scholarly article | Q13442814 |
P50 | author | ??? | Q16075062 |
Barbara S Slusher | Q63959262 | ||
Niyada Hin | Q125271226 | ||
P2093 | author name string | Qin Liu | |
Yun Wang | |||
Qian Xu | |||
Srinivasa N Raja | |||
Zhe Li | |||
Takashi Tsukamoto | |||
Feng Wei | |||
Liang Han | |||
Zongxiang Tang | |||
Fei Yang | |||
Xiaowei Guan | |||
Shao-Qiu He | |||
Vinod Tiwari | |||
Yun Guan | |||
Yu-Xia Chu | |||
P2860 | cites work | Atypical expansion in mice of the sensory neuron-specific Mrg G protein-coupled receptor family | Q24681230 |
A diverse family of GPCRs expressed in specific subsets of nociceptive sensory neurons | Q28215950 | ||
Short-term synaptic plasticity | Q28217342 | ||
Suppression of inflammatory and neuropathic pain symptoms in mice lacking the N-type Ca2+ channel | Q28364912 | ||
Impaired nociception and pain sensation in mice lacking the capsaicin receptor | Q28511370 | ||
A subpopulation of nociceptors specifically linked to itch | Q30533337 | ||
Proenkephalin A gene products activate a new family of sensory neuron--specific GPCRs | Q30674748 | ||
Multiple G-protein-coupled pathways inhibit N-type Ca channels of neurons. | Q33585453 | ||
Calcium-antagonist drugs | Q33765714 | ||
Sensory neuron-specific receptor activation elicits central and peripheral nociceptive effects in rats | Q33783377 | ||
Mas-related G-protein–coupled receptors inhibit pathological pain in mice | Q34115658 | ||
Orphan G protein-coupled receptors MrgA1 and MrgC11 are distinctively activated by RF-amide-related peptides through the Galpha q/11 pathway | Q34379315 | ||
Alternative splicing controls G protein-dependent inhibition of N-type calcium channels in nociceptors | Q34523190 | ||
BAM8-22 peptide produces itch and nociceptive sensations in humans independent of histamine release | Q35034301 | ||
TRP vanilloid 2 knock-out mice are susceptible to perinatal lethality but display normal thermal and mechanical nociception. | Q35335148 | ||
Suppression of inflammatory and neuropathic pain by uncoupling CRMP-2 from the presynaptic Ca²⁺ channel complex | Q35561043 | ||
The neurobiology of antiepileptic drugs for the treatment of nonepileptic conditions. | Q35824087 | ||
Opioid effectiveness, addiction, and depression in chronic pain | Q35833658 | ||
Targeting Ca2+ channels to treat pain: T-type versus N-type. | Q35960328 | ||
Targeting N-type and T-type calcium channels for the treatment of pain | Q36437519 | ||
Intrathecal therapy with ziconotide: clinical experience and considerations on its use. | Q37335009 | ||
Drug development from marine natural products | Q37354836 | ||
MrgC agonism at central terminals of primary sensory neurons inhibits neuropathic pain | Q37622078 | ||
Temporal changes in MrgC expression after spinal nerve injury | Q37622877 | ||
Ziconotide for treatment of severe chronic pain | Q37736046 | ||
Modulation of Ca2+-channel currents in sensory neurons by pertussis toxin-sensitive G-proteins | Q38275862 | ||
TRPA1 is required for histamine-independent, Mas-related G protein-coupled receptor-mediated itch | Q38573328 | ||
Mechanism of Action of Calcium-Channel-Blocking Agents | Q40131998 | ||
Modulation of Ca2+ channels by G-protein beta gamma subunits | Q41214714 | ||
Sensory neuron-specific GPCR Mrgprs are itch receptors mediating chloroquine-induced pruritus | Q41686577 | ||
Depression of presynaptic excitation by the activation of vanilloid receptor 1 in the rat spinal dorsal horn revealed by optical imaging | Q41830053 | ||
Effect of Mas-related gene (Mrg) receptors on hyperalgesia in rats with CFA-induced inflammation via direct and indirect mechanisms | Q42062642 | ||
α2δ expression sets presynaptic calcium channel abundance and release probability | Q42202772 | ||
