Gap junctions in inherited human disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physiology (medical),Clinical Biochemistry,Physiology
Link
http://link.springer.com/content/pdf/10.1007/s00424-010-0789-1.pdf
Reference166 articles.
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2. Ahmad S, Tang W, Chang Q, Qu Y, Hibshman J, Li Y, Sohl G, Willecke K, Chen P, Lin X (2007) Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness. Proc Natl Acad Sci USA 104:1337–1341
3. Altevogt BM, Kleopa KA, Postma FR, Scherer SS, Paul DL (2002) Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems. J Neurosci 22:6458–6470
4. Arita K, Akiyama M, Tsuji Y, McMillan JR, Eady RA, Shimizu H (2002) Changes in gap junction distribution and connexin expression pattern during human fetal skin development. J Histochem Cytochem 50:1493–1500
5. Arora A, Minogue PJ, Liu X, Addison PK, Russel-Eggitt I, Webster AR, Hunt DM, Ebihara L, Beyer EC, Berthoud VM, Moore AT (2008) A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts. J Med Genet 45:155–160
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