Catenin delta-1 (CTNND1) phosphorylation controls the mesenchymal to epithelial transition in astrocytic tumors

Inactivating mutations of the TSC1/TSC2 complex (TSC1/2) cause tuberous sclerosis (TSC), a hereditary syndrome with neurological symptoms and benign hamartoma tumours in the brain. Since TSC effectors are largely unknown in the human brain, TSC patient cortical tubers were used to uncover hyperphosp...

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Publicado no:Hum Mol Genet
Main Authors: Yang, Jin, Bassuk, Alexander G., Merl-Pham, Juliane, Hsu, Chun-Wei, Colgan, Diana F., Li, Xiaorong, Au, Kit Sing, Zhang, Lijuan, Smemo, Scott, Justus, Sally, Nagahama, Yasunori, Grossbach, Andrew J., Howard, Matthew A., Kawasaki, Hiroto, Feldstein, Neil A., Dobyns, William B., Northrup, Hope, Hauck, Stefanie M., Ueffing, Marius, Mahajan, Vinit B., Tsang, Stephen H.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2016
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5291196/
https://ncbi.nlm.nih.gov/pubmed/27516388
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw253
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