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   1  recognition by insect ORs, a novel class of ligand-gated channel.                                   
     2 mechanisms for the superfamily of pentameric ligand-gated channels.                                  
     3 channels, but not sodium (Na(+)) channels or ligand-gated channels.                                  
     4 , a common theme for activating mutations in ligand-gated channels.                                  
     5  data of ethanol action on a wide variety of ligand-gated channels.                                  
     6 of the OFF bipolar that arises directly from ligand-gated channels.                                  
     7 tivity modulators or downstream effectors of ligand-gated channels.                                  
  
     9 ction of a variety of ion channels including ligand-gated channels activated by ATP, acetylcholine, G
    10    The P2X receptors (P2XRs) are a family of ligand-gated channels activated by extracellular ATP thr
    11 re are three forms of IP3R, all of which are ligand-gated channels activated by the second messenger 
  
    13  allostery that are shared with conventional ligand-gated channels and (ii) the R domain modulates CF
    14 fects that have been observed for pentameric ligand-gated channels and may represent a previously unk
  
  
  
  
    19 TR gating is distinct from that of a typical ligand-gated channel because its ligand (ATP) is usually
  
    21 c Ca(2+)-gated K(+) channel that, like other ligand-gated channels, converts the chemical energy of l
    22 c properties that are common to conventional ligand-gated channels (e.g. unliganded openings and cons
  
    24 hosphorylated CFTR behaves as a conventional ligand-gated channel employing cytoplasmic ATP as a read
    25 forms are a family of ubiquitously expressed ligand-gated channels encoded by three individual genes.
    26 +]i increases result from Ca2+ entry through ligand-gated channels, entry through voltage-gated chann
    27  to menthol or cold, TRPM8 behaves like many ligand-gated channels, exhibiting rapid activation follo
    28 ated ion channels (5-HT3) are members of the ligand-gated channel family, which includes channels tha
  
    30  show that the binding domains of tetrameric ligand-gated channels form either a 4-fold symmetric gat
  
    32 butyric acid) exerts its effects through two ligand-gated channels, GABA(A) and GABA(C) receptors, an
  
    34 RPV1 or vanilloid receptor is a nonselective ligand-gated channel highly expressed in primary sensory
  
    36 Q) due to each of the different voltage- and ligand-gated channels in the cells in the presence of fa
  
    38 cognized that this small molecule influences ligand-gated channels, including the GABAA receptor and 
    39 an affect neuronal excitability by acting on ligand-gated channels, including those gated by glutamat
  
  
  
    43 ty of crystallographic information for these ligand-gated channels, little is known about the structu
  
  
  
    47 c [Ca2+]i can result from Ca2+ entry through ligand-gated channels or voltage-gated Ca2+ channels, or
    48 c activation opening voltage gated channels, ligand gated channels, or mobilizing Ca(2+) release from
    49 P receptors can modulate voltage- as well as ligand-gated channels permeable to calcium and may play 
  
    51 ctance expands the complex repertoire of the ligand-gated channel properties associated with EAAT4.  
  
    53 y inference, other members of the homologous ligand-gated channel superfamily, which include the iono
  
    55 oned vanilloid receptor subtype 1 (VR1) is a ligand-gated channel that is activated by capsaicin, pro
    56 2+ release channel (ryanodine receptor) is a ligand-gated channel that is activated by micromolar cyt
    57 f ADPR or AMPCPR, identify TRPM2 as a simple ligand-gated channel that obeys an equilibrium gating me
  
    59  loop receptors (CLRs) are commonly known as ligand-gated channels that transiently open upon binding
  
    61 esumably occupy overlapping binding sites on ligand-gated channels, these interactions cannot be iden
    62 dulate T currents but not other voltage- and ligand-gated channels thought to mediate pain sensitivit
    63 ge-gated Ca(2+) channels, various Ca(2+)- or ligand-gated channels, Trp family channels, and even the
    64 tamate receptors are postsynaptic tetrameric ligand-gated channels whose activity mediates fast excit
    65 alized by considering CFTR as a hydrolyzable-ligand-gated channel with cytoplasmic ATP as ligand.    
    66 TR gating that combines the allosterism of a ligand-gated channel with its unique enzymatic activity.
    67 2+) permeable isoform, is by far the fastest ligand-gated channel with the channel-opening and -closi
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