...COL1A2, TAC1, SST, and GALR1) were analyzed in 133 HNSCC cases using quantitative methylation-specific PCR. We detected ...
...COL1A2). Tooth agenesis is a common feature of OI. We investigated the association between tooth agenesis and collagen t...
...COL1A2 transcription by HIF-1α occurred in the absence of hypoxia and is strongly enhanced by TGF-β signaling. TGF-β, in...
...COL1A2. In moderate to severe OI, dominant mutations were found in COL1A1/COL1A2 (77 %), IFITM5 (9 %), and P4HB (0.6 %)....
...COL1A2, the two genes coding for collagen type I alpha chains, but in the past 10 years defects in at least 17 other gen...
...col1a2, col3a1, and TGF-β. Moreover, pirfenidone inhibited the activation of TGF-β-related smad and MAPK pathways both i...
...COL1A2 genes, leading to a deficit of quality and/or quantity in the synthesis of procollagen-α type 1. Seven different ...
...Col1a2 (p = 0.01) and Fn1 (p = 0.04), than non SM-derived CD68(+) cells.,These results demonstrate that smooth muscle ce...
...COL1A2). Genomic structural variations involving type I collagen genes are extremely rare in OI.,In this study, we chara...
...COL1A2. Bruck Syndrome (BS) is a further recessively-inherited OI-like phenotype in which bone fragility is associated w...
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