A Soluble Form of Fibroblast Growth Factor Receptor 2 (FGFR2) with S252W Mutation Acts as an Efficient Inhibitor for the Enhanced Osteoblastic Differentiation Caused by FGFR2 Activation in Apert Syndrome

詳細情報 詳細情報について

• CRID

  1363107368427305088

• NII論文ID

  80017019211

• DOI

  10.1074/jbc.m404824200

• ISSN

  00219258

• Web Site

  https://api.elsevier.com/content/article/PII:S0021925820725287?httpAccept=text/xml

  https://api.elsevier.com/content/article/PII:S0021925820725287?httpAccept=text/plain

  https://syndication.highwire.org/content/doi/10.1074/jbc.M404824200

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