Papers associated with cranium (and gjb1)

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	Structural studies of N-terminal mutants of Connexin 26 and Connexin 32 using (1)H NMR spectroscopy., Batir Y., Arch Biochem Biophys. October 15, 2016; 608 8-19.
	Role of connexin 32 hemichannels in the release of ATP from peripheral nerves., Nualart-Marti A., Glia. December 1, 2013; 61 (12): 1976-89.
	The carboxyl terminal residues 220-283 are not required for voltage gating of a chimeric connexin32 hemichannel., Kwon T., Biophys J. September 17, 2013; 105 (6): 1376-82.
	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.
	Prolonged FGF signaling is necessary for lung and liver induction in Xenopus., Shifley ET., BMC Dev Biol. September 18, 2012; 12 27.
	Unusual slow gating of gap junction channels in oocytes expressing connexin32 or its COOH-terminus truncated mutant., Peracchia C., J Membr Biol. February 1, 2007; 215 (2-3): 161-8.
	Severe neuropathy with leaky connexin32 hemichannels., Liang GS., Ann Neurol. May 1, 2005; 57 (5): 749-54.
	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.
	Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32., Abrams CK., J Neurosci. November 19, 2003; 23 (33): 10548-58.
	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.
	Voltage opens unopposed gap junction hemichannels formed by a connexin 32 mutant associated with X-linked Charcot-Marie-Tooth disease., Abrams CK., Proc Natl Acad Sci U S A. March 19, 2002; 99 (6): 3980-4.
	Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease., Dubourg O., Brain. October 1, 2001; 124 (Pt 10): 1958-67.
	Functional alterations in gap junction channels formed by mutant forms of connexin 32: evidence for loss of function as a pathogenic mechanism in the X-linked form of Charcot-Marie-Tooth disease., Abrams CK., Dev Biol. May 4, 2001; 900 (1): 9-25.
	Molecular dissection of transjunctional voltage dependence in the connexin-32 and connexin-43 junctions., Revilla A., Biophys J. September 1, 1999; 77 (3): 1374-83.
	The role of a conserved proline residue in mediating conformational changes associated with voltage gating of Cx32 gap junctions., Ri Y., Biophys J. June 1, 1999; 76 (6): 2887-98.
	Hetero-domain interactions as a mechanism for the regulation of connexin channels., Stergiopoulos K., Circ Res. May 28, 1999; 84 (10): 1144-55.
	Altered formation of hemichannels and gap junction channels caused by C-terminal connexin-32 mutations., Castro C., J Neurosci. May 15, 1999; 19 (10): 3752-60.
	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.
	Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease., Oh S., Neuron. October 1, 1997; 19 (4): 927-38.
	Positive charges of the initial C-terminus domain of Cx32 inhibit gap junction gating sensitivity to CO2., Wang XG., Biophys J. August 1, 1997; 73 (2): 798-806.
	Connexin domains relevant to the chemical gating of gap junction channels., Peracchia C., Braz J Med Biol Res. May 1, 1997; 30 (5): 577-90.
	Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease., Bruzzone R., Neuron. November 1, 1994; 13 (5): 1253-60.
	A structural basis for the unequal sensitivity of the major cardiac and liver gap junctions to intracellular acidification: the carboxyl tail length., Liu S., Biophys J. May 1, 1993; 64 (5): 1422-33.

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