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Summary Expression Phenotypes Gene Literature (109) GO Terms (5) Nucleotides (94) Proteins (45) Interactants (174) Wiki
XB-GENEPAGE-876601

Papers associated with gja1



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Directional coupling of oligodendrocyte connexin-47 and astrocyte connexin-43 gap junctions., Fasciani I, Pluta P, González-Nieto D, Martínez-Montero P, Molano J, Paíno CL, Millet O, Barrio LC., Glia. November 1, 2018; 66 (11): 2340-2352.

Connexin43 mutations linked to skin disease have augmented hemichannel activity., Srinivas M, Jannace TF, Cocozzelli AG, Li L, Slavi N, Sellitto C, White TW., Sci Rep. January 10, 2019; 9 (1): 19.              

Structural determinants underlying permeant discrimination of the Cx43 hemichannel., Nielsen BS, Zonta F, Farkas T, Litman T, Nielsen MS, MacAulay N., J Biol Chem. November 8, 2019; 294 (45): 16789-16803.              

S-nitrosylation of connexin43 hemichannels elicits cardiac stress-induced arrhythmias in Duchenne muscular dystrophy mice., Lillo MA, Himelman E, Shirokova N, Xie LH, Fraidenraich D, Contreras JE., JCI Insight. December 19, 2019; 4 (24):                                 

Bioelectric signaling: Reprogrammable circuits underlying embryogenesis, regeneration, and cancer., Levin M., Cell. April 15, 2021;               

Cellular responses in the FGF10-mediated improvement of hindlimb regenerative capacity in Xenopus laevis revealed by single-cell transcriptomics., Yanagi N, Kato S, Fukazawa T, Kubo T., Dev Growth Differ. August 1, 2022; 64 (6): 266-278.      

GJA1 depletion causes ciliary defects by affecting Rab11 trafficking to the ciliary base., Jang DG, Kwon KY, Kweon YC, Kim BG, Myung K, Lee HS, Young Park C, Kwon T, Park TJ., Elife. August 25, 2022; 11                                       

Understanding the Role of ATP Release through Connexins Hemichannels during Neurulation., Tovar LM, Burgos CF, Yévenes GE, Moraga-Cid G, Fuentealba J, Coddou C, Bascunan-Godoy L, Catrupay C, Torres A, Castro PA., Int J Mol Sci. January 21, 2023; 24 (3):                     

Increased Hemichannel Activity Displayed by a Connexin43 Mutation Causing a Familial Connexinopathy Exhibiting Hypotrichosis with Follicular Keratosis and Hyperostosis., Crouthamel OE, Li L, Dilluvio MT, White TW., Int J Mol Sci. January 22, 2023; 24 (3):           

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