Etude des possibilités d’utilisation du sarcome TG 180 de la Souris. Application à la Toxoplasmose
Ann. Parasitol. Hum. Comp., 44 3 (1969) 217-224
Published online: 2017-10-12
Articles citing this article
The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).
Cited article:
This article has been cited by the following article(s):
The microneme protein MIC3 of Toxoplasma gondii is a secretory adhesin that binds to both the surface of the host cells and the surface of the parasite
Nathalie Garcia-Reguet, Maryse Lebrun, Marie-Noelle Fourmaux, et al.Cellular Microbiology 2 (4) 353 (2000)
https://doi.org/10.1046/j.1462-5822.2000.00064.x
IgG recognizing 21-24 kDa and 30-33 kDa tachyzoite antigens show maximum avidity maturation during natural and accidental human toxoplasmosis
Margarita VILLAVEDRA, Julio BATTISTONI and Alberto NIETORevista do Instituto de Medicina Tropical de São Paulo 41 (5) 297 (1999)
https://doi.org/10.1590/S0036-46651999000500006
Evolution of IgG antibody response against Toxoplasma gondii tissue cyst in acute and chronic human infections
Margarita VILLAVEDRA, Hernán CAROL and Alberto NIETORevista do Instituto de Medicina Tropical de São Paulo 40 (2) 77 (1998)
https://doi.org/10.1590/S0036-46651998000200003
Immunolocalization and characterization of the low molecular weight antigen (4–5 kDa) ofToxoplasma gondiithat elicits an early IgM response upon primary infection
S. Tomavo, G. Couvreur, M. A. Leriche, et al.Parasitology 108 (2) 139 (1994)
https://doi.org/10.1017/S0031182000068220
Oral immunization with Toxoplasma gondii antigens in association with cholera toxin induces enhanced protective and cell-mediated immunity in C57BL/6 mice
I Bourguin, T Chardès and D BoutInfection and Immunity 61 (5) 2082 (1993)
https://doi.org/10.1128/iai.61.5.2082-2088.1993
Differential targeting of dense granule proteins in the parasitophorous vacuole ofToxoplasma gondii
A. Achbarou, O. Mercereau-Puijalon, A. Sadak, et al.Parasitology 103 (3) 321 (1991)
https://doi.org/10.1017/S0031182000059837
In vitro culture and cloning of Toxoplasma gondii in a newly established cell line derived from TG180
A. Couatarmanach, P. Andre, D. Le Minous, et al.International Journal for Parasitology 21 (1) 129 (1991)
https://doi.org/10.1016/0020-7519(91)90133-R
Amplification of the secretory IgA response toToxoplasma gondiiusing cholera toxin
Isabelle Bourguin, Thierry Chardes, Marie-Noelle Mevelec, Julia P. Woodman and Daniel BoutFEMS Microbiology Letters 81 (3) 265 (1991)
https://doi.org/10.1111/j.1574-6968.1991.tb04770.x
Characterization of microneme proteins of Toxoplasma gondii
Abderrahim Achbarou, Odile Mercereau-Puijalon, Jean Michel Autheman, et al.Molecular and Biochemical Parasitology 47 (2) 223 (1991)
https://doi.org/10.1016/0166-6851(91)90182-6
Characterization of bradyzoite-specific antigens of Toxoplasma gondii
S Tomavo, B Fortier, M Soete, et al.Infection and Immunity 59 (10) 3750 (1991)
https://doi.org/10.1128/iai.59.10.3750-3753.1991
Isolation of the pellicle ofToxoplasma gondii (Protozoa, Coccidia): Characterization by electron microscopy and protein composition
F. Foussard, Y. Gallois, G. Tronchin, R. Robert and G. MaurasParasitology Research 76 (7) 563 (1990)
https://doi.org/10.1007/BF00932561
Evidence for Glycosyl-Phosphatidylinositol Anchoring of Toxoplasma gondii Major Surface Antigens
Stanislas Tomavo, Ralph T. Schwarz and Jean François DubremetzMolecular and Cellular Biology 9 (10) 4576 (1989)
https://doi.org/10.1128/mcb.9.10.4576-4580.1989
Toxoplasma gondii: Redistribution of monoclonal antibodies on tachyzoites during host cell invasion
J.F. Dubremetz, C. Rodriguez and E. FerreiraExperimental Parasitology 59 (1) 24 (1985)
https://doi.org/10.1016/0014-4894(85)90053-0
Rapid, large-scale production and isolation forLeishmaniaamastigotes
L. Monjour, I. Vouldoukis, O. Brandicourt, et al.Annals of Tropical Medicine & Parasitology 78 (4) 423 (1984)
https://doi.org/10.1080/00034983.1984.11811840
Isolement de fractions antigéniques membranaires de Toxoplasma gondii par l'intermédiaire de microsphères de méthacrylate
G Mauras, P Laget, A Girault and J.M SenetAnnales de l'Institut Pasteur / Immunologie 132 (2) 219 (1981)
https://doi.org/10.1016/0769-2625(81)90030-1
Partial resolution of the sugar content of Toxoplasma gondii membrane
Geneviève Mauras, Michèle Dodeur, Patrice Laget, Jean-Marcel Senet and Roland BourrillonBiochemical and Biophysical Research Communications 97 (3) 906 (1980)
https://doi.org/10.1016/0006-291X(80)91462-X
Application de la réaction d'hémagglutination indirecte au sérodiagnostic de la toxoplasmose
J.P. Seguela, M.H. Bessieres, C. Foisy, et al.Médecine et Maladies Infectieuses 6 (8) 268 (1976)
https://doi.org/10.1016/S0399-077X(76)80102-3
Hémagglutination indirecte utilisant un antigène particulaire, appliquée au diagnostic immunologique de la toxoplasmose
J.M. Senet and R. RobertMédecine et Maladies Infectieuses 4 (1) 21 (1974)
https://doi.org/10.1016/S0399-077X(74)80044-2
Valeurs comparées de l'agglutination directe et de l'immunofluorescence indirecte pour le titrage des anticorps toxoplasmiques
J.M. Doby and M. Kombila-FavryMédecine et Maladies Infectieuses 4 (7) 397 (1974)
https://doi.org/10.1016/S0399-077X(74)80216-7