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Items: 1 to 20 of 186

1.

Mutation of a conserved threonine in the third transmembrane helix of alpha- and beta-connexins creates a dominant-negative closed gap junction channel.

Beahm DL, Oshima A, Gaietta GM, Hand GM, Smock AE, Zucker SN, Toloue MM, Chandrasekhar A, Nicholson BJ, Sosinsky GE.

J Biol Chem. 2006 Mar 24;281(12):7994-8009. Epub 2005 Dec 28.

2.

Analysis of trafficking, stability and function of human connexin 26 gap junction channels with deafness-causing mutations in the fourth transmembrane helix.

Ambrosi C, Walker AE, Depriest AD, Cone AC, Lu C, Badger J, Skerrett IM, Sosinsky GE.

PLoS One. 2013 Aug 15;8(8):e70916. doi: 10.1371/journal.pone.0070916. eCollection 2013.

3.

Analysis of four connexin26 mutant gap junctions and hemichannels reveals variations in hexamer stability.

Ambrosi C, Boassa D, Pranskevich J, Smock A, Oshima A, Xu J, Nicholson BJ, Sosinsky GE.

Biophys J. 2010 May 19;98(9):1809-19. doi: 10.1016/j.bpj.2010.01.019.

4.

Emerging issues of connexin channels: biophysics fills the gap.

Harris AL.

Q Rev Biophys. 2001 Aug;34(3):325-472. Review. Erratum in: Q Rev Biophys 2002 Feb;35(1):109.

PMID:
11838236
5.

Roles of Met-34, Cys-64, and Arg-75 in the assembly of human connexin 26. Implication for key amino acid residues for channel formation and function.

Oshima A, Doi T, Mitsuoka K, Maeda S, Fujiyoshi Y.

J Biol Chem. 2003 Jan 17;278(3):1807-16. Epub 2002 Oct 15.

6.

Connexin mutation that causes dominant congenital cataracts inhibits gap junctions, but not hemichannels, in a dominant negative manner.

Banks EA, Toloue MM, Shi Q, Zhou ZJ, Liu J, Nicholson BJ, Jiang JX.

J Cell Sci. 2009 Feb 1;122(Pt 3):378-88. doi: 10.1242/jcs.034124. Epub 2009 Jan 6.

7.

Functional rescue of defective mutant connexons by pairing with wild-type connexons.

Hülser DF, Rütz ML, Eckert R, Traub O.

Pflugers Arch. 2001 Jan;441(4):521-8.

PMID:
11212216
8.

Targeting motifs and functional parameters governing the assembly of connexins into gap junctions.

Martin PE, Steggles J, Wilson C, Ahmad S, Evans WH.

Biochem J. 2000 Jul 1;349(Pt 1):281-7.

9.

Pannexin1 and Pannexin2 channels show quaternary similarities to connexons and different oligomerization numbers from each other.

Ambrosi C, Gassmann O, Pranskevich JN, Boassa D, Smock A, Wang J, Dahl G, Steinem C, Sosinsky GE.

J Biol Chem. 2010 Aug 6;285(32):24420-31. doi: 10.1074/jbc.M110.115444. Epub 2010 Jun 1.

10.

Asymmetric configurations and N-terminal rearrangements in connexin26 gap junction channels.

Oshima A, Tani K, Toloue MM, Hiroaki Y, Smock A, Inukai S, Cone A, Nicholson BJ, Sosinsky GE, Fujiyoshi Y.

J Mol Biol. 2011 Jan 21;405(3):724-35. doi: 10.1016/j.jmb.2010.10.032. Epub 2010 Nov 20.

11.

A novel missense mutation in GJB2 disturbs gap junction protein transport and causes focal palmoplantar keratoderma with deafness.

de Zwart-Storm EA, Hamm H, Stoevesandt J, Steijlen PM, Martin PE, van Geel M, van Steensel MA.

J Med Genet. 2008 Mar;45(3):161-6. Epub 2007 Nov 9.

PMID:
17993581
12.

A quantitative analysis of connexin-specific permeability differences of gap junctions expressed in HeLa transfectants and Xenopus oocytes.

Cao F, Eckert R, Elfgang C, Nitsche JM, Snyder SA, H-ulser DF, Willecke K, Nicholson BJ.

J Cell Sci. 1998 Jan;111 ( Pt 1):31-43.

13.

The cataract related mutation N188T in human connexin46 (hCx46) revealed a critical role for residue N188 in the docking process of gap junction channels.

Schadzek P, Schlingmann B, Schaarschmidt F, Lindner J, Koval M, Heisterkamp A, Preller M, Ngezahayo A.

Biochim Biophys Acta. 2016 Jan;1858(1):57-66. doi: 10.1016/j.bbamem.2015.10.001. Epub 2015 Oct 9.

14.

A dominant negative mutation of neuronal connexin 36 that blocks intercellular permeability.

Placantonakis D, Cicirata F, Welsh JP.

Brain Res Mol Brain Res. 2002 Jan 31;98(1-2):15-28.

PMID:
11834292
15.

Autosomal recessive GJA1 (Cx43) gene mutations cause oculodentodigital dysplasia by distinct mechanisms.

Huang T, Shao Q, MacDonald A, Xin L, Lorentz R, Bai D, Laird DW.

J Cell Sci. 2013 Jul 1;126(Pt 13):2857-66. doi: 10.1242/jcs.123315. Epub 2013 Apr 19.

16.

A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts.

Arora A, Minogue PJ, Liu X, Addison PK, Russel-Eggitt I, Webster AR, Hunt DM, Ebihara L, Beyer EC, Berthoud VM, Moore AT.

J Med Genet. 2008 Mar;45(3):155-60. Epub 2007 Nov 15.

17.

Isolation and characterization of gap junctions from tissue culture cells.

Hand GM, Müller DJ, Nicholson BJ, Engel A, Sosinsky GE.

J Mol Biol. 2002 Jan 25;315(4):587-600.

PMID:
11812132
18.

The role of a conserved proline residue in mediating conformational changes associated with voltage gating of Cx32 gap junctions.

Ri Y, Ballesteros JA, Abrams CK, Oh S, Verselis VK, Weinstein H, Bargiello TA.

Biophys J. 1999 Jun;76(6):2887-98.

19.

trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation.

Rouan F, White TW, Brown N, Taylor AM, Lucke TW, Paul DL, Munro CS, Uitto J, Hodgins MB, Richard G.

J Cell Sci. 2001 Jun;114(Pt 11):2105-13.

20.

Connexin diversity and gap junction regulation by pHi.

Francis D, Stergiopoulos K, Ek-Vitorín JF, Cao FL, Taffet SM, Delmar M.

Dev Genet. 1999;24(1-2):123-36.

PMID:
10079516

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