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Results 51 - 60 of 87 for vitamin D
  1. SLC6A19 gene 
    ... these features are related to a deficiency of vitamin B3 (niacin) and one of its main components, the amino acid tryptophan. ... Citation on PubMed Camargo SM, Singer D, Makrides V, Huggel K, Pos KM, Wagner CA, ...
    https://medlineplus.gov/genetics/gene/slc6a19 - Genetics
  2. Thiamine-responsive megaloblastic anemia syndrome 
    ... without the help of a transporter when the vitamin is present in large amounts.It remains unclear exactly how ... Baron D, Assaraf YG, Cohen N, Aronheim A. Lack of ...
    https://medlineplus.gov/...-responsive-megaloblastic-anemia-syndrome - Genetics
  3. SLC19A3 gene 
    ... into cells, resulting in decreased absorption of the vitamin and leading to neurological ... Depienne C, Rastetter A, Bellanger A, Degos B, Galanaud D, Keren B, Lyon-Caen O, Brice A, Sedel ...
    https://medlineplus.gov/genetics/gene/slc19a3 - Genetics
  4. PROS1 gene 
    ... PS21 PS22 PS23 PS24 PS25 PSA THPH5 THPH6 vitamin K-dependent plasma protein S ... on PubMed Pintao MC, Garcia AA, Borgel D, Alhenc-Gelas M, Spek CA, de Visser MC, ...
    https://medlineplus.gov/genetics/gene/pros1 - Genetics
  5. MMUT gene 
    ... called adenosylcobalamin (AdoCbl), which is a form of vitamin B12, methylmalonyl CoA mutase converts ... JF, Pereira S, Callebaut I, Koskas T, Porquet D, Elion J. Molecular basis of methylmalonyl-CoA mutase ...
    https://medlineplus.gov/genetics/gene/mmut - Genetics
  6. PCCB gene 
    ... a molecule called propionyl-CoA. Using the B vitamin biotin, propionyl-CoA carboxylase then converts propionyl-CoA ... Citation on PubMed Gupta D, Bijarnia-Mahay S, Kohli S, Saxena R, Puri ...
    https://medlineplus.gov/genetics/gene/pccb - Genetics
  7. Nonketotic hyperglycinemia 
    ... molecule is added to and used by a vitamin called folate. Folate is required for many functions in the cell ... Aliefendioglu D, Tana Aslan Ay, Coskun T, Dursun A, Cakmak ...
    https://medlineplus.gov/.../condition/nonketotic-hyperglycinemia - Genetics
  8. MCCC1 gene 
    ... includes a region for binding to the B vitamin biotin, which is required for the enzyme to ... C, Cole RN, Packman S, Baumgartner ER, Valle D. The molecular basis of human 3-methylcrotonyl-CoA ...
    https://medlineplus.gov/genetics/gene/mccc1 - Genetics
  9. Hartnup disease 
    ... be lacking (deficient) in certain amino acids and vitamins. However, individuals who are nutrient-deficient due to their ... Citation on PubMed Camargo SM, Singer D, Makrides V, Huggel K, Pos KM, Wagner CA, ...
    https://medlineplus.gov/genetics/condition/hartnup-disease - Genetics
  10. ARSL gene 
    ... chemical pathway involving vitamin K. Evidence suggests that vitamin K normally plays a role in bone ... on PubMed Daniele A, Parenti G, d'Addio M, Andria G, Ballabio A, Meroni G. ...
    https://medlineplus.gov/genetics/gene/arsl - Genetics
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