Roles of Met-34, Cys-64, and Arg-75 in the Assembly of Human Connexin 26
暂无分享,去创建一个
Y. Fujiyoshi | K. Mitsuoka | S. Maeda | A. Oshima | T. Doi
[1] J. Shin,et al. Identification of amino acid residues lining the pore of a gap junction channel , 2002, The Journal of cell biology.
[2] K. Willecke,et al. Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death , 2002, Current Biology.
[3] R. Errington,et al. Multiple pathways in the trafficking and assembly of connexin 26, 32 and 43 into gap junction intercellular communication channels. , 2001, Journal of cell science.
[4] M. Falk,et al. Expression of fluorescently tagged connexins: a novel approach to rescue function of oligomeric DsRed‐tagged proteins1 , 2001, FEBS letters.
[5] D. Kelsell,et al. Connexin mutations in skin disease and hearing loss. , 2001, American journal of human genetics.
[6] D. Weil,et al. Functional Analysis of a Dominant Mutation of Human Connexin26 Associated with Nonsyndromic Deafness , 2001, Cell communication & adhesion.
[7] A. Pagnamenta,et al. Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss , 2001, Journal of medical genetics.
[8] M. Falk,et al. Connexin-specific distribution within gap junctions revealed in living cells. , 2000, Journal of cell science.
[9] C. Berlin,et al. Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT. , 2000, American journal of human genetics.
[10] Joe C. Adams,et al. Gap junction systems in the mammalian cochlea , 2000, Brain Research Reviews.
[11] M. Bennett,et al. Clustering of connexin 43-enhanced green fluorescent protein gap junction channels and functional coupling in living cells. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[12] A Forge,et al. Properties of connexin26 gap junctional proteins derived from mutations associated with non-syndromal heriditary deafness. , 1999, Human molecular genetics.
[13] D. Laird,et al. Trafficking, assembly, and function of a connexin43-green fluorescent protein chimera in live mammalian cells. , 1999, Molecular biology of the cell.
[14] W. H. Evans,et al. Assembly of heteromeric connexons in guinea-pig liver en route to the Golgi apparatus, plasma membrane and gap junctions. , 1999, European journal of biochemistry.
[15] J. Kendall,et al. Intracellular Trafficking Pathways in the Assembly of Connexins into Gap Junctions* , 1999, The Journal of Biological Chemistry.
[16] M. Yeager,et al. Three-dimensional structure of a recombinant gap junction membrane channel. , 1999, Science.
[17] A. Pfahnl,et al. Gating of cx46 gap junction hemichannels by calcium and voltage , 1999, Pflügers Archiv.
[18] A. Campbell,et al. Connexin-Aequorin Chimerae Report Cytoplasmic Calcium Environments along Trafficking Pathways Leading to Gap Junction Biogenesis in Living COS-7 Cells* , 1998, The Journal of Biological Chemistry.
[19] A. Pfahnl,et al. Localization of a voltage gate in connexin46 gap junction hemichannels. , 1998, Biophysical journal.
[20] Thomas W. White,et al. Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma , 1998, Human Genetics.
[21] D. Kelsell,et al. Connexin mutations in deafness , 1998, Nature.
[22] J. W. Askew,et al. Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss. , 1998, American journal of human genetics.
[23] G. Perkins,et al. Formation of the gap junction intercellular channel requires a 30 degree rotation for interdigitating two apposing connexons. , 1998, Journal of molecular biology.
[24] B. Nicholson,et al. The Pattern of Disulfide Linkages in the Extracellular Loop Regions of Connexin 32 Suggests a Model for the Docking Interface of Gap Junctions , 1998, The Journal of cell biology.
[25] V. Sheffield,et al. Connexin mutations and hearing loss , 1998, Nature.
[26] A Chakravarti,et al. Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations. , 1997, Human molecular genetics.
[27] M. Bennett,et al. Changes in Permeability Caused by Connexin 32 Mutations Underlie X-Linked Charcot-Marie-Tooth Disease , 1997, Neuron.
[28] A. Hudder,et al. Identification of a pore lining segment in gap junction hemichannels. , 1997, Biophysical journal.
