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  1. MT-ND6 - Wikipedia

    MT-ND6 is a gene of the mitochondrial genome coding for the NADH-ubiquinone oxidoreductase chain 6 protein (ND6). [5] The ND6 protein is a subunit of NADH dehydrogenase (ubiquinone), …

  2. MT-ND6 Gene - GeneCards | NU6M Protein | NU6M Antibody

    Mar 30, 2025 · Complete information for MT-ND6 gene (Protein Coding), Mitochondrially Encoded NADH:Ubiquinone Oxidoreductase Core Subunit 6, including: function, proteins, disorders, …

  3. ND6 NADH dehydrogenase subunit 6 [ (human)] - National …

    Maternally inherited non-syndromic hearing loss is linked with a novel mitochondrial ND6 gene mutation. Reduced mitochondrial-encoded NADH dehydrogenase 6 gene expression drives …

  4. MT-ND6 mitochondrially encoded NADH dehydrogenase 6

    Feb 8, 2025 · Reduced mitochondrial-encoded NADH dehydrogenase 6 gene expression drives inflammatory CD4 (+)T cells in patients with systemic lupus erythematosus. Pediatric-onset …

  5. MT-ND6 gene - MedlinePlus

    The MT-ND6 gene provides instructions for making a protein called NADH dehydrogenase 6. This protein is part of a large enzyme complex known as complex I, which is active in mitochondria. …

  6. Optimized allotopic expression of mitochondrial ND6 transgene …

    Aug 3, 2023 · We demonstrated that allotopic expression of nucleus-versions of ND6 restored complex I, apoptosis and mitophagy deficiencies caused by the m.14484T > C mutation. The …

  7. Hypermethylation of Hepatic Mitochondrial ND6 Provokes …

    ND6 is a Primary Target of mtDNA Methylation in the Liver of Insulin Resistant Mice. Given the central role of liver during the onset of IR, we further explore the involvement of hepatic ND6 …

  8. MT-ND6 mitochondrially encoded NADH dehydrogenase 6

    Jan 4, 2025 · Title: Maternally inherited non-syndromic hearing loss is linked with a novel mitochondrial ND6 gene mutation. Reduced mitochondrial-encoded NADH dehydrogenase 6 …

  9. ND6 (human) | Gene Target - PubChem

    Sep 14, 2016 · Gene target information for ND6 - NADH dehydrogenase subunit 6 (human). Find diseases associated with this biological target and compounds tested against it in bioassay …

  10. Systematic analysis of a mitochondrial disease-causing ND6

    Our data revealed that m.14487T>C mutation is insufficient to cause mitochondrial deficiency; additional modifier genes may be involved in m.14487T>C-associated mitochondrial disease. …

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