Liver-specific knockout of arginase-1 leads to a profound phenotype similar to inducible whole body arginase-1 deficiency-Reference-Cited by-同舟云学术

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Liver-specific knockout of arginase-1 leads to a profound phenotype similar to inducible whole body arginase-1 deficiency

Published:2016-12 Issue: Volume:9 Page:54-60
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Ballantyne Laurel L.,Sin Yuan Yan,Al-Dirbashi Osama Y.,Li Xinzhi,Hurlbut David J.,Funk Colin D.

Funder

Canada Research Chairs

Canadian Institutes of Health Research

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference22 articles.

1. Arginase-1 deficiency;Sin;J. Mol. Med.,2015

2. The human arginases and arginase deficiency;Iyer;J. Inherit. Metab. Dis.,1998

3. Mouse model for human arginase deficiency;Iyer;Mol. Cell. Biol.,2002

4. Inducible arginase 1 deficiency in mice leads to hyperargininemia and altered amino acid metabolism;Sin;PLoS One,2013

5. Lethal phenotype in conditional late-onset arginase 1 deficiency in the mouse;Kasten;Mol. Genet. Metab.,2013

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