Injury type-specific calcium channel alpha 2 delta-1 subunit up-regulation in rat neuropathic pain models correlates with antiallodynic effects of gabapentin. | Q44220892 | ||
Inhibition of Ca2+ currents by a mu-opioid in a defined subset of rat sensory neurons | Q44334341 | ||
Analgesic alpha-conotoxins Vc1.1 and Rg1A inhibit N-type calcium channels in rat sensory neurons via GABAB receptor activation. | Q44676738 | ||
Peptide leads new class of chronic pain drugs | Q46426170 | ||
Modulation of NMDA receptors by intrathecal administration of the sensory neuron-specific receptor agonist BAM8-22. | Q46772096 | ||
Morphological characterization of rat Mas-related G-protein-coupled receptor C and functional analysis of agonists. | Q46861794 | ||
Modulation of ion channels and synaptic transmission by a human sensory neuron-specific G-protein-coupled receptor, SNSR4/mrgX1, heterologously expressed in cultured rat neurons. | Q47428149 | ||
Intrathecal combination of ziconotide and morphine for refractory cancer pain: a rapidly acting and effective choice | Q48214498 | ||
Endocannabinoid-dependent plasticity at spinal nociceptor synapses | Q48639515 | ||
Changes in voltage-gated calcium channel alpha(1) gene expression in rat dorsal root ganglia following peripheral nerve injury | Q48698113 | ||
Cloning and expression of MRG receptors in macaque, mouse, and human | Q49050477 | ||
Mechanisms of compartmentalized expression of Mrg class G-protein-coupled sensory receptors. | Q51968003 | ||
Distinct mechanisms underlying pronociceptive effects of opioids. | Q53690404 | ||
Adverse effects associated with the intrathecal administration of ziconotide | Q73487816 | ||
Calcium channel gating and modulation by transmitters depend on cellular compartmentalization | Q73914504 | ||
Intrathecal sensory neuron-specific receptor agonists bovine adrenal medulla 8-22 and (Tyr6)-gamma2-MSH-6-12 inhibit formalin-evoked nociception and neuronal Fos-like immunoreactivity in the spinal cord of the rat | Q83378454 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1613-1621 | |
P577 | publication date | 2014-05-09 | |
P1433 | published in | Pain | Q2317902 |
P1476 | title | Activation of MrgC receptor inhibits N-type calcium channels in small-diameter primary sensory neurons in mice | |
P478 | volume | 155 |
Q42504892 | A Rapid Induction Mechanism for Lin28a in Trophic Responses |
Q42707296 | Activation of cannabinoid CB1 receptor contributes to suppression of spinal nociceptive transmission and inhibition of mechanical hypersensitivity by Aβ-fiber stimulation |
Q34772357 | Discovery and characterization of 2-(cyclopropanesulfonamido)-N-(2-ethoxyphenyl)benzamide, ML382: a potent and selective positive allosteric modulator of MrgX1. |
Q35623116 | Electrical stimulation of low-threshold afferent fibers induces a prolonged synaptic depression in lamina II dorsal horn neurons to high-threshold afferent inputs in mice |
Q55465669 | Involvement of MrgprC in Electroacupuncture Analgesia for Attenuating CFA-Induced Thermal Hyperalgesia by Suppressing the TRPV1 Pathway. |
Q64944700 | Oligomerization of MrgC11 and μ-opioid receptors in sensory neurons enhances morphine analgesia. |
Q36945667 | Phosphoinositide signaling in somatosensory neurons |
Q42174123 | Targeting human Mas-related G protein-coupled receptor X1 to inhibit persistent pain |
Q90084665 | The Ubiquitination of Spinal MrgC Alleviates Bone Cancer Pain and Reduces Intracellular Calcium Concentration in Spinal Neurons in Mice |
Q35798251 | The inhibition of high-voltage-activated calcium current by activation of MrgC11 involves phospholipase C-dependent mechanisms |
Search more.