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Results 1 - 10 of 14 for AMBERGRIS OR LEAD OR MAGNESIUM CATION OR PHOSPHATE ION
  1. ... and the accumulation of iron in the liver lead to the signs and symptoms of hypochromic ... (proton-coupled divalent metal ion transporter), member 2 solute carrier family 11 (proton- ...
  2. ... acts as a channel, which allows charged atoms (ions) of magnesium (Mg2+) to flow into cells; the channel may also allow small amounts of calcium ions (Ca2+) to pass through cells. Magnesium is involved in many cell processes, including production ...
  3. ... channel, sperm associated 1 CATSPER CTSR1_HUMAN sperm ion channel sperm-associated cation channel 1 Tests of CATSPER1 PubMed CATION CHANNEL, ...
  4. ... TRPV4 calcium channel, preventing it from transporting calcium ions effectively. It is unclear how a loss of channel function leads to the specific features of this condition.Common ...
  5. ... 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 ( ...
  6. ... 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 ...
  7. ... of these impaired cardiac cells over time can lead to a buildup of scar tissue (fibrosis), worsening ... calcium-activated non-selective cation channel 1 hTRPM4 long transient receptor potential channel ...
  8. ... polycystin-1, the channel transports positively charged atoms (ions), particularly calcium ions, into the cell. This influx of calcium ions triggers a cascade of chemical reactions inside the ...
  9. ... channels that allow positively charged sodium atoms (Na+ ions) into the cell or cellular compartment in exchange for positively charged hydrogen ions (H+, also known as protons), which are removed. ...
  10. ... caused by mutations in a gene encoding sodium ion-dependent carnitine transporter. Nat Genet. 1999 Jan;21( ...
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