Krieg T, Kirsch E, Matzen K, Müller P K
Klin Wochenschr. 1981 Jan 15;59(2):91-3. doi: 10.1007/BF01477288.
Skin fibroblasts were cultured from 13 patients with Osteogenesis imperfecta and collagen biosynthesis was investigated in vitro. In those patients characterised by only mild manifestations of the disease, the ratio of collagen types I and III was disturbed. By contrast, fibroblasts obtained from patients with Osteogenesis imperfecta of a more severe type synthesised collagen types I/III in a normal ratio.
从13名成骨不全患者身上培养皮肤成纤维细胞,并在体外研究胶原蛋白的生物合成。在那些仅表现出该疾病轻微症状的患者中,I型和III型胶原蛋白的比例受到干扰。相比之下,从更严重类型的成骨不全患者身上获得的成纤维细胞以正常比例合成I/III型胶原蛋白。