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Hyperactive transforming growth factor-ß1 signaling potentiates skeletal defects in a neurofibromatosis type 1 mouse model.
Rhodes, Steven D; Wu, Xiaohua; He, Yongzheng; Chen, Shi; Yang, Hao; Staser, Karl W; Wang, Jiapeng; Zhang, Ping; Jiang, Chang; Yokota, Hiroki; Dong, Ruizhi; Peng, Xianghong; Yang, Xianlin; Murthy, Sreemala; Azhar, Mohamad; Mohammad, Khalid S; Xu, Mingjiang; Guise, Theresa A; Yang, Feng-Chun.
Affiliation
  • Rhodes SD; Department of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, IN, USA; Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
J Bone Miner Res ; 28(12): 2476-89, 2013 Dec.
Article in En | MEDLINE | ID: mdl-23703870

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone and Bones / Signal Transduction / Neurofibromatosis 1 / Transforming Growth Factor beta1 Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: J Bone Miner Res Journal subject: METABOLISMO / ORTOPEDIA Year: 2013 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone and Bones / Signal Transduction / Neurofibromatosis 1 / Transforming Growth Factor beta1 Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: J Bone Miner Res Journal subject: METABOLISMO / ORTOPEDIA Year: 2013 Document type: Article Affiliation country: United States