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Results 1 - 7 of 7 for EPINEPHRINE OR SODIUM CATION OR LIDOCAINE OR IODINE
  1. SLC22A5 gene 
    ... More About This Health Condition CDSP high-affinity sodium dependent carnitine cotransporter novel organic cation transporter 2 OCTN2 organic cation transporter 5 organic ...
    https://medlineplus.gov/genetics/gene/slc22a5 - Genetics
  2. SLC9A6 gene 
    ... sodium/hydrogen exchanger 6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 solute carrier family 9 member 6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6 Tests of SLC9A6 ...
    https://medlineplus.gov/genetics/gene/slc9a6 - Genetics
  3. SLC5A5 gene 
    ... gene provides instructions for making a protein called sodium (Na)-iodide symporter or NIS. This protein transports iodide, a negatively charged version of iodine, into cells of certain tissues. The NIS protein ...
    https://medlineplus.gov/genetics/gene/slc5a5 - Genetics
  4. HCN4 gene 
    ... Condition HCN4_HUMAN hyperpolarization activated cyclic nucleotide-gated cation channel 4 hyperpolarization activated cyclic nucleotide-gated potassium channel 4 potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4 SSS2 ...
    https://medlineplus.gov/genetics/gene/hcn4 - Genetics
  5. UNC80 gene 
    ... to that caused by mutations in its interacting cation channel NALCN. J Med Genet. 2016 Jun;53( ...
    https://medlineplus.gov/genetics/gene/unc80 - Genetics
  6. UNC80 deficiency 
    ... to that caused by mutations in its interacting cation channel NALCN. J Med Genet. 2016 Jun;53( ...
    https://medlineplus.gov/genetics/condition/unc80-deficiency - Genetics
  7. Progressive familial heart block 
    ... genes are channels that allow positively charged atoms (cations) into and out of cells. Both channels are ... Aizawa Y, Wilde AA, Roden DM, Bezzina CR. Sodium channel beta1 subunit mutations associated with Brugada syndrome ...
    https://medlineplus.gov/.../progressive-familial-heart-block - Genetics