Epigenetic changes of the thioredoxin system in the tx-j mouse model and in patients with Wilson disease

Wilson disease (WD) is caused by mutations in the copper transporter ATP7B, leading to copper accumulation in the liver and brain. Excess copper inhibits S-adenosyl-L-homocysteine hydrolase, leading to variable WD phenotypes from widespread alterations in DNA methylation and gene expression. Previou...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Mordaunt, Charles E, Shibata, Noreene M, Kieffer, Dorothy A, Członkowska, Anna, Litwin, Tomasz, Weiss, Karl Heinz, Gotthardt, Daniel N, Olson, Kristin, Wei, Dongguang, Cooper, Stewart, Wan, Yu-Jui Yvonne, Ali, Mohamed R, LaSalle, Janine M, Medici, Valentina
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
Assuntos:
General Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6216211/
https://ncbi.nlm.nih.gov/pubmed/30010856
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy262
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