Nav1.7 is essential for nociceptor action potentials in the mouse in a manner independent of endogenous opioids
暂无分享,去创建一个
J. Kaminker | K. Stark | D. Hackos | S. Shields | M. Roose-Girma | O. Foreman | Victory Joseph | L. Deng | Hai Ngu | J. Allard | P. Karila | Lucinda Tam | Janet Tao | M. Dourado | Rebecca M. Reese | Linnea Strid Orrhult | James Maksymetz | Han Lin | Kevin Huang | Susanne Lardell | M. Jung
[1] S. McMahon,et al. Examination of the contribution of Nav1.7 to axonal propagation in nociceptors. , 2021, Pain.
[2] D. Henze,et al. Nav1.7 target modulation and efficacy can be measured in nonhuman primate assays , 2021, Science Translational Medicine.
[3] F. Zufall,et al. A central mechanism of analgesia in mice and humans lacking the sodium channel NaV1.7 , 2021, Neuron.
[4] G. King,et al. Fifteen years of NaV1.7 channels as an analgesic target: Why has excellent in vitro pharmacology not translated into in vivo analgesic efficacy? , 2020, British journal of pharmacology.
[5] D. Kohane,et al. Polymer-tetrodotoxin conjugates to induce prolonged duration local anesthesia with minimal toxicity , 2019, Nature Communications.
[6] M. Rothenberg,et al. Safety, Tolerability, and Pharmacokinetics of GDC-0276, a Novel NaV1.7 Inhibitor, in a First-in-Human, Single- and Multiple-Dose Study in Healthy Volunteers , 2019, Clinical Drug Investigation.
[7] D. Hackos,et al. Insensitivity to Pain upon Adult-Onset Deletion of Nav1.7 or Its Blockade with Selective Inhibitors , 2018, The Journal of Neuroscience.
[8] D. Sutherlin,et al. Selective NaV1.7 Antagonists with Long Residence Time Show Improved Efficacy against Inflammatory and Neuropathic Pain. , 2018, Cell reports.
[9] Ben Sidders,et al. Network-Based Drug Discovery: Coupling Network Pharmacology with Phenotypic Screening for Neuronal Excitability. , 2018, Journal of molecular biology.
[10] Brian E Marron,et al. Highly potent and selective NaV1.7 inhibitors for use as intravenous agents and chemical probes. , 2017, Bioorganic & medicinal chemistry letters.
[11] Dong Liu,et al. Pharmacologic Characterization of AMG8379, a Potent and Selective Small Molecule Sulfonamide Antagonist of the Voltage-Gated Sodium Channel NaV1.7 , 2017, The Journal of Pharmacology and Experimental Therapeutics.
[12] J. Wood,et al. Synergistic regulation of serotonin and opioid signaling contributes to pain insensitivity in Nav1.7 knockout mice , 2017, Science Signaling.
[13] Jun-Ming Zhang,et al. Localized Sympathectomy Reduces Mechanical Hypersensitivity by Restoring Normal Immune Homeostasis in Rat Models of Inflammatory Pain , 2016, The Journal of Neuroscience.
[14] Jun Li,et al. Structural basis of Nav1.7 inhibition by an isoform-selective small-molecule antagonist , 2015, Science.
[15] Flavia Mancini,et al. Endogenous opioids contribute to insensitivity to pain in humans and mice lacking sodium channel Nav1.7 , 2015, Nature Communications.
[16] H. Hioki,et al. Dorsal Horn Circuits for Persistent Mechanical Pain , 2015, Neuron.
[17] Matthew E. Ritchie,et al. limma powers differential expression analyses for RNA-sequencing and microarray studies , 2015, Nucleic acids research.
[18] S. Linnarsson,et al. Unbiased classification of sensory neuron types by large-scale single-cell RNA sequencing , 2014, Nature Neuroscience.
[19] W. Huber,et al. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2 , 2014, Genome Biology.
