De Baetselier P - Search Results

1

Reactive oxygen species and 12/15-lipoxygenase contribute to the antiproliferative capacity of alternatively activated myeloid cells elicited during helminth infection.

Brys L, Beschin A, Raes G, Ghassabeh GH, Noël W, Brandt J, Brombacher F, De Baetselier P. Brys L, et al. Among authors: de baetselier p. J Immunol. 2005 May 15;174(10):6095-104. doi: 10.4049/jimmunol.174.10.6095. J Immunol. 2005. PMID: 15879104

2

Differential expression of FIZZ1 and Ym1 in alternatively versus classically activated macrophages.

Raes G, De Baetselier P, Noël W, Beschin A, Brombacher F, Hassanzadeh Gh G. Raes G, et al. Among authors: de baetselier p. J Leukoc Biol. 2002 Apr;71(4):597-602. J Leukoc Biol. 2002. PMID: 11927645

3

Nitric oxide-independent CTL suppression during tumor progression: association with arginase-producing (M2) myeloid cells.

Liu Y, Van Ginderachter JA, Brys L, De Baetselier P, Raes G, Geldhof AB. Liu Y, et al. Among authors: de baetselier p. J Immunol. 2003 May 15;170(10):5064-74. doi: 10.4049/jimmunol.170.10.5064. J Immunol. 2003. PMID: 12734351

4

FIZZ1 and Ym as tools to discriminate between differentially activated macrophages.

Raes G, Noël W, Beschin A, Brys L, de Baetselier P, Hassanzadeh GH. Raes G, et al. Among authors: de baetselier p. Dev Immunol. 2002 Sep;9(3):151-9. doi: 10.1080/1044667031000137629. Dev Immunol. 2002. PMID: 12892049 Free PMC article.

5

Macrophage galactose-type C-type lectins as novel markers for alternatively activated macrophages elicited by parasitic infections and allergic airway inflammation.

Raes G, Brys L, Dahal BK, Brandt J, Grooten J, Brombacher F, Vanham G, Noël W, Bogaert P, Boonefaes T, Kindt A, Van den Bergh R, Leenen PJ, De Baetselier P, Ghassabeh GH. Raes G, et al. Among authors: de baetselier p. J Leukoc Biol. 2005 Mar;77(3):321-7. doi: 10.1189/jlb.0304212. Epub 2004 Dec 9. J Leukoc Biol. 2005. PMID: 15591125

6

Identification of a common gene signature for type II cytokine-associated myeloid cells elicited in vivo in different pathologic conditions.

Ghassabeh GH, De Baetselier P, Brys L, Noël W, Van Ginderachter JA, Meerschaut S, Beschin A, Brombacher F, Raes G. Ghassabeh GH, et al. Among authors: de baetselier p. Blood. 2006 Jul 15;108(2):575-83. doi: 10.1182/blood-2005-04-1485. Epub 2006 Mar 23. Blood. 2006. PMID: 16556895 Free article.

7

The tumor-promoting effect of TNF-alpha involves the induction of secretory leukocyte protease inhibitor.

Devoogdt N, Revets H, Kindt A, Liu YQ, De Baetselier P, Ghassabeh GH. Devoogdt N, et al. Among authors: de baetselier p. J Immunol. 2006 Dec 1;177(11):8046-52. doi: 10.4049/jimmunol.177.11.8046. J Immunol. 2006. PMID: 17114478

8

Alternatively activated macrophages in protozoan infections.

Raes G, Beschin A, Ghassabeh GH, De Baetselier P. Raes G, et al. Among authors: de baetselier p. Curr Opin Immunol. 2007 Aug;19(4):454-9. doi: 10.1016/j.coi.2007.05.007. Epub 2007 Jul 12. Curr Opin Immunol. 2007. PMID: 17628461 Review.

9

African trypanosomiasis: naturally occurring regulatory T cells favor trypanotolerance by limiting pathology associated with sustained type 1 inflammation.

Guilliams M, Oldenhove G, Noel W, Hérin M, Brys L, Loi P, Flamand V, Moser M, De Baetselier P, Beschin A. Guilliams M, et al. Among authors: de baetselier p. J Immunol. 2007 Sep 1;179(5):2748-57. doi: 10.4049/jimmunol.179.5.2748. J Immunol. 2007. PMID: 17709488

10

Alternatively activated myeloid cells limit pathogenicity associated with African trypanosomiasis through the IL-10 inducible gene selenoprotein P.

Bosschaerts T, Guilliams M, Noel W, Hérin M, Burk RF, Hill KE, Brys L, Raes G, Ghassabeh GH, De Baetselier P, Beschin A. Bosschaerts T, et al. Among authors: de baetselier p. J Immunol. 2008 May 1;180(9):6168-75. doi: 10.4049/jimmunol.180.9.6168. J Immunol. 2008. PMID: 18424738

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