Mutations of integrin-interacting protein Kindlin-1 cause Kindler syndrome and deregulation of Kindlin-1 is implicated in human cancers. The Kindlin-1-related diseases are confined in limited tissue types. However, Kindlin-1 tissue distribution and the dogma that governs Kindlin-1 expression in normal human body are elusive. This study examined Kindlin-1 expression in normal human adult organs, human and mouse embryonic organs by immunohistochemical analyses. We identified a general principle th...

【文章頁(yè)數(shù)】：10 頁(yè)

【文章目錄】：
1 Materials and methods
    1.1 Normal and tumor tissues
    1.2 Animal experiment
    1.3 Immunohistochemistry(IHC)
2 Results
    2.1 Kindlin-1 was highly expressed in ectoderm/endoderm-derived tissues of human adults
    2.2 Kindlin-1 was highly expressed in ectoderm/endoderm-derived tissues of human embryos
    2.3 Kindlin-1 was weakly expressed in mesoderm-derived tissues of human embryos
    2.4 Kindlin-1 was highly expressed in ectoderm/endo-derm-derived but not mesoderm-derived tissues of mouse embryos
    2.5 Kindlin-1 and Kindlin-2 were conversely expressed in human tissues
3 Discussion



本文編號(hào)：4048674