Functional analysis of connexin-32 mutants associated with X-linked dominant Charcot-Marie-Tooth disease
Authors:
- Hung-Li WangHWHung-Li Wang
- Wen-Teng ChangWCWen-Teng Chang
- Tu-Hsueh YehTYTu-Hsueh Yeh
- Tony WuTWTony Wu
- Mei-Shin ChenMCMei-Shin Chen
- Ching-Yi WuChing-Yi Wu
- 1 March 2004
- journal article
- Published by Elsevier in Neurobiology of Disease
- Vol. 15 (2) , 361-370
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Cx32 but Not Cx26 Is Associated with Tight Junctions in Primary Cultures of Rat HepatocytesExperimental Cell Research, 2001
- Calmodulin Directly Gates Gap Junction ChannelsJournal of Biological Chemistry, 2000
- Connexin channels in Schwann cells and the development of the X-linked form of Charcot-Marie-Tooth diseaseBrain Research Reviews, 2000
- Mutations in connexin 32: the molecular and biophysical bases for the X-linked form of Charcot–Marie–Tooth diseaseBrain Research Reviews, 2000
- Connexin32-null mice develop demyelinating peripheral neuropathyGlia, 1998
- Molecular Genetics of Demyelination: New Wrinkles on an Old MembraneNeuron, 1997
- Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth diseaseNeuron, 1994
- A connexin‐32 mutation associated with Charcot‐Marie‐Tooth disease does not affect channel formation in oocytesFEBS Letters, 1994
- Refined localization of human connexin32 gene locus, GJB1, to Xq13.1Genomics, 1992
- Molecular cloning of cDNA for rat liver gap junction protein.Journal of Cell Biology, 1986