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Divergence between Hemichannel and Gap Junction Permeabilities of Connexin 30 and 26. , Xu J., Life (Basel). January 31, 2023; 13 (2):
Structural determinants underlying permeant discrimination of the Cx43 hemichannel. , Nielsen BS., J Biol Chem. November 8, 2019; 294 (45): 16789-16803.
The syndromic deafness mutation G12R impairs fast and slow gating in Cx26 hemichannels. , García IE., J Gen Physiol. May 7, 2018; 150 (5): 697-711.
Syndromic deafness mutations at Asn 14 differentially alter the open stability of Cx26 hemichannels. , Sanchez HA., J Gen Physiol. July 1, 2016; 148 (1): 25-42.
RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance. , Ramírez-Gordillo D., BMC Res Notes. November 18, 2015; 8 691.
Extracellular gentamicin reduces the activity of connexin hemichannels and interferes with purinergic Ca(2+) signaling in HeLa cells. , Figueroa VA., Front Cell Neurosci. May 27, 2014; 8 265.
Mechanism of inhibition of connexin channels by the quinine derivative N-benzylquininium. , Rubinos C., J Gen Physiol. January 1, 2012; 139 (1): 69-82.
Asymmetric configurations and N-terminal rearrangements in connexin26 gap junction channels. , Oshima A., J Mol Biol. January 21, 2011; 405 (3): 724-35.
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.
GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf. , Tekin M., Ann Hum Genet. March 1, 2010; 74 (2): 155-64.
Mutations of connexin 26 at position 75 and dominant deafness: essential role of arginine for the generation of functional gap-junctional channels. , Deng Y., Hear Res. October 1, 2006; 220 (1-2): 87-94.
Loss of function mutations of the GJB2 gene detected in patients with DFNB1-associated hearing impairment. , Palmada M ., Neurobiol Dis. April 1, 2006; 22 (1): 112-8.
Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss. , Meşe G., Hum Genet. August 1, 2004; 115 (3): 191-9.
Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness. , Bruzzone R., FEBS Lett. January 2, 2003; 533 (1-3): 79-88.
Structure of the amino terminus of a gap junction protein. , Purnick PE., Arch Biochem Biophys. September 15, 2000; 381 (2): 181-90.