap Junction Protein, Connexin43, in the Formation and Function of Invadopodia in the Human U251 Glioblastoma Cell Line
Amandine Chepied, Zeinaba Daoud-Omar, Annie-Claire Meunier-Balandre, et al.
Page
of 14