Ornithine

origin recognition complex subunit 1 ; Homo sapiens







5 Article(s)
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PMID
Title
Pub. Year
#Total Relationships
1 25874378 The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome. 2015 Mar 11 2
2 26002808 Mitochondrial transporters for ornithine and related amino acids: a review. 2015 Sep 1
3 24721342 A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: functional analysis of the mutant protein. 2014 May 2
4 22262851 Substrate specificity of the two mitochondrial ornithine carriers can be swapped by single mutation in substrate binding site. 2012 Mar 9 1
5 12807890 The mitochondrial ornithine transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms. 2003 Aug 29 3