Department of Dermatology, University of Michigan Medical School, Medical Science I, 1150 W. Medical Center Dr., Ann Arbor, MI, 48109-0609, USA,
J Cell Commun Signal. 2007 Dec;1(3-4):229-30. doi: 10.1007/s12079-008-0020-8. Epub 2008 Jun 4.
A recent manuscript reported phenotypic alterations associated to the expression of a CCN3 protein deleted for the Von Willebrand type C repeat that is common to the various members of the CCN family of proteins. In this comment, the biological significance of these alterations is briefly discussed.
最近的一篇手稿报道了与 CCN3 蛋白表达相关的表型改变,该蛋白缺失了 Von Willebrand 类型 C 重复序列,该序列是 CCN 蛋白家族成员共有的。在这篇评论中,简要讨论了这些改变的生物学意义。