Cell Biology and Pathology of Myelin: Evolving Biological by R. H. Quarles, R. G. Farrer, S. H. Yim (auth.), Bernhard H. PDF

By R. H. Quarles, R. G. Farrer, S. H. Yim (auth.), Bernhard H. J. Juurlink, Richard M. Devon, J. Ronald Doucette, Adil J. Nazarali, David J. Schreyer, Valerie M. K. Verge (eds.)

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BioI. 103:2439-2448 36 Xinghua Yin and B. D. Trapp McKerracher L, David S, Jackson DL, Kottis Y, Dunn RJ, Braun PE (1994) Identification of myelin-associated glycoprotein as a major myelin-derived inhibitor of neurite growth. Neuron 13:805--811 Montag D, Giese KP, Bartsch U, Martini R, Land Y, Bliithmann H, Karthigasan J, Kirschner DA, Wintergerst ES, Nave K-A, Zielasek J, Toyka KY, Lipp H, Schachner M (1994) Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin.

Guarnieri M. Himmelstein 1. McKhann G (1974): Isolated myelin quantitatively adsorbs antIbody to basic protein. Brain Res 72: 172-176. Halliday K (1984): Regional homology in GTP binding proto oncogene products and elongation factors. J Cyc Nuc Res 9:435--448. Herndon RW. Rauch HC. Einstein ER (1973): Immunoelectron microscopic localization of the encephalitogenic basic protein in myelin. Immunol Commun 2: 163-172. Inouye H. Kirschner DA (1984): Effects of ZnCI, on membrane interactions in myelin of normal and shiverer mice.

First, MOG transcripts utilize a series of overlapping, rare polyadenylation signals, each of which has been shown in other models to be very inefficient at mRNA cleavage and polyadenylation, suggesting that MOG mRNA may be inherently unstable. Second, this Ig superfamily member contains two extremely hydrophobic domains and was the first Ig-like molecule identified with more than a single potential membrane spanning domain. , 1996). This membrane topology has interesting ramifications relative to another surprising observation we made regarding alternative splice variants of MOG.

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