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Formation of cartilage by non-chondrogenic cell types.

作者信息

Nathanson M A, Hilfer S R, Searls R L

出版信息

Dev Biol. 1978 May;64(1):99-117. doi: 10.1016/0012-1606(78)90063-5.

DOI:10.1016/0012-1606(78)90063-5
PMID:658598
Abstract
摘要

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Formation of cartilage by non-chondrogenic cell types.非软骨生成细胞类型形成软骨。
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Effects of moniliformin and selenium on human articular cartilage metabolism and their potential relationships to the pathogenesis of Kashin-Beck disease.玉米赤霉烯酮和硒对人关节软骨代谢的影响及其与大骨节病发病机制的潜在关系。
J Zhejiang Univ Sci B. 2010 Mar;11(3):200-8. doi: 10.1631/jzus.B0900074.
2
Pluripotent mesenchymal stem cells reside within avian connective tissue matrices.多能间充质干细胞存在于鸟类结缔组织基质中。
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Laminin provides a better substrate than fibronectin for attachment, growth, and differentiation of 1003 embryonal carcinoma cells.
层粘连蛋白比纤连蛋白能为1003个胚胎癌细胞的附着、生长和分化提供更好的底物。
In Vitro. 1982 Dec;18(12):997-1003. doi: 10.1007/BF02796374.
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In vitro induction of cartilage-specific macromolecules by a bone extract.骨提取物对软骨特异性大分子的体外诱导作用。
J Cell Biol. 1983 Dec;97(6):1950-3. doi: 10.1083/jcb.97.6.1950.
5
In vitro transformation of mesenchymal cells derived from embryonic muscle into cartilage in response to extracellular matrix components of bone.胚胎肌肉来源的间充质细胞在体外对骨细胞外基质成分作出反应转化为软骨。
Proc Natl Acad Sci U S A. 1984 Jun;81(11):3419-23. doi: 10.1073/pnas.81.11.3419.
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An osteo-inductive bone matrix extract stimulates the in vitro conversion of mesenchyme into chondrocytes.一种骨诱导性骨基质提取物可刺激间充质在体外转化为软骨细胞。
Calcif Tissue Int. 1984 Sep;36(5):625-7. doi: 10.1007/BF02405378.
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Posttranscriptional control of embryonic rat skeletal muscle protein synthesis. Control at the level of translation by endogenous RNA.胚胎大鼠骨骼肌蛋白质合成的转录后调控。内源性RNA在翻译水平的调控。
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Vitamin D deficiency causes a selective reduction in deposition of transforming growth factor beta in rat bone: possible mechanism for impaired osteoinduction.维生素D缺乏导致大鼠骨骼中转化生长因子β的沉积选择性减少：骨诱导受损的可能机制。
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Cartilage tissue differentiation from mesenchymal cells derived from mature muscle in tissue culture.组织培养中源自成熟肌肉的间充质细胞的软骨组织分化。
In Vitro. 1978 Aug;14(8):697-706. doi: 10.1007/BF02616166.