[29] D. Kelsell,et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness , 1997, nature.
[30] G. Perkins,et al. Three-dimensional structure of the gap junction connexon. , 1997, Biophysical journal.
[31] P. Hackett,et al. Expression of zebrafish connexin43.4 in the notochord and tail bud of wild-type and mutant no tail embryos. , 1996, Developmental biology.
[32] T. Tsukamoto,et al. Gap junction genes Cx26 and Cx43 individually suppress the cancer phenotype of human mammary carcinoma cells and restore differentiation potential. , 1996, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.
[33] N. Gilula,et al. The Gap Junction Communication Channel , 1996, Cell.
[34] D. Friend,et al. Synthesis and assembly of human beta 1 gap junctions in BHK cells by DNA transfection with the human beta 1 cDNA. , 1995, Journal of cell science.
[35] L. K. Buehler,et al. Single channel behavior of recombinant beta 2 gap junction connexons reconstituted into planar lipid bilayers. , 1995, Biophysical journal.
[36] Joe C. Adams,et al. Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis , 1995, Anatomy and Embryology.
[37] K. Willecke,et al. Negative growth control of HeLa cells by connexin genes: connexin species specificity. , 1995, Cancer research.
[38] H. Khorana,et al. Structure and function in rhodopsin: replacement by alanine of cysteine residues 110 and 187, components of a conserved disulfide bond in rhodopsin, affects the light-activated metarhodopsin II state. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[39] Sam W. Lee,et al. Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines , 1992, The Journal of cell biology.
[40] R. Werner,et al. Mutational analysis of gap junction formation. , 1992, Biophysical journal.
[41] S. Rahman,et al. Topography of connexin32 in rat liver gap junctions. Evidence for an intramolecular disulphide linkage connecting the two extracellular peptide loops. , 1991, Journal of cell science.
[42] N. Unwin,et al. Isolation and purification of gap junction channels , 1991, The Journal of cell biology.
[43] S. John,et al. Connexon integrity is maintained by non-covalent bonds: intramolecular disulfide bonds link the extracellular domains in rat connexin-43. , 1991, Biochemical and biophysical research communications.
[44] R. Werner,et al. Cell/cell channel formation involves disulfide exchange. , 1991, European journal of biochemistry.
[45] Jian-ting,et al. Sequence and tissue distribution of a second protein of hepatic gap junctions, Cx26, as deduced from its cDNA , 1989, The Journal of cell biology.
[46] E. Hertzberg,et al. Topology of the Mr 27,000 liver gap junction protein. Cytoplasmic localization of amino- and carboxyl termini and a hydrophilic domain which is protease-hypersensitive. , 1988, The Journal of biological chemistry.
[47] R. Houghten,et al. Topology of the 32‐kd liver gap junction protein determined by site‐directed antibody localizations. , 1988, The EMBO journal.
[48] D. Paul,et al. Connexin43: a protein from rat heart homologous to a gap junction protein from liver , 1987, The Journal of cell biology.
[49] C. Green,et al. Topological analysis of the major protein in isolated intact rat liver gap junctions and gap junction-derived single membrane structures. , 1987, The Journal of biological chemistry.
[50] P. N. Unwin,et al. Two configurations of a channel-forming membrane protein , 1984, Nature.
[51] W. Loewenstein,et al. Junctional intercellular communication: the cell-to-cell membrane channel. , 1981, Physiological reviews.
[52] G. Zampighi,et al. Structure of the junction between communicating cells , 1980, Nature.
[53] L. Makowski,et al. Gap junction structures. I. Correlated electron microscopy and x-ray diffraction , 1977, The Journal of cell biology.
[54] L. Makowski,et al. Gap junction structures: Analysis of the x-ray diffraction data , 1977, The Journal of cell biology.
[55] R. Williamson,et al. High frequency hearing loss correlated with mutations in the GJB2 gene , 2000, Human Genetics.
[56] M. Yeager,et al. Structure of cardiac gap junction intercellular channels. , 1998, Journal of structural biology.