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30403179 | Overexpression of SLC25A15 is involved in the proliferation of cutaneous melanoma and leads to poor prognosis. | 2018 Oct |
1 |
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26589310 | Heterologous Expression in Yeast of Human Ornithine Carriers ORNT1 and ORNT2 and of ORNT1 Alleles Implicated in HHH Syndrome in Humans. | 2016 |
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| 3 |
25874378 | The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome. | 2015 Mar 11 |
2 |
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24721342 | A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: functional analysis of the mutant protein. | 2014 May |
1 |
| 5 |
23430880 | Adult-onset presentation of a hyperornithinemia-hyperammonemia-homocitrullinuria patient without prior history of neurological complications. | 2012 |
2 |
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19287344 | The human and mouse SLC25A29 mitochondrial transporters rescue the deficient ornithine metabolism in fibroblasts of patients with the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. | 2009 Jul |
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18978333 | Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15. | 2008 Nov |
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10369256 | Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. | 1999 Jun |
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22649802 | Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome | 1993 |
2 |