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Results 1 - 10 of 28 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. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. KCNJ1 gene 
    ... of kidney cells. In particular, the transport of potassium ions by ROMK is necessary ... of salt (sodium chloride or NaCl) from the urine back into the ...
    https://medlineplus.gov/genetics/gene/kcnj1 - Genetics
  9. WNK1 gene 
    ... the kidneys helps maintain the correct levels of sodium and potassium for ... (chloride ions). These channels maintain the proper amount of chloride ...
    https://medlineplus.gov/genetics/gene/wnk1 - Genetics
  10. SLC12A1 gene 
    ... it moves charged atoms (ions) of sodium (Na+), potassium (K+), and chlorine (Cl-) ... reabsorb salt (sodium chloride or NaCl) from the urine back into the ...
    https://medlineplus.gov/genetics/gene/slc12a1 - Genetics
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