Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (80) GO Terms (12) Nucleotides (59) Proteins (32) Interactants (170) Wiki
XB--494160

Papers associated with gja3 (and Disease Ontology)

Search for gja3 morpholinos using Textpresso

Limit to papers also referencing gene:
Show all gja3 papers

Results 1 - 4 of 4 results

Page(s): 1

Sort Newest To Oldest Sort Oldest To Newest

The cataract related mutation N188T in human connexin46 (hCx46) revealed a critical role for residue N188 in the docking process of gap junction channels., Schadzek P, Schlingmann B, Schaarschmidt F, Lindner J, Koval M, Heisterkamp A, Preller M, Ngezahayo A., Biochim Biophys Acta. January 1, 2016; 1858 (1): 57-66.                        


Mechanism of inhibition of connexin channels by the quinine derivative N-benzylquininium., Rubinos C, Sánchez HA, Verselis VK, Srinivas M., J Gen Physiol. January 1, 2012; 139 (1): 69-82.                    


A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts., Arora A, Minogue PJ, Liu X, Addison PK, Russel-Eggitt I, Webster AR, Hunt DM, Ebihara L, Beyer EC, Berthoud VM, Moore AT., J Med Genet. March 1, 2008; 45 (3): 155-60.


Single-channel SCAM identifies pore-lining residues in the first extracellular loop and first transmembrane domains of Cx46 hemichannels., Kronengold J, Trexler EB, Bukauskas FF, Bargiello TA, Verselis VK., J Gen Physiol. October 1, 2003; 122 (4): 389-405.                    

Page(s): 1