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Understanding the Role of ATP Release through Connexins Hemichannels during Neurulation. , Tovar LM., Int J Mol Sci. January 21, 2023; 24 (3):
Aberrant connexin26 hemichannels underlying keratitis-ichthyosis-deafness syndrome are potently inhibited by mefloquine. , Levit NA., J Invest Dermatol. April 1, 2015; 135 (4): 1033-1042.
The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity. , Mhaske PV., Am J Physiol Cell Physiol. June 15, 2013; 304 (12): C1150-8.
Connexins in epidermal homeostasis and skin disease. , Scott CA., Biochim Biophys Acta. August 1, 2012; 1818 (8): 1952-61.
Connexin26-mediated transfer of laterality cues in Xenopus. , Beyer T., Biol Open. May 15, 2012; 1 (5): 473-81.
Zebrafish cx30.3: identification and characterization of a gap junction gene highly expressed in the skin. , Tao L., Dev Dyn. October 1, 2010; 239 (10): 2627-36.
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.
Connexin mutations causing skin disease and deafness increase hemichannel activity and cell death when expressed in Xenopus oocytes. , Lee JR , Lee JR ., J Invest Dermatol. April 1, 2009; 129 (4): 870-8.
Aberrant hemichannel properties of Cx26 mutations causing skin disease and deafness. , Gerido DA., Am J Physiol Cell Physiol. July 1, 2007; 293 (1): C337-45.
Species specificity of mammalian connexin-26 to form open voltage-gated hemichannels. , González D., FASEB J. November 1, 2006; 20 (13): 2329-38.
Cloning, embryonic expression, and functional characterization of two novel connexins from Xenopus laevis. , de Boer TP., Biochem Biophys Res Commun. October 20, 2006; 349 (2): 855-62.
Global analysis of the transcriptional network controlling Xenopus endoderm formation. , Sinner D ., Development. May 1, 2006; 133 (10): 1955-66.
An atlas of differential gene expression during early Xenopus embryogenesis. , Pollet N ., Mech Dev. March 1, 2005; 122 (3): 365-439.
A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triad. , Montgomery JR., J Am Acad Dermatol. September 1, 2004; 51 (3): 377-82.
trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation. , Rouan F., J Cell Sci. June 1, 2001; 114 (Pt 11): 2105-13.
Gap junctions are involved in the early generation of left- right asymmetry. , Levin M ., Dev Biol. November 1, 1998; 203 (1): 90-105.
Molecular cloning and functional expression of mouse connexin-30,a gap junction gene highly expressed in adult brain and skin. , Dahl E., J Biol Chem. July 26, 1996; 271 (30): 17903-10.
Molecular cloning and characterization of a new member of the gap junction gene family, connexin-31. , Hoh JH., J Biol Chem. April 5, 1991; 266 (10): 6524-31.