Latent transforming growth factor binding protein 4 regulates transforming growth factor beta receptor stability

Mutations in the gene for the latent transforming growth factor beta binding protein 4 (LTBP4) cause autosomal recessive cutis laxa type 1C. To understand the molecular disease mechanisms of this disease, we investigated the impact of LTBP4 loss on transforming growth factor beta (TGFβ) signaling. D...

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Publié dans:Hum Mol Genet
Auteurs principaux: Su, Chi-Ting, Huang, Jenq-Wen, Chiang, Chih-Kang, Lawrence, Elizabeth C., Levine, Kara L., Dabovic, Branka, Jung, Christine, Davis, Elaine C., Madan-Khetarpal, Suneeta, Urban, Zsolt
Format: Artigo
Langue:Inglês
Publié: Oxford University Press 2015
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Articles
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4476448/
https://ncbi.nlm.nih.gov/pubmed/25882708
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv139
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