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Items: 1 to 20 of 100

1.

The gap junction communication channel.

Kumar NM, Gilula NB.

Cell. 1996 Feb 9;84(3):381-8. Review. No abstract available.

3.

Altered assembly of gap junction channels caused by COOH-terminal connexin32 mutants of CMTX.

Barrio LC, Castro C, Gómez-Hernandez JM.

Ann N Y Acad Sci. 1999 Sep 14;883:526-9. No abstract available.

PMID:
10586291
4.

Learning the language of cell-cell communication through connexin channels.

Bruzzone R.

Genome Biol. 2001;2(11):REPORTS4027. Epub 2001 Oct 15.

5.

Beyond the gap: functions of unpaired connexon channels.

Goodenough DA, Paul DL.

Nat Rev Mol Cell Biol. 2003 Apr;4(4):285-94. Review.

PMID:
12671651
6.

Analysis of gap junction assembly using mutated connexins detected in Charcot-Marie-Tooth X-linked disease.

Martin PE, Mambetisaeva ET, Archer DA, George CH, Evans WH.

J Neurochem. 2000 Feb;74(2):711-20.

7.

X-linked Charcot-Marie-Tooth disease and connexin32.

Fischbeck KH, Abel A, Lin GS, Scherer SS.

Ann N Y Acad Sci. 1999 Sep 14;883:36-41. Review.

PMID:
10586227
8.

Gap junction channels: new roles in disease.

Donaldson P, Eckert R, Green C, Kistler J.

Histol Histopathol. 1997 Jan;12(1):219-31. Review.

PMID:
9046057
9.

Connexins in disease.

Bennett MV.

Nature. 1994 Mar 3;368(6466):18-9. No abstract available.

PMID:
8107878
10.

Connexin channels in Schwann cells and the development of the X-linked form of Charcot-Marie-Tooth disease.

Ressot C, Bruzzone R.

Brain Res Brain Res Rev. 2000 Apr;32(1):192-202. Review.

PMID:
10751670
11.

Connexins and information transfer through glia.

Bruzzone R, Giaume C.

Adv Exp Med Biol. 1999;468:321-37. Review. No abstract available.

PMID:
10635040
12.

Regulation and function of liver gap junctions and their genes.

Spray DC, Bai S, Burk RD, Saez JC.

Prog Liver Dis. 1994;12:1-18. Review. No abstract available.

PMID:
7746869
13.

Cell-cell communication beyond connexins: the pannexin channels.

Barbe MT, Monyer H, Bruzzone R.

Physiology (Bethesda). 2006 Apr;21:103-14. Review.

14.

Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease.

Oh S, Ri Y, Bennett MV, Trexler EB, Verselis VK, Bargiello TA.

Neuron. 1997 Oct;19(4):927-38.

15.

Mutations in connexin 32: the molecular and biophysical bases for the X-linked form of Charcot-Marie-Tooth disease.

Abrams CK, Oh S, Ri Y, Bargiello TA.

Brain Res Brain Res Rev. 2000 Apr;32(1):203-14. Review.

PMID:
10751671
16.

Altered formation of hemichannels and gap junction channels caused by C-terminal connexin-32 mutations.

Castro C, Gómez-Hernandez JM, Silander K, Barrio LC.

J Neurosci. 1999 May 15;19(10):3752-60.

17.

Transfer of biologically important molecules between cells through gap junction channels.

Alexander DB, Goldberg GS.

Curr Med Chem. 2003 Oct;10(19):2045-58. Review.

PMID:
12871102
18.

Connexin32 in the peripheral nervous system. Functional analysis of mutations associated with X-linked Charcot-Marie-Tooth syndrome and implications for the pathophysiology of the disease.

Nicholson SM, Ressot C, Gomès D, D'Andrea P, Perea J, Duval N, Bruzzone R.

Ann N Y Acad Sci. 1999 Sep 14;883:168-85. Review. No abstract available.

PMID:
10586243
19.

Connexins, gap junctions and cell-cell signalling in the nervous system.

Bruzzone R, Ressot C.

Eur J Neurosci. 1997 Jan;9(1):1-6. Review.

PMID:
9042562
20.

Gap junctions and the propagation of cell survival and cell death signals.

Krysko DV, Leybaert L, Vandenabeele P, D'Herde K.

Apoptosis. 2005 May;10(3):459-69. Review.

PMID:
15909108

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