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  2. Experts Reveal Exactly What You Should Eat When You Have COVID-19

    www.aol.com/experts-reveal-exactly-eat-covid...

    Focus on fiber-rich foods like whole grains, add fruits and vegetables whenever possible, include probiotic-rich foods like kimchi or kefir, cook with fats like canola and olive oil, and keep ...

  3. These Anti-Inflammatory Foods May Reduce COVID-19 Risk and ...

    www.aol.com/mediterranean-diet-may-reduce-risk...

    Now, a new review study published in the journal PLOS ONE on August 21, 2024, suggests that the Mediterranean diet might help prevent you from getting COVID-19. Yes, the virus is still around. Yes ...

  4. Diamine oxidase - Wikipedia

    en.wikipedia.org/wiki/Diamine_oxidase

    Diamine oxidase (DAO), also known "amine oxidase, copper-containing, 1" (AOC1), formerly called histaminase, [1] is an enzyme (EC 1.4.3.22) involved in the metabolism, oxidation, and inactivation of histamine and other polyamines such as putrescine or spermidine. The enzyme belongs to the amine oxidase (copper-containing) (AOC) family of amine ...

  5. D-amino acid oxidase - Wikipedia

    en.wikipedia.org/wiki/D-amino_acid_oxidase

    The genetic background of DAO involvement in schizophrenia is highly debated, and no compulsatory evidence has been found for DAO genes being strongly linked to schizophrenia. Although, the G72 gene, which reportedly encodes the D-amino acid oxidase activator, may be involved in the development of schizophrenia.

  6. FAD dependent oxidoreductase family - Wikipedia

    en.wikipedia.org/wiki/FAD_dependent...

    In molecular biology, the FAD dependent oxidoreductase family of proteins is a family of FAD dependent oxidoreductases.Members of this family include Glycerol-3-phosphate dehydrogenase EC 1.1.99.5, Sarcosine oxidase beta subunit EC 1.5.3.1, D-amino-acid dehydrogenase EC 1.4.99.1, D-aspartate oxidase EC 1.4.3.1.

  7. Adenosine monophosphate deaminase deficiency type 1

    en.wikipedia.org/wiki/Adenosine_monophosphate...

    AMPD1 deficiency is caused by a defect in the mechanism for production of AMP deaminase – an enzyme that converts adenosine monophosphate (AMP) to inosine monophosphate (IMP). [3] While the deficiency affects approximately 1–2% of people in populations of predominantly European descent, [ 3 ] the disorder appears to be considerably rarer in ...

  8. Kwashiorkor - Wikipedia

    en.wikipedia.org/wiki/Kwashiorkor

    However, Jamaican pediatrician Cicely Williams introduced the term in 1935, two years after she published the disease's first formal description. Williams was the first to research kwashiorkor and differentiate it from other dietary deficiencies. She was the first to suggest that this might be a protein deficiency.

  9. Adenosine deaminase deficiency - Wikipedia

    en.wikipedia.org/wiki/Adenosine_deaminase_deficiency

    The enzyme adenosine deaminase is encoded by the ADA gene on chromosome 20. [1] ADA deficiency is inherited in an autosomal recessive manner. This means the defective gene responsible for the disorder is located on an autosome (chromosome 20 is an autosome), and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder.