All Stories

  1. In vitro Characterization of a novel murine model of cancerous progression
  2. Effect of Cell Cycle on Cell Surface Expression of Voltage-Gated Sodium Channels and Na+,K+-ATPase
  3. Cancer as a Channelopathy—Appreciation of Complimentary Pathways Provides a Different Perspective for Developing Treatments
  4. The Role of Targeted Osmotic Lysis in the Treatment of Advanced Carcinoma in Companion Animals: A Case Series
  5. Targeted Osmotic Lysis: A Novel Approach to Targeted Cancer Therapies
  6. Emergency Use of Targeted Osmotic Lysis for the Treatment of a Patient with Aggressive Late-Stage Squamous Cell Carcinoma of the Cervix
  7. A novel pipeline of 2-(benzenesulfonamide)-N-(4-hydroxyphenyl) acetamide analgesics that lack hepatotoxicity and retain antipyresis
  8. Targeted Osmotic Lysis of Highly Invasive Breast Carcinomas Using Pulsed Magnetic Field Stimulation of Voltage-Gated Sodium Channels and Pharmacological Blockade of Sodium Pumps
  9. Selective lysis of breast carcinomas by simultaneous stimulation of sodium channels and blockade of sodium pumps
  10. Extended-release hydrocodone patient considerations
  11. Oxidation-sensitive nociception involved in endometriosis-associated pain
  12. Hydrocodone extended-release: Pharmacodynamics, pharmacokinetics and behavioral pharmacology of a controversy
  13. Ranolazine Attenuates Mechanical Allodynia Associated with Demyelination Injury
  14. Regulation and pharmacological blockade of sodium-potassium ATPase: A novel pathway to neuropathy
  15. PDZK1 Is a Novel Factor in Breast Cancer That Is Indirectly Regulated by Estrogen through IGF-1R and Promotes Estrogen-Mediated Growth
  16. Measurement of CFA-Induced Hyperalgesia and Morphine-Induced Analgesia in Rats: Dorsal vs Plantar Mechanical Stimulation of the Hindpaw
  17. Experimental Designs for the Study of Receptor–Receptor Interactions
  18. Insulin Is Essential for the Recovery from Allodynia Induced by Complete Freund's Adjuvant
  19. Ranolazine Attenuation of CFA-induced Mechanical Hyperalgesia
  20. Ranolazine attenuates behavioral signs of neuropathic pain
  21. Medications of abuse in pain management
  22. Synthesis and in vivo evaluation of non-hepatotoxic acetaminophen analogs
  23. Classical Models for Drug Receptor Interactions
  24. Drug-Receptor Interactions
  25. Quantitative Parameters of Drug Action
  26. Ibuprofen blocks changes in nav 1.7 and 1.8 sodium channels associated with complete freund's adjuvant–induced inflammation in rat
  27. Synthesis and Biological Evaluation at Nicotinic Acetylcholine Receptors ofN-Arylalkyl- andN-Aryl-7-Azabicyclo[2.2.1]heptanes
  28. Cross-tolerance between analgesia produced by xylazine and selective opioid receptor subtype treatments
  29. A possible role for nerve growth factor in the augmentation of sodium channels in models of chronic pain
  30. Development of inflammatory hypersensitivity and augmentation of sodium channels in rat dorsal root ganglia
  31. The effects of postmortem delay on mu, delta and kappa opioid receptor subtypes in rat brain and guinea pig cerebellum evaluated by radioligand receptor binding
  32. Analgesic effects of Tyr-W-MIF-1: a mixed μ2-opioid receptor receptor antagonist
  33. Binding of Tyr-W-MIF-1 (Tyr-Pro-Trp-Gly-NH2) and related peptides to μ1 and μ2 opiate receptors
  34. Intrathecal Tyr-W-MIF-1 produces potent, naloxone-reversible analgesia modulated by α2-adrenoceptors
  35. Effects of κ-opioid receptor agonists on stimulated phosphoinositide hydrolysis in rat kidney
  36. Differential cross-tolerance between analgesia produced by α2-adrenoceptor agonists and receptor subtype selective opioid treatments
  37. Potentiation of intrathecal DAMGO antinociception, but not gastrointestinal transit inhibition, by 5-hydroxytryptamine and norepinephrine uptake blockade
  38. Analgesic potency of TRIMU-5: A mixed μ2 opioid receptor agonists/μ1 opioid receptor antagonist
  39. Potentiation of opioid analgesia by the antidepressant nefazodone
  40. Evidence of hyperglycemic hyperalgesia by quinpirole
  41. Genetic influences in opioid analgesic sensitivity in mice
  42. Synergistic analgesic interactions between the periaqueductal gray and the locus coeruleus
  43. Gender effects and central opioid analgesia
  44. Comparison of naloxonazine and β-funaltrexamine antagonism of μ1 and μ2 opioid actions
  45. Blockade of morphine analgesia by both pertussis and cholera toxins in the periaqueductal gray and locus coeruleus
  46. Proglumide selectively potentiates supraspinal μ1 opioid analgesia in mice
  47. The serotonin type-2 receptors that inhibit opioid analgesia are in the brain.
  48. Associative factors in tolerance to analgesia produced by electrical stimulation in the brainstem.
  49. Reduction in opioid and non-opioid forms of swim analgesia by 5-HT2 receptor antagonists
  50. Different μ receptor subtypes mediate spinal and supraspinal analgesia in mice
  51. Contingent tolerance and cross-tolerance to anticonvulsant drug effects: Pentobarbital and ethanol
  52. Chronic opioid antagonist treatment increases μ and δ receptor mediated spinal cord opioid analgesia
  53. Differential development of acute tolerance to analgesia, respiratory depression, gastrointestinal transit and hormone release in a morphine infusion model
  54. Serotonin type-2 receptors that mediate morphine analgesia are in the central nervous system
  55. Erratum to: Observations
  56. Differential blockade by naloxonazine of two μ opiate actions: Analgesia and inhibition of gastrointestinal transit
  57. Observations
  58. Serotonin type-2 receptors mediate opioid analgesia.