Heat Shock Response Associated with Hepatocarcinogenesis in a Murine Model of Hereditary Tyrosinemia Type I

Hereditary Tyrosinemia type 1 (HT1) is a metabolic liver disease caused by genetic defects of fumarylacetoacetate hydrolase (FAH), an enzyme necessary to complete the breakdown of tyrosine. The severe hepatic dysfunction caused by the lack of this enzyme is prevented by the therapeutic use of NTBC (...

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Detalles Bibliográficos
Autores principales: Angileri, Francesca, Morrow, Geneviève, Roy, Vincent, Orejuela, Diana, Tanguay, Robert M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074813/
https://www.ncbi.nlm.nih.gov/pubmed/24762634
http://dx.doi.org/10.3390/cancers6020998

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074813/
https://www.ncbi.nlm.nih.gov/pubmed/24762634
http://dx.doi.org/10.3390/cancers6020998

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