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Results 1 - 7 of 7 for S -Methylmalonic acid semialdehyde
Did you mean S -Methylmalonic acid "semi aldehyde"?
  1. ALDH5A1 gene 
    ... disrupts the conversion of succinic semialdehyde to succinic acid. Instead, succinic semialdehyde is converted back into GABA or a related ... A, Gibson KM, Jakobs C, Hogema B, Akaboshi S, Loreni F, Malaspina P. ... dehydrogenase gene: identification of promoter region and alternatively ...
    https://medlineplus.gov/genetics/gene/aldh5a1 - Genetics
  2. ALDH18A1 gene 
    ... step in this process by converting the amino acid glutamate to glutamate 5-semialdehyde. Subsequent steps convert this intermediate product to the amino acid proline. The conversion of glutamate to proline is ...
    https://medlineplus.gov/genetics/gene/aldh18a1 - Genetics
  3. AASS gene 
    ... block (amino acid) of many different proteins. Amino acids are broken down when they are no longer needed. Alpha-aminoadipic semialdehyde synthase is called a bifunctional enzyme because it ...
    https://medlineplus.gov/genetics/gene/aass - Genetics
  4. Succinic semialdehyde dehydrogenase deficiency 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD PubMed Akaboshi S, Hogema BM, Novelletto A, Malaspina P, Salomons GS, ...
    https://medlineplus.gov/...nic-semialdehyde-dehydrogenase-deficiency - Genetics
  5. ALDH7A1 gene 
    ... the breakdown of the protein building block (amino acid) lysine in the brain. In one step in the breakdown of lysine to other molecules, antiquitin facilitates the conversion of α-aminoadipic semialdehyde to α-aminoadipate. The breakdown of lysine in ...
    https://medlineplus.gov/genetics/gene/aldh7a1 - Genetics
  6. Pyridoxine-dependent epilepsy 
    ... instructions for making an enzyme called α-aminoadipic semialdehyde (α-AASA) dehydrogenase, also known as antiquitin. This enzyme is involved in the breakdown of the protein building block (amino acid) lysine in the brain.When antiquitin is deficient, ...
    https://medlineplus.gov/.../condition/pyridoxine-dependent-epilepsy - Genetics
  7. Hyperlysinemia 
    ... the building blocks (amino acids) of proteins. Amino acids are not stored in the body and must be broken down when they are no longer needed. When the body's ability to break down lysine is impaired, lysine ...
    https://medlineplus.gov/genetics/condition/hyperlysinemia - Genetics