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Results 1 - 10 of 141 for Enzyme activity finding
  1. Polymyositis: Diagnosis (Muscular Dystrophy Association)  
    Myositis/Diagnosis and Tests ... Myositis ... MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, ...
    https://www.mda.org/disease/polymyositis/diagnosis - External Health Links
  2. Inclusion-Body Myositis: Diagnosis (Muscular Dystrophy Association)  
    Myositis/Diagnosis and Tests ... Myositis ... MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, ...
    https://www.mda.org/disease/inclusion-body-myositis/diagnosis - External Health Links
  3. SDHB gene 
    ... a result, there is little or no SDH enzyme activity. Without the SDH enzyme, succinate is not converted ... a result, there is little or no SDH enzyme activity. As in GIST (described above), the reduction of ...
    https://medlineplus.gov/genetics/gene/sdhb - Genetics
  4. SDHD gene 
    ... a result, there is little or no SDH enzyme activity. Without the SDH enzyme, succinate is not converted ... a result, there is little or no SDH enzyme activity. As in GIST (described above), the reduction of ...
    https://medlineplus.gov/genetics/gene/sdhd - Genetics
  5. SDHC gene 
    ... a result, there is little or no SDH enzyme activity. Without the SDH enzyme, succinate is not converted ... a result, there is little or no SDH enzyme activity. As in GIST (described above), the reduction of ...
    https://medlineplus.gov/genetics/gene/sdhc - Genetics
  6. SDHAF2 gene 
    ... function. The FAD cofactor is required for SDH enzyme activity.The SDH enzyme plays a critical role in mitochondria, which are ...
    https://medlineplus.gov/genetics/gene/sdhaf2 - Genetics
  7. Hereditary paraganglioma-pheochromocytoma 
    ... lead to the loss or reduction of SDH enzyme activity. Because the mutated SDH enzyme cannot convert succinate to fumarate, succinate accumulates in the cell. As a result, the hypoxia pathways are triggered in normal oxygen conditions, which lead ... chain with loss of enzymatic activity and abnormal mitochondrial morphology. J Pathol. 2003 Nov; ...
    https://medlineplus.gov/...hereditary-paraganglioma-pheochromocytoma - Genetics
  8. What are the different types of genetic tests?: MedlinePlus Genetics 
    ... genetic disorder. (For example, low levels of biotinidase enzyme activity is suggestive of biotinidase deficiency , which is caused ...
    https://medlineplus.gov/genetics/understanding/testing/types - Genetics
  9. Learning about Gaucher Disease From the National Institutes of Health (National Human Genome Research Institute)  
    Gaucher Disease/Learn More ... Gaucher Disease ... National Human Genome Research Institute ... From the National Institutes of Health ... Gaucher disease is an autosomal ...
    https://www.genome.gov/Genetic-Disorders/Gaucher-Disease - External Health Links
  10. Learning about Trimethylaminuria From the National Institutes of Health (National Human Genome Research Institute)  
    Metabolic Disorders/Specifics ... Metabolic Disorders ... National Human Genome Research Institute ... From the National Institutes of Health ... Trimethylaminuria is a metabolic ...
    https://www.genome.gov/Genetic-Disorders/Trimethylaminuria - External Health Links
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