Pages that link to "Q39419727"

The following pages link to A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: functional analysis of the mutant protein (Q39419727):

Displaying 11 items.

• Power(2): the power of yeast genetics applied to the powerhouse of the cell (Q27005796) (← links)
• Characterization of Human and Yeast Mitochondrial Glycine Carriers with Implications for Heme Biosynthesis and Anemia. (Q29568201) (← links)
• The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (Q35174229) (← links)
• Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies (Q35687142) (← links)
• Mitochondrial transporters of the SLC25 family and associated diseases: a review (Q38209474) (← links)
• Mitochondrial transporters for ornithine and related amino acids: a review (Q38499421) (← links)
• Three mitochondrial transporters of Saccharomyces cerevisiae are essential for ammonium fixation and lysine biosynthesis in synthetic minimal medium (Q38636436) (← links)
• Heterologous Expression in Yeast of Human Ornithine Carriers ORNT1 and ORNT2 and of ORNT1 Alleles Implicated in HHH Syndrome in Humans (Q40295242) (← links)
• Aminoacidopathies: Prevalence, Etiology, Screening, and Treatment Options (Q47389266) (← links)
• Pathogenic potential of SLC25A15 mutations assessed by transport assays and complementation of Saccharomyces cerevisiae ORT1 null mutant (Q87011960) (← links)
• Mitochondrial Carriers for Aspartate, Glutamate and Other Amino Acids: A Review (Q90062078) (← links)