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The Journal of Cell Biology|August 29, 1998
Functional gap junctions in the schwann cell myelin sheathR J Balice-Gordon, L J Bone, S S SchererJournal of Neuropathology and Experimental Neurology|July 20, 1999
Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-Tooth diseaseA Abel, L J Bone, A Messing, et al.Glia|August 13, 1998
Connexin32-null mice develop demyelinating peripheral neuropathyS S Scherer, Y T Xu, E Nelles, et al.Neurobiology of Disease|January 1, 1997
Connexin32 and X-linked Charcot-Marie-Tooth diseaseL J Bone, S M Deschênes, R J Balice-Gordon, et al.Novartis Foundation Symposium|April 20, 1999
The role of the gap junction protein connexin32 in the pathogenesis of X-linked Charcot-Marie-Tooth diseaseS S Scherer, L J Bone, S M Deschênes, et al.Neurology|October 1, 1995
New connexin32 mutations associated with X-linked Charcot-Marie-Tooth diseaseL J Bone, N Dahl, M W Lensch, et al.American Journal of Human Genetics|November 1, 1995
Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndromeM Muenke, L J Bone, H F Mitchell, et al.Science (New York, N.Y.)|December 24, 1993
Connexin mutations in X-linked Charcot-Marie-Tooth diseaseJ Bergoffen, S S Scherer, S Wang, et al.Pageof 1