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PUBMED FOR HANDHELDS

Journal Abstract Search


317 related items for PubMed ID: 18024079

  • 1. Phenotype of CD4+ T cell subsets that develop following mouse facial nerve axotomy.
    Xin J, Wainwright DA, Serpe CJ, Sanders VM, Jones KJ.
    Brain Behav Immun; 2008 May; 22(4):528-37. PubMed ID: 18024079
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  • 2. Immune-mediated neuroprotection of axotomized mouse facial motoneurons is dependent on the IL-4/STAT6 signaling pathway in CD4(+) T cells.
    Deboy CA, Xin J, Byram SC, Serpe CJ, Sanders VM, Jones KJ.
    Exp Neurol; 2006 Sep; 201(1):212-24. PubMed ID: 16806176
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  • 3. CD4+ Th2 cells function alike effector Tr1 and Th1 cells through the deletion of a single cytokine IL-6 and IL-10 gene.
    Ankathatti Munegowda M, Xu S, Freywald A, Xiang J.
    Mol Immunol; 2012 Jun; 51(2):143-9. PubMed ID: 22424785
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  • 5. CD4+ T, but not CD8+ or B, lymphocytes mediate facial motoneuron survival after facial nerve transection.
    Serpe CJ, Coers S, Sanders VM, Jones KJ.
    Brain Behav Immun; 2003 Oct; 17(5):393-402. PubMed ID: 12946661
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  • 9. Immune cell-mediated neuroprotection is independent of estrogen action through estrogen receptor-alpha.
    Xin J, Fargo KN, Tanzer L, Sanders VM, Jones KJ.
    Metab Brain Dis; 2012 Mar; 27(1):23-8. PubMed ID: 21975535
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  • 10. Impact of peripheral immune status on central molecular responses to facial nerve axotomy.
    Setter DO, Runge EM, Schartz ND, Kennedy FM, Brown BL, McMillan KP, Miller WM, Shah KM, Haulcomb MM, Sanders VM, Jones KJ.
    Brain Behav Immun; 2018 Feb; 68():98-110. PubMed ID: 29030217
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  • 11. In Vitro Differentiation of Effector CD4+ T Helper Cell Subsets.
    Read KA, Powell MD, Sreekumar BK, Oestreich KJ.
    Methods Mol Biol; 2019 Feb; 1960():75-84. PubMed ID: 30798522
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  • 12. CD4+ T cell expression of the IL-10 receptor is necessary for facial motoneuron survival after axotomy.
    Runge EM, Iyer AK, Setter DO, Kennedy FM, Sanders VM, Jones KJ.
    J Neuroinflammation; 2020 Apr 17; 17(1):121. PubMed ID: 32303238
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  • 13. CCR8 expression identifies CD4 memory T cells enriched for FOXP3+ regulatory and Th2 effector lymphocytes.
    Soler D, Chapman TR, Poisson LR, Wang L, Cote-Sierra J, Ryan M, McDonald A, Badola S, Fedyk E, Coyle AJ, Hodge MR, Kolbeck R.
    J Immunol; 2006 Nov 15; 177(10):6940-51. PubMed ID: 17082609
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  • 14. Identity and Diversity of Human Peripheral Th and T Regulatory Cells Defined by Single-Cell Mass Cytometry.
    Kunicki MA, Amaya Hernandez LC, Davis KL, Bacchetta R, Roncarolo MG.
    J Immunol; 2018 Jan 01; 200(1):336-346. PubMed ID: 29180490
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  • 15. IL-10 within the CNS is necessary for CD4+ T cells to mediate neuroprotection.
    Xin J, Wainwright DA, Mesnard NA, Serpe CJ, Sanders VM, Jones KJ.
    Brain Behav Immun; 2011 Jul 01; 25(5):820-9. PubMed ID: 20723599
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  • 16. Existence of Th22 in children and evaluation of IL-22 + CD4 + T, Th17, and other T cell effector subsets from healthy children compared to adults.
    Shen E, Wang M, Xie H, Zou R, Lin Q, Lai L, Li F, Liang Z, Xu Y, Zhou M.
    BMC Immunol; 2016 Jun 23; 17(1):20. PubMed ID: 27338754
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  • 18. Brain-derived neurotrophic factor supports facial motoneuron survival after facial nerve transection in immunodeficient mice.
    Serpe CJ, Byram SC, Sanders VM, Jones KJ.
    Brain Behav Immun; 2005 Mar 23; 19(2):173-80. PubMed ID: 15664790
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  • 19. SOD1(G93A) transgenic mouse CD4(+) T cells mediate neuroprotection after facial nerve axotomy when removed from a suppressive peripheral microenvironment.
    Mesnard-Hoaglin NA, Xin J, Haulcomb MM, Batka RJ, Sanders VM, Jones KJ.
    Brain Behav Immun; 2014 Aug 23; 40():55-60. PubMed ID: 24911596
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  • 20. CD73 and Ly-6A/E distinguish in vivo primed but uncommitted mouse CD4 T cells from type 1 or type 2 effector cells.
    Yang L, Kobie JJ, Mosmann TR.
    J Immunol; 2005 Nov 15; 175(10):6458-64. PubMed ID: 16272299
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