...COL1A1) and osteocalcin [bone gamma-carboxyglutamate protein (BGLAP)] osteoblastogenesis-related genes in MSC differenti...
...COL1A1 or COL1A2. Bruck Syndrome (BS) is a further recessively-inherited OI-like phenotype in which bone fragility is as...
...COL1A1), alpha smooth muscle actin (α-SMA) expression was determined by immunoblot analysis.,We first profiled the expre...
...COL1A1 was almost undetectable on cultured chondrocytes; likewise, COL2 and SOX9 proteins were detected by immunofluores...
...Col1a1 were also decreased. The apoA-1(-/-) phenotype also included augmented CEPBa levels, suggesting complex changes i...
...Col1a1, which are known to play roles in scar formation. The knockdown of CTGF within the healing burn wounds resulted i...
...COL1A1 gene in patients with osteogenesis imperfecta (OI).,Molecular genetic analysis of the COL1A1 gene was performed i...
...col1a1, and dentin sialophosphoprotein (Dspp); and apoptosis assay. For the loss and gain of function experiments, an in...
...Col1a1, Acta2 and Tnfa.,Intervention with a caspase-1 inhibitor attenuated the development of NASH, liver fibrosis and i...
...COL1A1, and decreased RASAL1 expression in NTM cells. 5-aza treatment decreased DNMT1, TGFβ1 and COL1A1 expression, and ...
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