Results 1 - 10 of 219 for ALANINE OR ARGININE OR ASPARTIC ACID OR glutamine ACID OR GLYCINE OR HISTIDINE OR ISOLEUCINE OR LEUCINE OR LYSINE OR METHIONINE OR "N-acetyl tyrosine" OR PHENYLALANINE OR PROLINE OR SERINE OR THREONINE OR TRYPTOPHAN OR VALINE
  1. Aspartic acid 
    Aspartic acid is a nonessential amino acid . Amino acids are building blocks of proteins. "Nonessential" means that our ... Aspartic acid helps every cell in the body work. It plays a role in: Hormone production and release ...
    https://medlineplus.gov/ency/article/002234.htm - Medical Encyclopedia
  2. RERE gene 
    ... are affected. More About This Health Condition ARG arginine-glutamic acid dipeptide (RE) repeats arginine-glutamic acid repeats-encoding gene ARP ATN1L atrophin 2 atrophin- ...
    https://medlineplus.gov/genetics/gene/rere - Genetics
  3. GSN gene 
    ... acid) in the gelsolin protein: the amino acid aspartic acid at position 187. The most common mutation replaces the aspartic acid with the amino acid asparagine (written as Asp187Asn ...
    https://medlineplus.gov/genetics/gene/gsn - Genetics
  4. DARS2 gene 
    ... Mitochondrial aspartyl-tRNA synthetase attaches the amino acid aspartic acid to the correct tRNA, which helps ensure that aspartic acid is added at the proper place in the ...
    https://medlineplus.gov/genetics/gene/dars2 - Genetics
  5. ASPA gene 
    ... breaks down a compound called N-acetyl-L-aspartic acid (NAA) into aspartic acid (an amino acid that is a building block ... the amino acid glutamic acid with the amino acid alanine at position 285 of the enzyme (written as ...
    https://medlineplus.gov/genetics/gene/aspa - Genetics
  6. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation 
    ... plays a role in adding the amino acid aspartic acid at the proper place in mitochondrial proteins.Mutations ... synthetase enzyme activity, which hinders the addition of aspartic acid to mitochondrial proteins. It is unclear how the ...
    https://medlineplus.gov/...al-cord-involvement-and-lactate-elevation - Genetics
  7. FGFR3 gene 
    ... that causes LADD syndrome replaces the amino acid aspartic acid with the amino acid asparagine at position 513 ... mutation that causes Muenke syndrome substitutes the amino acid arginine for the amino acid proline at position 250 ...
    https://medlineplus.gov/genetics/gene/fgfr3 - Genetics
  8. Arginase deficiency 
    ... is an inherited disorder that causes the amino acid arginine (a building block of proteins) and ammonia to ...
    https://medlineplus.gov/genetics/condition/arginase-deficiency - Genetics
  9. ATP7B gene 
    ... have a mutation that replaces the amino acid aspartic acid with the amino acid serine at position 1270 ( ...
    https://medlineplus.gov/genetics/gene/atp7b - Genetics
  10. Canavan disease 
    ... affects how the body breaks down and uses aspartic acid . ... MRI scan Urine or blood chemistry for elevated aspartic acid DNA analysis
    https://medlineplus.gov/ency/article/001586.htm - Medical Encyclopedia
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