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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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Autori principali: Angileri, Francesca, Morrow, Geneviève, Roy, Vincent, Orejuela, Diana, Tanguay, Robert M.
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2014
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4074813/
https://ncbi.nlm.nih.gov/pubmed/24762634
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cancers6020998
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