Prisca Honore

Overview

Best Publications

• Inhibition of hyperalgesia by ablation of lamina I spinal neurons expressing the substance P receptor.

  Patrick W. Mantyh;Scott D. Rogers;Scott D. Rogers;Prisca Honore;Prisca Honore;Brian J. Allen;Brian J. Allen

  735
  Citations

• Neurochemical and cellular reorganization of the spinal cord in a murine model of bone cancer pain

  Matthew J. Schwei;Prisca Honore;Scott D. Rogers;Janeen L. Salak-Johnson

  706
  Citations

• Murine models of inflammatory, neuropathic and cancer pain each generates a unique set of neurochemical changes in the spinal cord and sensory neurons.

  P Honore;S.D Rogers;M.J Schwei;J.L Salak-Johnson

  704
  Citations

• A-803467, a potent and selective Nav1.8 sodium channel blocker, attenuates neuropathic and inflammatory pain in the rat

  Michael F. Jarvis;Prisca Honore;Char Chang Shieh;Mark Chapman

  638
  Citations

• Osteoprotegerin blocks bone cancer-induced skeletal destruction, skeletal pain and pain-related neurochemical reorganization of the spinal cord

  Prisca Honore;Nancy M. Luger;Nancy M. Luger;Mary Ann C. Sabino;Mary Ann C. Sabino;Matthew J. Schwei;Matthew J. Schwei

  619
  Citations

• A-740003 [N-(1-{[(Cyanoimino)(5-quinolinylamino) methyl]amino}-2,2-dimethylpropyl)-2-(3,4-dimethoxyphenyl)acetamide], a Novel and Selective P2X7 Receptor Antagonist, Dose-Dependently Reduces Neuropathic Pain in the Rat

  Prisca Honore;Diana Donnelly-Roberts;Marian T. Namovic;Gin Hsieh

  573
  Citations

• A-317491, a novel potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 receptors, reduces chronic inflammatory and neuropathic pain in the rat

  Michael F. Jarvis;Edward C. Burgard;Steve McGaraughty;Prisca Honore

  560
  Citations

• Transmission of chronic nociception by spinal neurons expressing the substance P receptor.

  Michael L. Nichols;Michael L. Nichols;Brian J. Allen;Brian J. Allen;Scott D. Rogers;Scott D. Rogers;Joseph R. Ghilardi;Joseph R. Ghilardi

  526
  Citations

• TRPV1 Receptors in the CNS Play a Key Role in Broad-Spectrum Analgesia of TRPV1 Antagonists

  M. Cui;P. Honore;C. Zhong;D. Gauvin

  394
  Citations

• A-425619 [1-Isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a Novel Transient Receptor Potential Type V1 Receptor Antagonist, Relieves Pathophysiological Pain Associated with Inflammation and Tissue Injury in Rats

  Prisca Honore;Carol T Wismer;Joseph P Mikusa;Chang Z Zhu

  377
  Citations

• Analgesic profile of intrathecal P2X3 antisense oligonucleotide treatment in chronic inflammatory and neuropathic pain states in rats

  Prisca Honore;Karen Kage;Joseph Mikusa;Andrew T. Watt

  322
  Citations

• Structure−Activity Relationship Studies on a Series of Novel, Substituted 1-Benzyl-5-phenyltetrazole P2X7 Antagonists

  Derek W. Nelson;Robert J. Gregg;Michael E. Kort;Arturo Perez-Medrano

  287
  Citations

• Osteoprotegerin Diminishes Advanced Bone Cancer Pain

  Nancy M. Luger;Prisca Honore;Mary Ann C. Sabino;Matthew J. Schwei

  284
  Citations

• Efficacy of systemic morphine suggests a fundamental difference in the mechanisms that generate bone cancer vs inflammatory pain.

  Nancy M. Luger;Mary Ann C. Sabino;Matthew J. Schwei;David B. Mach

  282
  Citations

• P2X7-related modulation of pathological nociception in rats

  S. McGaraughty;K.L. Chu;M.T. Namovic;D.L. Donnelly-Roberts

  275
  Citations

• Effects of A‐317491, a novel and selective P2X3/P2X2/3 receptor antagonist, on neuropathic, inflammatory and chemogenic nociception following intrathecal and intraplantar administration

  Steve McGaraughty;Carol T Wismer;Chang Z Zhu;Joseph Mikusa

  257
  Citations

• Involvement of the TTX-resistant sodium channel Nav 1.8 in inflammatory and neuropathic, but not post-operative, pain states.

  S K Joshi;Joseph P Mikusa;Gricelda Hernandez;Scott Baker

  256
  Citations

• Spinal Substance P Receptor Expression and Internalization in Acute, Short-Term, and Long-Term Inflammatory Pain States

  Prisca Honoré;Prisca Honoré;Patrick M. Menning;Patrick M. Menning;Scott D. Rogers;Scott D. Rogers;Michael L. Nichols;Michael L. Nichols

  254
  Citations

• Electrophysiological and in vivo characterization of A-317567, a novel blocker of acid sensing ion channels.

  G.R. Dubé;Sonya G. Lehto;Nicole M. Breese;Scott J. Baker

  251
  Citations

• Novel transient receptor potential vanilloid 1 receptor antagonists for the treatment of pain: structure-activity relationships for ureas with quinoline, isoquinoline, quinazoline, phthalazine, quinoxaline, and cinnoline moieties.

  Arthur Gomtsyan;Erol K Bayburt;Robert G Schmidt;Guo Zhu Zheng

  225
  Citations