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Items: 1 to 20 of 101

1.

Histone deacetylase 3 is an epigenomic brake in macrophage alternative activation.

Mullican SE, Gaddis CA, Alenghat T, Nair MG, Giacomin PR, Everett LJ, Feng D, Steger DJ, Schug J, Artis D, Lazar MA.

Genes Dev. 2011 Dec 1;25(23):2480-8. doi: 10.1101/gad.175950.111.

2.

Schistosoma mansoni hemozoin modulates alternative activation of macrophages via specific suppression of Retnla expression and secretion.

Truscott M, Evans DA, Gunn M, Hoffmann KF.

Infect Immun. 2013 Jan;81(1):133-42. doi: 10.1128/IAI.00701-12. Epub 2012 Oct 22.

3.

Th2 Cytokines Augment IL-31/IL-31RA Interactions via STAT6-dependent IL-31RA Expression.

Edukulla R, Singh B, Jegga AG, Sontake V, Dillon SR, Madala SK.

J Biol Chem. 2015 May 22;290(21):13510-20. doi: 10.1074/jbc.M114.622126. Epub 2015 Apr 6.

PMID:
25847241
4.

Epigenetic regulation of the alternatively activated macrophage phenotype.

Ishii M, Wen H, Corsa CA, Liu T, Coelho AL, Allen RM, Carson WF 4th, Cavassani KA, Li X, Lukacs NW, Hogaboam CM, Dou Y, Kunkel SL.

Blood. 2009 Oct 8;114(15):3244-54. doi: 10.1182/blood-2009-04-217620. Epub 2009 Jun 30.

5.

A systemic granulomatous response to Schistosoma mansoni eggs alters responsiveness of bone-marrow-derived macrophages to Toll-like receptor agonists.

Joshi AD, Raymond T, Coelho AL, Kunkel SL, Hogaboam CM.

J Leukoc Biol. 2008 Feb;83(2):314-24. Epub 2007 Nov 20.

6.

Helminth 2-Cys peroxiredoxin drives Th2 responses through a mechanism involving alternatively activated macrophages.

Donnelly S, Stack CM, O'Neill SM, Sayed AA, Williams DL, Dalton JP.

FASEB J. 2008 Nov;22(11):4022-32. doi: 10.1096/fj.08-106278. Epub 2008 Aug 15.

7.

Targeting macrophage Histone deacetylase 3 stabilizes atherosclerotic lesions.

Hoeksema MA, Gijbels MJ, Van den Bossche J, van der Velden S, Sijm A, Neele AE, Seijkens T, Stöger JL, Meiler S, Boshuizen MC, Dallinga-Thie GM, Levels JH, Boon L, Mullican SE, Spann NJ, Cleutjens JP, Glass CK, Lazar MA, de Vries CJ, Biessen EA, Daemen MJ, Lutgens E, de Winther MP.

EMBO Mol Med. 2014 Jul 9;6(9):1124-32. doi: 10.15252/emmm.201404170.

8.

Histone deacetylase 9 deficiency protects against effector T cell-mediated systemic autoimmunity.

Yan K, Cao Q, Reilly CM, Young NL, Garcia BA, Mishra N.

J Biol Chem. 2011 Aug 19;286(33):28833-43. doi: 10.1074/jbc.M111.233932. Epub 2011 Jun 27.

9.

The IL-21 receptor augments Th2 effector function and alternative macrophage activation.

Pesce J, Kaviratne M, Ramalingam TR, Thompson RW, Urban JF Jr, Cheever AW, Young DA, Collins M, Grusby MJ, Wynn TA.

J Clin Invest. 2006 Jul;116(7):2044-55. Epub 2006 Jun 15.

10.

Using eggs from Schistosoma mansoni as an in vivo model of helminth-induced lung inflammation.

Joyce KL, Morgan W, Greenberg R, Nair MG.

J Vis Exp. 2012 Jun 5;(64):e3905. doi: 10.3791/3905.

11.

T cell-derived IL-4/IL-13 protects mice against fatal Schistosoma mansoni infection independently of basophils.

Schwartz C, Oeser K, Prazeres da Costa C, Layland LE, Voehringer D.

J Immunol. 2014 Oct 1;193(7):3590-9. doi: 10.4049/jimmunol.1401155. Epub 2014 Aug 29.

12.

Macrophage polarization: the epigenetic point of view.

Van den Bossche J, Neele AE, Hoeksema MA, de Winther MP.

Curr Opin Lipidol. 2014 Oct;25(5):367-73. doi: 10.1097/MOL.0000000000000109. Review.

PMID:
25188918
13.

IL-10 regulates Il12b expression via histone deacetylation: implications for intestinal macrophage homeostasis.

Kobayashi T, Matsuoka K, Sheikh SZ, Russo SM, Mishima Y, Collins C, deZoeten EF, Karp CL, Ting JP, Sartor RB, Plevy SE.

J Immunol. 2012 Aug 15;189(4):1792-9. doi: 10.4049/jimmunol.1200042. Epub 2012 Jul 11.

14.

IL-4 receptor signaling is required for mannose receptor expression by macrophages recruited to granulomata but not resident cells in mice infected with Schistosoma mansoni.

Linehan SA, Coulson PS, Wilson RA, Mountford AP, Brombacher F, Martínez-Pomares L, Gordon S.

Lab Invest. 2003 Aug;83(8):1223-31.

PMID:
12920251
15.

IL-4 blocks TH1-polarizing/inflammatory cytokine gene expression during monocyte-derived dendritic cell differentiation through histone hypoacetylation.

López-Bravo M, Minguito de la Escalera M, Domínguez PM, González-Cintado L, del Fresno C, Martín P, Martínez del Hoyo G, Ardavín C.

J Allergy Clin Immunol. 2013 Dec;132(6):1409-19. doi: 10.1016/j.jaci.2013.08.039. Epub 2013 Oct 17.

PMID:
24139608
16.

Emergence of fibroblasts with a proinflammatory epigenetically altered phenotype in severe hypoxic pulmonary hypertension.

Li M, Riddle SR, Frid MG, El Kasmi KC, McKinsey TA, Sokol RJ, Strassheim D, Meyrick B, Yeager ME, Flockton AR, McKeon BA, Lemon DD, Horn TR, Anwar A, Barajas C, Stenmark KR.

J Immunol. 2011 Sep 1;187(5):2711-22. doi: 10.4049/jimmunol.1100479. Epub 2011 Aug 3.

17.

Cigarette smoke induces proinflammatory cytokine release by activation of NF-kappaB and posttranslational modifications of histone deacetylase in macrophages.

Yang SR, Chida AS, Bauter MR, Shafiq N, Seweryniak K, Maggirwar SB, Kilty I, Rahman I.

Am J Physiol Lung Cell Mol Physiol. 2006 Jul;291(1):L46-57. Epub 2006 Feb 10.

18.

IL-4Ralpha-independent expression of mannose receptor and Ym1 by macrophages depends on their IL-10 responsiveness.

Dewals BG, Marillier RG, Hoving JC, Leeto M, Schwegmann A, Brombacher F.

PLoS Negl Trop Dis. 2010 May 18;4(5):e689. doi: 10.1371/journal.pntd.0000689.

19.

HDAC2 deacetylates class II transactivator and suppresses its activity in macrophages and smooth muscle cells.

Kong X, Fang M, Li P, Fang F, Xu Y.

J Mol Cell Cardiol. 2009 Mar;46(3):292-9. doi: 10.1016/j.yjmcc.2008.10.023. Epub 2008 Nov 7.

PMID:
19041327
20.
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