Mouse Models of Pain in Sickle Cell Disease

scientific article published on 28 September 2018

Mouse Models of Pain in Sickle Cell Disease is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/CPNS.54
P698PubMed publication ID30265442

P2093author name stringKalpna Gupta
Varun Sagi
Barbara A Benson
Sonal S Joshi
Waogwende L Song-Naba
P2860cites workBlood sample collection in small laboratory animalsQ24616699
From Individualized Treatment of Sickle Cell Pain to Precision Medicine: A 40-Year JourneyQ26747771
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The impact of a multidisciplinary pain management model on sickle cell disease pain hospitalizationsQ34752970
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Sensitization of nociceptive spinal neurons contributes to pain in a transgenic model of sickle cell diseaseQ35196490
Transient receptor potential vanilloid 1 mediates pain in mice with severe sickle cell diseaseQ35230235
Safety and Utility of Quantitative Sensory Testing among Adults with Sickle Cell Disease: Indicators of Neuropathic Pain?Q35843541
Pathology of Berkeley sickle cell mice: similarities and differences with human sickle cell diseaseQ35848672
The endothelial biology of sickle cell disease: inflammation and a chronic vasculopathyQ35848692
Acute and chronic administration of the cannabinoid receptor agonist CP 55,940 attenuates tumor-evoked hyperalgesiaQ36015427
Comparative Analysis of Pain Behaviours in Humanized Mouse Models of Sickle Cell Anemia.Q36096001
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Patients with sickle cell disease have increased sensitivity to cold and heatQ36554754
Patient-reported outcomes: descriptors of nociceptive and neuropathic pain and barriers to effective pain management in adult outpatients with sickle cell diseaseQ36809000
Clinical Interpretation of Quantitative Sensory Testing as a Measure of Pain Sensitivity in Patients With Sickle Cell DiseaseQ36868088
Quantitative sensory testing and pain-evoked cytokine reactivity: comparison of patients with sickle cell disease to healthy matched controlsQ37064951
Sickle cell disease in mice is associated with sensitization of sensory nerve fibersQ37070937
Frequency of Hospitalizations for Pain and Association With Altered Brain Network Connectivity in Sickle Cell DiseaseQ37179797
Cannabinoid receptor-specific mechanisms to alleviate pain in sickle cell anemia via inhibition of mast cell activation and neurogenic inflammationQ37216210
Heme triggers TLR4 signaling leading to endothelial cell activation and vaso-occlusion in murine sickle cell diseaseQ37489028
Chronic Opioid Therapy and Central Sensitization in Sickle Cell DiseaseQ37736976
Frequently asked questions by hospitalists managing pain in adults with sickle cell diseaseQ37887687
Health-related quality of life in sickle cell disease: past, present, and futureQ38004362
The delay time in sickle cell disease after 40 years: A paradigm assessedQ38341763
Common gynecological challenges in adolescents with sickle cell diseaseQ38650270
Sickle cell disease in the older adultQ39028346
Sensory and Thermal Quantitative Testing in Children With Sickle Cell DiseaseQ39161218
How we manage iron overload in sickle cell patientsQ39179372
A new staining technique for proteins in polyacrylamide gels using coomassie brilliant blue G250.Q39456868
Hypoxia/reoxygenation causes inflammatory response in transgenic sickle mice but not in normal miceQ40431909
Small-molecule nociceptin receptor agonist ameliorates mast cell activation and pain in sickle miceQ40620939
Substance P is increased in patients with sickle cell disease and associated with haemolysis and hydroxycarbamide use.Q41635275
Mouse models for studying pain in sickle disease: effects of strain, age, and acutenessQ41996084
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Pulmonary hypertension and NO in sickle cellQ42558017
Mast cell activation contributes to sickle cell pathobiology and pain in miceQ42612548
Daily Opioid Use Fluctuates as a Function of Pain, Catastrophizing, and Affect in Patients with Sickle Cell Disease: an Electronic Daily Diary AnalysisQ44349172
Endothelial cell expression of tissue factor in sickle mice is augmented by hypoxia/reoxygenation and inhibited by lovastatinQ44836521
Targeting novel mechanisms of pain in sickle cell diseaseQ46051242
A monocyte-TNF-endothelial activation axis in sickle transgenic mice: Therapeutic benefit from TNF blockade.Q46081377
Transgenic knockout mice with exclusively human sickle hemoglobin and sickle cell diseaseQ46264390
Prospective evaluation of chronic organ damage in adult sickle cell patients: A seven-year follow-up studyQ48140774
Mouse models of sickle cell disease.Q50648124
Pain in sickle cell disease: the future of acute treatment.Q51701658
Quantitative sensory testing is feasible and is well-tolerated in patients with sickle cell disease following a vaso-occlusive episode.Q52728984
Sickle cell disease.Q52795486
Sensitization of C-fiber nociceptors in mice with sickle cell disease is decreased by local inhibition of anandamide hydrolysis.Q53692390
Simplified typing of mouse hemoglobin (Hbb) phenotypes using cystamineQ67427060
High-performance liquid chromatography of human hemoglobins on a new cation exchangerQ71071184
Knockout-transgenic mouse model of sickle cell diseaseQ73823833
Assessment of sickle cell pain in children and young adults using the adolescent pediatric pain toolQ77639254
Transgenic sickle mice have vascular inflammationQ78835117
Hospital readmission for adult acute sickle cell painful episodes: frequency, etiology, and prognostic significanceQ81682302
Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemiaQ89125129
P433issue1
P304page(s)e54
P577publication date2018-09-28
P1433published inCurrent protocols in neuroscienceQ27721712
P1476titleMouse Models of Pain in Sickle Cell Disease
P478volume85

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cites work (P2860)
Q91594586Diet and gender influence survival of transgenic Berkley sickle cell mice
Q64078541Effect of chronic opioid therapy on pain and survival in a humanized mouse model of sickle cell disease
Q64228738Mast Cells Induce Blood Brain Barrier Damage in SCD by Causing Endoplasmic Reticulum Stress in the Endothelium
Q91842406Sensitization of nociceptors by prostaglandin E2-glycerol contributes to hyperalgesia in mice with sickle cell disease

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