How do you pronounce phenylalanine in English (1 out of 65).

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Translation of phenylalanine

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IPA (International Phonetic Alphabet) of phenylalanine

The International Phonetic Alphabet (IPA) is an alphabetic system of phonetic notation based primarily on the Latin alphabet. With phonetic transcriptions, dictionarie tell you about the pronunciation of words, because the spelling of an English word does not tell you how you should pronounce it. Below is the phonetic transcription of phenylalanine:

Derived Form of phenylalanine

plural: phenylalanines
an essential amino acid found in proteins and needed for growth of children and for protein metabolism in children and adults; abundant in milk and eggs; it is normally converted to tyrosine in the human body
Type ofessential amino acid,

phenylalanine on Youtube

  1. D Phenylalanine or L Phenylalanine or Tyracine will raise your Catecholamines. It's another
  2. Phenylalanine with the phenylalanine deaminase enzyme they don't it doesn't have that enzyme
  3. that occurs in the body called phenylalanine,
  4. made of protein which turns phenylalanine into something
  5. And as a result, this phenylalanine
  6. the phenylalanine into something safer.
  7. oxide booster arginine, and others such as lysine, glycine, phenylalanine, and aspartic
  8. Leucine, isoleucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine are all
  9. Aspartame is quickly and completely broken down into by-products including phenylalanine,
  10. So, tryptophan, phenylalanine, tyrosine, the aromatic amino acids are the ones in shorter
  11. break down phenylalanine. And so that's a great example where we understand
  12. must code for a fee or phenylalanine.
  13. radioactive phenylalanine, and he still had to prove chemically
  14. isoleucine, valine, threonine, phenylalanine and tryptophan.
  15. Glutamine, Alpha-Lipoic Acid which also helps with blood sugar stabilization and DL-Phenylalanine
  16. break down or you can't do well with a diet that's rich in phenylalanine. And so they
  17. Look at the size of the R group on phenylalanine.
  18. The gene for phenylalanine hydroxylase, a metabolic gene that converts the amino acid
  19. L-phenylalanine to L-tyrosine. Why does the absence of this enzyme cause this severe disorder?
  20. The gene, a mutation in phenylalanine hydroxylase, leads to the production of toxic products.