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Summary Anatomy Item Literature (84) Expression Attributions Wiki
XB-ANAT-412

Papers associated with tooth (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. January 1, 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.


Severe neuropathy with leaky connexin32 hemichannels., Liang GS., Ann Neurol. May 1, 2005; 57 (5): 749-54.


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.


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.


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.


Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease., Bruzzone R., Neuron. November 1, 1994; 13 (5): 1253-60.

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