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Results 1 - 10 of 38 for GLYCINE OR PROLINE OR HISTIDINE OR THREONINE OR LYSINE OR VALINE OR PHENYLALANINE OR LEUCINE OR TYROSINE OR SODIUM CATION OR ISOLEUCINE OR TRYPTOPHAN OR POTASSIUM CATION OR DEXTROSE OR METHIONINE OR ALANINE OR SERINE OR CHLORIDE ION OR ARGININE
  1. Ions 
    ... Many normal substances exist in the body as ions. Common examples include sodium, potassium, calcium, chloride, and bicarbonate. These substances are known as electrolytes . ...
    https://medlineplus.gov/ency/article/002385.htm - Medical Encyclopedia
  2. Corticosterone methyloxidase deficiency 
    ... which impairs the kidneys' ability to reabsorb salt (sodium chloride or NaCl) into the blood and release potassium in the urine. As a result, excessive amounts of salt in the form of charged atoms (ions) of sodium (Na+) and chlorine (Cl-) leave the ...
    https://medlineplus.gov/.../corticosterone-methyloxidase-deficiency - Genetics
  3. CYP11B2 gene 
    ... which impairs the kidneys' ability to reabsorb salt (sodium chloride or NaCl) into the blood and release potassium in the urine. As a result, excessive amounts of salt in the form of charged atoms (ions) of sodium (Na+) and chlorine (Cl-) leave the ...
    https://medlineplus.gov/genetics/gene/cyp11b2 - Genetics
  4. GRIN2B gene 
    ... combinations of proteins.NMDA receptors are glutamate-gated ion channels. When brain chemicals called glutamate and glycine attach to the receptor, a channel opens, allowing positively charged particles (cations) to flow through. The flow of cations activates ( ...
    https://medlineplus.gov/genetics/gene/grin2b - Genetics
  5. GRIN2A gene 
    ... of protein components. NMDA receptors are glutamate-gated ion channels; when brain chemicals called glutamate and glycine attach to the receptor, a channel opens, allowing positively charged particles (cations) to flow through. The flow of cations generates ...
    https://medlineplus.gov/genetics/gene/grin2a - Genetics
  6. FGFR2 gene 
    ... FGFR2 protein. One mutation replaces the amino acid serine with the amino acid tryptophan at protein position 252 (written as Ser252Trp). The other mutation replaces the amino acid proline with the amino acid arginine at position 253 (written as Pro253Arg). These changes ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  7. Aminoaciduria 
    ... normal ranges in 24 hours urine for adults. Alanine: 9 to 98 Arginine: 0 ... 49 to 413 Isoleucine: 30 to 186 Leucine: 1 to 9 Lysine: ...
    https://medlineplus.gov/ency/article/003366.htm - Medical Encyclopedia
  8. ACADS gene 
    ... One of these polymorphisms replaces the amino acid arginine with the amino acid tryptophan at protein position 147 (written as Arg147Trp or R147W). The other polymorphism switches the amino acid glycine with the amino acid serine at protein position 185 (written as Gly185Ser or ...
    https://medlineplus.gov/genetics/gene/acads - Genetics
  9. Amino acids 
    ... are: histidine, isoleucine, leucine, lysine, methionine, ... aspartic acid, cysteine, glutamic acid, glutamine, glycine, ...
    https://medlineplus.gov/ency/article/002222.htm - Medical Encyclopedia
  10. Gitelman syndrome 
    ... are involved in the kidneys' reabsorption of salt (sodium chloride or ... ions of potassium, magnesium, and calcium. The resulting imbalance of ions ...
    https://medlineplus.gov/genetics/condition/gitelman-syndrome - Genetics
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