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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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| Udgivet i: | Hum Mol Genet |
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| Main Authors: | , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2015
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| Fag: | |
| Online adgang: | 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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