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Titlebook: Cell Biology and Pathology of Myelin; Evolving Biological Bernhard H. J. Juurlink,Richard M. Devon,Valerie M Book 1997 Springer Science+Bu

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書目名稱Cell Biology and Pathology of Myelin
副標(biāo)題Evolving Biological
編輯Bernhard H. J. Juurlink,Richard M. Devon,Valerie M
視頻videohttp://file.papertrans.cn/223/222736/222736.mp4
叢書名稱Altschul Symposia Series
圖書封面Titlebook: Cell Biology and Pathology of Myelin; Evolving Biological  Bernhard H. J. Juurlink,Richard M. Devon,Valerie M Book 1997 Springer Science+Bu
出版日期Book 1997
關(guān)鍵詞Nervous System; biology; cell; cell biology; glycoprotein; membrane; pathology; regulation; transcription
版次1
doihttps://doi.org/10.1007/978-1-4615-5949-8
isbn_softcover978-1-4613-7726-9
isbn_ebook978-1-4615-5949-8
copyrightSpringer Science+Business Media New York 1997
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M. J. Waldock,J. E. Thain,M. E. Waited by compacted multilamellar membranes. A single oligodendrocyte in the central nervous system (CNS) has the capacity to extend numerous processes, which develop into elaborate specialized membranes that ensheathe multiple larger diameter axonal segments. Historically, CNS myelin had been characteri
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Michael A. Champ,Peter F. SeligmanS and in adulthood, the continuous bi-directional dialogue between axon and Schwann cell regulates a temporally and spatially precise pattern of myelin protein expression in the complex myelin structure as a prerequisite for the correct function of the various myelin proteins (reviewed by Snipes and
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M. J. Waldock,J. E. Thain,M. E. Waiteelin component has been difficult to define. The primary structure of PLP has been determined by direct protein sequencing and through cDNA cloning: PLP comprises 276 residues and its primary translation product lacks a N-terminal signal peptide (Milner et al., 1985 and references herein). Four high
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