...COL1A2 CCAAT box and CME-binding proteins demonstrated that they were distinct unrelated transcription factors. These re...
...COL1A2 genes of type I collagen. Amelogenesis imperfecta (AI) is a diverse group of hereditary disorders characterized b...
...COL1A2 upstream sequence. Intraperitoneal CCl4 administration activated the -17 kb COL1A2 promoter more than 10-fold, wh...
...COL1A2 allele, resulting in a Gly922 --> Ser substitution in the alpha2(I) chain. The proband's mutation was demonstrate...
Although >90% of patients with osteogenesis imperfecta (OI) have been estimated to have mutations in the COL1A1 and COL1...
...COL1A2) promoter. Specifically, we have identified a segment of the proximal promoter region, located between nucleotide...
...COL1A2 gene. These results establish COL1A2 as an early growth responsive gene, and that its regulation is PKC dependent...
...COL1A2. Collectively, our results exclude the structural genes of FBN1, elastin, and COL1A2 as candidate genes within th...
...COL1A2 gene activation were examined in fibroblasts grown from lung biopsy specimens obtained from 16 scleroderma patien...
...COL1A2 as the disease locus. Heteroduplex analysis of reverse transcription-polymerase chain reaction (RT-PCR) amplifica...
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