期刊
FEBS LETTERS
卷 550, 期 1-3, 页码 1-4出版社
WILEY
DOI: 10.1016/S0014-5793(03)00854-8
关键词
membrane traffic; spondyloepiphyseal dysplasia tarda; transport protein particle; sedlin
The ability of cells to synthesize and secrete proteins is essential for numerous cellular functions. Therefore, when mutations in one component of the secretory pathway result in a tissue-specific defect, a unique opportunity arises to examine the molecular mechanisms at play. The recent finding that a defect in the protein sedlin, whose yeast counterpart is involved in the first step of the secretory pathway, leads to a cartilage-specific disorder in humans raises numerous questions and interesting possibilities for understanding both the pathobiology involved and the role of membrane traffic in normal cartilage development. (C) 2003 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
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