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Results 1 - 10 of 1,116 for amino acids
  1. Amino Acid Metabolism Disorders (National Library of Medicine)  
    ... this process. One group of these disorders is amino acid metabolism disorders. They include phenylketonuria (PKU) and maple syrup urine disease. Amino acids are "building blocks" that join together to form ...
    https://medlineplus.gov/aminoacidmetabolismdisorders.html - Health Topics
  2. Aromatic l-amino acid decarboxylase deficiency 
    Aromatic l-amino acid decarboxylase (AADC) deficiency is an inherited disorder that affects the way nerve cells (neurons) transmit information to other cells.Signs ...
    https://medlineplus.gov/...tic-l-amino-acid-decarboxylase-deficiency - Genetics
  3. Aminoaciduria 
    Aminoaciduria is an abnormally high amount of amino acids in the urine. Amino acids are the building blocks for proteins in the body.
    https://medlineplus.gov/ency/article/003366.htm - Medical Encyclopedia
  4. Plasma amino acids 
    Plasma amino acids is a screening test, usually done on infants that looks at the amounts of amino acids in the blood. Amino acids are the building ...
    https://medlineplus.gov/ency/article/003361.htm - Medical Encyclopedia
  5. Amino acids 
    Amino acids are molecules that combine to form proteins . Amino acids and proteins are the building blocks of life. When proteins are digested or broken down, amino acids are the result. The human body then uses ...
    https://medlineplus.gov/ency/article/002222.htm - Medical Encyclopedia
  6. SLC6A19 gene 
    ... making a protein called system B(0) neutral amino acid transporter 1 (B0AT1). This protein transports certain protein building blocks (amino acids), namely those with a neutral charge, into cells. ...
    https://medlineplus.gov/genetics/gene/slc6a19 - Genetics
  7. SLC3A1 gene 
    ... this protein complex absorbs particular protein building blocks (amino acids) back into the blood. In particular, the amino acids cystine, ornithine, arginine, and lysine are absorbed back ...
    https://medlineplus.gov/genetics/gene/slc3a1 - Genetics
  8. Phenylketonuria (National Library of Medicine)  
    Phenylketonuria (PKU) is a type of amino acid metabolism disorder. It is inherited. If you have it, your body can't process phenylalanine (Phe). Phe is an amino acid, a ...
    https://medlineplus.gov/phenylketonuria.html - Health Topics
  9. SLC7A7 gene 
    ... instructions for producing a protein called y+L amino acid transporter 1 (y+LAT-1), which is involved in transporting certain protein building blocks (amino acids), namely lysine, arginine, and ornithine. The transportation of ...
    https://medlineplus.gov/genetics/gene/slc7a7 - Genetics
  10. Overview of Amino Acid Metabolism Disorders (Merck & Co., Inc.)  
    Overview of Amino Acid Metabolism Disorders - Learn about the causes, symptoms, diagnosis & treatment from the Merck Manuals - Medical Consumer Version. ... amino acids,metabolic disorder,inherited disorders,hereditary disorders,metabolic,metabolism
    https://www.merckmanuals.com/...w-of-amino-acid-metabolism-disorders - External Health Links
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