...COL1A2 are known to be the causal genes. In this work,we performed linkage analysis in a kindred with autosomal dominant...
...COL1A2) gene, encoding type I procollagen chains. We describe here the clinical, biochemical, and molecular characteriza...
...COL1A2), collagen type 2 (COL2A1) was analyzed through semi-quantitative reverse transcription-polymerase chain reaction...
...COL1A2 gene. In contrast to dominant negative point mutations, which cause osteogenesis imperfecta with bone fractures, ...
...COL1A2, COL6A3), 'ECM-receptor interaction' pathway (THBS2, COL1A2, COL6A3, FN1) and 'TGF-beta signaling' (THBS2, MAPK1,...
...COL1A2, and DSPP), and ameloblasts (AMELX, ENAM, MMP20, and KLK4) during the crown formation stage, are associated with ...
COL1A2 and COL2A1 genes are expressed at high levels in many cochlear cells of 16- to 23-week-old human fetuses. Given t...
...COL1A2 and CYP1A1 and short tandem repeats of HS1,2 Ig enhancer genes. In order to provide a clearer picture of COL1A2, ...
...COL1A2 promoter luciferase assay was performed in human dermal fibroblast cells. CJ oil was determined to activate human...
...Col1a2 levels. These results uncover a role for miRs in the kidney and DN in controlling TGF-beta-induced Col1a2 express...
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