Page last updated: 2024-08-23

substance p and Anemia, Sickle Cell

substance p has been researched along with Anemia, Sickle Cell in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (14.29)18.2507
2000's2 (28.57)29.6817
2010's4 (57.14)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ericson, ME; Gupta, K; Gupta, M; Luk, K; Nguyen, J; Simone, DA; Vang, D; Vincent, L1
Douglas, SD2
Brandow, AM; Dasgupta, M; Hillery, CA; Hoffmann, RG; Panepinto, JA; Stucky, CL; Wandersee, NJ1
Ericson, ME; Gupta, K; Gupta, P; Gupta, V; Hebbel, RP; Kehl, LJ; Khasabov, SG; Kohli, DR; Li, Y; Nguyen, J; Simone, DA1
Pepple, DJ1
Douglas, SD; Michaels, LA; Ohene-Frempong, K; Zhao, H1

Other Studies

7 other study(ies) available for substance p and Anemia, Sickle Cell

ArticleYear
Mast cell activation contributes to sickle cell pathobiology and pain in mice.
    Blood, 2013, Sep-12, Volume: 122, Issue:11

    Topics: Anemia, Sickle Cell; Animals; Benzamides; Cells, Cultured; Cytokines; Ganglia, Spinal; Granulocyte-Macrophage Colony-Stimulating Factor; Humans; Hyperalgesia; Hypoxia; Imatinib Mesylate; Leukocyte Count; Mast Cells; Mice; Mice, Knockout; Mice, Transgenic; Microscopy, Confocal; Neurogenic Inflammation; Nociceptors; Pain; Piperazines; Protein Kinase Inhibitors; Pyrimidines; Skin; Substance P

2013
Substance P and sickle cell disease-a marker for pain and novel therapeutic approaches.
    British journal of haematology, 2016, Volume: 175, Issue:2

    Topics: Anemia, Sickle Cell; Biomarkers; Humans; Morpholines; Pain; Substance P

2016
Substance P is increased in patients with sickle cell disease and associated with haemolysis and hydroxycarbamide use.
    British journal of haematology, 2016, Volume: 175, Issue:2

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Antisickling Agents; Biomarkers; Black or African American; Case-Control Studies; Child; Female; Hemolysis; Humans; Hydroxyurea; Male; Risk Factors; Substance P; Young Adult

2016
Pain-related behaviors and neurochemical alterations in mice expressing sickle hemoglobin: modulation by cannabinoids.
    Blood, 2010, Jul-22, Volume: 116, Issue:3

    Topics: Anemia, Sickle Cell; Animals; Behavior, Animal; Calcitonin Gene-Related Peptide; Cannabinoid Receptor Agonists; Cannabinoids; Cyclohexanols; Disease Models, Animal; Female; Hemoglobin, Sickle; Humans; Hyperalgesia; Male; Mice; Mice, Knockout; Mice, Transgenic; Morphine; Neuroglia; Pain; Receptors, Opioid, mu; Recombinant Proteins; Skin; Spinal Cord; Substance P

2010
The role of hypoxia and substance P in the painful crisis of homozygous sickle cell disease.
    Medical hypotheses, 2008, Volume: 70, Issue:4

    Topics: Anemia, Sickle Cell; Hematocrit; Homozygote; Humans; Hypoxia; Models, Biological; Models, Theoretical; Oxygen; Pain; Substance P

2008
Elevated plasma substance P in sickle cell disease and vaso-occlusive crisis.
    Medical hypotheses, 2008, Volume: 70, Issue:6

    Topics: Anemia, Sickle Cell; Antiemetics; Aprepitant; Clinical Trials, Phase I as Topic; Humans; Models, Immunological; Morpholines; Neurokinin-1 Receptor Antagonists; Pain; Substance P

2008
Serum levels of substance P are elevated in patients with sickle cell disease and increase further during vaso-occlusive crisis.
    Blood, 1998, Nov-01, Volume: 92, Issue:9

    Topics: Acute Disease; Adolescent; Anemia, Sickle Cell; Child; Child, Preschool; Female; Humans; Interleukin-8; Ischemia; Male; Pain; Substance P; Tumor Necrosis Factor-alpha

1998