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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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Bibliografiske detaljer
Udgivet i:Hum Mol Genet
Main Authors: 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
Sprog:Inglês
Udgivet: Oxford University Press 2015
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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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