Papers associated with oocyte (and gja8)

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	Molecular mechanisms underlying enhanced hemichannel function of a cataract-associated Cx50 mutant., Tong JJ., Biophys J. December 21, 2021; 120 (24): 5644-5656.
	A novel voltage-clamp/dye uptake assay reveals saturable transport of molecules through CALHM1 and connexin channels., Gaete PS., J Gen Physiol. November 2, 2020; 152 (11):
	The connexin46 mutant, Cx46T19M, causes loss of gap junction function and alters hemi-channel gating., Tong JJ., J Membr Biol. February 1, 2015; 248 (1): 145-55.
	Bisphenol A and 4-tert-Octylphenol Inhibit Cx46 Hemichannel Currents., Oh S., Korean J Physiol Pharmacol. January 1, 2015; 19 (1): 73-9.
	Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion., Kumari SS., Exp Eye Res. November 1, 2013; 116 371-85.
	Properties of two cataract-associated mutations located in the NH2 terminus of connexin 46., Tong JJ., Am J Physiol Cell Physiol. May 1, 2013; 304 (9): C823-32.
	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.
	Mechanism of inhibition of connexin channels by the quinine derivative N-benzylquininium., Rubinos C., J Gen Physiol. January 1, 2012; 139 (1): 69-82.
	Cataracts and microphthalmia caused by a Gja8 mutation in extracellular loop 2., Xia CH., PLoS One. January 1, 2012; 7 (12): e52894.
	Pannexin1 and Pannexin2 channels show quaternary similarities to connexons and different oligomerization numbers from each other., Ambrosi C., J Biol Chem. August 6, 2010; 285 (32): 24420-31.
	Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome., Sánchez HA., J Gen Physiol. July 1, 2010; 136 (1): 47-62.
	The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutation., Graw J., Mol Vis. May 18, 2009; 15 1881-5.
	The cataract-inducing S50P mutation in Cx50 dominantly alters the channel gating of wild-type lens connexins., DeRosa AM., J Cell Sci. December 1, 2007; 120 (Pt 23): 4107-16.
	Regulation of connexin hemichannels by monovalent cations., Srinivas M., J Gen Physiol. January 1, 2006; 127 (1): 67-75.
	Interplay between cystic fibrosis transmembrane regulator and gap junction channels made of connexins 45, 40, 32 and 50 expressed in oocytes., Kotsias BA., J Membr Biol. January 1, 2006; 214 (1): 1-8.
	Exchange of gating properties between rat cx46 and chicken cx45.6., Tong JJ., Biophys J. October 1, 2004; 87 (4): 2397-406.
	Hemichannel and junctional properties of connexin 50., Beahm DL., Biophys J. April 1, 2002; 82 (4): 2016-31.
	Characterization of a mouse Cx50 mutation associated with the No2 mouse cataract., Xu X., Invest Ophthalmol Vis Sci. July 1, 1999; 40 (8): 1844-50.
	Molecular mechanism underlying a Cx50-linked congenital cataract., Pal JD., Am J Physiol. June 1, 1999; 276 (6): C1443-6.
	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.
	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 lens connexin expression lead to increased gap junctional voltage dependence and conductance., Donaldson PJ., Am J Physiol. September 1, 1995; 269 (3 Pt 1): C590-600.
	Bovine connexin44, a lens gap junction protein: molecular cloning, immunologic characterization, and functional expression., Gupta VK., Invest Ophthalmol Vis Sci. September 1, 1994; 35 (10): 3747-58.

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