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1
A novel persistent tetrodotoxin-resistant sodium current in SNS-null and wild-type small primary sensory neurons.
J Neurosci. 1999 Dec 15;19(24):RC43. doi: 10.1523/JNEUROSCI.19-24-j0001.1999.
2
alpha-SNS produces the slow TTX-resistant sodium current in large cutaneous afferent DRG neurons.
J Neurophysiol. 2000 Aug;84(2):710-8. doi: 10.1152/jn.2000.84.2.710.
4
Differential role of GDNF and NGF in the maintenance of two TTX-resistant sodium channels in adult DRG neurons.
Brain Res Mol Brain Res. 1999 Apr 20;67(2):267-82. doi: 10.1016/s0169-328x(99)00070-4.
6
Two tetrodotoxin-resistant sodium channels in human dorsal root ganglion neurons.
FEBS Lett. 1999 Nov 26;462(1-2):117-20. doi: 10.1016/s0014-5793(99)01519-7.
10
Analysis of the variation in use-dependent inactivation of high-threshold tetrodotoxin-resistant sodium currents recorded from rat sensory neurons.
Neuroscience. 2006 Dec 28;143(4):923-38. doi: 10.1016/j.neuroscience.2006.08.052. Epub 2006 Oct 4.

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2
Mechanism-based nonopioid analgesic targets.
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A robust expression system reveals distinct gating mechanisms and calmodulin regulation of Na1.9 channels.
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Modulation of human dorsal root ganglion neuron firing by the Nav1.8 inhibitor suzetrigine.
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Non-invasive in vivo bidirectional magnetogenetic modulation of pain circuits.
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Voltage-gated sodium channels in excitable cells as drug targets.
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The μ-opioid receptor differentiates two distinct human nociceptive populations relevant to clinical pain.
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Na V 1.8/Na V 1.9 double deletion mildly affects acute pain responses in mice.
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