Cargando…
Liver-specific knockout of arginase-1 leads to a profound phenotype similar to inducible whole body arginase-1 deficiency
Arginase-1 (Arg1) converts arginine to urea and ornithine in the distal step of the urea cycle in liver. We previously generated a tamoxifen-inducible Arg1 deficient mouse model (Arg1-Cre) that disrupts Arg1 expression throughout the whole body and leads to lethality ≈ 2 weeks after gene disruption....
Autores principales: | Ballantyne, Laurel L., Sin, Yuan Yan, Al-Dirbashi, Osama Y., Li, Xinzhi, Hurlbut, David J., Funk, Colin D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065044/ https://www.ncbi.nlm.nih.gov/pubmed/27761413 http://dx.doi.org/10.1016/j.ymgmr.2016.10.003 |
Ejemplares similares
-
Inducible Arginase 1 Deficiency in Mice Leads to Hyperargininemia and Altered Amino Acid Metabolism
por: Sin, Yuan Yan, et al.
Publicado: (2013) -
Proof-of-Concept Gene Editing for the Murine Model of Inducible Arginase-1 Deficiency
por: Sin, Yuan Yan, et al.
Publicado: (2017) -
Strategies to Rescue the Consequences of Inducible Arginase-1 Deficiency in Mice
por: Ballantyne, Laurel L., et al.
Publicado: (2015) -
Transplantation of Gene-Edited Hepatocyte-like Cells Modestly Improves Survival of Arginase-1-Deficient Mice
por: Sin, Yuan Yan, et al.
Publicado: (2017) -
The role and control of arginine levels in arginase 1 deficiency
por: Diaz, George A., et al.
Publicado: (2022)