Papers associated with skeletal element (and gja3)

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	The role of the C-terminus in functional expression and internalization of rat connexin46 (rCx46)., Schlingmann B., J Bioenerg Biomembr. February 1, 2013; 45 (1-2): 59-70.
	Connexin mutation that causes dominant congenital cataracts inhibits gap junctions, but not hemichannels, in a dominant negative manner., Banks EA., J Cell Sci. February 1, 2009; 122 (Pt 3): 378-88.
	Single-channel SCAM identifies pore-lining residues in the first extracellular loop and first transmembrane domains of Cx46 hemichannels., Kronengold J., J Gen Physiol. October 1, 2003; 122 (4): 389-405.
	Inhibition of gap junction hemichannels by chloride channel blockers., Eskandari S., J Membr Biol. January 15, 2002; 185 (2): 93-102.
	Biological functions of connexin genes revealed by human genetic defects, dominant negative approaches and targeted deletions in the mouse., Willecke K., Novartis Found Symp. January 1, 1999; 219 76-88; discussion 88-96.
	Connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease show two distinct behaviors: loss of function and altered gating properties., Ressot C., J Neurosci. June 1, 1998; 18 (11): 4063-75.

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