{"title":"在体外研究中,Sclerostin不影响BMP2/SMAD1/5或Wnt3a/β-catenin信号,而是通过激活血小板来源的生长因子受体信号来抑制成骨细胞分化。","authors":"C. Thouverey, J. Caverzasio","doi":"10.1038/bonekey.2015.126","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":72441,"journal":{"name":"BoneKEy reports","volume":"4 1","pages":"757"},"PeriodicalIF":0.0000,"publicationDate":"2015-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1038/bonekey.2015.126","citationCount":"21","resultStr":"{\"title\":\"Sclerostin inhibits osteoblast differentiation without affecting BMP2/SMAD1/5 or Wnt3a/β-catenin signaling but through activation of platelet-derived growth factor receptor signaling in vitro.\",\"authors\":\"C. Thouverey, J. Caverzasio\",\"doi\":\"10.1038/bonekey.2015.126\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":72441,\"journal\":{\"name\":\"BoneKEy reports\",\"volume\":\"4 1\",\"pages\":\"757\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-11-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1038/bonekey.2015.126\",\"citationCount\":\"21\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BoneKEy reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1038/bonekey.2015.126\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BoneKEy reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/bonekey.2015.126","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Sclerostin inhibits osteoblast differentiation without affecting BMP2/SMAD1/5 or Wnt3a/β-catenin signaling but through activation of platelet-derived growth factor receptor signaling in vitro.