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Restoring Ureagenesis in Hepatocytes by CRISPR/Cas9-mediated Genomic Addition to Arginase-deficient Induced Pluripotent Stem Cells
Urea cycle disorders are incurable enzymopathies that affect nitrogen metabolism and typically lead to hyperammonemia. Arginase deficiency results from a mutation in Arg1, the enzyme regulating the final step of ureagenesis and typically results in developmental disabilities, seizures, spastic diple...
Autores principales: | Lee, Patrick C, Truong, Brian, Vega-Crespo, Agustin, Gilmore, W Blake, Hermann, Kip, Angarita, Stephanie AK, Tang, Jonathan K, Chang, Katherine M, Wininger, Austin E, Lam, Alex K, Schoenberg, Benjamen E, Cederbaum, Stephen D, Pyle, April D, Byrne, James A, Lipshutz, Gerald S |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155330/ https://www.ncbi.nlm.nih.gov/pubmed/27898091 http://dx.doi.org/10.1038/mtna.2016.98 |
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