(2-sulfonatoethyl)methanethiosulfonate

Known as: MTSES cpd, methanethiosulfonate ethylsulfonate 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1994-2012
0246819942012

Papers overview

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Highly Cited
2013
Highly Cited
2013
P2X receptors are widely distributed in the nervous system, and P2X7 receptors have roles in neuropathic pain and in the release… (More)
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2012
2012
P2X receptors for ATP have a wide range of physiological roles and comprise a structurally distinct family of ligand-gated… (More)
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2003
2003
The GABA-binding site undergoes structural rearrangements during the transition from agonist binding to channel opening. To… (More)
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2001
2001
Slow inactivation in voltage-gated sodium channels (NaChs) occurs in response to depolarizations of seconds to minutes and is… (More)
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2000
2000
Membrane-impermeant quaternary derivatives of lidocaine (QX222 and QX314) block cardiac Na(+) channels when applied from either… (More)
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2000
2000
The excitatory neurotransmitter glutamate is removed from the synaptic cleft by several related sodium- and potassium-coupled… (More)
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2000
2000
Depolarization of sodium channels initiates at least three gating pathways: activation, fast inactivation, and slow inactivation… (More)
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1997
1997
The second and third basic residues of the S4 segment of domain 4 (D4:R2 and D4:R3) of the human skeletal muscle Na+ channel are… (More)
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1996
1996
MinK has neither the P region nor signature sequence that characterizes pore-forming subunits of all known K+ channels. A… (More)
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Highly Cited
1994
Highly Cited
1994
All of the potent agonists and competitive antagonists of the acetylcholine receptors are positively charged, onium compounds… (More)
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