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Complement (Basel, Switzerland)|January 1, 1984
Quantification of large C3 fragments as an index of complement activation in mice. I. In vitro studiesJ Lulé, G J Fournié, C Bousquet, et al.
Journal of Virology|October 12, 2000
Incoming human cytomegalovirus pp65 (UL83) contained in apoptotic infected fibroblasts is cross-presented to CD8(+) T cells by dendritic cellsG Arrode, C Boccaccio, J Lulé, et al.
American Journal of Nephrology|January 1, 1989
Plasma DNA in patients undergoing hemodialysis or hemofiltration: cytolysis in artificial kidney is responsible for the release of DNA in circulationG J Fournié, J Lulé, J M Dueymes, et al.
International Journal of Immunopharmacology|January 1, 1991
The beta-blocker acebutolol down modulates the spontaneous polyclonal activation of lymphocytes in NZB X NZW lupus miceS In, J Lulé, H f1noist, et al.
Nephrologie|January 1, 1981
[Hypothesis: immune complex glomerulonephritis and auto-immunity (author's transl)]G J Fournié, J Lulé, M Gayral-Ta Minh, et al.
Journal of Clinical & Laboratory Immunology|July 1, 1989
The spontaneous development of immune complex type glomerular lesions in outbred mice is dependent on environmental factors and sexJ Lulé, F Puginier-Carentz, J P Basile, et al.
Cytotherapy|April 16, 2002
IE1-pp65 recombinant protein from human CMV combined with a nanoparticulate carrier, SMBV, as a potential source for the development of anti-human CMV adoptive immunotherapyJ Vaz-Santiago, J Lulé, P Rohrlich, et al.
Nephrologie|January 1, 1981
[Experimental approach to the treatment of lupus nephritis by use of an accelerated model of the NZBxNZW mouse disease (author's transl)]M Gayral-Ta Minh, J Lulé, G J Fournié, et al.
Clinical and Experimental Immunology|October 1, 1980
Immune complex glomerulonephritis in mice infected with Escherichia coliG J Fournié, M A Mignon-Conté, J Lulé, et al.
Journal of Virology|August 3, 2001
Ex vivo stimulation and expansion of both CD4(+) and CD8(+) T cells from peripheral blood mononuclear cells of human cytomegalovirus-seropositive blood donors by using a soluble recombinant chimeric protein, IE1-pp65J Vaz-Santiago, J Lulé, P Rohrlich, et al.
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