The majority of Osteogenesis Imperfecta (OI) cases are caused by mutations in one of the two genes, COL1A1 and COL1A2 en...
...COL1A1 or COL1A2 genes, respectively. The overall phenotypic features were consistent with the diagnosis of osteogenesis...
...COL1A1 gene with ACL ruptures in Polish male recreational skiers in a case-control study.,A total of 138 male recreation...
...COL1A1), fibronectin, and versican before and after treatment with liarozole, and confirmatory immunohistochemical stain...
...COL1A1), and α -smooth muscle actin ( α SMA). One method of regulating fibrosis is through epigenetics; the study of her...
...Col1A1) mRNA in response to activation on plastic. Expression of mRNA for C5aR, but not C5L2, a second C5a receptor that...
To investigate mutation of COL1A1 gene and analyze the relationship between genotype and clinical phenotype in a family ...
...COL1A1 and COL6A1 genes showed increased expression, whereas decreased expression mainly occurred for the following gene...
...COL1A1), alpha 1 (III) procollagen (COL3A1), matrix metalloproteinase (MMP)-1 and tissue inhibitor of matrix metalloprot...
...COL1A1), COL2A1, aggrecan (ACAN), and MMP-13 gene expression were measured in cartilage by quantitative RT-PCR.,Media TN...
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