Mouse models for studying pain in sickle disease: effects of strain, age, and acuteness.
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Cold hypersensitivity increases with age in mice with sickle cell diseaseMorphine for the treatment of pain in sickle cell diseaseCognitive and behavior deficits in sickle cell mice are associated with profound neuropathologic changes in hippocampus and cerebellum.Sensitization of nociceptive spinal neurons contributes to pain in a transgenic model of sickle cell disease.Dexmedetomidine ameliorates nocifensive behavior in humanized sickle cell mice.Updated Mechanisms of Sickle Cell Disease-Associated Chronic painComparative Analysis of Pain Behaviours in Humanized Mouse Models of Sickle Cell Anemia.Quantification of pain in sickle mice using facial expressions and body measurements.N-ethylmaleimide activates a Cl(-)-independent component of K(+) flux in mouse erythrocytesSickle cell disease in mice is associated with sensitization of sensory nerve fibers.Original Research: Diametric effects of hypoxia on pathophysiology of sickle cell disease in a murine model.Cannabinoid receptor-specific mechanisms to alleviate pain in sickle cell anemia via inhibition of mast cell activation and neurogenic inflammation.An overview of animal models of pain: disease models and outcome measures.Electroacupuncture in conscious free-moving mice reduces pain by ameliorating peripheral and central nociceptive mechanisms.Thinking beyond sickling to better understand pain in sickle cell disease.Small-molecule nociceptin receptor agonist ameliorates mast cell activation and pain in sickle mice.Spinal glial activation and oxidative stress are alleviated by treatment with curcumin or coenzyme Q in sickle mice.Mast cell activation contributes to sickle cell pathobiology and pain in miceDoes cold hypersensitivity increase with age in sickle cell disease?State of the Art Management of Acute Vaso-occlusive Pain in Sickle Cell Disease.Targeting novel mechanisms of pain in sickle cell disease.Transcriptomic analysis of gene signatures associated with sickle pain.Characterization of a mouse model of sickle cell trait: parallels to human trait and a novel finding of cutaneous sensitization.Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia.Mast cell-neural interactions contribute to pain and itch.Functional MRI BOLD response in sickle mice with hyperalgesia.Bivalent ligand MCC22 potently attenuates nociception in a murine model of sickle cell disease.Endothelin-Type A receptors mediate pain in a mouse model of sickle cell disease.Quantitative sensory testing is feasible and is well-tolerated in patients with sickle cell disease following a vaso-occlusive episode.Sensitization of C-fiber nociceptors in mice with sickle cell disease is decreased by local inhibition of anandamide hydrolysis.Sickle cell disease: a natural model of acute and chronic pain.Iron Chelation with Transdermal Deferoxamine Accelerates Healing of Murine Sickle Cell Ulcers
P2860
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P2860
Mouse models for studying pain in sickle disease: effects of strain, age, and acuteness.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Mouse models for studying pain in sickle disease: effects of strain, age, and acuteness.
@en
type
label
Mouse models for studying pain in sickle disease: effects of strain, age, and acuteness.
@en
prefLabel
Mouse models for studying pain in sickle disease: effects of strain, age, and acuteness.
@en
P2093
P2860
P1476
Mouse models for studying pain in sickle disease: effects of strain, age, and acuteness.
@en
P2093
David M Cain
Derek Vang
Donald A Simone
Kalpna Gupta
Robert P Hebbel
P2860
P304
P356
10.1111/J.1365-2141.2011.08977.X
P407
P577
2011-12-15T00:00:00Z