Maturation of the filaria Litomosoides sigmodontis in BALB/c mice; comparative susceptibility of nine other inbred strains
Ann. Parasitol. Hum. Comp., 67 5 (1992) 144-150
Published online: 2016-08-15
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https://doi.org/10.1016/j.exppara.2011.09.003
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J. KOLBAUM, U. RITTER, N. ZIMARA, N. BREWIG, M.‐L. ESCHBACH and M. BRELOERParasite Immunology 33 (4) 226 (2011)
https://doi.org/10.1111/j.1365-3024.2010.01273.x
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https://doi.org/10.4049/jimmunol.1004136
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https://doi.org/10.1016/j.exppara.2009.05.009
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https://doi.org/10.1002/eji.200838727
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K. M. HOUSTON, S. A. BABAYAN, J. E. ALLEN and W. HARNETTParasitology 135 (1) 55 (2008)
https://doi.org/10.1017/S0031182007003642
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Tarik Attout, Coralie Martin, Simon A. Babayan, et al.Parasitology International 57 (2) 201 (2008)
https://doi.org/10.1016/j.parint.2008.01.001
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https://doi.org/10.1371/journal.pntd.0000217
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https://doi.org/10.4049/jimmunol.179.7.4626
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Sabine Specht, Michael Saeftel, Manuela Arndt, et al.Infection and Immunity 74 (9) 5236 (2006)
https://doi.org/10.1128/IAI.00329-06
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https://doi.org/10.4049/jimmunol.176.11.6918
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https://doi.org/10.1017/S0031182004006651
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https://doi.org/10.1111/j.1365-3024.2005.00779.x
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Matthew D. Taylor, Laetitia LeGoff, Anjanette Harris, et al.The Journal of Immunology 174 (8) 4924 (2005)
https://doi.org/10.4049/jimmunol.174.8.4924
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https://doi.org/10.1016/j.micinf.2004.12.019
Increased early local immune responses and altered worm development in high-dose infections of mice susceptible to the filaria Litomosoides sigmodontis
Simon Babayan, Tarik Attout, Sabine Specht, et al.Medical Microbiology and Immunology 194 (3) 151 (2005)
https://doi.org/10.1007/s00430-004-0226-1
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Simon A Babayan, Tarik Attout, Phat N Vuong, Laetitia Le Goff, Jean-Charles Gantier and Odile BainFilaria Journal 4 (1) (2005)
https://doi.org/10.1186/1475-2883-4-3
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A. HOERAUF, J. SATOGUINA, M. SAEFTEL and S. SPECHTParasite Immunology 27 (10-11) 417 (2005)
https://doi.org/10.1111/j.1365-3024.2005.00792.x
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https://doi.org/10.1111/j.0105-2896.2004.00191.x
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Simon Babayan, Marie-Noëlle Ungeheuer, Coralie Martin, et al.Infection and Immunity 71 (12) 6820 (2003)
https://doi.org/10.1128/IAI.71.12.6820-6829.2003
Impaired clearance of primary but not secondary Brugia infections in IL-5 deficient mice
Thirumalai Ramalingam, Lisa Ganley-Leal, Patricia Porte and T.V RajanExperimental Parasitology 105 (2) 131 (2003)
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T.V Rajan, Lisa Ganley, Natalia Paciorkowski, et al.Experimental Parasitology 100 (4) 235 (2002)
https://doi.org/10.1016/S0014-4894(02)00015-2
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https://doi.org/10.1006/expr.1999.4475
Litomosoides sigmodontis in Mice: Reappraisal of an Old Model for Filarial Research
Wolfgang Hoffmann, Gilles Petit, Hartwig Schulz-Key, et al.Parasitology Today 16 (9) 387 (2000)
https://doi.org/10.1016/S0169-4758(00)01738-5
Interleukin-5 Is Essential for Vaccine-Mediated Immunity but Not Innate Resistance to a Filarial Parasite
Laetitia Le Goff, J. M. Mansfield, P'ng Loke, et al.Infection and Immunity 68 (5) 2513 (2000)
https://doi.org/10.1128/IAI.68.5.2513-2517.2000
Drastic Reduction of a Filarial Infection in Eosinophilic Interleukin-5 Transgenic Mice
Coralie Martin, W. A. Petri, Laëtitia Le Goff, et al.Infection and Immunity 68 (6) 3651 (2000)
https://doi.org/10.1128/IAI.68.6.3651-3656.2000
The role of nitric oxide in the innate resistance to microfilariae of Litomosoides sigmodontis in mice
Alexander W. Pfaff, Hartwig Schulz‐Key, Peter T. Soboslay, Stefan M. Geiger and Wolfgang H. HoffmannParasite Immunology 22 (8) 397 (2000)
https://doi.org/10.1046/j.1365-3024.2000.00317.x
A new mechanism for IL-5-dependent helminth control: neutrophil accumulation and neutrophil-mediated worm encapsulation in murine filariasis are abolished in the absence of IL-5
Khaled M. Al-Qaoud, Eric Pearlman, Thomas Hartung, et al.International Immunology 12 (6) 899 (2000)
https://doi.org/10.1093/intimm/12.6.899
Infection of BALB/c mice with the filarial nematode Litomosoides sigmodontis: role of CD4+ T cells in controlling larval development
K M Al-Qaoud, A Taubert, H Zahner, B Fleischer and A HoeraufInfection and Immunity 65 (6) 2457 (1997)
https://doi.org/10.1128/iai.65.6.2457-2461.1997
Early reduction of the challenge recovery rate following immunization with irradiated infective larvae in a filaria mouse system
L. Le Goff, P. Maréchal, G. Petit, D.W. Taylor, W. Hoffmann and O. BainTropical Medicine & International Health 2 (12) 1170 (1997)
https://doi.org/10.1046/j.1365-3156.1997.d01-218.x
Genetic control of susceptibility toTaenia crassicepscysticercosis
G. Fragoso, E. Lamoyi, A. Mellor, et al.Parasitology 112 (1) 119 (1996)
https://doi.org/10.1017/S003118200006515X
Molecular characterisation and localisation of an Onchocerca volvulus π-class glutathione S-transferase
Gustavo Salinas, Gabriele Braun and David W. TaylorMolecular and Biochemical Parasitology 66 (1) 1 (1994)
https://doi.org/10.1016/0166-6851(94)90030-2