Chronic Phenotype Characterization of a Large-Animal Model of Hereditary Tyrosinemia Type 1

Hereditary tyrosinemia type 1 (HT1) is an autosomal recessive disease caused by deficiency in fumarylacetoacetate hydrolase, the last enzyme in the tyrosine catabolic pathway. In this study, we investigated whether fumarylacetoacetate hydrolase deficient (FAH(−/−)) pigs, a novel large-animal model o...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Am J Pathol
Päätekijät: Elgilani, Faysal, Mao, Shennen A., Glorioso, Jaime M., Yin, Meng, Iankov, Ianko D., Singh, Anisha, Amiot, Bruce, Rinaldo, Piero, Marler, Ronald J., Ehman, Richard L., Grompe, Markus, Lillegard, Joseph B., Hickey, Raymond D., Nyberg, Scott L.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society for Investigative Pathology 2017
Aiheet:
Regular Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5225308/
https://ncbi.nlm.nih.gov/pubmed/27855279
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajpath.2016.09.013
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