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Published in 2019 at "Experimental cell research"
DOI: 10.1016/j.yexcr.2019.111673
Abstract: Mitochondrial dysfunction causes various diseases. Mutations in the SLC25A46 gene have been identified in mitochondrial diseases that are sometimes classified as Charcot-Marie-Tooth disease type 2, optic atrophy, and Leigh syndrome. A homolog of SLC25A46 was…
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Keywords:
drosophila;
mitochondrial diseases;
reduction rpd3;
slc25a46 ... See more keywords
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Published in 2017 at "Human Molecular Genetics"
DOI: 10.1093/hmg/ddx262
Abstract: Recently, we identified biallelic mutations of SLC25A46 in patients with multiple neuropathies. Functional studies revealed that SLC25A46 may play an important role in mitochondrial dynamics by mediating mitochondrial fission. However, the cellular basis and pathogenic…
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Keywords:
slc25a46 causes;
mice;
slc25a46;
mitochondrial dynamics ... See more keywords
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Published in 2023 at "Journal of cell science"
DOI: 10.1242/jcs.260049
Abstract: Glucose sensing in pancreatic beta-cells depends on oxidative phosphorylation and mitochondria-derived signals that promote insulin secretion. Using mass spectrometry-based phosphoproteomics to search for down-stream effectors of glucose dependent signal transduction in INS-1E insulinoma cells, we…
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Keywords:
stress;
secreting cells;
slc25a46;
insulin secreting ... See more keywords