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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.