[20] A. Winterpacht,et al. Inherited Pain , 2013, The Journal of Biological Chemistry.
[21] Eli J. Fine,et al. DNA targeting specificity of RNA-guided Cas9 nucleases , 2013, Nature Biotechnology.
[22] James E. DiCarlo,et al. RNA-Guided Human Genome Engineering via Cas9 , 2013, Science.
[23] Le Cong,et al. Multiplex Genome Engineering Using CRISPR/Cas Systems , 2013, Science.
[24] S. Waxman,et al. Membrane properties and electrogenesis in the distal axons of small dorsal root ganglion neurons in vitro. , 2012, Journal of neurophysiology.
[25] S. Dib-Hajj,et al. Gain of function NaV1.7 mutations in idiopathic small fiber neuropathy , 2012, Annals of neurology.
[26] Wenqin Luo,et al. The Functional Organization of Cutaneous Low-Threshold Mechanosensory Neurons , 2011, Cell.
[27] S. Dib-Hajj,et al. Sodium channels in normal and pathological pain. , 2010, Annual review of neuroscience.
[28] Serban Nacu,et al. Fast and SNP-tolerant detection of complex variants and splicing in short reads , 2010, Bioinform..
[29] S. Dib-Hajj,et al. Early- and late-onset inherited erythromelalgia: genotype-phenotype correlation. , 2009, Brain : a journal of neurology.
[30] S. Dib-Hajj,et al. NaV1.7 Gain-of-Function Mutations as a Continuum: A1632E Displays Physiological Changes Associated with Erythromelalgia and Paroxysmal Extreme Pain Disorder Mutations and Produces Symptoms of Both Disorders , 2008, The Journal of Neuroscience.
[31] Yi Dai,et al. Comparative study of the distribution of the α‐subunits of voltage‐gated sodium channels in normal and axotomized rat dorsal root ganglion neurons , 2008, The Journal of comparative neurology.
[32] S. Dib-Hajj,et al. Paroxysmal extreme pain disorder M1627K mutation in human Nav1.7 renders DRG neurons hyperexcitable , 2008, Molecular pain.
[33] M. Dubé,et al. Loss‐of‐function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations , 2007, Clinical genetics.
[34] Hussain Jafri,et al. An SCN9A channelopathy causes congenital inability to experience pain , 2006, Nature.
[35] D. Kohane,et al. Tetrodotoxin for prolonged local anesthesia with minimal myotoxicity , 2006, Muscle & nerve.
[36] A. M. Rush,et al. A single sodium channel mutation produces hyper- or hypoexcitability in different types of neurons. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[37] Sulayman D. Dib-Hajj,et al. Electrophysiological Properties of Mutant Nav1.7 Sodium Channels in a Painful Inherited Neuropathy , 2004, The Journal of Neuroscience.
[38] R. Langer,et al. A Re‐examination of Tetrodotoxin for Prolonged Duration Local Anesthesia , 1998, Anesthesiology.
[39] T. Yaksh,et al. Quantitative assessment of tactile allodynia in the rat paw , 1994, Journal of Neuroscience Methods.
[40] R. Dubner,et al. A new and sensitive method for measuring thermal nociception in cutaneous hyperalgesia , 1987, Pain.
[41] OUP accepted manuscript , 2021, Brain.
[42] D. Hackos,et al. Selective Ligands and Drug Discovery Targeting the Voltage-Gated Sodium Channel Nav1.7. , 2018, Handbook of experimental pharmacology.
[43] S. Waxman,et al. Altered sodium channel gating as molecular basis for pain: contribution of activation, inactivation, and resurgent currents. , 2014, Handbook of experimental pharmacology.
[44] S. Dib-Hajj,et al. Paroxysmal extreme pain disorder: a molecular lesion of peripheral neurons , 2011, Nature Reviews Neurology.
[45] A. Hodgkin,et al. A quantitative description of membrane current and its application to conduction and excitation in nerve , 1990, Bulletin of mathematical biology.