search:mcad gene相關網頁資料

      • www.ncbi.nlm.nih.gov
        Clinical Diagnosis Medium-chain acyl-coenzyme A dehydrogenase (MCAD) deficiency is a disorder of fatty acid oxidation. Fatty acid oxidation fuels hepatic ketogenesis, a major source of energy for peripheral tissues once glycogen stores become depleted dur
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      • ghr.nlm.nih.gov
        Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a condition that prevents the body from converting certain fats to energy, particularly during periods without food (fasting). Signs and symptoms of MCAD deficiency typically appear during infancy o
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    日期:2024-05-04
    Sequencing of the medium chain acyl-CoA dehydrogenase ( MCAD) gene can confirm the diagnosis of MCAD defi ......
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    日期:2024-05-05
    Complete information for ACADM gene (protein-coding), acyl-CoA dehydrogenase, C-4 to C-12 straight chain, ......
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    日期:2024-05-03
    Gene ID 34 Official Symbol ACADM Locus RP4-682C21.1 Gene Type protein-coding Synonyms ACAD1; FLJ18227; F ......
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    日期:2024-05-06
    The ACADM gene provides instructions for making an enzyme called medium-chain acyl-CoA dehydrogenase ( MC ......
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    日期:2024-05-07
    A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase ( MCAD) gene changes a cons ......
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    日期:2024-05-04
    Publication » A985G mutation incidence in the medium-chain acyl-CoA dehydrogenase ( MCAD) gene in Brazil. ......
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    日期:2024-05-08
    The MCAD gene contains 12 exons (Zhang et al., 1992). Gene Function Medium-chain acyl-CoA dehydrogenase c ......
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    日期:2024-05-05
    How to Cite Tanaka, K., Yokota, I., Coates, P. M., Strauss, A. W., Kelly, D. P., Zhang, Z., Gregersen, N. ......