Ptpn11 Deletion in A Novel Cartilage Cell Causes Metachondromatosis by Activating Hedgehog Signaling

SHP2, encoded by PTPN11, is required for survival, proliferation and differentiation of various cell types(1,2). Germ line activating mutations in PTPN11 cause Noonan Syndrome, while somatic PTPN11 mutations cause childhood myeloproliferative disease and contribute to some solid tumors. Recently, he...

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Detalhes bibliográficos
Main Authors: Yang, Wentian, Wang, Jianguo, Moore, Douglas C., Liang, Haipei, Dooner, Mark, Wu, Qian, Terek, Richard, Chen, Qian, Ehrlich, Michael G., Quesenberry, Peter J., Neel, Benjamin G.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4148013/
https://ncbi.nlm.nih.gov/pubmed/23863940
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature12396
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