Papers associated with skeletal element (and gja8)

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	Voltage-dependent gating of the Cx32*43E1 hemichannel: conformational changes at the channel entrances., Kwon T., J Gen Physiol. February 1, 2013; 141 (2): 243-59.
	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.
	CO(2) sensitivity of voltage gating and gating polarity of gapjunction channels--connexin40 and its COOH-terminus-truncated mutant., Peracchia C., J Membr Biol. July 15, 2004; 200 (2): 105-13.
	Inhibition of gap junction hemichannels by chloride channel blockers., Eskandari S., J Membr Biol. January 15, 2002; 185 (2): 93-102.
	Hetero-domain interactions as a mechanism for the regulation of connexin channels., Stergiopoulos K., Circ Res. May 28, 1999; 84 (10): 1144-55.
	Functional and morphological correlates of connexin50 expressed in Xenopus laevis oocytes., Zampighi GA., J Gen Physiol. April 1, 1999; 113 (4): 507-24.
	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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